Comparison of Standard of Care Treatment With a Triplet Combination of Targeted Immunotherapeutic Agents

Sponsor
National Cancer Institute (NCI) (NIH)
Overall Status
Recruiting
CT.gov ID
NCT04739800
Collaborator
NRG Oncology (Other)
164
374
4
31.6
0.4
0

Study Details

Study Description

Brief Summary

This phase II trial studies the possible benefits of treatment with different combinations of the drugs durvalumab, olaparib and cediranib vs. the usual treatment in patients with ovarian, primary peritoneal, or fallopian tube cancer that has come back after a period of improvement with platinum therapy (recurrent platinum resistant). Usual treatment is the type of treatment most patients with this condition receive if they are not part of a clinical study. Combination therapies studied in this trial include MEDI4736 (durvalumab) plus olaparib and cediranib, durvalumab and cediranib, or olaparib and cediranib. Monoclonal antibodies, such as durvalumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumors cells to grow and spread. Olaparib is an inhibitor of PARP, an enzyme that helps repair deoxyribonucleic acid (DNA) when it becomes damaged. Blocking PARP may help keep cancer cells from repairing their damaged DNA, causing them to die. PARP inhibitors are a type of targeted therapy. Cediranib may stop the growth of tumor cells by blocking VEGF (an enzyme). needed for cell growth. Giving different combinations of durvalumab, olaparib and cediranib may work better in increasing the duration of time that the cancer does not progress compared to the usual treatment.

Condition or Disease Intervention/Treatment Phase
  • Drug: Cediranib Maleate
  • Biological: Durvalumab
  • Drug: Olaparib
  • Drug: Paclitaxel
  • Drug: Pegylated Liposomal Doxorubicin Hydrochloride
  • Drug: Topotecan Hydrochloride
Phase 2

Detailed Description

PRIMARY OBJECTIVE:
  1. To assess the efficacy of the combinations durvalumab (MEDI4736) plus olaparib and cediranib, durvalumab (MEDI4736) plus cediranib, or olaparib and cediranib, as measured by progression-free survival (PFS), as compared to physician's choice standard of care chemotherapy, in patients with recurrent platinum-resistant ovarian, primary peritoneal or fallopian tube cancer who had prior bevacizumab.
SECONDARY OBJECTIVES:
  1. To assess the efficacy of the combinations durvalumab (MEDI4736) plus olaparib and cediranib, durvalumab (MEDI4736) plus cediranib, or olaparib and cediranib, as measured by overall response rate (ORR) by Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1, as compared to physician's choice standard of care chemotherapy, in patients with recurrent platinum-resistant ovarian, primary peritoneal or fallopian tube cancer who had prior bevacizumab.

  2. To assess the efficacy of the combinations durvalumab (MEDI4736) plus olaparib and cediranib, durvalumab (MEDI4736) plus cediranib, or olaparib and cediranib, as measured by overall survival (OS), as compared to physician's choice standard of care chemotherapy, in patients with recurrent platinum-resistant ovarian, primary peritoneal or fallopian tube cancer who had prior bevacizumab.

OUTLINE: Patients are randomized to 1 of 4 arms.

ARM I: Patients receive paclitaxel intravenously (IV) over 60 minutes on days 1, 8, and 15, or pegylated liposomal doxorubicin hydrochloride IV over 60 minutes on day 1, or topotecan hydrochloride IV over 30 minutes on days 1, 8 and 15 or days 1-5 per the discretion of the treating physician. Cycles repeat every 21 or 28 days in the absence of disease progression or unacceptable toxicity.

ARM II: Patients receive durvalumab IV over 60 minutes on day 1, cediranib maleate orally (PO) once daily (QD) Monday through Friday, and olaparib PO twice daily (BID) on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

ARM III: Patients receive durvalumab IV over 60 minutes on day 1 and cediranib maleate PO QD Monday through Friday. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

ARM IV: Patients receive cediranib maleate PO QD on days 1-28 and olaparib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up periodically for up to 5 years.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
164 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
A Randomized Phase II Trial of Triplet Therapy (A PD-L1 Inhibitor Durvalumab (MEDI4736) in Combination With Olaparib and Cediranib) Compared to Olaparib and Cediranib or Durvalumab (MEDI4736) and Cediranib or Standard of Care Chemotherapy in Women With Platinum-Resistant Recurrent Epithelial Ovarian Cancer, Primary Peritoneal or Fallopian Cancer Who Have Received Prior Bevacizumab
Actual Study Start Date :
Apr 28, 2021
Anticipated Primary Completion Date :
Dec 15, 2023
Anticipated Study Completion Date :
Dec 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Arm I (paclitaxel, doxorubicin, topotecan hydrochloride))

Patients receive paclitaxel IV over 60 minutes on days 1, 8, and 15, or pegylated liposomal doxorubicin hydrochloride IV over 60 minutes on day 1, or topotecan hydrochloride IV over 30 minutes on days 1, 8 and 15 or days 1-5 per the discretion of the treating physician. Cycles repeat every 21 or 28 days in the absence of disease progression or unacceptable toxicity.

Drug: Paclitaxel
Given IV
Other Names:
  • Anzatax
  • Asotax
  • Bristaxol
  • Praxel
  • Taxol
  • Taxol Konzentrat
  • Drug: Pegylated Liposomal Doxorubicin Hydrochloride
    Given IV
    Other Names:
  • ATI-0918
  • Caelyx
  • Dox-SL
  • Doxil
  • Doxilen
  • Doxorubicin HCl Liposomal
  • Doxorubicin HCl Liposome
  • Doxorubicin Hydrochloride Liposome
  • Duomeisu
  • Evacet
  • LipoDox
  • Lipodox 50
  • Liposomal Adriamycin
  • Liposomal Doxorubicin Hydrochloride
  • Liposomal-Encapsulated Doxorubicin
  • Pegylated Doxorubicin HCl Liposome
  • S-Liposomal Doxorubicin
  • Stealth Liposomal Doxorubicin
  • TLC D-99
  • Drug: Topotecan Hydrochloride
    Given IV
    Other Names:
  • Hycamptamine
  • Hycamtin
  • SKF S-104864-A
  • Topotecan HCl
  • topotecan hydrochloride (oral)
  • Experimental: Arm II (durvalumab, cediranib maleate, olaparib)

    Patients receive durvalumab IV over 60 minutes on day 1, cediranib maleate PO QD Monday through Friday, and olaparib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

    Drug: Cediranib Maleate
    Given PO
    Other Names:
  • AZD2171
  • AZD2171 Maleate
  • Recentin
  • Biological: Durvalumab
    Given IV
    Other Names:
  • Imfinzi
  • Immunoglobulin G1, Anti-(Human Protein B7-H1) (Human Monoclonal MEDI4736 Heavy Chain), Disulfide with Human Monoclonal MEDI4736 Kappa-chain, Dimer
  • MEDI-4736
  • MEDI4736
  • Drug: Olaparib
    Given PO
    Other Names:
  • AZD 2281
  • AZD-2281
  • AZD2281
  • KU-0059436
  • Lynparza
  • PARP Inhibitor AZD2281
  • Experimental: Arm III (durvalumab, cediranib maleate)

    Patients receive durvalumab IV over 60 minutes on day 1 and cediranib maleate PO QD Monday through Friday. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

    Drug: Cediranib Maleate
    Given PO
    Other Names:
  • AZD2171
  • AZD2171 Maleate
  • Recentin
  • Biological: Durvalumab
    Given IV
    Other Names:
  • Imfinzi
  • Immunoglobulin G1, Anti-(Human Protein B7-H1) (Human Monoclonal MEDI4736 Heavy Chain), Disulfide with Human Monoclonal MEDI4736 Kappa-chain, Dimer
  • MEDI-4736
  • MEDI4736
  • Experimental: Arm IV (cediranib maleate, olaparib)

    Patients receive cediranib maleate PO QD on days 1-28 and olaparib PO BID on days 1-28. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity.

    Drug: Cediranib Maleate
    Given PO
    Other Names:
  • AZD2171
  • AZD2171 Maleate
  • Recentin
  • Drug: Olaparib
    Given PO
    Other Names:
  • AZD 2281
  • AZD-2281
  • AZD2281
  • KU-0059436
  • Lynparza
  • PARP Inhibitor AZD2281
  • Outcome Measures

    Primary Outcome Measures

    1. Progression free survival [From study entry to time of progression or death, whichever occurs first, assessed up to 5 years]

      Will be presented by Kaplan Meier methods.

    Secondary Outcome Measures

    1. Objective response rate [From the start of the treatment until disease progression/recurrence, assessed up to 5 years]

      Quantified as the binomial proportion of patients with measurable disease at enrollment who have a best overall response of complete response (CR) or partial response (PR).

    2. Duration of response [From the time measurement criteria are met for CR or PR (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, assessed up to 5 years]

      Will be presented by Kaplan Meier methods.

    3. Overall survival [Time from study entry to date of death from any cause, assessed up to 5 years]

      Will be presented by Kaplan Meier methods.

    4. Incidence of adverse events [Up to 30 days post treatment]

      All adverse events, including severe adverse events and treatment-related adverse events, will be categorized and graded for severity according to National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Women with recurrent/persistent platinum-resistant ovarian, primary peritoneal, or fallopian tube cancers; platinum-resistant disease is defined as progression within < 6 months from completion of platinum based therapy. The date should be calculated from the last administered dose of platinum therapy

    • Patients must have histologically or cytologically confirmed ovarian cancer, peritoneal cancer or fallopian tube cancer and must have a histological diagnosis of high grade serous, grade 3 endometrioid or clear cell carcinoma based on local histopathological findings. Patients with low grade serous, grade 1 or 2 endometrioid, mixed epithelial, undifferentiated carcinoma, or mucinous carcinoma histologies are also eligible, provided that the patient has a known deleterious BRCA1 or BRCA2 mutation identified through testing at a clinical laboratory. Histologic confirmation of the original primary tumor is required via the pathology report (upload of report required). Confirmation of BRCA1 and BRCA2 germline and/or somatic mutation status and hormone receptor (HR) status is required for all entered patients (if available) via testing report (upload of report[s] required)

    • Evaluable disease - defined as RECIST 1.1 measurable disease OR non-measurable disease (defined as solid and/or cystic abnormalities on radiographic imaging that do not meet RECIST 1.1 definitions for target lesions OR ascites and/or pleural effusion that has been pathologically demonstrated to be disease-related in the setting of a CA125 >= 2 x upper limit of normal [ULN])

    • Prior therapy:

    • At least two prior treatment regimens (including primary therapy) but up to 5 lines of systemic anticancer therapy. Hormonal therapy (such as tamoxifen, aromatase inhibitors) will not count as a previous treatment regimen.

    • Prior use of bevacizumab in the upfront or recurrent setting is required.

    • Prior use of PARP inhibitor is allowed.

    • Prior use of immune checkpoint blockade (e.g., a PD-L1/PD-1inhibitor or a CTLA-4 inhibitor) is allowed

    • Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2

    • Absolute neutrophil count (ANC) >= 1,500/mcL

    • Hemoglobin > 10 g/dL

    • Platelets >= 100,000/mcL

    • Creatinine clearance (CrCL) or estimated glomerular filtration rate (eGFR) of > 50 mL/min estimated using either the Cockcroft-Gault equation, the Modification of Diet in Renal Disease Study, or as reported in the comprehensive metabolic panel/basic metabolic panel (eGFR)

    • Urine protein: creatinine ratio (UPC) of =< 1

    • Total serum bilirubin level =< 1.5 x ULN (patients with known Gilbert's disease who have bilirubin level =< 3 x ULN may be enrolled)

    • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =< 3 x ULN

    • Age >= 18 years

    • Body weight > 30 kg

    • Adequately controlled blood pressure (systolic blood pressure [SBP] =< 140; diastolic blood pressure [DBP] =< 90 mmHg) on a maximum of three antihypertensive medications. Patients must have a BP of =< 140/90 mmHg taken in the clinic setting by a medical professional within 2 weeks prior to study registration. It is strongly recommended that patients who are on three antihypertensive medications be followed by a cardiologist or a primary care physician for management of BP while on protocol. Patients must be willing and able to check and record daily blood pressure readings. BP cuffs will be provided to patients randomized to the cediranib-containing arms

    • Adequately controlled thyroid dysfunction with no symptoms of thyroid dysfunction and normal thyroid stimulating hormone (TSH). If TSH is not within normal range despite no symptoms of thyroid dysfunction, normal free T4 level is required

    • Able to swallow and retain oral medications and no gastrointestinal (GI) illnesses that would preclude absorption of olaparib and cediranib as judged by treating physician

    • Toxicities of prior therapy (excepting alopecia and vitiligo), should be resolved to less than or equal to grade 1 as per Common Terminology Criteria for Adverse Events (CTCAE) v5.0

    • Women of childbearing potential (WOCBP) must agree to use two forms of birth control (hormonal or barrier method of birth control; abstinence). Note: Definition of women of no longer having childbearing potential: Postmenopausal or evidence of non-childbearing status for women of childbearing potential as confirmed by a negative urine or serum pregnancy test within 7 days prior to start of study treatment. Postmenopausal is defined as: Age >= 60 years, or age < 60 with any one or more of the conditions below:

    • Amenorrhoeic for >= 1 year in the absence of chemotherapy and/or hormonal treatments,

    • Luteinizing hormone and/or follicle stimulating hormone and/or estradiol levels in the post-menopausal range,

    • Radiation-induced oophorectomy with last menses > 1 year ago,

    • Chemotherapy-induced menopause with > 1 year interval since last menses,

    • Surgical sterilization (bilateral oophorectomy or hysterectomy)

    • The patient or a legally authorized representative must provide study-specific informed consent prior to study entry and authorization permitting release of personal health information

    Exclusion Criteria:
    • Primary platinum-refractory disease defined as progression during first-line platinum-based chemotherapy

    • Rising CA-125 only without RECIST 1.1 evaluable disease

    • Prior therapy:

    • Patients who have had chemotherapy, investigational drugs or radiotherapy within 3 weeks prior to study registration or those who have not recovered from adverse events due to agents administered more than 3 weeks earlier.

    • Patients may not have had hormonal therapy within 2 weeks of study registration. Patients receiving raloxifene for bone health as per Food and Drug Administration (FDA) indication may remain on raloxifene absent other drug interactions.

    • Prior use of concurrent olaparib and cediranib combination.

    • Patients who have had prior PARP inhibitor or immune checkpoint blockade requiring dose modifications as they cannot start this study at full dose

    • History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 3 months prior to study registration

    • Current signs and/or symptoms of bowel obstruction or signs and/or symptoms of bowel obstruction within 3 months of study registration except temporary (< 24 hr) improved with medical management, within last 3 months

    • Any prior grade >= 3 immune-related adverse event (irAE) while receiving any previous immunotherapy agent, or any unresolved irAE > grade 1

    • Dependency on IV hydration or total parenteral nutrition (TPN)

    • Pregnant women. Because there is an unknown but potential risk of adverse events in nursing infants secondary to treatment of the mother with these drugs, breastfeeding should be discontinued. These potential risks may also apply to other agents used in this study

    • Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial

    • Patients with untreated brain metastases, spinal cord compression, or evidence of symptomatic brain metastases or leptomeningeal disease as noted on computed tomography (CT) or magnetic resonance imaging (MRI) scans should not be included on this study, since neurologic dysfunction may confound the evaluation of neurologic and other adverse events. Patients with treated brain metastases and resolution of any associated symptoms must demonstrate stable post-therapeutic imaging for at least 6 months following therapy prior to starting study registration

    • Patients who have the following clinical conditions are considered to be at increased risk for cardiac toxicities. Patients with any cardiac history of the following conditions:

    • History of myocardial infarction or myocarditis within six months of study registration

    • Unstable angina

    • Resting electrocardiogram (ECG) with clinically significant abnormal findings.

    • New York Heart Association functional classification of III or IV

    • If cardiac function assessment is clinically indicated or performed: left ventricular ejection fraction (LVEF) less than normal per institutional guidelines, or < 55%, if threshold for normal not otherwise specified by institutional guidelines. Patients with the following risk factors should have a baseline cardiac function assessment:

    • Prior treatment with anthracyclines

    • Prior treatment with trastuzumab or T-DM1

    • Prior central thoracic radiation therapy (RT), including RT to the heart

    • History of myocardial infarction within 6 to 12 months (Patients with history of myocardial infarction within 6 months are excluded from the study)

    • Prior history of impaired cardiac function

    • History of stroke or transient ischemic attack within six months of study registration

    • Clinically significant peripheral vascular disease or vascular disease (aortic aneurysm or aortic dissection)

    • Major surgical procedure (as defined by the Investigator) within 28 days prior to the first dose of study treatment. Patients must have recovered from any effects of any major surgery and surgical wound should have healed prior to starting treatment. Note: Local surgery of isolated lesions for palliative intent is acceptable

    • Evidence of coagulopathy or bleeding diathesis. Therapeutic anticoagulation for prior thromboembolic events, including warfarin, is permitted. Patients receiving warfarin are recommended to have careful monitoring of international normalized ratio (INR)

    • Evidence suggestive of myelodysplastic syndrome (MDS) or acute myelogenous leukemia (AML) on peripheral blood smear or bone marrow biopsy, if clinically indicated. No prior allogeneic bone marrow transplant or double umbilical cord blood transplantation (dUBCT)

    • Human immunodeficiency virus (HIV) positive patients due to potential drug and drug interactions

    • Patients may not use any complementary or alternative medicines including natural herbal products or folk remedies as they may interfere with the effectiveness of the study treatments

    • Receipt of live attenuated vaccine within 30 days prior to the first dose of study treatment. Note: Patients, if enrolled, should not receive live vaccine whilst receiving study treatment and up to 30 days after the last dose of study treatment

    • Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia (other than atrial fibrillation with controlled ventricular rate), or psychiatric illness/social situations that would limit compliance with study requirements, substantially increase risk of incurring adverse events or compromise the ability of the patient to given written informed consent

    • Patients receiving any medications or substances that are strong inhibitors or inducers of CYP3A4. Dihydropyridine calcium-channel blockers are permitted for management of hypertension

    • Current or prior use of immunosuppressive medication within 14 days of study registration. The following are exceptions to this criterion:

    • Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra articular injection)

    • Systemic corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or its equivalent

    • Steroids as premedication for hypersensitivity reactions (e.g., CT scan premedication)

    • History of allergic reactions attributed to compounds of similar chemical or biologic composition to durvalumab, olaparib, or cediranib

    • Patients with active autoimmune disease that has required systemic treatment in the past 2 years (i.e., with use of disease modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment

    • Active infection including tuberculosis (clinical evaluation that includes clinical history, physical examination and radiographic findings, and tuberculosis [TB] testing in line with local practice), hepatitis B (known positive hepatitis B virus [HBV] surface antigen (HBsAg) result), or hepatitis C. Patients with a past or resolved HBV infection (defined as the presence of hepatitis B core antibody [anti-HBc] and absence of HBsAg) are eligible. Patients positive for hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for hepatitis C virus (HCV) ribonucleic acid (RNA)

    • Patients who have a history of (non-infectious) pneumonitis that required steroids, or current pneumonitis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Anchorage Associates in Radiation Medicine Anchorage Alaska United States 98508
    2 Anchorage Radiation Therapy Center Anchorage Alaska United States 99504
    3 Alaska Breast Care and Surgery LLC Anchorage Alaska United States 99508
    4 Alaska Oncology and Hematology LLC Anchorage Alaska United States 99508
    5 Alaska Women's Cancer Care Anchorage Alaska United States 99508
    6 Anchorage Oncology Centre Anchorage Alaska United States 99508
    7 Katmai Oncology Group Anchorage Alaska United States 99508
    8 Providence Alaska Medical Center Anchorage Alaska United States 99508
    9 Fairbanks Memorial Hospital Fairbanks Alaska United States 99701
    10 CTCA at Western Regional Medical Center Goodyear Arizona United States 85338
    11 Cancer Center at Saint Joseph's Phoenix Arizona United States 85004
    12 Mercy Hospital Fort Smith Fort Smith Arkansas United States 72903
    13 CHI Saint Vincent Cancer Center Hot Springs Hot Springs Arkansas United States 71913
    14 University of Arkansas for Medical Sciences Little Rock Arkansas United States 72205
    15 Mission Hope Medical Oncology - Arroyo Grande Arroyo Grande California United States 93420
    16 Sutter Auburn Faith Hospital Auburn California United States 95602
    17 Sutter Cancer Centers Radiation Oncology Services-Auburn Auburn California United States 95603
    18 Alta Bates Summit Medical Center-Herrick Campus Berkeley California United States 94704
    19 Providence Saint Joseph Medical Center/Disney Family Cancer Center Burbank California United States 91505
    20 Sutter Cancer Centers Radiation Oncology Services-Cameron Park Cameron Park California United States 95682
    21 Eden Hospital Medical Center Castro Valley California United States 94546
    22 John Muir Medical Center-Concord Campus Concord California United States 94520
    23 Sutter Davis Hospital Davis California United States 95616
    24 City of Hope Comprehensive Cancer Center Duarte California United States 91010
    25 Palo Alto Medical Foundation-Fremont Fremont California United States 94538
    26 City of Hope Antelope Valley Lancaster California United States 93534
    27 Los Angeles County-USC Medical Center Los Angeles California United States 90033
    28 USC / Norris Comprehensive Cancer Center Los Angeles California United States 90033
    29 Memorial Medical Center Modesto California United States 95355
    30 Palo Alto Medical Foundation-Camino Division Mountain View California United States 94040
    31 Palo Alto Medical Foundation-Gynecologic Oncology Mountain View California United States 94040
    32 Palo Alto Medical Foundation Health Care Palo Alto California United States 94301
    33 Sutter Cancer Centers Radiation Oncology Services-Roseville Roseville California United States 95661
    34 Sutter Roseville Medical Center Roseville California United States 95661
    35 Sutter Medical Center Sacramento Sacramento California United States 95816
    36 California Pacific Medical Center-Pacific Campus San Francisco California United States 94115
    37 Pacific Central Coast Health Center-San Luis Obispo San Luis Obispo California United States 93401
    38 Palo Alto Medical Foundation-Santa Cruz Santa Cruz California United States 95065
    39 Mission Hope Medical Oncology - Santa Maria Santa Maria California United States 93444
    40 Sutter Pacific Medical Foundation Santa Rosa California United States 95403
    41 City of Hope South Pasadena South Pasadena California United States 91030
    42 Palo Alto Medical Foundation-Sunnyvale Sunnyvale California United States 94086
    43 City of Hope Upland Upland California United States 91786
    44 Sutter Cancer Centers Radiation Oncology Services-Vacaville Vacaville California United States 95687
    45 Sutter Solano Medical Center/Cancer Center Vallejo California United States 94589
    46 John Muir Medical Center-Walnut Creek Walnut Creek California United States 94598
    47 Rocky Mountain Cancer Centers-Aurora Aurora Colorado United States 80012
    48 Rocky Mountain Cancer Centers-Boulder Boulder Colorado United States 80304
    49 Rocky Mountain Cancer Centers - Centennial Centennial Colorado United States 80112
    50 Penrose-Saint Francis Healthcare Colorado Springs Colorado United States 80907
    51 Rocky Mountain Cancer Centers-Penrose Colorado Springs Colorado United States 80907
    52 Porter Adventist Hospital Denver Colorado United States 80210
    53 Mercy Medical Center Durango Colorado United States 81301
    54 Southwest Oncology PC Durango Colorado United States 81301
    55 Saint Anthony Hospital Lakewood Colorado United States 80228
    56 Rocky Mountain Cancer Centers-Littleton Littleton Colorado United States 80120
    57 Littleton Adventist Hospital Littleton Colorado United States 80122
    58 Rocky Mountain Cancer Centers-Sky Ridge Lone Tree Colorado United States 80124
    59 Longmont United Hospital Longmont Colorado United States 80501
    60 Rocky Mountain Cancer Centers-Longmont Longmont Colorado United States 80501
    61 McKee Medical Center Loveland Colorado United States 80539
    62 Parker Adventist Hospital Parker Colorado United States 80138
    63 Saint Mary Corwin Medical Center Pueblo Colorado United States 81004
    64 Northside Hospital Atlanta Georgia United States 30342
    65 CTCA at Southeastern Regional Medical Center Newnan Georgia United States 30265
    66 Saint Alphonsus Cancer Care Center-Boise Boise Idaho United States 83706
    67 Saint Luke's Cancer Institute - Boise Boise Idaho United States 83712
    68 Saint Alphonsus Cancer Care Center-Caldwell Caldwell Idaho United States 83605
    69 Kootenai Health - Coeur d'Alene Coeur d'Alene Idaho United States 83814
    70 Walter Knox Memorial Hospital Emmett Idaho United States 83617
    71 Saint Luke's Cancer Institute - Fruitland Fruitland Idaho United States 83619
    72 Idaho Urologic Institute-Meridian Meridian Idaho United States 83642
    73 Saint Luke's Cancer Institute - Meridian Meridian Idaho United States 83642
    74 Saint Alphonsus Medical Center-Nampa Nampa Idaho United States 83686
    75 Saint Luke's Cancer Institute - Nampa Nampa Idaho United States 83686
    76 Kootenai Clinic Cancer Services - Post Falls Post Falls Idaho United States 83854
    77 Kootenai Cancer Clinic Sandpoint Idaho United States 83864
    78 Saint Luke's Cancer Institute - Twin Falls Twin Falls Idaho United States 83301
    79 Saint Anthony's Health Alton Illinois United States 62002
    80 Rush - Copley Medical Center Aurora Illinois United States 60504
    81 Illinois CancerCare-Bloomington Bloomington Illinois United States 61704
    82 Illinois CancerCare-Canton Canton Illinois United States 61520
    83 Memorial Hospital of Carbondale Carbondale Illinois United States 62902
    84 SIH Cancer Institute Carterville Illinois United States 62918
    85 Illinois CancerCare-Carthage Carthage Illinois United States 62321
    86 Centralia Oncology Clinic Centralia Illinois United States 62801
    87 John H Stroger Jr Hospital of Cook County Chicago Illinois United States 60612
    88 Rush University Medical Center Chicago Illinois United States 60612
    89 University of Chicago Comprehensive Cancer Center Chicago Illinois United States 60637
    90 Carle on Vermilion Danville Illinois United States 61832
    91 Cancer Care Specialists of Illinois - Decatur Decatur Illinois United States 62526
    92 Decatur Memorial Hospital Decatur Illinois United States 62526
    93 Illinois CancerCare-Dixon Dixon Illinois United States 61021
    94 Carle Physician Group-Effingham Effingham Illinois United States 62401
    95 Crossroads Cancer Center Effingham Illinois United States 62401
    96 Illinois CancerCare-Eureka Eureka Illinois United States 61530
    97 NorthShore University HealthSystem-Evanston Hospital Evanston Illinois United States 60201
    98 Illinois CancerCare-Galesburg Galesburg Illinois United States 61401
    99 Western Illinois Cancer Treatment Center Galesburg Illinois United States 61401
    100 NorthShore University HealthSystem-Glenbrook Hospital Glenview Illinois United States 60026
    101 Ingalls Memorial Hospital Harvey Illinois United States 60426
    102 NorthShore University HealthSystem-Highland Park Hospital Highland Park Illinois United States 60035
    103 Sudarshan K Sharma MD Limited-Gynecologic Oncology Hinsdale Illinois United States 60521
    104 Illinois CancerCare-Kewanee Clinic Kewanee Illinois United States 61443
    105 Illinois CancerCare-Macomb Macomb Illinois United States 61455
    106 Carle Physician Group-Mattoon/Charleston Mattoon Illinois United States 61938
    107 Good Samaritan Regional Health Center Mount Vernon Illinois United States 62864
    108 UC Comprehensive Cancer Center at Silver Cross New Lenox Illinois United States 60451
    109 Cancer Care Center of O'Fallon O'Fallon Illinois United States 62269
    110 University of Chicago Medicine-Orland Park Orland Park Illinois United States 60462
    111 Illinois CancerCare-Ottawa Clinic Ottawa Illinois United States 61350
    112 Illinois CancerCare-Pekin Pekin Illinois United States 61554
    113 Illinois CancerCare-Peoria Peoria Illinois United States 61615
    114 Methodist Medical Center of Illinois Peoria Illinois United States 61636
    115 Illinois CancerCare-Peru Peru Illinois United States 61354
    116 Valley Radiation Oncology Peru Illinois United States 61354
    117 Illinois CancerCare-Princeton Princeton Illinois United States 61356
    118 Southern Illinois University School of Medicine Springfield Illinois United States 62702
    119 Springfield Clinic Springfield Illinois United States 62702
    120 Memorial Medical Center Springfield Illinois United States 62781
    121 Carle Cancer Center Urbana Illinois United States 61801
    122 The Carle Foundation Hospital Urbana Illinois United States 61801
    123 Northwestern Medicine Cancer Center Warrenville Warrenville Illinois United States 60555
    124 Illinois CancerCare - Washington Washington Illinois United States 61571
    125 Rush-Copley Healthcare Center Yorkville Illinois United States 60560
    126 Midwestern Regional Medical Center Zion Illinois United States 60099
    127 Mary Greeley Medical Center Ames Iowa United States 50010
    128 McFarland Clinic PC - Ames Ames Iowa United States 50010
    129 McFarland Clinic PC-Boone Boone Iowa United States 50036
    130 Mercy Hospital Cedar Rapids Iowa United States 52403
    131 Oncology Associates at Mercy Medical Center Cedar Rapids Iowa United States 52403
    132 Medical Oncology and Hematology Associates-West Des Moines Clive Iowa United States 50325
    133 Mercy Cancer Center-West Lakes Clive Iowa United States 50325
    134 Alegent Health Mercy Hospital Council Bluffs Iowa United States 51503
    135 Greater Regional Medical Center Creston Iowa United States 50801
    136 Medical Oncology and Hematology Associates-Laurel Des Moines Iowa United States 50314
    137 Mercy Medical Center - Des Moines Des Moines Iowa United States 50314
    138 McFarland Clinic PC-Trinity Cancer Center Fort Dodge Iowa United States 50501
    139 University of Iowa/Holden Comprehensive Cancer Center Iowa City Iowa United States 52242
    140 McFarland Clinic PC-Jefferson Jefferson Iowa United States 50129
    141 McFarland Clinic PC-Marshalltown Marshalltown Iowa United States 50158
    142 Mercy Medical Center-West Lakes West Des Moines Iowa United States 50266
    143 Central Care Cancer Center - Garden City Garden City Kansas United States 67846
    144 Central Care Cancer Center - Great Bend Great Bend Kansas United States 67530
    145 Flaget Memorial Hospital Bardstown Kentucky United States 40004
    146 Commonwealth Cancer Center-Corbin Corbin Kentucky United States 40701
    147 Saint Joseph Radiation Oncology Resource Center Lexington Kentucky United States 40504
    148 Saint Joseph Hospital East Lexington Kentucky United States 40509
    149 Saint Joseph London London Kentucky United States 40741
    150 Jewish Hospital Louisville Kentucky United States 40202
    151 Saints Mary and Elizabeth Hospital Louisville Kentucky United States 40215
    152 UofL Health Medical Center Northeast Louisville Kentucky United States 40245
    153 Jewish Hospital Medical Center South Shepherdsville Kentucky United States 40165
    154 Our Lady of the Lake Medical Oncology Baton Rouge Louisiana United States 70817
    155 Harold Alfond Center for Cancer Care Augusta Maine United States 04330
    156 Lafayette Family Cancer Center-EMMC Brewer Maine United States 04412
    157 Maine Medical Center- Scarborough Campus Scarborough Maine United States 04074
    158 Greater Baltimore Medical Center Baltimore Maryland United States 21204
    159 National Institutes of Health Clinical Center Bethesda Maryland United States 20892
    160 University of Michigan Comprehensive Cancer Center Ann Arbor Michigan United States 48109
    161 Fairview Ridges Hospital Burnsville Minnesota United States 55337
    162 Minnesota Oncology - Burnsville Burnsville Minnesota United States 55337
    163 Cambridge Medical Center Cambridge Minnesota United States 55008
    164 Mercy Hospital Coon Rapids Minnesota United States 55433
    165 Fairview Southdale Hospital Edina Minnesota United States 55435
    166 Unity Hospital Fridley Minnesota United States 55432
    167 Fairview Clinics and Surgery Center Maple Grove Maple Grove Minnesota United States 55369
    168 Minnesota Oncology Hematology PA-Maplewood Maplewood Minnesota United States 55109
    169 Saint John's Hospital - Healtheast Maplewood Minnesota United States 55109
    170 Abbott-Northwestern Hospital Minneapolis Minnesota United States 55407
    171 Hennepin County Medical Center Minneapolis Minnesota United States 55415
    172 Health Partners Inc Minneapolis Minnesota United States 55454
    173 Monticello Cancer Center Monticello Minnesota United States 55362
    174 New Ulm Medical Center New Ulm Minnesota United States 56073
    175 Fairview Northland Medical Center Princeton Minnesota United States 55371
    176 North Memorial Medical Health Center Robbinsdale Minnesota United States 55422
    177 Park Nicollet Clinic - Saint Louis Park Saint Louis Park Minnesota United States 55416
    178 Regions Hospital Saint Paul Minnesota United States 55101
    179 United Hospital Saint Paul Minnesota United States 55102
    180 Saint Francis Regional Medical Center Shakopee Minnesota United States 55379
    181 Lakeview Hospital Stillwater Minnesota United States 55082
    182 Ridgeview Medical Center Waconia Minnesota United States 55387
    183 Rice Memorial Hospital Willmar Minnesota United States 56201
    184 Minnesota Oncology Hematology PA-Woodbury Woodbury Minnesota United States 55125
    185 Fairview Lakes Medical Center Wyoming Minnesota United States 55092
    186 Saint Louis Cancer and Breast Institute-Ballwin Ballwin Missouri United States 63011
    187 Central Care Cancer Center - Bolivar Bolivar Missouri United States 65613
    188 Saint Francis Medical Center Cape Girardeau Missouri United States 63703
    189 Southeast Cancer Center Cape Girardeau Missouri United States 63703
    190 Parkland Health Center - Farmington Farmington Missouri United States 63640
    191 Capital Region Southwest Campus Jefferson City Missouri United States 65109
    192 Freeman Health System Joplin Missouri United States 64804
    193 Mercy Hospital Joplin Joplin Missouri United States 64804
    194 Delbert Day Cancer Institute at PCRMC Rolla Missouri United States 65401
    195 Mercy Clinic-Rolla-Cancer and Hematology Rolla Missouri United States 65401
    196 Heartland Regional Medical Center Saint Joseph Missouri United States 64506
    197 Saint Louis Cancer and Breast Institute-South City Saint Louis Missouri United States 63109
    198 Washington University School of Medicine Saint Louis Missouri United States 63110
    199 Mercy Hospital South Saint Louis Missouri United States 63128
    200 Missouri Baptist Medical Center Saint Louis Missouri United States 63131
    201 Mercy Hospital Saint Louis Saint Louis Missouri United States 63141
    202 Sainte Genevieve County Memorial Hospital Sainte Genevieve Missouri United States 63670
    203 Mercy Hospital Springfield Springfield Missouri United States 65804
    204 CoxHealth South Hospital Springfield Missouri United States 65807
    205 Missouri Baptist Sullivan Hospital Sullivan Missouri United States 63080
    206 Missouri Baptist Outpatient Center-Sunset Hills Sunset Hills Missouri United States 63127
    207 Mercy Hospital Washington Washington Missouri United States 63090
    208 Community Hospital of Anaconda Anaconda Montana United States 59711
    209 Billings Clinic Cancer Center Billings Montana United States 59101
    210 Bozeman Deaconess Hospital Bozeman Montana United States 59715
    211 Benefis Healthcare- Sletten Cancer Institute Great Falls Montana United States 59405
    212 Great Falls Clinic Great Falls Montana United States 59405
    213 Kalispell Regional Medical Center Kalispell Montana United States 59901
    214 Saint Patrick Hospital - Community Hospital Missoula Montana United States 59802
    215 Community Medical Hospital Missoula Montana United States 59804
    216 CHI Health Saint Francis Grand Island Nebraska United States 68803
    217 CHI Health Good Samaritan Kearney Nebraska United States 68847
    218 Saint Elizabeth Regional Medical Center Lincoln Nebraska United States 68510
    219 Cancer Partners of Nebraska - Pine Lake Lincoln Nebraska United States 68516
    220 Southeast Nebraska Cancer Center - 68th Street Place Lincoln Nebraska United States 68516
    221 Nebraska Methodist Hospital Omaha Nebraska United States 68114
    222 Alegent Health Immanuel Medical Center Omaha Nebraska United States 68122
    223 Alegent Health Bergan Mercy Medical Center Omaha Nebraska United States 68124
    224 Alegent Health Lakeside Hospital Omaha Nebraska United States 68130
    225 Creighton University Medical Center Omaha Nebraska United States 68131
    226 Midlands Community Hospital Papillion Nebraska United States 68046
    227 Women's Cancer Center of Nevada Las Vegas Nevada United States 89106
    228 Jersey Shore Medical Center Neptune New Jersey United States 07753
    229 University of New Mexico Cancer Center Albuquerque New Mexico United States 87102
    230 Memorial Medical Center - Las Cruces Las Cruces New Mexico United States 88011
    231 Presbyterian Rust Medical Center/Jorgensen Cancer Center Rio Rancho New Mexico United States 87124
    232 Northwell Health Imbert Cancer Center Bay Shore New York United States 11706
    233 Island Gynecologic Oncology Brightwaters New York United States 11718
    234 Roswell Park Cancer Institute Buffalo New York United States 14263
    235 Northwell Health/Center for Advanced Medicine Lake Success New York United States 11042
    236 State University of New York Upstate Medical University Syracuse New York United States 13210
    237 Dickstein Cancer Treatment Center White Plains New York United States 10601
    238 Southeastern Medical Oncology Center-Clinton Clinton North Carolina United States 28328
    239 Southeastern Medical Oncology Center-Goldsboro Goldsboro North Carolina United States 27534
    240 Southeastern Medical Oncology Center-Jacksonville Jacksonville North Carolina United States 28546
    241 Summa Health System - Akron Campus Akron Ohio United States 44304
    242 Aultman Alliance Community Hospital Alliance Ohio United States 44601
    243 UHHS-Chagrin Highlands Medical Center Beachwood Ohio United States 44122
    244 Strecker Cancer Center-Belpre Belpre Ohio United States 45714
    245 Aultman Health Foundation Canton Ohio United States 44710
    246 Geauga Hospital Chardon Ohio United States 44024
    247 Adena Regional Medical Center Chillicothe Ohio United States 45601
    248 Good Samaritan Hospital - Cincinnati Cincinnati Ohio United States 45220
    249 Bethesda North Hospital Cincinnati Ohio United States 45242
    250 TriHealth Cancer Institute-Westside Cincinnati Ohio United States 45247
    251 TriHealth Cancer Institute-Anderson Cincinnati Ohio United States 45255
    252 Case Western Reserve University Cleveland Ohio United States 44106
    253 Cleveland Clinic Cancer Center/Fairview Hospital Cleveland Ohio United States 44111
    254 Cleveland Clinic Foundation Cleveland Ohio United States 44195
    255 Ohio State University Comprehensive Cancer Center Columbus Ohio United States 43210
    256 Mount Carmel East Hospital Columbus Ohio United States 43213
    257 Columbus Oncology and Hematology Associates Inc Columbus Ohio United States 43214
    258 Riverside Methodist Hospital Columbus Ohio United States 43214
    259 Grant Medical Center Columbus Ohio United States 43215
    260 The Mark H Zangmeister Center Columbus Ohio United States 43219
    261 Mount Carmel Health Center West Columbus Ohio United States 43222
    262 Doctors Hospital Columbus Ohio United States 43228
    263 Delaware Health Center-Grady Cancer Center Delaware Ohio United States 43015
    264 Grady Memorial Hospital Delaware Ohio United States 43015
    265 Dublin Methodist Hospital Dublin Ohio United States 43016
    266 Central Ohio Breast and Endocrine Surgery Gahanna Ohio United States 43230
    267 Mount Carmel Grove City Hospital Grove City Ohio United States 43123
    268 Fairfield Medical Center Lancaster Ohio United States 43130
    269 Saint Rita's Medical Center Lima Ohio United States 45801
    270 OhioHealth Mansfield Hospital Mansfield Ohio United States 44903
    271 Marietta Memorial Hospital Marietta Ohio United States 45750
    272 OhioHealth Marion General Hospital Marion Ohio United States 43302
    273 Hillcrest Hospital Cancer Center Mayfield Heights Ohio United States 44124
    274 UH Seidman Cancer Center at Lake Health Mentor Campus Mentor Ohio United States 44060
    275 Knox Community Hospital Mount Vernon Ohio United States 43050
    276 Licking Memorial Hospital Newark Ohio United States 43055
    277 Newark Radiation Oncology Newark Ohio United States 43055
    278 Mercy Health Perrysburg Cancer Center Perrysburg Ohio United States 43551
    279 Southern Ohio Medical Center Portsmouth Ohio United States 45662
    280 Saint Vincent Mercy Medical Center Toledo Ohio United States 43608
    281 Mercy Health - Saint Anne Hospital Toledo Ohio United States 43623
    282 University Hospitals Sharon Health Center Wadsworth Ohio United States 44281
    283 Saint Ann's Hospital Westerville Ohio United States 43081
    284 UH Seidman Cancer Center at Saint John Medical Center Westlake Ohio United States 44145
    285 Genesis Healthcare System Cancer Care Center Zanesville Ohio United States 43701
    286 Cancer Centers of Southwest Oklahoma Research Lawton Oklahoma United States 73505
    287 University of Oklahoma Health Sciences Center Oklahoma City Oklahoma United States 73104
    288 Mercy Hospital Oklahoma City Oklahoma City Oklahoma United States 73120
    289 Oklahoma Cancer Specialists and Research Institute-Tulsa Tulsa Oklahoma United States 74146
    290 Saint Alphonsus Medical Center-Baker City Baker City Oregon United States 97814
    291 Saint Charles Health System Bend Oregon United States 97701
    292 Clackamas Radiation Oncology Center Clackamas Oregon United States 97015
    293 Providence Cancer Institute Clackamas Clinic Clackamas Oregon United States 97015
    294 Bay Area Hospital Coos Bay Oregon United States 97420
    295 Providence Newberg Medical Center Newberg Oregon United States 97132
    296 Saint Alphonsus Medical Center-Ontario Ontario Oregon United States 97914
    297 Legacy Good Samaritan Hospital and Medical Center Portland Oregon United States 97210
    298 Providence Portland Medical Center Portland Oregon United States 97213
    299 Providence Saint Vincent Medical Center Portland Oregon United States 97225
    300 Saint Charles Health System-Redmond Redmond Oregon United States 97756
    301 Legacy Meridian Park Hospital Tualatin Oregon United States 97062
    302 Paoli Memorial Hospital Paoli Pennsylvania United States 19301
    303 Thomas Jefferson University Hospital Philadelphia Pennsylvania United States 19107
    304 UPMC-Magee Womens Hospital Pittsburgh Pennsylvania United States 15213
    305 West Penn Hospital Pittsburgh Pennsylvania United States 15224
    306 University of Pittsburgh Cancer Institute (UPCI) Pittsburgh Pennsylvania United States 15232
    307 Asplundh Cancer Pavilion Willow Grove Pennsylvania United States 19090
    308 Lankenau Medical Center Wynnewood Pennsylvania United States 19096
    309 Women and Infants Hospital Providence Rhode Island United States 02905
    310 Medical University of South Carolina Charleston South Carolina United States 29425
    311 Saint Francis Hospital Greenville South Carolina United States 29601
    312 Saint Francis Cancer Center Greenville South Carolina United States 29607
    313 Bristol Regional Medical Center Bristol Tennessee United States 37620
    314 Ballad Health Cancer Care - Kingsport Kingsport Tennessee United States 37660
    315 Wellmont Holston Valley Hospital and Medical Center Kingsport Tennessee United States 37660
    316 Thompson Cancer Survival Center Knoxville Tennessee United States 37916
    317 Thompson Cancer Survival Center - West Knoxville Tennessee United States 37932
    318 Saint Joseph Regional Cancer Center Bryan Texas United States 77802
    319 Parkland Memorial Hospital Dallas Texas United States 75235
    320 UT Southwestern/Simmons Cancer Center-Dallas Dallas Texas United States 75390
    321 Houston Methodist Hospital Houston Texas United States 77030
    322 Methodist Willowbrook Hospital Houston Texas United States 77070
    323 Houston Methodist West Hospital Houston Texas United States 77094
    324 Houston Methodist Sugar Land Hospital Sugar Land Texas United States 77479
    325 Houston Methodist The Woodlands Hospital The Woodlands Texas United States 77385
    326 Wellmont Medical Associates-Bristol Bristol Virginia United States 24201
    327 Southwest VA Regional Cancer Center Norton Virginia United States 24273
    328 Providence Regional Cancer System-Aberdeen Aberdeen Washington United States 98520
    329 PeaceHealth Saint Joseph Medical Center Bellingham Washington United States 98225
    330 Harrison Medical Center Bremerton Washington United States 98310
    331 Highline Medical Center-Main Campus Burien Washington United States 98166
    332 Providence Regional Cancer System-Centralia Centralia Washington United States 98531
    333 Swedish Cancer Institute-Edmonds Edmonds Washington United States 98026
    334 Saint Elizabeth Hospital Enumclaw Washington United States 98022
    335 Providence Regional Cancer Partnership Everett Washington United States 98201
    336 Saint Francis Hospital Federal Way Washington United States 98003
    337 Swedish Cancer Institute-Issaquah Issaquah Washington United States 98029
    338 Kadlec Clinic Hematology and Oncology Kennewick Washington United States 99336
    339 Providence Regional Cancer System-Lacey Lacey Washington United States 98503
    340 Saint Clare Hospital Lakewood Washington United States 98499
    341 PeaceHealth Saint John Medical Center Longview Washington United States 98632
    342 Jefferson Healthcare Port Townsend Washington United States 98368
    343 Pacific Gynecology Specialists Seattle Washington United States 98104
    344 Swedish Medical Center-Ballard Campus Seattle Washington United States 98107
    345 Swedish Medical Center-First Hill Seattle Washington United States 98122-4307
    346 Swedish Medical Center-Cherry Hill Seattle Washington United States 98122-5711
    347 PeaceHealth United General Medical Center Sedro-Woolley Washington United States 98284
    348 Providence Regional Cancer System-Shelton Shelton Washington United States 98584
    349 Franciscan Research Center-Northwest Medical Plaza Tacoma Washington United States 98405
    350 PeaceHealth Southwest Medical Center Vancouver Washington United States 98664
    351 Legacy Salmon Creek Hospital Vancouver Washington United States 98686
    352 Providence Saint Mary Regional Cancer Center Walla Walla Washington United States 99362
    353 Providence Regional Cancer System-Yelm Yelm Washington United States 98597
    354 West Virginia University Charleston Division Charleston West Virginia United States 25304
    355 Saint Vincent Hospital Cancer Center Green Bay Green Bay Wisconsin United States 54301
    356 Saint Vincent Hospital Cancer Center at Saint Mary's Green Bay Wisconsin United States 54303
    357 Gundersen Lutheran Medical Center La Crosse Wisconsin United States 54601
    358 Medical College of Wisconsin Milwaukee Wisconsin United States 53226
    359 ProHealth D N Greenwald Center Mukwonago Wisconsin United States 53149
    360 Cancer Center of Western Wisconsin New Richmond Wisconsin United States 54017
    361 ProHealth Oconomowoc Memorial Hospital Oconomowoc Wisconsin United States 53066
    362 Saint Vincent Hospital Cancer Center at Oconto Falls Oconto Falls Wisconsin United States 54154
    363 Saint Vincent Hospital Cancer Center at Sturgeon Bay Sturgeon Bay Wisconsin United States 54235-1495
    364 ProHealth Waukesha Memorial Hospital Waukesha Wisconsin United States 53188
    365 UW Cancer Center at ProHealth Care Waukesha Wisconsin United States 53188
    366 Billings Clinic-Cody Cody Wyoming United States 82414
    367 Welch Cancer Center Sheridan Wyoming United States 82801
    368 Cancer Center-Metro Medical Center Bayamon Bayamon Puerto Rico 00959-5060
    369 HIMA San Pablo Oncologic Hospital Caguas Puerto Rico 00726
    370 Doctors Cancer Center Manati Puerto Rico 00674
    371 Instituto Oncologia Moderna Ponce Ponce Puerto Rico 00716
    372 San Juan Community Oncology Group San Juan Puerto Rico 00917
    373 Centro Comprensivo de Cancer de UPR San Juan Puerto Rico 00927
    374 San Juan City Hospital San Juan Puerto Rico 00936

    Sponsors and Collaborators

    • National Cancer Institute (NCI)
    • NRG Oncology

    Investigators

    • Principal Investigator: Jung-min Lee, NRG Oncology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    National Cancer Institute (NCI)
    ClinicalTrials.gov Identifier:
    NCT04739800
    Other Study ID Numbers:
    • NCI-2021-00615
    • NCI-2021-00615
    • NRG-GY023
    • NRG-GY023
    • U10CA180868
    First Posted:
    Feb 5, 2021
    Last Update Posted:
    Aug 24, 2022
    Last Verified:
    May 1, 2022

    Study Results

    No Results Posted as of Aug 24, 2022