Multi-arm Multi-modality Therapy for Very High Risk Localized and Low Volume Metastatic Prostatic Adenocarcinoma

Sponsor
Memorial Sloan Kettering Cancer Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT03436654
Collaborator
Dana-Farber Cancer Institute (Other)
76
Enrollment
11
Locations
2
Arms
55.8
Anticipated Duration (Months)
6.9
Patients Per Site
0.1
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The purpose of this study is to test if treatment with medications that reduce the male hormone level in the participant's body for a few months before surgery can shrink prostate cancer as much as possible, which might reduce the chances of the cancer coming back in the future. These treatments include a hormone injection given monthly or every three months and the study drugs, which include abiraterone acetate, prednisone, and apalutamide.

These medications are being used in combination with surgery and maybe radiotherapy because studies have shown that any single approach on its own is not sufficient to control or get rid of the cancer especially if they have high risk or aggressive features. The researchers hope to learn if combining the study drugs with surgery and radiation will get rid of the cancer from participants' prostates and reduce their prostate-specific antigen (PSA) to an undetectable level.

Condition or DiseaseIntervention/TreatmentPhase
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
76 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Multi-arm Multi-modality Therapy for Very High Risk Localized and Low Volume Metastatic Prostatic Adenocarcinoma
Actual Study Start Date :
Jun 21, 2018
Anticipated Primary Completion Date :
Feb 14, 2023
Anticipated Study Completion Date :
Feb 14, 2023

Arms and Interventions

ArmIntervention/Treatment
Experimental: ADT + Apalutamide

Drug: Apalutamide
240mg daily orally
Other Names:
  • ARN-509, ERLEADA™
  • Procedure: Radical Prostatectomy
    A laparoscopic, robotic-assisted, or open approach to RP is permitted at the discretion of the operating surgeon.

    Procedure: Extended Pelvic lymphadenectomy
    To be performed concurrently with prostatectomy. Bilateral pelvic lymphadenectomy should include complete removal of all pelvic lymph nodes within the broad template described and includes the external iliac, hypogastric, obturator, and pre-sacral lymph nodes

    Drug: GnRH agonist/antagonist
    Physician's choice, for a total duration not to extend beyond the treatment phase of the protocol or 10 months from the start of investigational agent(s)

    Experimental: ADT + Apalutamide + Abiraterone Acetate + Prednisone

    Drug: Apalutamide
    240mg daily orally
    Other Names:
  • ARN-509, ERLEADA™
  • Drug: Abiraterone Acetate
    1000mg daily orally
    Other Names:
  • ZYTIGA
  • Drug: Prednisone
    5mg BID orally

    Procedure: Radical Prostatectomy
    A laparoscopic, robotic-assisted, or open approach to RP is permitted at the discretion of the operating surgeon.

    Procedure: Extended Pelvic lymphadenectomy
    To be performed concurrently with prostatectomy. Bilateral pelvic lymphadenectomy should include complete removal of all pelvic lymph nodes within the broad template described and includes the external iliac, hypogastric, obturator, and pre-sacral lymph nodes

    Drug: GnRH agonist/antagonist
    Physician's choice, for a total duration not to extend beyond the treatment phase of the protocol or 10 months from the start of investigational agent(s)

    Outcome Measures

    Primary Outcome Measures

    1. Pathologic complete response [24 months]

      The primary efficacy measure of pathological complete response and minimal residual disease is defined as the less than or equal to 5 mm of morphologically identifiable carcinoma in the RP specimen.

    2. Minimal residual disease (MRD) [24 months]

      ≤ 5mm tumor

    Secondary Outcome Measures

    1. PSA Response Rate [10 months from randomization]

      defined as percentage of patients with an undetectable PSA at 10 months from randomization (after completion of all protocol treatment)

    2. Time to PSA Progression [24 months]

      Time from the start of treatment to the date of first evidence of disease progression (serum PSA ≥0.2ng/mL, which is confirmed by a second determination with a PSA ≥0.2 ng/mL, according to the 2007 American Urological Association Prostate Guidelines). This will be estimated by the cumulative incidence function. For each arm, time to PSA progression will be presented for all patients as well as by metastatic status

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Willing and able to provide written informed consent and Authorization for Use and Release of Health and Research Study Information (HIPAA authorization) NOTE: HIPAA authorization may be either included in the informed consent or obtained separately

    • Male aged 18 years and above

    • Serum testosterone of ≥150 ng/dL (For cohorts A and B1, testosterone level requirement is exempted if they are already on ADT prior to treatment start. For cohort B2, patients will be considered eligible if their testosterone is currently ≥150 ng/dl).

    • Histologically confirmed adenocarcinoma of the prostate, who meet the following criteria:

    Cohort A

    • Clinically localized disease with histologically confirmed adenocarcinoma of the prostate with either ≥3 positive cores or 2 positive cores if >1cm in length with at least 50% tumor content WITH

    • With Gleason score 8-10 OR

    • Gleason 4+3 with one of the following features:

    • PSA ≥ 20 mg/mL within 2 months prior to diagnostic biopsy

    • MRI suspicious for radiographic ≥T3 disease (as long as urologist deems tumor is resectable at baseline); defined as >75% probability of extracapsular extension or seminal vesicle invasion in the opinion of the reading radiologist.

    OR

    • Gleason 3+4 or 4+3 and Oncotype DX Genomic Prostate Score of >40

    • With or without clinical N1 (size >1.5cm in the short axis) (Gleason score requirement can be omitted if node positive)

    OR

    Cohort B1

    • Newly diagnosed low-volume metastatic disease with either.

    • Bone metastases as documented by CT, MRI or radionuclide bone scan amenable to treatment with a maximum of 3 radiation isocenters*

    *(note: patients with PET scans that show osseous metastases that would not be amenable to 3-isocenter radiation treatment are still eligible as long as conventional imaging shows osseous disease that can be treated with 3 radiation isocenters) And/or

    • Retroperitoneal nodes up to the level of the renal hilum with/without pelvic nodal metastasis ≥1.5cm in the short axis

    OR

    Cohort B2

    • Rising PSA after RP with:

    • Osseous or nodal metastases (up to the level of renal hila) as documented by FACBC or

    PSMA PET which are:
    • amenable to treatment with a maximum of 3 radiation isocenters* These lesions should have structural correlates on CT or MRI. Lesions without structural correlates will be viewed as equivocal and not need to be irradiated but will be followed.

    • With associated CT or MRI correlate

    • No evidence of local recurrence within prior radiation field on MRI or other imaging studies i.e. local recurrence is acceptable in patients without prior salvage radiation.

    • Prior salvage radiotherapy is permitted.

    • Multiple lesions within one isocenter may be permitted upon review by the sponsor's radiation oncologist;
    • ECOG performance status of ≤ 1

    • Adequate bone marrow, hepatic and renal function, as evidenced within 28 days prior to treatment start by:

    • ANC ≥ 1500/µl

    • Hemoglobin ≥ 9g/dL

    • Platelet count ≥ 100,000/µl

    • Serum Creatinine GFR >45 mL/min

    • Porassium within institutional normal range

    • Total Bilirubin ≤ 1.5 x ULN (Note: In subjects with Gilbert's syndrome, if total bilirubin is >1.5 x ULN, measure direct and indirect bilirubin and if direct bilirubin is ≤ 1.5 x ULN, subject may be eligible)

    • Albumin ≥ 3.0 g/dL

    • SGOT (AST) ≤ 2.5 x ULN

    • SGPT (ALT) ≤ 2.5 x ULN

    • Patients must have a clinical T stage documented by the treating urologist/medical oncologist within 90 days prior to treatment start using the 7th edition AJCC staging system, recorded as the urologist's/medical oncologist's best clinical assessment of extent of local disease by digital rectal examination and/or available imaging studies such as transrectral ultrasound, CT scan, and/or MRI. Applicable to Cohort A and B1.

    • The primary tumor must be considered unresectable by RP based on initial imaging with gross negative margins as determined by a urologist and documented as such. (applicable to cohorts A and B1 only)

    • Recovery of reversible effects of prior surgery (i.e., incisional pain, wound drainage) to Grade ≤1, and at least 4 weeks from prior surgery to treatment start. (biopsy excluded)

    • Able to swallow the study drug(s) whole as a tablet

    • Willing to take abiraterone acetate on an empty stomach; no food should be consumed at least one hour before and for at least two hours after the dose of abiraterone acetate is taken (Note: apalutamide does not have to be taken on an empty stomach.)

    • Agrees to use a condom (even men with vasectomies) and another effective method of birth control if he is having sex with a woman of childbearing potential or agrees to use a condom if he is having sex with a woman who is pregnant while on study drug and for 3 months following the last dose of study drug. Must also agree not to donate sperm during the study and for 3 months after receiving the last dose of study drug.

    • For Cohorts B1 and B2 only, biopsy confirmation of metastases (strongly encouraged; if safe and feasible at treating center)

    Exclusion Criteria:
    • Prior treatment for prostate cancer including prior surgery (excluding TURP and patients with rising PSA after RP), pelvic lymph node dissection, radiation therapy unless the patient is eligible for Cohort B2.

    • Prior cytotoxic chemotherapy or biologic therapy for prostate cancer

    • More than 2 months of prior ADT with GnRH antagonist/agonist at time of treatment start. Bicalutamide given for < 2 months at the time of registration as flare prevention is allowed. For Cohort B2, prior ADT and/or first generation anti-androgen treatment in the (neo)adjuvant and/or salvage setting in conjunction with radiation or surgery is allowed provided last effective dose of ADT and/or first generation anti-androgen is > 12 months prior to the date of randomization and total duration of prior therapy is 12 months or lesser, and their testosterone is currently >150ng/dL.

    • Prior exposure to ketoconazole (systemic), abiraterone acetate, enzalutamide or other agents targeting the AR signaling pathway

    • Concomitant therapy with any other experimental drug

    • Known brain, liver, lung or other visceral metastasis (with the exception of retroperitoneal and / or pelvic nodal metastases as per inclusion criteria)

    • Prior prostate cancer metastasis-directed therapies

    • Currently active second malignancy or past history of malignancies diagnosed within the last 5 years that require active therapy and/or in remission with life expectancy of < 5 years, with the exception of resected non-melanoma skin cancers, non-muscle invasive bladder cancer, state I head and neck cancer, or stage I colorectal cancer

    • Significant medical condition other than cancer, that would prevent consistent and compliant participation in the study that would, in the opinion of the investigator, make this protocol unreasonably hazardous including but not limited to:

    • Any medical condition requiring a higher dose of corticosteroid than 10mg prednisone/prednisolone once daily

    • History of gastrointestinal disordered (medical disorders or extensive surgery) that may interfere with the absorption of the study agents

    • Uncontrolled hypertension (systolic BP ≥ 160 mmHg or diastolic BP ≥ 95 mmHg); patients with a history of hypertension are allowed provided blood pressure is controlled by anti-hypertensive treatment (systolic BP < 160 mmHg or diastolic BP <95 mmHg)

    • Active or symptomatic viral hepatitis of chronic liver disease

    • Known active HIV, Hepatitis B or Hepatitis C infection. (HIV testing is not mandatory)

    • History of pituitary or adrenal dysfunction

    • History of hypogonadism

    • Clinically significant heart disease as evidenced by myocardial infarction, or arterial thrombotic events in the past 6 months, severe or unstable angina, or New York Heart Association (NYHA) Class III or IV heart disease or cardiac ejection fraction measurement of <50% at baseline, or clinically significant ventricular arrhythmias within 6 months prior to treatment start.

    • History of seizure or any condition that may predispose to seizure (including, but not limited to prior stroke, transient ischemic attack or loss of consciousness </= 1 year prior to treatment start; brain arteriovenous malformation; or intracranial masses such as schawnnomas and meningiomas that are causing edema or mass effect)

    • Uncontrolled diabetes mellitus

    • History of inflammatory bowel disease

    • Baseline moderate and severe hepatic impairment (Child Pugh Class B & C)

    • Use of any prohibited concomitant medications within 14 days prior to treatment start, or use of prohibited concomitant medication listed in section 7.9.1 within the outlined windows NOTE: Medications known to lower the seizure threshold must be discontinued or substituted at least 4 weeks prior to treatment start

    • Pre-existing condition that warrants long-term corticosteroid use in excess of 10 mg prednisone/prednisolone daily

    • Known allergies, hypersensitivity or intolerance to apalutamide, abiraterone acetate, prednisone, or GBRH agonist or GNRH antagonist

    • Administration of an investigational therapeutic within 30 days of treatment start

    • Patients that cannot tolerate MRI

    • Any condition which, in the opinion of the investigator, would preclude participation in this trial

    Contacts and Locations

    Locations

    SiteCityStateCountryPostal Code
    1University of ChicagoChicagoIllinoisUnited States60637
    2Northwestern UniversityEvanstonIllinoisUnited States60208
    3Dana Farber Cancer InstituteBostonMassachusettsUnited States02115
    4Memoral Sloan Kettering Basking Ridge (Limited Protocol Activities)Basking RidgeNew JerseyUnited States07920
    5Memoral Sloan Kettering Monmouth (Limited Protocol Activities)MiddletownNew JerseyUnited States07748
    6Memorial Sloan Kettering Bergen (Limited Protocol Activities)MontvaleNew JerseyUnited States07645
    7Memorial Sloan Kettering Commack (Limited Protocol Activities)CommackNew YorkUnited States11725
    8Memorial Sloan Kettering Westchester (Limited Protocol Activities)HarrisonNew YorkUnited States10604
    9Memorial Sloan Kettering Cancer CenterNew YorkNew YorkUnited States10065
    10Memorial Sloan Kettering Nassau (Limited Protocol Activities)UniondaleNew YorkUnited States11553
    11Cleveland ClinicClevelandOhioUnited States44195

    Sponsors and Collaborators

    • Memorial Sloan Kettering Cancer Center
    • Dana-Farber Cancer Institute

    Investigators

    • Principal Investigator: Howard Scher, MD, Memorial Sloan Kettering Cancer Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Memorial Sloan Kettering Cancer Center
    ClinicalTrials.gov Identifier:
    NCT03436654
    Other Study ID Numbers:
    • 17-646
    • PCCTC #: c16-183
    First Posted:
    Feb 19, 2018
    Last Update Posted:
    Nov 18, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Memorial Sloan Kettering Cancer Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 18, 2021