Tislelizumab for the Treatment of Recurrent Mismatch Repair Deficient Endometrial Cancer

NCT ID: NCT04906382

Last Updated: 2025-02-13

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

EARLY_PHASE1

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-07-01

Study Completion Date

2022-09-01

Brief Summary

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This clinical trial evaluates the effect of tislelizumab in treating patients with mismatch repair deficient endometrial cancer that has come back (recurrent). Deoxyribonucleic acid (DNA) mismatch repair (MMR) is a system for recognizing and repairing DNA errors and damage. Mismatch repair deficient tumors (dMMR) may have difficulty repairing DNA mutations during replication that may affect tumor's response to therapy. Immunotherapy with monoclonal antibodies, such as tislelizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving tislelizumab may help treat patients with mismatch repair deficient endometrial cancer.

Detailed Description

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PRIMARY OBJECTIVE:

I. To evaluate the effect of tislelizumab (BGB-A317) on the diversity and dynamics of the T cell receptor repertoire in responders versus non-responders.

SECONDARY OBJECTIVES:

I. To evaluate the effect of tislelizumab on tumor mutational profiles between responders and non-responders.

II. To evaluate the effect of tislelizumab +/- carboplatin/paclitaxel on PD-1/PD-L1 expression and other immune markers in tumor biopsies between responders and non-responders.

III. To evaluate the safety and tolerability of tislelizumab +/- carboplatin/paclitaxel in patients with MMR deficient recurrent endometrial cancer.

EXPLORATORY OBJECTIVES:

I. To explore the effect of adding carboplatin/paclitaxel to tislelizumab on tumor mutational profiles.

II. To explore the effect of adding carboplatin/paclitaxel to tislelizumab (BGB-A317) on the diversity and dynamics of the T cell receptor repertoire.

III. To explore the objective antitumor activity (complete and partial response) of tislelizumab as measured by Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1 criteria.

IV. To explore the objective antitumor activity (complete and partial response) of tislelizumab/carboplatin/paclitaxel after single agent tislelizumab as measured by RECIST v1.1 criteria V. To explore the progression free survival in patients with mismatch repair deficiency (dMMR) recurrent endometrial cancer treated with tislelizumab +/- carboplatin/paclitaxel.

OUTLINE:

Patients receive tislelizumab intravenously (IV) over 30-60 minutes on day 1. Cycles repeat every 21 days for up to 24 months in the absence of disease progression or unacceptable toxicity. Beginning cycle 4, patients who are chemotherapy naive with progressive disease, stable disease, or partial response, also receive carboplatin IV and paclitaxel IV every 21 days per standard of care for 6-9 cycles at the discretion of the treating physician.

After completion of study treatment, patients are followed up at 30, 60, and 90 days, and then periodically thereafter.

Conditions

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Lynch Syndrome Recurrent Endometrial Carcinoma Recurrent Endometrial Clear Cell Adenocarcinoma Recurrent Uterine Corpus Carcinosarcoma Mismatch Repair Deficiency Recurrent Endometrial Cancer Metastatic Endometrial Cancer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Treatment (tislelizumab)

Chemo naïve patients receive tislelizumab IV over 30-60 minutes on day 1. Cycles repeat every 21 days for up to 24 months in the absence of disease progression or unacceptable toxicity. Beginning cycle 4, patients who are chemotherapy naive with progressive disease, stable disease, or partial response, also receive carboplatin IV and paclitaxel IV every 21 days per standard of care for 6-9 cycles at the discretion of the treating physician.

Patients who have received prior chemotherapy will receive single agent tislelizumab IV over 30-60 minutes on day 1. Cycles repeat every 21 days for up to 24 months in the absence of disease progression or unacceptable toxicity.

Group Type EXPERIMENTAL

Biopsy

Intervention Type PROCEDURE

Undergo biopsy

Carboplatin

Intervention Type DRUG

Given IV

Paclitaxel

Intervention Type DRUG

Given IV

Tislelizumab

Intervention Type BIOLOGICAL

Given IV

Interventions

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Biopsy

Undergo biopsy

Intervention Type PROCEDURE

Carboplatin

Given IV

Intervention Type DRUG

Paclitaxel

Given IV

Intervention Type DRUG

Tislelizumab

Given IV

Intervention Type BIOLOGICAL

Other Intervention Names

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BIOPSY_TYPE Bx Blastocarb Carboplat Carboplatin Hexal Carboplatino Carboplatinum Carbosin Carbosol Carbotec CBDCA Displata Ercar JM-8 Nealorin Novoplatinum Paraplatin Paraplatin AQ Paraplatine Platinwas Ribocarbo Anzatax Asotax Bristaxol Praxel Taxol Taxol Konzentrat BGB-A317

Eligibility Criteria

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Inclusion Criteria

* Able to provide written informed consent and can understand and agree to comply with the requirements of the study and the schedule of assessments
* Age \>= 18 years on the day of signing the informed consent form (or the legal age of consent in the jurisdiction in which the study is taking place)
* All patients with recurrent endometrial carcinoma, of any histology including clear cell, serous papillary carcinomas, and carcinosarcoma, whose disease is not amenable to definitive local therapy (including surgery and/or radiation therapy)
* Patients must have deficient mismatch repair as demonstrated by lack of expression of at least 1 mismatch repair protein by immunohistochemistry, or evidence of microsatellite instability (MSI) high, or evidence of Lynch syndrome
* The patient must have a lesion that is amenable to safe biopsy and the patient must agree to pre-and post-treatment biopsies
* Patients may have received radiation for the treatment of endometrial cancer
* Patient must have recovered from toxicity related to prior treatment to grade 2 or less
* At least two weeks should have elapsed since completion of prior chemotherapy or 5 half-lives (whichever is shorter), or 4 weeks from radiation involving the whole pelvis or over 50% of the spine
* At least 1 measurable lesion as defined per RECIST v1.1 that is amenable to biopsy
* Eastern Cooperative Oncology Group (ECOG) performance status =\< 1
* Absolute neutrophil count (ANC) \>= 1.5 x 10\^9/L (must not have required a blood transfusion or growth factor support =\< 14 days before sample collection at screening) (during screening or =\< 14 days prior to first dose of study drug)
* Platelets \>= 75 x 10\^9/L (must not have required a blood transfusion or growth factor support =\< 14 days before sample collection at screening) (during screening or =\< 14 days prior to first dose of study drug)
* Hemoglobin \>= 9.0 g/dL (must not have required a blood transfusion or growth factor support =\< 14 days before sample collection at screening) (during screening or =\< 14 days prior to first dose of study drug)
* Serum creatinine =\< 1.5 x ULN (upper limit of normal) or estimated glomerular filtration rate \>= 30 mL/min/1.73 m\^2 by Chronic Kidney Disease Epidemiology Collaboration equation (during screening or =\< 14 days prior to first dose of study drug)
* Serum total bilirubin =\< 1.5 x ULN (total bilirubin must be \< 3 x ULN for patients with Gilberts syndrome) (during screening or =\< 14 days prior to first dose of study drug)
* Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 x ULN (during screening or =\< 14 days prior to first dose of study drug)
* Females of childbearing potential must be willing to use a highly effective method of birth control for the duration of the study, and \>= 120 days after the last dose of tislelizumab, and have a negative urine or serum pregnancy test =\< 7 days of first dose of study drug

Exclusion Criteria

* Prior therapies targeting PD-1 or PD-L1
* Patients with symptomatic pleural effusion are excluded
* Active leptomeningeal disease or uncontrolled brain metastasis.

* Following treatment, these patients may then be eligible, provided all other criteria, including those for patients with a history of brain metastases, are met
* Active autoimmune diseases or history of autoimmune diseases that may relapse.
* Any active malignancy =\< 2 years before first dose of study drug except for the specific cancer under investigation in this study and any locally recurring cancer that has been treated curatively (e.g., resected basal or squamous cell skin cancer, superficial bladder cancer, carcinoma in situ of the cervix or breast)
* Any condition that required systemic treatment with either corticosteroids (\> 10 mg daily of prednisone or equivalent) or other immunosuppressive medication =\< 14 days before first dose of study drug
* With uncontrolled diabetes or laboratory test abnormalities \> grade 1 in potassium, sodium, or corrected calcium despite standard medical management or \>= grade 3 hypoalbuminemia =\< 14 days before first dose of study drug
* With history of interstitial lung disease, non-infectious pneumonitis or uncontrolled diseases including pulmonary fibrosis, acute lung diseases, etc.
* With severe chronic or active infections (including tuberculosis infection, etc.) requiring systemic antibacterial, antifungal or antiviral therapy within 14 days prior to randomization or first dose of study drugs
* Human immunodeficiency virus (HIV) testing is not required by protocol unless clinically indicated. Known HIV positive patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
* Known clinically significant liver disease, including active viral, alcoholic, or other hepatitis; and cirrhosis. For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated. Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load
* Any major surgical procedure requiring general anesthesia =\< 28 days before first dose of study drug
* Prior allogeneic stem cell transplantation or organ transplantation
* Any of the following cardiovascular risk factors:

* Cardiac chest pain, defined as moderate pain that limits instrumental activities of daily living, =\< 28 days before first dose of study drug
* Symptomatic pulmonary embolism =\< 28 days before first dose of study drug
* Any history of acute myocardial infarction =\< 6 months before first dose of study drug
* Any history of heart failure meeting New York Heart Association (NYHA) classification III or IV =\< 6 months before first dose of study drug
* Any event of ventricular arrhythmia \>= grade 2 in severity =\< 6 months before first dose of study drug
* Any history of cerebrovascular accident =\< 6 months before first dose of study drug
* Uncontrolled hypertension: systolic pressure \>= 160 mmHg or diastolic pressure \>= 100 mmHg despite anti-hypertension medications =\< 28 days before randomization or first dose of drug
* Any episode of syncope or seizure =\< 28 days before first dose of study drug
* A history of severe hypersensitivity reactions to tislelizumab
* Has received any chemotherapy, immunotherapy (e.g., interleukin, interferon, thymoxin) or any investigational therapies within 14 days or 5 half-lives (whichever is shorter) of the first study drug administration
* Has received any herbal medicine used to control cancer within 14 days of the first study drug administration
* Was administered a live vaccine =\< 4 weeks before first dose of study drug

* Note: Seasonal vaccines for influenza are generally inactivated vaccines and are allowed. Intranasal vaccines are live vaccines, and are not allowed
* Underlying medical conditions (including laboratory abnormalities) or alcohol or drug abuse or dependence that, will be unfavorable for the administration of study drug or affect the explanation of drug toxicity or AEs or result in insufficient or might impair compliance with study conduct
* Concurrent participation in another therapeutic clinical study
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Floor Backes, MD

OTHER

Sponsor Role lead

Responsible Party

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Floor Backes, MD

Principal Investigator

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Floor Backes, MD

Role: PRINCIPAL_INVESTIGATOR

Ohio State University Comprehensive Cancer Center

Locations

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Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Informed Consent Form

View Document

Related Links

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Other Identifiers

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NCI-2021-01367

Identifier Type: REGISTRY

Identifier Source: secondary_id

OSU-20173

Identifier Type: -

Identifier Source: org_study_id

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