Gastric or Gastroesophageal Junction Adenocarcinoma
Conditions
Interventions
Sponsors
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Be willing and able to provide written informed consent/assent for the trial. The subject may also provide consent for Future Biomedical Research. However, the subject may participate in the main trial without participating in Future Biomedical Research. 2. Be 18 years of age on day of signing informed consent (or acceptable age according to local regulations, whichever is older). 3. Have histologically or cytologically-confirmed diagnosis of gastric or GEJ adenocarcinoma. 4. Have metastatic disease or locally advanced, unresectable disease. 5. Have measurable disease as defined by RECIST 1.1 as determined by investigator. Tumor lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions. 6. Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group (ECOG) Performance Scale. 7. Has experienced documented objective radiographic or clinical disease progression during or after first-line therapy containing any platinum/fluoropyrimidine doublet. i. To be considered as second-line, the subject needs to have the documentation of disease progression on first-line treatment. The disease progression can be confirmed by CT scan or by clinical evidence (such as cytology report from newly developed ascites and plural effusion). ii. Any new or worsening malignant effusion (documented by ultrasound) may be confirmed by pathologic criteria (histology and/or cytology) if appropriate. iii. A subject experiencing clinical disease progression during or within 6 months following the last dose of adjuvant therapy will be eligible for enrollment provided they received a platinum/fluoropyrimidine doublet as required. iv. To be eligible, the subject is required to have received at least one dose of platinum and fluoropyrimidine therapy. 8. Be willing to provide tissue for PD-L1 biomarker analysis from a newly obtained core, excisional, or endoscopic biopsy and, based on the adequacy of the tissue sample quality for assessment of PD-L1 status, received permission for enrollment from the Core Lab. Repeat samples may be required if adequate tissue is not provided. Formalin-fixed, paraffin-embedded (FFPE) block specimens are preferred to slides. i. Newly-obtained is defined as a specimen obtained up to 6 weeks (42 days) prior to initiation of treatment on Day 1. No additional anti-cancer treatment should be administered after tumor sample is obtained. Subjects for whom newly-obtained samples cannot be provided (e.g. inaccessible or subject safety concern) may submit an archived specimen only upon agreement from the Sponsor. ii. Collection of an archived tissue sample will also be requested (where available) to support evaluation of the clinical utility of PD-L1 assessment in newly obtained vs. archived tissue samples; however, a subject will not be precluded from participating in the study if an archived tissue sample is not available for collection or is otherwise insufficient for analysis. iii. The following inclusion criteria is only applicable after the results from the interim futility analysis: If at the time of enrollment, only subjects with PD-L1 positive expression are being enrolled, then subject must have a confirmed PD-L1 positive expression sample per central laboratory evaluation to be eligible for enrollment. 9. Subjects with HER-2/neu negative tumors are eligible. For subjects with HER2/neu positive tumors or have an unknown tumor
Exclusion criteria
Exclusion criteria: 1. Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigation device within 4 weeks of the first dose of treatment. 2. Has squamous cell or undifferentiated gastric cancer. 3. Has active autoimmune disease that has required systemic treatment in past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). 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. 4. Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment. The use of physiologic doses of corticosteroids may be approved after consultation with the Sponsor. 5. Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study Day 1 or who has not recovered (i.e., = Grade 1 or at baseline) from adverse events due to agents administered more than 4 weeks earlier. 6. Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered (i.e., = Grade 1 or at baseline) from adverse events due to a previously administered agent. Note: Subjects with = Grade 2 neuropathy or = Grade 2 alopecia are an exception to this criterion and may qualify for the study. a. If subject received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy. 7. Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or in situ cervical cancer that has undergone potentially curative therapy. 8. Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Subjects with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging for at least four weeks prior to the first dose of trial treatment and any neurologic symptoms have returned to baseline), have no evidence of new or enlarging brain metastases, and are not using steroids for at least 7 days prior to trial treatment. This exception does not include carcinomatous meningitis which is excluded regardless of clinical stability. 9. Has history or evidence of interstitial lung disease or active non-infectious pneumonitis. 10. Has an active infection requiring systemic therapy. 11. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject’s participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator. 12. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial. 13. Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 120 days after the last dose of trial treatment. 14. Has received prior immunotherapy including anti-PD-1, anti-PD-L1, or anti-PD-L2 agent, or if the subject has previously participate
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Main Objective: 1. To evaluate Progression Free Survival (PFS) per RECIST 1.1 by blinded central radiologists’ review of subjects with PD-L1 positive expression with advanced gastric or GEJ adenocarcinoma who have progressed on one previous line of therapy, when treated with pembrolizumab compared to paclitaxel. 2. To evaluate Overall Survival (OS) of subjects with PD-L1 positive expression with advanced gastric or GEJ adenocarcinoma who have progressed on one previous line of therapy, when treated with pembrolizumab compared to paclitaxel. ;Secondary Objective: 1. To evaluate PFS per RECIST 1.1 by blinded central radiologists’ review of all subjects who have progressed on 1 previous line of therapy.. 2. To evaluate OS of all subjects with advanced gastric or GEJ adenocarcinoma who have progressed on one previous line of therapy.. 3. To evaluate PFS per RECIST 1.1 by investigator assessment and PFS per irRECIST by blinded central radiologists’ review, among subjects with PD-L1 positive expression and all subjects.. 4. To evaluate the Time to Progression (TTP), Overall Response Rate (ORR), and Duration of Response (DOR), per RECIST 1.1 by blinded central radiologists’ review and per RECIST 1.1 by investigator assessment among subjects with PD-L1 positive expression and all subjects.. 5. To evaluate the safety and tolerability profile of pembrolizumab in subjects with PD-L1 positive expression and all subjects. ;Primary end point(s): This trial will use progression free survival (PFS) and overall survival (OS) as a dual primary endpoint. The endpoint of OS is the standard for demonstrating superiority of antineoplastic therapy in clinical studies in the area of oncology. Additionally, PFS is an acceptable scientific endpoint for a randomized Phase III trial to demonstrate superiority of a new antineoplastic therapy. RECIST 1.1 will be used to determine progression, as this methodology is uniformly accepted by regulatory authorities. Because the treatment ass | — |
Secondary
| Measure | Time frame |
|---|---|
| Timepoint(s) of evaluation of this end point: Response will be assessed throughout the entire study. The first protocol defined response assessment is scheduled for Week 6, with additional assessments following at 6 week intervals. Safety will be assessed at all study visits conducted either in person or by phone. ;Secondary end point(s): PFS – RECIST 1.1 by investigator assessment, and irRECIST by blinded central radiologists’ review. Progression-free-survival (PFS) is defined as the time from randomization to the first documented disease progression or death due to any cause, whichever occurs first. Time to Progression (TTP) – RECIST 1.1 by blinded central radiologists’ review, and RECIST 1.1 by investigator assessment. Time to Progression (TTP) is defined as the time from randomization to the first documented disease progression. If there is no documented disease progression, TTP is censored at last tumor assessment date. Overall Response Rate (ORR) – RECIST 1.1 by blinded central radiologists’ review, and RECIST 1.1 by investigator assessment. Overall response rate is defined as the proportion of the subjects in the analysis population who have a complete response (CR) or partial response (PR). Duration of Response (DOR) – RECIST 1.1 by blinded central radiologists’ review, and RECIST 1.1 by investigator assessment For subjects who demonstrated CR or PR, response duration is defined as the time from first documented evidence of CR or PR until disease progression or death due to any cause, whichever occurs first. Response duration for subjects who have not progressed or died at the time of analysis will be censored a t the date of their last tumor assessment. The primary safety objective of this trial is to characterize the safety and tolerability of pembrolizumab in subjects with metastatic gastric cancer. The primary safety analysis will be based on subjects who experienced toxicities as defined by CTCAE criteria. Safety will be assessed by quantifying | — |
Countries
Argentina, Australia, Belgium, Brazil, Canada, Chile, Colombia, Denmark, Estonia, Finland, France, Germany, Guatemala, Hong Kong, Ireland, Israel, Italy, Japan, Korea, Republic of, Lithuania, Malaysia, Mexico, New Zealand, Norway, Philippines, Poland, Puerto Rico, Russian Federation, Singapore, South Africa, Spain, Taiwan, Turkey, United Kingdom, United States
Contacts
Public ContactGlobal Clinical Trials Operations
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
Outcome results
None listed