Tislelizumab With Anlotinib and Chemotherapy for Second-line Treatment of Pancreatic Cancer

Xi'an Jiaotong University

Status and phase

Enrolling

Phase 2

Conditions

Pancreatic Neoplasms

Treatments

Drug: Tislelizumab

Study type

Interventional

Funder types

Other

Identifiers

NCT05681390

XJTU1AF2020LSL-010X1

Details and patient eligibility

About

This is a prospective, one-arm, phase II clinical study of Tislelizumab Combined With Anlotinib and Chemotherapy for Second-line Treatment of Advanced or Metastatic Pancreatic Cancer

Full description

This is a single-arm, open-label, clinical trial of tislelizumab in combination with anlotinib and investigator-selected chemotherapy for second-line treatment of patients with advanced or metastatic pancreatic cancer. Patients with histopathologically or cytologically confirmed unresectable, recurrent or metastatic pancreatic cancer are planned to be recruited. Systemic medical antineoplastic therapy previously treated with first-line chemotherapy, meeting the inclusion and exclusion criteria of this study, and giving tislelizumab and anlotinib in combination with investigator 's choice of second-line chemotherapy regimen

Enrollment

30 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Advanced or metastatic pancreatic adenocarcinoma diagnosed by pathology;
Previously received a standard first-line chemotherapy regimen of pancreatic cancer
Age ≥ 18 and≤ 75 years old;
Expected survival ≥ 3 months;
ECOG score 0-1;
Child-Pugh score < 8;
There is at least one measurable tumor lesion: the long diameter is ≥10 mm, and the short diameter of lymph nodes is ≥15 mm;
The results of liver and kidney function and blood routine examination within 1 week before enrollment meet the following conditions:

Neutrophils (ANC) ≥ 1.5×109/L, platelets (PLT) ≥ 80×109/L, hemoglobin (HGB) ≥ 80g/L; Serum creatinine (Cr) ≤ 1.5 × upper limit of normal value; total bilirubin (TBIL) ≤ 2.5 × upper limit of normal value, Alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) ≤2.5× upper limit of normal value;

The patient voluntarily participated in this study and signed the informed consent form.

Exclusion criteria

Received other immunotherapy previously(including immune checkpoint inhibitor PD-1/PDL1 and other immune checkpoint inhibitors) and/or anti-angiogenic drugs (including anti-VEGFR monoclonal antibody and anti-angiogenic small molecule kinase inhibitors) ; Known to be severely allergic to the drugs used in the study of tislelizumab and anlotinib;
Patients with obstructive jaundice who cannot reach TBIL ≤ 2.5 times the upper limit of normal value after surgical intervention;
Patients with biliary obstruction that may occur or worsen within 4 to 6 weeks;
Obvious blood coagulation disorder, active bleeding and bleeding tendency;
There is a history of other malignant tumors within 5 years (adequately treated skin basal cell carcinoma, cervical in situ);
Interstitial pneumonia or pulmonary fibrosis;
Uncontrollable pleural effusion or ascites;
Severe uncontrolled medical diseases, acute infections, recent history of myocardial infarction (within 3 months);
During pregnancy or breastfeeding, and those who refuse to take appropriate contraceptive measures during the test;
Patients judged by the investigator to be inappropriate to participate in this study.