MC200708 Pemetrexed and Pembrolizumab for the Treatment of Recurrent and/or Metastatic Salivary Gland Cancer

Mayo Clinic

Status and phase

Active, not recruiting

Phase 2

Conditions

Recurrent Salivary Gland Carcinoma

Adenoid Cystic Carcinoma

Metastatic Salivary Gland Carcinoma

Stage IV Major Salivary Gland Cancer AJCC v8

Treatments

Procedure: Computed Tomography

Biological: Pembrolizumab

Procedure: Biospecimen Collection

Procedure: Positron Emission Tomography

Drug: Pemetrexed Disodium

Procedure: PSMA PET Scan

Procedure: Magnetic Resonance Imaging

Study type

Interventional

Funder types

Other

NIH

Identifiers

NCT04895735

MC200708 (Other Identifier)

20-010144 (Other Identifier)

NCI-2021-04161 (Registry Identifier)

Details and patient eligibility

About

This phase II trial studies the effect of pemetrexed and pembrolizumab in treating patients with salivary gland cancer that has come back (recurrent) and/or has spread to other places in the body (metastatic). Chemotherapy drugs, such as pemetrexed, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. The purpose of this study is to evaluate whether pembrolizumab, an immunotherapy drug, in combination with the chemotherapy drug, pemetrexed, has an effect on advanced salivary gland cancer.

Full description

PRIMARY OBJECTIVE:

I. To determine the clinical benefit rate (CBR) of the combination of pembrolizumab and pemetrexed in patients with recurrent or metastatic adenoid cystic salivary gland cancer. (Group A1, adenoid cystic carcinoma [ACC]) II. To determine the response rate of the combination of pembrolizumab and pemetrexed in patients with recurrent or metastatic salivary gland cancer (recurrent/metastatic salivary gland cancer [R/M SGC]). (Groups A and B, ACC and non-ACC)

SECONDARY OBJECTIVES:

I. To determine the progression-free survival (PFS), overall survival (OS), response rate (ACC cohort), CBR rate (non-ACC), and adverse events of the combination of pembrolizumab and pemetrexed in patients with recurrent or metastatic salivary gland cancer (R/M SGC).

II. To assess safety and tolerability of the combination of pembrolizumab and pemetrexed in patients with recurrent or metastatic salivary gland cancer (R/M SGC).

CORRELATIVE RESEARCH OBJECTIVES:

I. To investigate the frequency of MTAP loss by immunohistochemistry in R/M SGC and whether it correlates with enhanced response to pemetrexed.

II. To measure the degree of PDL1 expression using formalin-fixed tumor samples, and determine the extent of PDL1 expression correlates with response to study treatment.

III. To investigate expression of thymidylate synthase by immunohistochemistry in R/M SGC and whether it correlates with enhanced response to pemetrexed.

IV. To investigate circulating tumor deoxyribonucleic acid (DNA) (ctDNA) and correlation with response to study treatment.

V. To prospectively investigate circulating prostate-specific membrane antigen (PSMA) extracellular vesibles (EVs) and correlate with disease burden and treatment response for patients with adenoid cystic carcinoma in Cohort A1.

VI. To prospectively investigate PSMA positron emission tomography (PET)/computed tomography (CT) as an imaging modality for patients with adenoid cystic carcinoma in Cohort A1.

OUTLINE:

Patients receive pembrolizumab intravenously (IV) over 30 minutes and pemetrexed disodium IV over 10 minutes on day 1. Treatment with pembrolizumab repeats every 21 days for up to 35 cycles (2 years) in the absence of disease progression or unacceptable toxicity. Cycles of pemetrexed disodium repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients who had stable disease, partial response, or complete response after completion of 35 cycles of pembrolizumab, may continue pembrolizumab for an additional 17 cycles (1 year) in the absence of disease progression or unacceptable toxicity. Patients additionally undergo blood sample collection, CT, PET/CT or magnetic resonance imaging (MRI) and may also undergo PSMA PET on study.

After completion of study intervention, patients are followed up at 30 days, and then every 3 months for up to 3 years.

Enrollment

45 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

REGISTRATION - INCLUSION CRITERIA
Age >= 18 years
Histologically confirmed diagnosis of recurrent or metastatic salivary gland cancer not amenable to curative-intent therapy
COHORT A1: Rochester Minnesota only: Diagnosis of adenoid cystic carcinoma (ACC)
Measurable disease as defined by Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1 criteria
- NOTE: Tumor lesions in a previously irradiated area are considered measurable disease if progression has been demonstrated in such lesions. Disease that is measurable by physical examination only is not eligible
Prior treatment:
- Prior treatment with checkpoint inhibitor(s) allowed
- Any number of lines of prior therapy in the recurrent/metastatic setting is permitted at the investigator's discretion
Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1
- NOTE: PS must be assessed again within 7 days prior to first dose of study drug
Hemoglobin >= 9.0 g/dL (obtained =< 8 days prior to registration)
- NOTE: Must be met without growth factor support and no transfusions <14 days prior to testing
Absolute neutrophil count (ANC) >= 1500/mm^3 (obtained =< 8 days prior to registration)
Platelet count >= 100,000/mm^3 (obtained =< 8 days prior to registration)
Total bilirubin =< 1.5 x upper limit of normal (ULN) (obtained =< 8 days prior to registration)
Alanine aminotransferase (ALT) and aspartate transaminase (AST) =< 2.5 x ULN (=< 5 x ULN for patients with liver involvement) (obtained =< 8 days prior to registration)
Prothrombin time (PT)/international normalized ratio (INR)/activated partial thromboplastin time (aPTT) =< 1.5 x ULN OR if patient is receiving anticoagulant therapy and INR or aPTT is within target range of therapy (obtained =< 8 days prior to registration)
Creatinine =< 1.5 x ULN OR calculated creatinine clearance >= 45 ml/min using the Cockcroft-Gault formula (obtained =< 8 days prior to registration)
Negative pregnancy test done =< 7 days prior to registration, for persons of childbearing potential only
- Note: If testing done for eligibility is > 72 hours prior to first dose, then pregnancy testing must be repeated and result must be negative for patient to receive treatment
Persons able to become pregnant OR able to father a child must be willing to use an adequate method of contraception while on treatment and for 180 days after last treatment
Life expectancy >= 12 weeks
Provide written informed consent
Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study)
Willingness to provide mandatory blood specimens for correlative research
Willingness to provide mandatory tissue specimens for correlative research

Exclusion criteria

REGISTRATION - EXCLUSION CRITERIA
Any of the following because this study involves an agent that has known genotoxic, mutagenic and teratogenic effects:
- Pregnant persons
- Nursing persons
- Persons of childbearing potential and persons able to father a child who are unwilling to employ adequate contraception
- Persons expecting to conceive or father children during study treatment or within 180 days (6 months) after the last treatment
Any of the following prior therapies:
- Surgery < 3 weeks prior to registration
- Systemic anti-cancer therapy < 3weeks prior to registration
- Radiotherapy < 2 weeks prior to registration OR Palliative radiation < 1 week prior to registration
  - NOTES: Must have recovered from all radiation related adverse effects (=< grade 1) Must not currently require corticosteroids Must not have had radiation pneumonitis
- Live vaccine < 4 weeks prior to registration
  - NOTES: Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guerin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist) are live attenuated vaccines and are not allowed
- Received an investigational agent or used an investigational device or participated in a study of an investigational agent < 4 weeks prior to registration
Known active human immunodeficiency virus (HIV) infection (defined as patients who are not on anti-retroviral treatment and have detectable viral load and CD4+ < 500/ml)
- NOTE: HIV-positive patients who are well controlled on anti-retroviral therapy are allowed to enroll
Active autoimmune disease requiring systemic treatment < 2 years prior to registration, documented history of severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents with use of disease modifying agents, corticosteroids or immunosuppressive drugs
- NOTE: Exceptions are allowed for:
  - Vitiligo
  - Resolved childhood asthma/atopy
  - Intermittent use of bronchodilators or inhaled steroids
  - Daily steroids at dose of =< 10 mg of prednisone (or equivalent)
  - Local steroid injections
  - Stable hypothyroidism on replacement therapy
  - Stable diabetes mellitus on therapy (with or without insulin)
  - Sjogren's syndrome
  - 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 and is allowed
Current or prior use of immunosuppressive medication < 14 days prior to registration
- NOTE: The following are exceptions to this criterion:
  - Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intraarticular 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., premedication for computed tomography [CT] scans)
Uncontrolled intercurrent illness including, but not limited to:
- Ongoing or active infection requiring systemic therapy
- Interstitial lung disease or clinically significant pleural effusion
- Clinically significant ascites
- Serious, chronic gastrointestinal conditions associated with diarrhea (e.g., Crohn's disease or others)
- Known history of hepatitis B (i.e., known positive hepatitis B virus [HBV] surface antigen [HBsAg] reactive)
- Known active hepatitis C (i.e., positive for hepatitis C virus [HCV] ribonucleic acid [RNA] detected by polymerase chain reaction [PCR])
- Known active tuberculosis (TB)
- Symptomatic congestive heart failure
- Unstable angina pectoris
- Unstable cardiac arrhythmia or
- Psychiatric illness/social situations that would limit compliance with study requirements (e.g., substance abuse)
Co-morbid systemic illnesses or other severe concurrent disease or current evidence of any condition, therapy, or laboratory abnormality which, in the judgment of the investigator, would make the patient inappropriate for entry into this study or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens
Failure to recover to =< grade 1 (or baseline) from adverse events due to previously administered therapies or prior surgery
- Exceptions: Neuropathy, fatigue, and/or alopecia may be grade 1
Known active central nervous system (CNS) metastases
- NOTE: Patients with previously treated brain metastases may participate provided all of the following are true:
  - They are stable (without evidence of progression by imaging =< 4 weeks prior to registration and any neurologic symptoms have returned to baseline)
  - Have no evidence of new or enlarging brain metastases, and
  - Are not using steroids =< 14 days prior to registration
Known leptomeningeal disease
Hypersensitivity (>= grade 3) to pembrolizumab or any of its excipients
Previous serious adverse event (>= grade 3) attributed to prior checkpoint inhibitor therapy
History of (non-infectious) pneumonitis that required steroids or has current pneumonitis
History of grade >= 3 immune-related adverse event or any grade of immune-related neurologic or ocular adverse event while receiving immunotherapy
- Note: Patients who had endocrine adverse events =< grade 2 are allowed to enroll if they are stable on appropriate replacement therapy and asymptomatic
Other active malignancy < 2 years prior to registration
- EXCEPTIONS: Non-melanotic skin cancer, superficial bladder cancer, papillary thyroid cancer, or carcinoma-in-situ of the cervix or others curatively treated and now considered to be at less than 30% risk of relapse
History of allogenic tissue/solid organ transplant

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

45 participants in 1 patient group

Treatment (pembrolizumab, pemetrexed)

Experimental group

Description:

Patients receive pembrolizumab IV over 30 minutes and pemetrexed disodium IV over 10 minutes on day 1. Treatment with pembrolizumab repeats every 21 days for up to 35 cycles (2 years) in the absence of disease progression or unacceptable toxicity. Cycles of pemetrexed disodium repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients who had stable disease, partial response, or complete response after completion of 35 cycles of pembrolizumab, may continue pembrolizumab for an additional 17 cycles (1 year) in the absence of disease progression or unacceptable toxicity. Patients additionally undergo blood sample collection, CT, PET/CT or MRI and may also undergo PSMA PET on study.