Curative Surgery After 3-Drug Chemotherapy Regimen Extends Survival in Patients with Locally Advanced CCA

Web Exclusives — March 22, 2022

The current standard first-line therapy for advanced cholangiocarcinoma (CCA) is the chemotherapy combination of gemcitabine plus cisplatin; only about 40% of patients are amenable to surgery. The objective of this retrospective study was to evaluate the clinical feasibility of the triplet chemotherapy regimen of nab-paclitaxel plus gemcitabine and cisplatin as first-line therapy in patients with locally advanced CCA.

The results were presented by Sung Hoon Choi, BA, CHA University, Seongnam-Si, South Korea, at the 2022 ASCO GI Cancers Symposium.

This retrospective analysis was based on a chart review of patients with locally advanced CCA who received the triplet regimen of nab-paclitaxel plus gemcitabine and cisplatin between October 2019 and December 2020. The feasibility of resection after induction chemotherapy was evaluated by a multidisciplinary team.

The investigators assessed the perioperative outcomes and pathologic results of surgical resection after induction chemotherapy.

Of the 85 patients in this study, 46 (54.1%) patients had measurable lesions, 24 patients had a diagnosis of intrahepatic CCA, 37 had extrahepatic/perihilar CCA, and 24 had extrahepatic/distal CCA.

In the overall population, after induction chemotherapy, the objective response rate in patients with measurable disease was 51.1%, and the disease control rate was 85.1%. Of the 85 patients in the study, 52 (61.2%) patients had resectable tumors.

Among all the patients in this study, 48 (56.5%) patients underwent subsequent curative surgery. In the subset of patients who underwent surgery, 6 (12.5%) achieved complete remissions (all in extrahepatic CCA); R0 resection was achieved in 43 (89.6%) patients.

The overall survival (OS) rates were significantly higher among patients who had induction chemotherapy followed by surgery compared with those who received chemotherapy alone, with a 12-month OS of 94.9% versus 72.6%, respectively (P = .009).

These data support the clinical feasibility of induction chemotherapy with nab-paclitaxel plus gemcitabine and cisplatin before curative surgery in patients with locally advanced CCA.

Source

Choi SH, Kang B, Cheon J, et al. Clinical feasibility of curative surgery after nab-paclitaxel plus gemcitabine-cisplatin chemotherapy in patients with locally advanced cholangiocarcinoma. Abstract 387.

Related Items

Tasurgratinib for Patients With FGFR2 Gene Fusion–Positive CCA: A Phase 2 Study
March 2024, Vol 5, No 1
Junji Furuse, MD, PhD, presented the results of a phase 2 study of tasurgratinib efficacy on patients with FGFR2 fusion-positive cholangiocarcinoma following gene fusion status confirmation by fluorescence in situ hybridization.
Safety and Efficacy of Telotristat Ethyl Plus First-Line Chemotherapy in Patients With Advanced BTC: A Phase 2, Open-Label Study
March 2024, Vol 5, No 1
Richard Kim, MD, presented the results of a phase 2, open-label study of patients who underwent telotristat ethyl plus first-line chemotherapy for the treatment of advanced biliary tract cancer.
Efficacy and Safety of Brigimadlin (BI 907828) in Patients With Advanced BTC: Data From 2 Phase 1a/1b Dose-Escalation/Expansion Trials
March 2024, Vol 5, No 1
Teresa Macarulla, MD, PhD, presented the results of 2 phase 1a/1b dose-escalation/expansion trials, studies that measured the efficacy and safety of brigimadlin in patients with advanced biliary tract cancer.
COMPANION-002: A Phase 2/3 Randomized Study Design of CTX-009 Combination in Second-Line BTC
March 2024, Vol 5, No 1
A recombinant bispecific antibody, CTX-009, is discussed regarding its role in an ongoing phase 2/3 open-label, randomized, controlled study—a study being conducted to measure the efficacy of CTX-009 in previously treated, advanced, or metastatic biliary tract cancer.
A Phase 2 Clinical Trial of Anlotinib Plus TQB2450 (PD-L1 Blockade) Plus Nab-Paclitaxel and Cisplatin as First-Line Treatment for Advanced BTC
March 2024, Vol 5, No 1
Cholangiocarcinoma experts presented the preliminary results of a phase 2 clinical trial regarding anlotinib plus TQB2450, nab-paclitaxel, and cisplatin—a study conducted for the treatment of advanced biliary tract cancer.
Preliminary Results of a Real-World Study of the Safety and Efficacy of Surufatinib in BTC
March 2024, Vol 5, No 1
Zongli Zhang, MD, PhD, presented the preliminary results of an ongoing single-arm, multicenter, open-label, real-world study analyzing the efficacy and safety of surufatinib as a second-line treatment option for patients with biliary tract cancer.
Genomic Factors Indicating Sensitivity to IO and Chemotherapy in CCA
March 2024, Vol 5, No 1
Riya Jayesh Patel, MD, presented how the impact of transcriptomic signatures related to chemotherapy and immunotherapy sensitivity in the cholangiocarcinoma (CCA) cohort of The Cancer Genome Atlas could serve as evidence supporting the effectiveness of metabolism-targeted therapies in overcoming CCA therapeutic resistance.
Examining Real-World Testing, Treatment Patterns, and Outcomes After Liquid Biopsy in aCCA
March 2024, Vol 5, No 1
Amit Mahipal, MD, presented results from a real-world data study examining the rates of molecular alterations detected using circulating tumor DNA (ctDNA) for patients receiving ivosidenib following circulating tumor ctDNA-detected IDH1 mutations.
A Phase 2 Primary Analysis of Tislelizumab Plus Lenvatinib and GEMOX as Conversion Therapy in Potentially Resectable Locally Advanced BTC (ZSAB-TransGOLP)
March 2024, Vol 5, No 1
Jia Fan, PhD, presented results from a phase 2 trial that investigated the efficacy and safety of lenvatinib and a programmed cell death protein-1 antibody as conversion therapy for the treatment of potentially resectable and locally advanced biliary tract cancer.
Role of CD27 Agonist in Combination With PD-L1 and MEK Inhibition on Antitumor Effect and CD8+ T Cells: Expanding Immunotherapy Options in CCA
March 2024, Vol 5, No 1
Frances J. Bennett, MD, presented the results of a phase 2 trial that tested the antitumor effect of dual programmed death-ligand 1 plus mitogen-activated protein kinase inhibition in patients with advanced biliary tract cancer.

Subscribe Today!

To sign up for our newsletter or print publications, please enter your contact information below.

I'd like to receive: