Study of Induction PD-1 Blockade in Subjects With Locally Advanced Mismatch Repair Deficient Solid Tumors

Solid Tumor Clinical Trial

Official title:

A Phase II Study of Induction PD-1 Blockade in Subjects With Locally Advanced Mismatch Repair Deficient Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04165772
• Other study ID #: 19-288
• Status: Recruiting
• Phase: Phase 2
• Start date: December 11, 2019
• Est. completion date: November 30, 2026

Study information

• Verified date: April 2024
• Source: Memorial Sloan Kettering Cancer Center
• Contact: Andrea Cercek, MD
• Phone: 646-888-4189
• Email: cerceka[@]mskcc.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to find out whether the study drug, TSR-042, followed by standard chemoradiotherapy (the chemotherapy drug capecitabine + radiation therapy) and standard surgery is an effective treatment for advanced dMMR solid tumors. The study will also look at the safety of the study drug.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: November 30, 2026
• Est. primary completion date: November 30, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Willing and able to provide written informed consent for the trial.

• Be =18 years of age on the date of signing informed consent.

• ECOG performance status of 0 or 1.

• Histologically confirmed locally advanced solid tumor

• Solid tumors that in standard practice would be treated with neoadjuvant therapy

• No evidence of distant metastases.

• Radiologically measurable or clinically evaluable disease

• Tumor specimen that demonstrates mismatch repair deficiency by Immunohistochemistry or microsatellite instability as demonstrated by NGS or PCR.

• Negative pregnancy test done 72 hours prior to beginning treatment, for women of childbearing potential only. Subjects of childbearing potential must be willing to use an adequate method of contraception. Appropriate methods of birth control include abstinence, oral contraceptives, implantable hormonal contraceptives, or double barrier method (diaphragm plus condom). Contraception, for the course of the study starting with the first dose of study medication through 150 days after the last dose of study medication. Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject.

Nonchildbearing potential is defined as follows (by other than medical reasons):

• =45 years of age and has not had menses for >1 year

• Patients who have been amenorrhoeic for <2 years without history of a hysterectomy and oophorectomy must have a follicle stimulating hormone value in the postmenopausal range upon screening evaluation

• Post-hysterectomy, post-bilateral oophorectomy, or post-tubal ligation. Documented hysterectomy or oophorectomy must be confirmed with medical records of the actual procedure or confirmed by an ultrasound. Tubal ligation must be confirmed with medical records of the actual procedure, otherwise the patient must be willing to use 2 adequate barrier methods throughout the study.

• Participant receiving corticosteroids may continue if their dose is stable for least 4 weeks prior to initiating protocol therapy.

• Has QTcF = 450 msec, or = 480 msec for participants with bundle branch block.

• Demonstrate adequate organ function as defined below within 14 days of Cycle 1, Day 1, all screening labs should be performed within 14 days of treatment initiation.

• Hematological

• Absolute neutrophil count (ANC) =1,500 /mcL

• Platelets =100,000 / mcL

• Hemoglobin >9 g/dL or =5.6 mmol/L

• Renal

• Serum creatinine OR Measured or calculated(a) creatinine clearance (GFR can also be used in place of creatinine or CrCl) =1.5 × upper limit of normal (ULN) OR =60 mL/min for subject with creatinine levels > 1.5 × institutional ULN

• Hepatic

• Serum total bilirubin = 1.5 × ULN OR Direct bilirubin = ULN for subjects with total bilirubin levels > 1.5 ULN

• AST (SGOT) and ALT (SGPT) = 2.5 × ULN

• Coagulation

• International Normalized Ratio (INR) or Prothrombin Time (PT) Activated Partial Thromboplastin Time (aPTT) =1.5 × ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants =1.5 × ULN unless subject is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended (a) Creatinine clearance should be calculated per institutional standard.

Exclusion Criteria:

• Presence of metastatic or recurrent disease

• Prior radiation therapy, chemotherapy, or surgery for tumor

• For patients with colorectal primary -Tumor is causing symptomatic bowel obstruction (patients who have a temporary diverting ostomy are eligible).

• Cohort 1 Only: Other invasive malignancy = 5 years prior to registration. Exceptions are non-melanoma skin cancer that has undergone potentially curative therapy and in situ cervical carcinoma.

• Diagnosis of immunodeficiency or receiving systemic steroid therapy or any other form of non- physiologic dose immunosuppressive therapy within 7 days prior to first dose of trial treatment.

• Active autoimmune disease requiring systemic treatment within the past 2 years or documented history of clinically severe autoimmune disease, or a syndrome that requires systemic steroids or immunosuppressive agents at non-physiologic doses.

• Active infection requiring systemic therapy.

• Cohort 1 Only: Received prior therapy with an antibody or drug specifically targeting T- cell co-stimulation or checkpoint pathways.

• Experienced = Grade 3 immune-related AE with prior immunotherapy, except for non-clinically significant lab abnormalities.

• Other Anticancer or Experimental Therapy. No other experimental therapies (including chemotherapy, radiation, hormonal treatment, antibody therapy, immunotherapy, gene therapy, vaccine therapy, angiogenesis inhibitors, matrix metalloprotease inhibitors, thalidomide, anti-VEGF/Flk-1 monoclonal antibody or other experimental drugs) of any kind are permitted while the patient is receiving study treatment.

• Known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies)

• Known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA [qualitative] is detected).

• Women who are pregnant or breastfeeding, or men expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening visit through 150 days after the last dose of study medication.

• Concurrent medical or psychiatric condition or disease which, in the investigator's judgement, would make them inappropriate candidates for entry into the study. Examples include, but are not limited to, uncontrolled ventricular arrhythmia, recent (within 90 days) myocardial infarction, chronic obstructive pulmonary disease, uncontrolled major seizure disorder, unstable spinal cord compression, superior vena cava syndrome, or any psychiatric disorder that prohibits obtaining informed consent.

• Received a live vaccine within 30 days of planned start of study medication.

• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to enrollment.

• History of interstitial lung disease.

• Known hypersensitivity to TSR-042 components or excipients.

Related Conditions & MeSH terms

• Clinical Stage: Stage II (T3-4, N-)
• Neoplasms
• Rectal Adenocarcinoma
• Solid Tumor
• Solid Tumor, Adult
• Stage III (Any T, N+)

Intervention

Drug:
• TSR-042 or Dostarlimab
Patients will be given TSR-042/Dostarlimab at a dose of 500mg IV, over 30 minutes Q 3 weeks.
• capecitabine or 5-FU
Capecitabine 825mg/m2 BID concurrently with radiation per standard radiation guidelines. If patient is unable to tolerate oral medication, infusional 5-FU is an acceptable alternative.

Radiation:
• Intensity Modulated Radiation Therapy (IMRT)
The radiation dose is 5400 cGy to the tumor and surrounding nodes 4700 cGy to the pelvis, with an integrated boost to the primary tumor and involved nodes of receiving 5400cGy in 27fx.

Locations

Country	Name	City	State
United States	Lehigh Valley Health Network (Data Collection Only)	Allentown	Pennsylvania
United States	New York Cancer and Blood Specialists	Babylon	New York
United States	Memorial Sloan Kettering Basking Ridge - Limited Protocol Activities	Basking Ridge	New Jersey
United States	Memorial Sloan Kettering Commack - Limited Protocol Activities	Commack	New York
United States	Memorial Sloan Kettering Westchester - Limited Protocol Activities	Harrison	New York
United States	Hartford Healthcare (Data Collection)	Hartford	Connecticut
United States	Baptist Alliance MCI (Data Collection Only)	Miami	Florida
United States	Memorial Sloan Kettering Monmouth - Limited Protocol Activities	Middletown	New Jersey
United States	Memorial Sloan Kettering Bergen - Limited Protocol Activities	Montvale	New Jersey
United States	Memorial Sloan Kettering Cancer Center	New York	New York
United States	Memorial Sloan Kettering Nassau - Limited Protocol Activities	Uniondale	New York

Sponsors (2)

Lead Sponsor	Collaborator
Memorial Sloan Kettering Cancer Center	Tesaro, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pathologic complete response (pCR) or complete clinical response (cCR) at 12 months	To determine the pathologic complete response rate (pCR) or complete clinical response (cCR) rate at 12 months, after PD-1 blockade and with or without chemoradiation in subjects with mismatch repair deficient locally advanced adenocarcinoma.	12 months

External Links

•   Memorial Sloan Kettering Cancer Center