Advanced Intrahepatic Cholangiocarcinoma: Post Hoc Analysis of the ABC-01, -02, and -03 Clinical Trials.


Journal

Journal of the National Cancer Institute
ISSN: 1460-2105
Titre abrégé: J Natl Cancer Inst
Pays: United States
ID NLM: 7503089

Informations de publication

Date de publication:
01 02 2020
Historique:
received: 12 12 2018
revised: 26 03 2019
accepted: 19 03 2019
pubmed: 12 5 2019
medline: 11 8 2020
entrez: 12 5 2019
Statut: ppublish

Résumé

The incidence of intrahepatic cholangiocarcinoma (iCCA) is increasing. The aim of the study was to provide reference survival data for patients with advanced iCCA treated with first-line cisplatin-gemcitabine chemotherapy (current standard of care). Individual data from patients with iCCA recruited into the prospective, random assignment Advanced Biliary Tract Cancer (ABC)-01, -02, and -03 studies were retrieved. The prevalence and survival of liver-only iCCA was also assessed. Survival analysis was performed using univariate and multivariable Cox regression. All statistical tests were two-sided. Of 534 patients recruited into the ABC-01, -02, and -03 studies, 109 (20.4%) had iCCA. Most patients (n = 86, 78.9%) had metastatic disease at the time of recruitment; 52 patients (47.7%) had liver-only disease. Following random assignment, 66 (60.6%) iCCA patients received cisplatin and gemcitabine. The median progression-free and overall survival (OS) were 8.4 months (95% confidence interval [CI] = 5.9 to 8.9 months) and 15.4 months (95% CI = 11.1 to 17.9 months), respectively. Of these 66 patients, 34 patients (51.5%) had liver-only disease. Following chemotherapy, 30 (45.5%) and 21 (31.8%) were progression-free at 3 and 6 months from chemotherapy commencement, respectively. The median OS for patients with liver-only iCCA at diagnosis and after 3 and 6 months of chemotherapy was 16.7 months (95% CI = 8.7 to 20.2 months), 17.9 months (95% CI = 11.7 to 20.9 months), and 18.9 months (95% CI = 16.7 to 25.9 months), respectively. Multivariable analysis confirmed that iCCA had a longer OS compared with other non-iCCA biliary tract cancers (hazard ratio = 0.58, 95% CI = 0.35 to 0.95, P value = .03); liver-only iCCA patients also showed longer OS even though findings did not reach statistical significance (hazard ratio = 0.65, 95% CI = 0.36 to 1.19, P value = .16). Patients diagnosed with advanced iCCA have a better OS compared with other biliary tract cancers; a similar trend was identified for patients diagnosed with liver-only iCCA. These findings are to be considered for future clinical trial design.

Sections du résumé

BACKGROUND
The incidence of intrahepatic cholangiocarcinoma (iCCA) is increasing. The aim of the study was to provide reference survival data for patients with advanced iCCA treated with first-line cisplatin-gemcitabine chemotherapy (current standard of care).
METHODS
Individual data from patients with iCCA recruited into the prospective, random assignment Advanced Biliary Tract Cancer (ABC)-01, -02, and -03 studies were retrieved. The prevalence and survival of liver-only iCCA was also assessed. Survival analysis was performed using univariate and multivariable Cox regression. All statistical tests were two-sided.
RESULTS
Of 534 patients recruited into the ABC-01, -02, and -03 studies, 109 (20.4%) had iCCA. Most patients (n = 86, 78.9%) had metastatic disease at the time of recruitment; 52 patients (47.7%) had liver-only disease. Following random assignment, 66 (60.6%) iCCA patients received cisplatin and gemcitabine. The median progression-free and overall survival (OS) were 8.4 months (95% confidence interval [CI] = 5.9 to 8.9 months) and 15.4 months (95% CI = 11.1 to 17.9 months), respectively. Of these 66 patients, 34 patients (51.5%) had liver-only disease. Following chemotherapy, 30 (45.5%) and 21 (31.8%) were progression-free at 3 and 6 months from chemotherapy commencement, respectively. The median OS for patients with liver-only iCCA at diagnosis and after 3 and 6 months of chemotherapy was 16.7 months (95% CI = 8.7 to 20.2 months), 17.9 months (95% CI = 11.7 to 20.9 months), and 18.9 months (95% CI = 16.7 to 25.9 months), respectively. Multivariable analysis confirmed that iCCA had a longer OS compared with other non-iCCA biliary tract cancers (hazard ratio = 0.58, 95% CI = 0.35 to 0.95, P value = .03); liver-only iCCA patients also showed longer OS even though findings did not reach statistical significance (hazard ratio = 0.65, 95% CI = 0.36 to 1.19, P value = .16).
CONCLUSIONS
Patients diagnosed with advanced iCCA have a better OS compared with other biliary tract cancers; a similar trend was identified for patients diagnosed with liver-only iCCA. These findings are to be considered for future clinical trial design.

Identifiants

pubmed: 31077311
pii: 5488118
doi: 10.1093/jnci/djz071
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

200-210

Subventions

Organisme : Cancer Research UK
ID : CRUK/04/012
Pays : United Kingdom
Organisme : Cancer Research UK
ID : CRUK/09/029
Pays : United Kingdom

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press.

Auteurs

Angela Lamarca (A)

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Division of Cancer Sciences, University of Manchester, Manchester, UK.
Cancer Research UK & UCL Cancer Centre, University College of London, London, UK.

Paul Ross (P)

Department of Medical Oncology, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Harpreet S Wasan (HS)

Department of Medical Oncology, Imperial College Healthcare, London, UK.

Richard A Hubner (RA)

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Division of Cancer Sciences, University of Manchester, Manchester, UK.

Mairéad G McNamara (MG)

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Division of Cancer Sciences, University of Manchester, Manchester, UK.

Andre Lopes (A)

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Division of Cancer Sciences, University of Manchester, Manchester, UK.
Cancer Research UK & UCL Cancer Centre, University College of London, London, UK.

Prakash Manoharan (P)

Department of Radiology and Nuclear Medicine, The Christie NHS Foundation Trust, Manchester, UK.

Daniel Palmer (D)

Department of Medical Oncology, Clatterbridge Cancer Centre, Liverpool, UK.

John Bridgewater (J)

Department of Medical Oncology, UCL Cancer Institute, London, UK.

Juan W Valle (JW)

Department of Medical Oncology, The Christie NHS Foundation Trust, Manchester, UK.
Division of Cancer Sciences, University of Manchester, Manchester, UK.

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