- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04777162
Tislelizumab Plus Anlotinib for Immunotherapy Resistant Gastrointestinal Cancer
Efficacy and Safety of Tislelizumab Plus Anlotinib in PD-1/PD-L1 Resistant Metastatic Gastric or Colorectal Cancer: a Single Arm Phase II Clinical Trial
연구 개요
상세 설명
연구 유형
등록 (예상)
단계
- 2 단계
연락처 및 위치
연구 장소
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Beijing
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Beijing, Beijing, 중국, 100142
- 모병
- Beijing Cancer Hospital
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- ECOG scored 0 or 1, ≥18 years old, expected OS≥3 months;
- Histology confirmed unresectable or metastatic gastric/gastroesophageal junction adenocarcinoma or colorectal cancer;
- ≥1 evaluable lesion based on RECIST 1.1;
Patients received PD-1/PD-L1 in the last treatment line, and should meet following conditions:
i) there was no severe immune-related adverse events, ii) the duration between tumor progression and screening should be 3-12 weeks, iii) the best evaluation results should be PR or CR when receiving PD-1/PD-L1 treatment but progression was confirmed in the latest evaluation, iv) patients were diagnosed with special pathology subtypes, that are sensitive to immunotherapy, such as dMMR, MSI-H tumors, or gastric cancer with PD-L1 CPS≥10, PFS≥6 months in the last treatment line;
- laboratory test should meet following standard: i) HB≥90g/l, neutrophils≥1.5*10^9/L, plt≥100*10^9, ii) ALT and AST<2.5xULN (5ULN for liver metastatic patients), TBIL≤2×ULN, Cr≤1.5×ULN, and Ccr>50μmol/L iii) APTT, INR and PT≤1.5×ULN iv) LVEF≥50%
- for female participants, Hcg should be negative and both male and female participants should have contraception measures
- participants should be informed consent, and voluntary.
Exclusion Criteria:
- received anlotinib or other TKIs previously;
- allergic to other monoclonal antibody before the treatment;
- diagnosed with other malignancy in last five years (cured skin basal carcinoma, prostate cancer or cervical caner in situ were excluded)
- concurrent with other active autoimmune disease;
- any condition that require immune suppressor, such as cortisol (>10mg/d prednisone equally), CTX;
- conditions affect oral absorption (eg: dysphagia, intestinal obstruction; chronic diarrhea);
- uncontrolled pleural effusion, hydropericardium and seroperitoneum;
- brain metastasis;
- received other anti-tumor treatment in past 3 weeks, eg: surgery, radiotherapy, target therapy, immunotherapy, and traditional Chinese therapy (target therapy less than 5 half-life period, 5-Fu less than 14 days were excluded);
- concurrent with uncontrolled other diseases, i) hypertension (>150/90mmHg) ii) unstable angina pectoris, ≥ level 2 heart failure, arrhythmia within last 6 months; iii) clinical meaningful liver disease, eg: active HBV/HCV hepatitis; iv) HIV positive; v) uncontrolled diabetes; vi) urine protein ≥++ or 24h urine protein >1g;
- injected vaccine in past 4 weeks, or administrated with antibiotics;
- investigator assumed improper conditions, such as mental disease, family or society factors.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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실험적: tislelizumab+anlotinib
patients will be administrate with dual drugs, tislelizumab plus anlotinib.
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For included participants, tislelizumab would be administrated 200mg q3w iv.
Patients will be administrated with Anlotinib 12mg p.o. d1-d14 q3w.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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objective response rate
기간: 2 years
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the rate of patients reached PR or CR based on RECIST 1.1
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2 years
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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progression-free survival
기간: Up to 2 years
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the time from recruiting to death or progression
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Up to 2 years
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overall survival
기간: Up to 2 years
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the time from recruiting to death
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Up to 2 years
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (예상)
기본 완료 (예상)
연구 완료 (예상)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .