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Clinical Trial Summary

This study were designed to verify the better method of survival for metastatic ICC. Since the traditional method for metastatic ICC was GEMOX(first-line treatment from NCCN guideline), our previous study found similar results from FOLFOX (second-line treatment from NCCN guideline) compared with GEMOX. Our current study were conducted for further investigation to verify the better method for metastatic ICC.


Clinical Trial Description

ICC(Intrahepatic CholangioCarcinoma) patients with metastasis has a short survival time and poor prognosis after diagnosis. Treatment methods was few and far from satisfaction. The treatment recommended from NCCN guideline was GEMOX(Systemic Chemotheray) and clinical trials. Our previous study has demonstrate FOLFOX (Systemic Chemotheray based on Oxaliplatin#5- fluorouracil) has a similar survival and tumor response compared with GEMOX. Further study was needed to intensive confirmation of the result. We designed this study to demonstrate the hypothesis. Metastasis ICCs were recruited and screened by our criteria. All patients were treated with FOLFOX (Systemic Chemotheray based on Oxaliplatin#5-fluorouracil ), apatinib (one of tyrosine kinase inhibitors) plus sintilimab (one of PD-1 antibody). Our study were designed to verify the better method of survival for metastatic ICC. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04682249
Study type Interventional
Source Sun Yat-sen University
Contact
Status Withdrawn
Phase Phase 2
Start date December 1, 2020
Completion date February 1, 2021

See also
  Status Clinical Trial Phase
Withdrawn NCT04398927 - Systemic Chemotherapy Plus PD-1 for Metastasis ICC Phase 2
Not yet recruiting NCT06447454 - Combining Chemoradiotherapy With Sintilimab in First-Line ICC
Recruiting NCT04769908 - Systemic Chemotherapy, Lenvatinib Plus Sintilimab for ICC With Distant Metastasis Phase 2
Recruiting NCT03940378 - Treatment of Advanced Intrahepatic Cholangiocarcinoma Phase 3