Safety and Feasibility of PD-1 Blockade in the Treatment of dMMR or MSI-H Rectal Cancer

NCT ID: NCT04357587

Last Updated: 2024-05-29

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 6 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-08-06
• Study Completion Date: 2023-09-25

Brief Summary

Colorectal cancer is the third most common cancer worldwide and the second leading cause of cancer mortality in the United States. The current standard of care (SOC) for locally advanced rectal cancer includes neoadjuvant chemotherapy and radiation followed by surgery. However, great variability exists in patient's response to neoadjuvant chemoradiotherapy with only about 20-25% of patients achieving a complete response while other patients achieve a partial or no treatment response. The purpose of this study is to test the investigational agent, Pembrolizumab, in combination with SOC radiation and Capecitabine (or 5-Fluorouacil) in treatment of patients with mismatch repair deficient locally advanced rectal cancer.

Detailed Description

This study investigates the safety, tolerability, and feasibility of Pembrolizumab, an immunotherapy agent, in combination with SOC radiation and Capecitabine (or 5-Fluorouacil) in treatment of patients with mismatch repair deficient locally advanced rectal cancer. Pembrolizumab is an investigational (experimental) drug that works by enhancing the functional activity of the target lymphocytes (immune cells) to facilitate tumor regression and ultimately immune rejection. Pembrolizumab in combination with radiation and Capcitabine (or 5-Fluorouacil) is experimental because it is not approved by the Food and Drug Administration (FDA) for this specific indication.

The primary objective of this study is to determine the safety, tolerability and feasibility of neoadjuvant pembrolizumab in combination with capectiabine (or 5-Fluorouracil ) in the treatment of patients with MMR-d locally advanced rectal cancer

The secondary objective of this study is to determine the treatment response in MMR-d rectal cancer patients treated with neoadjuvant chemoradiotherapy and Pembrolizumab.

Conditions

Rectal Neoplasms

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Pembrolizumab

Experimental pembrolizumab and SOC external beam radiation and capecitabine

Group Type: EXPERIMENTAL

Pembrolizumab

Intervention Type: DRUG

200 mg intravenously (IV) on days 1, 22, and 43

External beam radiation

Intervention Type: RADIATION

Daily fractions of 200 cGy, 5 days a week for the first 5 weeks of the study, excluding weekends

Capecitabine

Intervention Type: DRUG

825 mg/m2 orally twice a day on days where radiation therapy is given

Interventions

Pembrolizumab

200 mg intravenously (IV) on days 1, 22, and 43

Intervention Type: DRUG

External beam radiation

Daily fractions of 200 cGy, 5 days a week for the first 5 weeks of the study, excluding weekends

Intervention Type: RADIATION

Capecitabine

825 mg/m2 orally twice a day on days where radiation therapy is given

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Must have confirmed rectal adenocarcinoma Defined as, MRI based clinical stage II (T3-4, N0), stage III (T1-4, N+), or oligometastatic locally advanced stage IV that are candidates for curative surgery
• Tumor location at and/or below the peritoneal reflection on MRI.
• Review and discussion at multidisciplinary tumor board with consensus recommendation for neoadjuvant chemoradiation followed by curative-intent surgery. Documented in EPIC tumor board.
• MMR-deficiency confirmed on immunohistochemistry or MSI status confirmed by PCR.
• ECOG Performance status 0-1
• Life expectancy of ≥ 6 months, in the opinion of and as documented by the treating physician.
• Must have normal organ and marrow function as defined below:

• Hemoglobin ≥ 8.0 g/dL
• Leukocytes ≥ 3,000/k/uL
• Absolute neutrophil count ≥ 1,500/k/uL
• Platelet count ≥ 100,000/k/uL
• Total bilirubin ≤ 1.3 x institutional upper limit of normal (ULN)
• AST (SGOT) ≤ 2.5 x institutional upper limit of normal (ULN)
• ALT (SGPT) ≤ 2.5 x institutional upper limit of normal (ULN)
• Must have the ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

• Prior treatment for rectal cancer or prior radiation for other diagnoses to the expected rectal cancer treatment fields.
• Participants receiving any other investigational agents.
• Unresectable primary tumor or unresectable metastatic disease as determined by imaging.
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to Pembrolizumab or other agents used in this study.
• Participants with uncontrolled intercurrent illness including, but not limited to:

• Ongoing or active infection
• Known history of pneumonitis
• Symptomatic congestive heart failure
• Unstable angina pectoris
• Cardiac arrhythmia
• Psychiatric illness/social situations that would limit compliance with study requirements.
• Pregnant or lactating females.
• Female participants who:

• Are postmenopausal for at least 1 year before the screening visit, OR
• Are surgically sterile, OR
• Agree to practice true abstinence from heterosexual contact or agree to use effective contraception without interruption during the study therapy and 90 days after the last dose
• Male participants who: Are surgically sterile, OR Agree to practice true abstinence from heterosexual contact or agree to use effective contraception without interruption during the study therapy and 90 days after the last dose
• HIV-positive participants on combination antiretroviral therapy, participants with active Hepatitis B or C, active tuberculosis, or administration of live vaccine within 30 days of planned start of study therapy will be excluded.
• Participants with a diagnosis of immunodeficiency, active autoimmune disease (including inflammatory bowel disease) or those receiving immunosuppressive therapy within 7 days (other than Prednisone ≤ 5mg daily) prior to the planned start of study treatment will be excluded.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Case Comprehensive Cancer Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David Liska, MD

Role: PRINCIPAL_INVESTIGATOR

Cleveland Clinic, Case Comprehensive Cancer Center

Locations

Cleveland Clinic, Case Comprehensive Cancer Center

Cleveland, Ohio, United States

Countries

United States

Other Identifiers

CASE1220

Identifier Type: -

Identifier Source: org_study_id