Clinical trial · Interventional
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
NCT04777162CI-TRIAL-00050457unknownPhase 2ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Immunotherapy acquired resistance was observed in clinical practice. The investigators intended to add anlotinib to PD-1 inhibitors, hoping reverse the resistance.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colo-rectal Cancer | — | UNRESOLVED | — |
| Gastric Cancer | Malignant Gastric Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Anlotinib | Drug | — | UNRESOLVED |
| Tislelizumab | Drug | Tislelizumab | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- tislelizumab+anlotinib
- description
- patients will be administrate with dual drugs, tislelizumab plus anlotinib.
- interventionNames
- Drug: Tislelizumab
- Drug: Anlotinib
Primary outcomes (1)
- measure
- objective response rate
- timeFrame
- 2 years
- description
- the rate of patients reached PR or CR based on RECIST 1.1
Secondary outcomes (2)
- measure
- progression-free survival
- timeFrame
- Up to 2 years
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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.
References
Publications (0)
Data not yet available
No reference posted for this study.