Pemigatinib for patients with previously treated, locally advanced or metastatic cholangiocarcinoma harboring FGFR2 fusions or rearrangements: A joint analysis of the French PEMI-BIL and Italian PEMI-REAL cohort studies.

BTC FGFR2 fusions/rearrangements Intrahepatic cholangiocarcinoma Real-world data Systemic treatment Targeted therapy

Journal

European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373

Informations de publication

Date de publication:
06 Feb 2024
Historique:
received: 13 11 2023
revised: 23 01 2024
accepted: 27 01 2024
medline: 10 2 2024
pubmed: 10 2 2024
entrez: 10 2 2024
Statut: aheadofprint

Résumé

Pemigatinib is approved for patients with pretreated, locally advanced or metastatic CCA harboring FGFR2 rearrangements or fusions. We aim to assess the effectiveness and safety of pemigatinib in real-world setting. A joint analysis of two multicentre observational retrospective cohort studies independently conducted in France and Italy was performed. All consecutive FGFR2-positive patients affected by CCA and treated with pemigatinib as second- or further line of systemic treatment in clinical practice, within or outside the European Expanded Access Program, were included. Between July 2020 and September 2022, 72 patients were treated with pemigatinib in 14 Italian and 25 French Centres. Patients had a median age of 57 years, 76% were female, 81% had ECOG-PS 0-1, 99% had intrahepatic CCA, 74% had ≥ 2 metastatic sites, 67% had metastatic disease at diagnosis, while 38.8% received ≥ 2 previous lines of systemic treatment. At data cut-off analysis (April 2023), ORR and DCR were 45.8% and 84.7%, respectively. Median DoR was 7 months (IQR: 5.8-9.3). Over a median follow-up time of 19.5 months, median PFS and 1-year PFS rate were 8.7 months and 32.8%. Median OS and 1-year OS rate were 17.1 months and 60.6%. Fatigue (69.4%), ocular toxicity (68%), nail toxicities (61.1%), dermatologic toxicity (41.6%) hyperphosphataemia (55.6%), stomatitis (48.6%), and diarrhea (36.1%) were the most frequent, mainly G1-G2 AEs. Overall incidence of G3 AEs was 22.2%, while no patient experienced G4 AE. Dose reduction and temporary discontinuation were needed in 33.3% and 40.3% of cases, with 1 permanent discontinuation due to AEs. These results confirm the effectiveness and safety of pemigatinib in a real-world setting.

Sections du résumé

BACKGROUND BACKGROUND
Pemigatinib is approved for patients with pretreated, locally advanced or metastatic CCA harboring FGFR2 rearrangements or fusions. We aim to assess the effectiveness and safety of pemigatinib in real-world setting.
MATERIAL AND METHODS METHODS
A joint analysis of two multicentre observational retrospective cohort studies independently conducted in France and Italy was performed. All consecutive FGFR2-positive patients affected by CCA and treated with pemigatinib as second- or further line of systemic treatment in clinical practice, within or outside the European Expanded Access Program, were included.
RESULTS RESULTS
Between July 2020 and September 2022, 72 patients were treated with pemigatinib in 14 Italian and 25 French Centres. Patients had a median age of 57 years, 76% were female, 81% had ECOG-PS 0-1, 99% had intrahepatic CCA, 74% had ≥ 2 metastatic sites, 67% had metastatic disease at diagnosis, while 38.8% received ≥ 2 previous lines of systemic treatment. At data cut-off analysis (April 2023), ORR and DCR were 45.8% and 84.7%, respectively. Median DoR was 7 months (IQR: 5.8-9.3). Over a median follow-up time of 19.5 months, median PFS and 1-year PFS rate were 8.7 months and 32.8%. Median OS and 1-year OS rate were 17.1 months and 60.6%. Fatigue (69.4%), ocular toxicity (68%), nail toxicities (61.1%), dermatologic toxicity (41.6%) hyperphosphataemia (55.6%), stomatitis (48.6%), and diarrhea (36.1%) were the most frequent, mainly G1-G2 AEs. Overall incidence of G3 AEs was 22.2%, while no patient experienced G4 AE. Dose reduction and temporary discontinuation were needed in 33.3% and 40.3% of cases, with 1 permanent discontinuation due to AEs.
CONCLUSIONS CONCLUSIONS
These results confirm the effectiveness and safety of pemigatinib in a real-world setting.

Identifiants

pubmed: 38340384
pii: S0959-8049(24)00063-7
doi: 10.1016/j.ejca.2024.113587
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

113587

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Alessandro Parisi (A)

Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, Azienda Ospedaliero-Universitaria delle Marche, Via Conca 71, 60126 Ancona, Italy. Electronic address: alexparis@hotmail.it.

Blandine Delaunay (B)

Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, Azienda Ospedaliero-Universitaria delle Marche, Via Conca 71, 60126 Ancona, Italy; Digestive Oncology Department, Centre Hospitalier Universitaire de Toulouse - Hopital Rangueil, Toulouse, France.

Giada Pinterpe (G)

Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, Azienda Ospedaliero-Universitaria delle Marche, Via Conca 71, 60126 Ancona, Italy.

Antoine Hollebecque (A)

Département d'Innovation Thérapeutique et Essais précoces (DITEP), Gustave Roussy, Villejuif Cedex, France.

Jean Frederic Blanc (JF)

Oncology Digestive Unit, Hôpital haut-Lévêque, CHU Bordeaux France, France.

Mohamed Bouattour (M)

Liver Oncology and Therapeutic Innovation Functional Unit, Beaujon Hospital APHP, Clichy, France.

Eric Assenat (E)

Medical oncology, ICM - Institut du Cancer de Montpellier, Montpellier Cedex, France.

Meher Ben Abdelghani (M)

Oncology Department, ICANS - Institut de Cancérologie Strasbourg Europe, Strasbourg, France.

Matthieu Sarabi (M)

Medical Oncology, Centre Léon Bérard, Lyon, GI Oncology Department, France; GI Oncology Department, Hôpital privé Jean Mermoz, Lyon, France.

Monica Niger (M)

Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Via Venezian 1, 20133 Milan, Italy.

Caterina Vivaldi (C)

Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, 56126 Pisa, Italy.

Mario Mandalà (M)

Unit of Medical Oncology, University of Perugia, Perugia, Italy.

Andrea Palloni (A)

Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Maria Bensi (M)

Oncologia Medica, Comprehensive Cancer Center, Fondazione Policlinico Universitario Agostino Gemelli-IRCCS, Italy; Università Cattolica del Sacro Cuore, Roma, Italy.

Silvio Ken Garattini (SK)

Department of Oncology, Academic Hospital of Udine ASUFC, Piazzale Santa Maria della Misericordia 15, Udine, UD 33100, Italy.

David Tougeron (D)

Université de Poitiers, Department of Gastroenterology and Hepatology, Poitiers University Hospital, Poitiers, France.

Pierre Combe (P)

Medical Oncology, CORT37, Pôle Santé Léonard de Vinci, Chambray-lès-Tours, France.

Massimiliano Salati (M)

Division of Oncology, Department of Oncology and Hematology, University Hospital Modena, Modena Cancer Centre, Via del Pozzo 71, 41125 Modena, Italy; Clinical and Experimental Medicine, University of Modena and Reggio Emilia, Modena, Italy.

Margherita Rimini (M)

Vita-Salute University San Raffaele, Milan, Italy; Department of Oncology, IRCCS San Raffaele Hospital, via Olgettina N. 60, Milan 20132, Italy.

Chiara Alessandra Cella (CA)

Division of Gastrointestinal Medical Oncology and Neuroendocrine Tumors, European Institute of Oncology, IEO IRCCS, Via Ripamonti 435, Milan, Italy.

Marco Tucci (M)

Department of Interdisciplinary Medicine, Oncology Unit, University of Bari "Aldo Moro", P.za Giulio Cesare, 11, 70124, Bari, Italy.

Anna Diana (A)

UOC Oncologia - Ospedale del Mare, Naples.

Elena Mori (E)

Department of Medical Oncology, New Hospital of Prato S. Stefano, 59100 Prato, Italy.

Raffaella Longarini (R)

Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Pascal Artru (P)

GI Oncology Department, Hôpital privé Jean Mermoz, Lyon, France.

Gael Roth (G)

Univ. Grenoble Alpes / Hepato-Gastroenterology and Digestive Oncology Department, CHU Grenoble Alpes / Institute for Advanced Biosciences, CNRS UMR 5309-INSERM, U1209, France.

Ludovic Evesque (L)

Medical Oncology Department, Centre Antoine-Lacassagne, Nice, France.

Agathe Vienne (A)

Oncology Department, CHU Sud Réunion, Saint Pierre, France.

Anthony Turpin (A)

Medical Oncology Department, Hopital Claude Huriez, Lille, France.

Sandrine Hiret (S)

Oncology Department, ICO Institut de Cancerologie de l'Ouest René Gauducheau, Saint-Herblain, France.

Vincent Bourgeois (V)

Digestive Oncology, Hopital duchenne Boulogne-sur-Mer, France.

Camille Herve (C)

Digestive Oncology, Groupe Hospitalier Mutualiste, Grenoble.

Rodolphe Paulon (R)

Medical Oncology, Clinique du Sidobre, Castres, France.

Marion Stacoffe (M)

Medical Oncology, CHRU Hopitaux de Tours - Hopital Bretonneau, Tours Cedex, France.

David Malka (D)

Medical Oncology, Institut Mutualiste Montsouris, Paris, France.

Cindy Neuzillet (C)

GI Oncology, Medical Oncology Department, Curie Institute, Paris, France.

Julien Edeline (J)

Medical Oncology Department, Centre Eugene - Marquis, Rennes, France.

Astrid Lievre (A)

Department of Gastroenterology, CHU de Rennes - Hopital Pontchaillou, Rennes Cedex, France.

Rosine Guimbaud (R)

Digestive Oncology Department, Centre Hospitalier Universitaire de Toulouse - Hopital Rangueil, Toulouse, France.

Marie Christelle Pajiep Chapda (MCP)

MeDatas, CIC (Centre d'Investigation Clinique), CHU Toulouse, Toulouse, France.

Lorenza Rimassa (L)

Department of Biomedical Sciences, Humanitas University, 20072 Pieve Emanuele, Milan, Italy; Medical Oncology and Hematology Unit, Humanitas Cancer Center, IRCCS Humanitas Research Hospital, 20089 Rozzano, Milan, Italy.

Riccardo Giampieri (R)

Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, Azienda Ospedaliero-Universitaria delle Marche, Via Conca 71, 60126 Ancona, Italy.

Juan Valle (J)

Cholangiocarcinoma Foundation, Salt Lake City, Utah, USA; Division of Cancer Sciences, University of Manchester, Manchester, UK.

Rossana Berardi (R)

Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, Azienda Ospedaliero-Universitaria delle Marche, Via Conca 71, 60126 Ancona, Italy.

Nadim Fares (N)

Digestive Oncology Department, Centre Hospitalier Universitaire de Toulouse - Hopital Rangueil, Toulouse, France.

Classifications MeSH