Pembrolizumab, Trastuzumab, HER2 Positive Gastric Cancer
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ClinicalTrials.gov Identifier: NCT02901301 |
Recruitment Status : Unknown
Verified April 2021 by Hyun Cheol Chung, Yonsei University.
Recruitment status was: Active, not recruiting
First Posted : September 15, 2016
Last Update Posted : April 6, 2021
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Gastric cancer is one of the major health problems worldwide, and one of the leading cause of death especially in Asia. Though the cytotoxic chemotherapy is the main treatment option, newer and molecularly targeted agents are recently incorporated to improve the survival outcome. Human epidermal growth factor receptor 2 (HER2, ErbB2) is a transmembrane tyrosine kinase receptor and is overexpressed or amplified in 10-20% of gastric cancer. Recently, Trastuzumab for Gastric Cancer (ToGA) study reported the clinical benefit of trastuzumab for HER2 positive gastric cancer patients. However, because the majority of patients develop intrinsic or acquired resistance within 1 year, elucidating the molecular mechanisms for trastuzumab resistance is warranted to improve the survival outcome of HER2 positive gastric cancer patients.
A growing body of preclinical and clinical evidence shows that the immune system contributes substantially to the therapeutic effects of "monoclonal antibody, trastuzumab" in solid tumors. Pembrolizumab is a potent and highly selective humanized monoclonal antibody designed to directly block the interaction between PD-1 and its ligands, PD-L1 and PD-L2.
Based on strong rationale in exploring the impact of combining trastuzumab with anti-PD-1 inhibitor in HER2 positive cancer, we suggest multicenter phase IB/II study to determine antitumor activity and safety of pembrolizumab in combination with standard treatment (trastuzumab, capecitabine, and cisplatin) in patients with HER2 positive gastric cancer.
Condition or disease | Intervention/treatment | Phase |
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Gastric Cancer | Drug: Pembrolizumab Drug: Trastuzumab Drug: Capecitabine Drug: Cisplatin | Phase 1 Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 41 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | A Phase Ib/II Study of First Line Pembrolizumab in Combination With Trastuzumab, Capecitabine, and Cisplatin in HER2 Positive Gastric Cancer |
Actual Study Start Date : | February 6, 2017 |
Actual Primary Completion Date : | October 31, 2020 |
Estimated Study Completion Date : | October 2021 |
Arm | Intervention/treatment |
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Experimental: 4 combination
pembrolizumab 200mg, IV, q3weeks, Day 1 trastuzumab 6mg/kg (8mg loading dose), IV, q3weeks, Day 1 capecitabine 1000mg/m2, PO, BID, Day 1-14 cisplatin 80mg/m2 (level 1), IV, q3weeks, Day 1
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Drug: Pembrolizumab
200mg, IV, q3weeks, Day 1 Drug: Trastuzumab 6mg/kg (8mg loading dose), IV, q3weeks, Day 1 Drug: Capecitabine 1000mg/m2, PO, BID, Day 1-14 Drug: Cisplatin 80mg/m2 (level 1), IV, q3weeks, Day 1 |
- The recommended dose of phase II [ Time Frame: 4 weeks ]
- The overall response rate using RECIST 1.1 [ Time Frame: 6 weeks ]
- Duration of response [ Time Frame: 1 year ]
- Time to response [ Time Frame: 6 weeks ]
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Ages Eligible for Study: | 19 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- HER2 positive advanced gastric cancer
- Be willing and able to provide written informed consent/assent for the trial.
- Be 19 years of age on day of signing informed consent.
- Have measurable disease based on RECIST 1.1.
- performance status of 0 or 1 on the Eastern Cooperative Oncology Group Performance Scale.
- Demonstrate adequate organ function
- Female subject of childbearing potential should have a negative urine or serum pregnancy or be willing to use birth control.
Exclusion Criteria:
- Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment.
- 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.
- Has a known history of active Bacillus Tuberculosis
- Hypersensitivity to pembrolizumab or any of its excipients.
- Has had a prior anti-cancer monoclonal antibody within 4 weeks prior to study Day 1 or who has not recovered from adverse events due to agents administered more than 4 weeks earlier.
- Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered from adverse events due to a previously administered agent.
- Has a known additional malignancy that is progressing or requires active treatment within 3 years.
- Has known active central nervous system metastases and/or carcinomatous meningitis.
- Has active autoimmune disease that has required systemic treatment in the past 2 years
- Has known history of, or any evidence of active, non-infectious pneumonitis.
- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.
- Has known active Hepatitis B or Hepatitis C
- Has received a live vaccine within 30 days of planned start of study therapy.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02901301
Korea, Republic of | |
Severance Hospital, Yonsei University Health System | |
Seoul, Korea, Republic of, 03722 |
Responsible Party: | Hyun Cheol Chung, Professor, Yonsei University |
ClinicalTrials.gov Identifier: | NCT02901301 |
Other Study ID Numbers: |
4-2016-0190 |
First Posted: | September 15, 2016 Key Record Dates |
Last Update Posted: | April 6, 2021 |
Last Verified: | April 2021 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Stomach Neoplasms Gastrointestinal Neoplasms Digestive System Neoplasms Neoplasms by Site Neoplasms Digestive System Diseases Gastrointestinal Diseases Stomach Diseases Pembrolizumab |
Capecitabine Trastuzumab Antineoplastic Agents Antineoplastic Agents, Immunological Immune Checkpoint Inhibitors Molecular Mechanisms of Pharmacological Action Antimetabolites, Antineoplastic Antimetabolites |