First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis.

FOLFIRI bile duct carcinoma cholangiocellular carcinoma first line palliative chemotherapy gemcitabine/cisplatin retrospective analysis second line palliative chemotherapy

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 30 05 2021
accepted: 22 10 2021
entrez: 3 12 2021
pubmed: 4 12 2021
medline: 4 12 2021
Statut: epublish

Résumé

Prognosis of patients with irresectable cholangiocarcinoma is still poor. The ABC-02 trial established the current first line (1L) standard systemic chemotherapy (CT) with gemcitabine/platinum derivate for advanced cholangiocarcinoma. However, the majority of patients needed therapy adaptions. Thus, the aim of this study was to evaluate 1L and second line (2L) therapy regimens and the impact of therapy adaptions in an unselected real-life cohort of patients with advanced cholangiocarcinoma. This is a single institution retrospective analysis of patients with irresectable cholangiocarcinoma who were treated with gemcitabine/platinum derivate from 2010 to 2018. Overall survival (OS), progression-free survival (PFS) and toxicity were analyzed for all patients, especially with regard to CT de-escalation. Fifty-eight patients receiving gemcitabine/platinum derivate were included in the analysis. Median OS and PFS were 12.2 and 6.9 months. Interestingly, 41 patients (71%) needed therapy de-escalation. However, despite reduced CT exposition, there was no-significant difference in OS (10.8 months vs. 15.6 months, p = 0.127), and patients suffered from less adverse events during CT. 21 (36%) patients reached 2L CT, most often with FOLFIRI (57%). Survival beyond the end of 1L CT was 7.1 months with 2L CT vs. 2.9 months with BSC. In our study, the combination of gemcitabine/platinum derivate showed similar OS and PFS as randomized prospective phase II/III trials. Therapy regimen adaptions were needed in the majority of patients. However, individualized modifications of the therapy regimen allowed better tolerance as well as continuation of therapy and did not significantly influence median OS. Furthermore, our study revealed a potential survival benefit with 2L CT for selected patients.

Identifiants

pubmed: 34858809
doi: 10.3389/fonc.2021.717397
pmc: PMC8631360
doi:

Types de publication

Journal Article

Langues

eng

Pagination

717397

Informations de copyright

Copyright © 2021 Möhring, Feder, Mohr, Sadeghlar, Bartels, Mahn, Zhou, Marinova, Feldmann, Brossart, von Websky, Matthaei, Manekeller, Glowka, Kalff, Weismüller, Strassburg and Gonzalez-Carmona.

Déclaration de conflit d'intérêts

Author MG-C has contributed to advisory boards for Roche, Eisai, MSD and AZ. However, these activities have no potential conflicts of interest with the manuscript. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Christian Möhring (C)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Jan Feder (J)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Raphael U Mohr (RU)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Farsaneh Sadeghlar (F)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Alexandra Bartels (A)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Robert Mahn (R)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Taotao Zhou (T)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Milka Marinova (M)

Department of Radiology, University Hospital, Bonn, Germany.

Georg Feldmann (G)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Peter Brossart (P)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Martin von Websky (M)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Hanno Matthaei (H)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Steffen Manekeller (S)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Tim Glowka (T)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Jörg C Kalff (JC)

Department of Internal Medicine III, University Hospital, Bonn, Germany.

Tobias J Weismüller (TJ)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Christian P Strassburg (CP)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Maria A Gonzalez-Carmona (MA)

Department of Internal Medicine I, University Hospital, Bonn, Germany.

Classifications MeSH