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

ObjectivePrognosis 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 adaptio...

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Autores principales: Christian Möhring, Jan Feder, Raphael U. Mohr, Farsaneh Sadeghlar, Alexandra Bartels, Robert Mahn, Taotao Zhou, Milka Marinova, Georg Feldmann, Peter Brossart, Martin von Websky, Hanno Matthaei, Steffen Manekeller, Tim Glowka, Jörg C. Kalff, Tobias J. Weismüller, Christian P. Strassburg, Maria A. Gonzalez-Carmona
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Publicado: Frontiers Media S.A. 2021
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spelling oai:doaj.org-article:3a0b0c8729054bd493c1b136c9000bca2021-11-10T06:33:21ZFirst Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis2234-943X10.3389/fonc.2021.717397https://doaj.org/article/3a0b0c8729054bd493c1b136c9000bca2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fonc.2021.717397/fullhttps://doaj.org/toc/2234-943XObjectivePrognosis 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.Materials and MethodsThis 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.ResultsFifty-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.ConclusionIn 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.Christian MöhringJan FederRaphael U. MohrFarsaneh SadeghlarAlexandra BartelsRobert MahnTaotao ZhouMilka MarinovaGeorg FeldmannPeter BrossartMartin von WebskyHanno MatthaeiSteffen ManekellerTim GlowkaJörg C. KalffTobias J. WeismüllerChristian P. StrassburgMaria A. Gonzalez-CarmonaFrontiers Media S.A.articlebile duct carcinomacholangiocellular carcinomafirst line palliative chemotherapysecond line palliative chemotherapyretrospective analysisgemcitabine/cisplatinNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENFrontiers in Oncology, Vol 11 (2021)
institution DOAJ
collection DOAJ
language EN
topic bile duct carcinoma
cholangiocellular carcinoma
first line palliative chemotherapy
second line palliative chemotherapy
retrospective analysis
gemcitabine/cisplatin
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle bile duct carcinoma
cholangiocellular carcinoma
first line palliative chemotherapy
second line palliative chemotherapy
retrospective analysis
gemcitabine/cisplatin
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Christian Möhring
Jan Feder
Raphael U. Mohr
Farsaneh Sadeghlar
Alexandra Bartels
Robert Mahn
Taotao Zhou
Milka Marinova
Georg Feldmann
Peter Brossart
Martin von Websky
Hanno Matthaei
Steffen Manekeller
Tim Glowka
Jörg C. Kalff
Tobias J. Weismüller
Christian P. Strassburg
Maria A. Gonzalez-Carmona
First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis
description ObjectivePrognosis 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.Materials and MethodsThis 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.ResultsFifty-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.ConclusionIn 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.
format article
author Christian Möhring
Jan Feder
Raphael U. Mohr
Farsaneh Sadeghlar
Alexandra Bartels
Robert Mahn
Taotao Zhou
Milka Marinova
Georg Feldmann
Peter Brossart
Martin von Websky
Hanno Matthaei
Steffen Manekeller
Tim Glowka
Jörg C. Kalff
Tobias J. Weismüller
Christian P. Strassburg
Maria A. Gonzalez-Carmona
author_facet Christian Möhring
Jan Feder
Raphael U. Mohr
Farsaneh Sadeghlar
Alexandra Bartels
Robert Mahn
Taotao Zhou
Milka Marinova
Georg Feldmann
Peter Brossart
Martin von Websky
Hanno Matthaei
Steffen Manekeller
Tim Glowka
Jörg C. Kalff
Tobias J. Weismüller
Christian P. Strassburg
Maria A. Gonzalez-Carmona
author_sort Christian Möhring
title First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis
title_short First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis
title_full First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis
title_fullStr First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis
title_full_unstemmed First Line and Second Line Chemotherapy in Advanced Cholangiocarcinoma and Impact of Dose Reduction of Chemotherapy: A Retrospective Analysis
title_sort first line and second line chemotherapy in advanced cholangiocarcinoma and impact of dose reduction of chemotherapy: a retrospective analysis
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/3a0b0c8729054bd493c1b136c9000bca
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