Alisertib and Pembrolizumab for the Treatment of Patients With Rb-deficient Head and Neck Squamous Cell Cancer
Study Details
Study Description
Brief Summary
This phase I/II trial investigates the best dose and effect of alisertib in combination with pembrolizumab in treating patients with Rb-deficient head and neck squamous cell cancer. Alisertib may help block the growth of cancer.. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the tumor, and may interfere with the ability of tumor cells to grow and spread. Giving alisertib in combination with pembrolizumab may help control Rb-deficient head and neck squamous cell cancer. HPV positive head and neck cancers are Rb-deficient.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1/Phase 2 |
Detailed Description
PRIMARY OBJECTIVES:
- To determine the recommend phase II dose of the combination of alisertib and pembrolizumab. (Phase I) II. To determine the overall response rate (ORR) and progression free survival (PFS) of patients with recurrent or metastatic Rb-deficient head and neck squamous cell carcinoma (HNSCC) treated with the combination of pembrolizumab and alisertib. (Phase II)
SECONDARY OBJECTIVES:
-
To evaluate the safety of the combination of pembrolizumab and alisertib in patients with solid tumors.
-
To determine the overall survival in HNSCC patients treated with the combination of pembrolizumab and alisertib.
-
To determine the relationship between pharmacokinetics, pharmacodynamics, baseline immune and tumor biomarkers and clinical responses in patients treated with alisertib and pembrolizumab.
-
To determine correlations between clinical responses and the effect of the treatment on human papilloma virus (HPV)-reactive T cells in HPV+ cancers.
-
To determine correlations between clinical responses and tumor infiltrating lymphocyte function and T cell repertoire.
OUTLINE: This is a phase I, dose-escalation study of alisertib in combination with fixed dose pembrolizumab followed by a phase II study.
Patients receive alisertib orally (PO) twice daily (BID) on days 1-7 and pembrolizumab intravenously (IV) over 30 minutes on day 1. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up every 2-3 months.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Treatment (alisertib, pembrolizumab) Patients receive alisertib PO BID on days 1-7 and pembrolizumab IV over 30 minutes on day 1. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. |
Drug: Alisertib
Given PO
Other Names:
Biological: Pembrolizumab
Given IV
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Maximum tolerated dose (Phase I) [Up to 18 weeks from start of study treatment]
To guide dose escalation decisions, if the observed dose-limiting toxicity (DLT) rate at the current dose is =< 0.236, the next cohort of patients will be treated at the next higher dose level; if it is >= 0.359, the next cohort of patients will be treated at the next lower dose level; otherwise the next cohort of patients will be treated at the same dose.
- (Overall response rate [ORR]) (Phase II) [Up to 2 years]
Measured using the Bayesian optimal phase 2 (BOP2) design.
- Progression free survival (PFS) (Phase II) [6 months]
Measured using the BOP2 design.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
PHASE II ONLY:
-
Histologically or cytological confirmed diagnosis of Rb-deficient HNSCC for which no standard curative therapy is available
-
Rb deficient HNSCC includes Clinical Laboratory Improvement Act (CLIA)-certified testing confirming one of the following:
-
Human papillomavirus (HPV) positive as determined by any one of the following: p16 immunohistochemistry (IHC), HPV ribonucleic acid (RNA) in situ hybridization (ISH), RNAscope (messenger RNA [mRNA] ISH), deoxyribonucleic acid (DNA) ISH, DNA polymerase chain reaction (PCR), or quantitative reverse transcriptase PCR (qRT PCR)
-
No Rb protein expression in the tumor as determined by IHC
-
No prior treatment with an anti-PD-1 antibody (e.g., nivolumab, pembrolizumab, cemiplimab), as well as anti-PD L1, anti-PD-L2, anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell co-stimulation or immune checkpoint pathways
-
Appropriate for single agent pembrolizumab:
-
Front line therapy for those whose tumors express PD-L1 (Control Preference Scale [CPS] >= 1)
-
Front line therapy for those who cannot tolerate chemotherapy per the judgement of the treating physician
-
As second line or greater line of therapy
-
PHASE I ONLY:
-
Histologically or cytological confirmed diagnosis of an invasive solid tumor malignancy, for which no standard curative or life prolonging therapy is available
-
PHASE I AND PHASE II:
-
Eastern Cooperative Oncology Group (ECOG) performance status of =< 2
-
Absolute neutrophil count (ANC) > 1500/mm^3 (within 22 days before the first dose of study drug)
-
Platelets > 100,000/mm^3 (within 22 days before the first dose study drug)
-
Hemoglobin (Hgb) > 9 g/dL (within 22 days before the first dose of study drug). Values must be obtained without need for myeloid growth factor or platelet transfusion support within 14 days, however, erythrocyte growth factor is allowed as per published American Society of Clinical Oncology (ASCO) guidelines
-
Total bilirubin =< 1.5 x upper limit of normal (ULN) (within 22 days before the first dose of study drug)
-
Serum glutamic-oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST]) and serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) < 2.5 x ULN (within 22 days before the first dose of study drug). AST and/or ALT may be up to 5 X ULN if with known liver mets or total 3 x ULN with direct bilirubin =< ULN in patients with well-documented Gilbert syndrome
-
Adequate renal function as defined by calculated creatinine clearance >= 30 ml/min (Cockcroft-Gault formula) (within 22 days before the first dose of study drug)
-
Measurable disease according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1
-
Voluntary written consent must be given before performance of any study related procedure not part of standard of care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care
-
Patients must be able to either swallow alisertib enteric coated tablets, swallow alisertib oral solution formulation, or administer alisertib oral solution formulation via a feeding tube that terminates in the stomach
-
Willing to provide blood and tissue for correlative research purposes
-
Female patients who:
-
Are postmenopausal for at least 1 year before the screening visit, OR
-
Are surgically sterile, OR
-
If they are of childbearing potential, agree to practice 1 highly effective method of contraception and 1 additional effective (barrier) method at the same time, from the time of signing the informed consent through 120 days after the last dose of study drug, OR
-
Agree to practice true abstinence, when this is in line with the preferred and usual lifestyle of the subject (Periodic abstinence [e.g, calendar, ovulation, symptothermal, postovulation methods], withdrawal, spermicides only, and lactational amenorrhea are not acceptable methods of contraception. Female and male condoms should not be used together)
-
Male patients, even if surgically sterilized (i.e., status postvasectomy), who:
-
Agree to practice effective barrier contraception during the entire study treatment period and through 120 after the last dose of study drug, OR
-
Agree to practice true abstinence, when this is in line with the preferred and usual lifestyle of the subject (Periodic abstinence [e.g., calendar, ovulation, symptothermal, postovulation methods], withdrawal, spermicides only, and lactational amenorrhea are not acceptable methods of contraception. Female and male condoms should not be used together)
Exclusion Criteria:
-
Radiation therapy to more than 25% of the bone marrow. Whole pelvic radiation is considered to be over 25%
-
Prior allogeneic bone marrow or organ transplantation
-
Known gastrointestinal (GI) disease or GI procedures that could interfere with the oral absorption or tolerance of alisertib. Examples include, but are not limited to partial gastrectomy, history of small intestine surgery, and celiac disease
-
Inability to swallow (or use a feeding tube to administer) oral medication or inability or unwillingness to comply with the administration requirements related to alisertib
-
Known history of uncontrolled sleep apnea syndrome and other conditions that could result in excessive daytime sleepiness, such as severe chronic obstructive pulmonary disease; requirement for supplemental oxygen
-
Requirement for constant administration of proton pump inhibitor, H2 antagonist, or pancreatic enzymes throughout the study. The intermittent use of H2-antagonists and antacids (including carafate) is only allowed within these guidelines:
-
H2 antagonists until D-1 and after the dosing of alisertib is done
-
Antacid formulations until 2 hours before doing and after 2 hours following dosing
-
Proton pump inhibitor (PPI) is allowed until D-5 of first alisertib dose. PPIs are prohibited throughout the study
-
Myocardial infarction within 6 months prior to enrollment or has New York Heart Association (NYHA) class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia or active conduction system abnormalities. Prior to study entry, any electrocardiogram (ECG) abnormality at screening has to be documented by the investigator as not medically relevant
-
Female subject who is pregnant or breast-feeding. Confirmation that the subject is not pregnant must be established by a negative urine or serum beta-human chorionic gonadotropin (beta-hCG) pregnancy test result obtained during screening. Pregnancy testing is not required for post-menopausal or surgically sterilized women
-
Female patient who intend to donate eggs (ova) during the course of this study or 120 days after receiving their last dose of study drug(s)
-
Male patients who intend to donate sperm during the course of this study or 120 days after receiving their last dose of study drug(s)
-
Other severe acute or chronic medical or psychiatric condition, including uncontrolled diabetes, malabsorption, resection of the pancreas or upper small bowel, requirement for pancreatic enzymes, any condition that would modify small bowel absorption of oral medications, or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for enrollment in this study
-
Diagnosed or treated for another invasive malignancy within 2 years of enrollment, with the exception of complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, an in situ malignancy, or low-risk prostate cancer after curative therapy
-
Has received any anti-cancer treatment including investigational agents within 21 days prior to first dose of alisertib
-
Patients who receive gamma knife radiosurgery for brain metastases or whole brain radiation are eligible if gamma knife radiosurgery was completed > 2 weeks before treatment is started or whole brain radiation was performed > 4 weeks before treatment is started, and are clinically stable (not requiring steroids or anti-epileptic drugs)
-
Known hypersensitivity to any of the excipients of alisertib enteric coated tablets or severe reaction to any human monoclonal antibody
-
Patients with a prior history of clinically significant metabolic acidosis (exclusion only for patients receiving alisertib oral solution)
-
Major surgery within 28 days prior to first dose of alisertib or persisting side effects that have not improved to National Cancer Institute - Common Terminology Criteria for Adverse Events (NCI-CTCAE) grade 1 or better
-
Patients who are on (or will require) prolonged systemic corticosteroid treatment during the study except for replacement dosing for adrenal insufficiency
-
Concurrent severe and/or uncontrolled medical conditions that would, in the investigator's judgment, contraindicate patient participation in the clinical study or require concomitant anti-cancer drugs (e.g. active or uncontrolled severe infection, chronic active hepatitis, immuno-compromised, acute or chronic pancreatitis, uncontrolled high blood pressure, interstitial lung disease)
-
Patients with active, known, diagnosed or suspected autoimmune disease. Patients suffering from vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune thyroiditis only requiring thyroid hormone replacement therapy, or psoriasis not requiring systemic treatment can be enrolled
-
Patients diagnosed with active interstitial lung disease (ILD)/pneumonitis or a history of ILD/pneumonitis or another condition requiring immunosuppressive doses of systemic medication such as systemic corticosteroids or absorbed topical corticosteroids (doses >= 10 mg/day prednisone or equivalent) or other immunosuppressive medications within 14 days of study drug administration. Inhaled or topical corticosteroids, adrenal replacement doses, or < 10 mg daily prednisone or equivalent are permitted
-
Administration of any live vaccine within 30 days before first dose of study drug
-
Uncontrolled infection with human immunodeficiency virus (HIV), hepatitis B virus or hepatitis C virus, except for: Patients with HIV who have controlled infection (undetectable viral load and CD4 count above 350 cells/mm3 either spontaneously or on a stable antiviral regimen) are permitted; Patients with hepatitis B (HepBsAg+) virus who have controlled infection (serum hepatitis B virus DNA PCR that is below the limit of detection AND receiving antiviral therapy for hepatitis B) are permitted; Patients who are hepatitis C virus antibody positive (HCV Ab +) who have controlled infection (undetectable HCV RNA by PCR either spontaneously or in response to a successful prior course of anti-HCV therapy) are permitted
-
Participating in another therapeutic clinical trial
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | M D Anderson Cancer Center | Houston | Texas | United States | 77030 |
Sponsors and Collaborators
- M.D. Anderson Cancer Center
- National Cancer Institute (NCI)
Investigators
- Principal Investigator: Faye M Johnson, MD, M.D. Anderson Cancer Center
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 2020-0210
- NCI-2020-05051
- 2020-0210