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Efficacy and Safety of Pembrolizumab in Patients with Refractory Advanced Biliary Tract Cancer: Tumor Proportion Score as a Potential Biomarker for Response

Authors :
Shin Hwang
Hee-Sang Hwang
Seung-Mo Hong
Dae Wook Hwang
Do Hyun Park
Ki-Hun Kim
Baek-Yeol Ryoo
Kyu-Pyo Kim
Jae Ho Jeong
Tae Jun Song
Changhoon Yoo
Dongwook Oh
Junho Kang
Sang Soo Lee
Song Cheol Kim
Jin-Hong Park
Source :
Cancer Research and Treatment : Official Journal of Korean Cancer Association
Publication Year :
2020
Publisher :
Korean Cancer Association, 2020.

Abstract

Purpose The current standard chemotherapy for advanced biliary tract cancer (BTC) has limited benefit, and novel therapies need to be investigated. Materials and MethodsIn this prospective cohort study, programmed death ligand-1 (PD-L1)–positive BTC patients who progressed on first-line gemcitabine plus cisplatin were enrolled. Pembrolizumab 200 mg was administered intravenously every 3 weeks. ResultsBetween May 2018 and February 2019, 40 patients were enrolled. Pembrolizumab was given as second-line (47.5%) or ≥ third-line therapy (52.5%). The objective response rate was 10% and 12.5% by Response Evaluation Criteria in Solid Tumor (RECIST) v1.1 and immune- modified RECIST (imRECIST) and median duration of response was 6.3 months. Among patients with progressive disease as best response, one patient (1/20, 5.0%) achieved complete response subsequently. The median progression-free survival (PFS) and overall survival (OS) were 1.5 months (95% confidence interval [CI], 0.0 to 3.0) and 4.3 months (95% CI, 3.5 to 5.1), respectively, and objective response per imRECIST was significantly associated with PFS (p < 0.001) and OS (p=0.001). Tumor proportion score ≥ 50% was significantly associated with higher response rates including the response after pseudoprogression (vs. < 50%; 37.5% vs. 6.5%; p=0.049). Conclusion Pembrolizumab showed modest anti-tumor activity in heavily pretreated PD-L1–positive BTC patients. In patients who showed objective response, durable response could be achieved.

Details

ISSN :
20059256 and 15982998
Volume :
52
Database :
OpenAIRE
Journal :
Cancer Research and Treatment
Accession number :
edsair.doi.dedup.....004d290cfb9a58293e19f877fa183039