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Tislelizumab Plus Anlotinib for Immunotherapy Resistant Gastrointestinal Cancer

Primary Purpose

Gastric Cancer, Colo-rectal Cancer

Status
Unknown status
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Tislelizumab
Anlotinib
Sponsored by
Peking University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gastric Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Beijing Cancer HospitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

tislelizumab+anlotinib

Arm Description

patients will be administrate with dual drugs, tislelizumab plus anlotinib.

Outcomes

Primary Outcome Measures

objective response rate
the rate of patients reached PR or CR based on RECIST 1.1

Secondary Outcome Measures

progression-free survival
the time from recruiting to death or progression
overall survival
the time from recruiting to death

Full Information

First Posted
February 25, 2021
Last Updated
March 2, 2021
Sponsor
Peking University
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1. Study Identification

Unique Protocol Identification Number
NCT04777162
Brief Title
Tislelizumab Plus Anlotinib for Immunotherapy Resistant Gastrointestinal Cancer
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
March 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 2021 (Anticipated)
Primary Completion Date
January 2023 (Anticipated)
Study Completion Date
May 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Immunotherapy acquired resistance was observed in clinical practice. The investigators intended to add anlotinib to PD-1 inhibitors, hoping reverse the resistance.
Detailed Description
Anti-angiogenesis seems have positive effects on tumor immune microenvironment. the combination of PD-1/PD-L1 inhibitors and TKIs exhibited favorable efficacy on gastrointestinal malignancies. Here the investigators want to examine the efficacy and survival benefit from the combination therapy to PD-1 acquired resistance patients, which turns out to be critical issues in recent years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Cancer, Colo-rectal Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
tislelizumab+anlotinib
Arm Type
Experimental
Arm Description
patients will be administrate with dual drugs, tislelizumab plus anlotinib.
Intervention Type
Drug
Intervention Name(s)
Tislelizumab
Intervention Description
For included participants, tislelizumab would be administrated 200mg q3w iv.
Intervention Type
Drug
Intervention Name(s)
Anlotinib
Intervention Description
Patients will be administrated with Anlotinib 12mg p.o. d1-d14 q3w.
Primary Outcome Measure Information:
Title
objective response rate
Description
the rate of patients reached PR or CR based on RECIST 1.1
Time Frame
2 years
Secondary Outcome Measure Information:
Title
progression-free survival
Description
the time from recruiting to death or progression
Time Frame
Up to 2 years
Title
overall survival
Description
the time from recruiting to death
Time Frame
Up to 2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Facility Information:
Facility Name
Beijing Cancer Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100142
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shen Lin, Professor
Phone
010-88196561
Email
Linshenpku@163.com
First Name & Middle Initial & Last Name & Degree
Shen Lin, professor

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Tislelizumab Plus Anlotinib for Immunotherapy Resistant Gastrointestinal Cancer

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