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Clinical Trials/NCT04361331
NCT04361331
Completed
Phase 2

A Randomized, Open, Two-cohort Phase 2 Study of Toripalimab(PD1) Combined with Lenvatnib, or Gemox Chemotherapy Combined with Lenvatinib As First-line Therapy in Patients with Advanced or Unresectable Intrahepatic Cholangiocarcinoma

Shanghai Zhongshan Hospital2 sites in 1 country61 target enrollmentMarch 6, 2020

Overview

Phase
Phase 2
Intervention
Toripalimab combined with lenvatinib
Conditions
Cholangiocarcinoma, Intrahepatic
Sponsor
Shanghai Zhongshan Hospital
Enrollment
61
Locations
2
Primary Endpoint
Objective response rate
Status
Completed
Last Updated
last year

Overview

Brief Summary

We aim to explore the effects and safety of the two cohorts of toripalimab combined with lenvatinib or gemox combined with lenvatinib as first-line therapy in advanced or unresectable intrahepatic cholangiocarcinoma

Detailed Description

For advanced intrahepatic cholangiocarcinoma (ICC) that cannot be surgically removed or accompanied by metastasis, the NCCN guidelines (NCCN guidelines hepatobiliary cancer, 2019) recommend that the current treatment options are limited, mainly recommending gemcitabine combined with platinum-based antitumor drugs (cisplatin, oxaliplatin, etc.) chemotherapy as first-line treatment. Adding targeted drugs can enhance the anti-tumor effect. For those with microsatellite instability, it is recommended to add anti-PD1(programmed cell death protein 1) antibody. Gemox chemotherapy (oxaliplatin + gemcitabine) has been used in the treatment of advanced intrahepatic cholangiocarcinoma, but the efficacy is still not satisfactory. Lenvatinib is a small-molecule multi-kinase inhibitor that is currently approved for first-line treatment of advanced hepatocellular carcinoma. In recent years, the anti-PD1 antibody has shown efficacy in the treatment of primary liver cancer. Lenvatinib combined with anti-PD1 antibody or chemotherapy may have a better effect than single use for advanced ICC. At present, lenvatinib combined with anti-PD1 antibody or lenvatinib combined with Gemox in the first-line treatment of advanced ICC has not been reported.

Registry
clinicaltrials.gov
Start Date
March 6, 2020
End Date
September 1, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shanghai Zhongshan Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • The patient must be required to sign an informed consent;
  • Age 18-75 years old, male or female;
  • ECOG performance status score (PS score) 0 or 1 point;
  • Child-Pugh score A;
  • Intrahepatic cholangiocarcinoma confirmed by histopathology; agree to provide previously stored tumor tissue samples or fresh biopsy tumor lesions;
  • Unresectable ICC patients or postoperative ICC recurrence and metastasis, without systematic treatment within 6 months;
  • The functional indicators of vital organs meet the following requirements
  • Neutrophils ≥1.5 \* 109 / L; platelets ≥100 \* 109 / L; hemoglobin ≥9g / dl; serum albumin ≥3g/dl;
  • Thyroid stimulating hormone (TSH) ≤ 1 times the upper limit of normal value(ULN), T3 and T4 are in the normal range;
  • Bilirubin ≤ 1.5 times ULN; ALT and AST ≤ 3 times ULN;

Exclusion Criteria

  • Pathological diagnosis of hepatocellular carcinoma, mixed hepatocellular carcinoma and other non-cholangiocarcinoma malignancies;
  • Existing or concurrently suffering from other malignant tumors, except for fully treated non-melanoma skin cancer, cervical carcinoma in situ, and papillary thyroid cancer;
  • Have used lenvatinib or gemcitabine-based chemotherapy within 6 months or have used PD1 monoclonal antibody and PD-L1 monoclonal antibody treatment;
  • Severe cardiopulmonary and renal dysfunction;
  • Hypertension that is difficult to control by the drug (systolic blood pressure (BP) ≥140 mmHg and / or diastolic blood pressure ≥90 mmHg) (based on the average of ≥3 BP readings obtained from ≥2 measurements);
  • Abnormal blood coagulation function (PT\> 14s), have bleeding tendency or are receiving thrombolysis or anticoagulation treatment;
  • HBV DNA\> 2000 copies/ml and HCV RNA\>1000 after antiviral treatment;
  • Have a history of esophagogastric varices, with significant clinically significant bleeding symptoms or a clear tendency to appear within 3 months before enrollment;
  • Active infection requiring systemic treatment and treatment; patients with active tuberculosis infection within 1 year before enrollment; a history of active tuberculosis infection more than 1 year before enrollment, have not received regular anti-TB treatment or tuberculosis Still in the active period;
  • Human immunodeficiency virus (HIV, HIV1/2 antibody) positive;

Arms & Interventions

Toripalimab combined with lenvatinib

1. Toripalimab: 240 mg, intravenous infusion, Q3W; 2. Lenvatinib: 8mg (body weight \<60kg) or 12mg (body weight ≥60kg), qd;

Intervention: Toripalimab combined with lenvatinib

Lenvatinib combined with gemox

1. Lenvatinib: 8mg (body weight \<60kg) or 12mg (body weight ≥60kg), qd 2. Gemox chemotherapy D1: Oxaliplatin 85mg / m2, Gemcitabine 1g / m2 D8: Gemcitabine 1g / m2 Three weeks are a course, a total of 6-8 courses

Intervention: Lenvatinib combined with gemox

Outcomes

Primary Outcomes

Objective response rate

Time Frame: 12 months

Objective response rate of advanced and unresectable intrahepatic cholangiocarcinoma

Secondary Outcomes

  • Safety: the potential side effects(12 months)
  • Overall survival(12 months)
  • Progression free survival(12 months)

Study Sites (2)

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