DCF versus doublet chemotherapy as first-line treatment of advanced squamous anal cell carcinoma: a multicenter propensity score-matching study.

Advanced Anal carcinoma Chemotherapy Docetaxel Metastatic

Journal

Experimental hematology & oncology
ISSN: 2162-3619
Titre abrégé: Exp Hematol Oncol
Pays: England
ID NLM: 101590676

Informations de publication

Date de publication:
21 Jul 2023
Historique:
received: 26 03 2023
accepted: 15 05 2023
medline: 22 7 2023
pubmed: 22 7 2023
entrez: 21 7 2023
Statut: epublish

Résumé

Triplet DCF (docetaxel, cisplatin and 5-flurouracil) and doublet CP/CF (carboplatin and paclitaxel/cisplatin and 5-fluorouracil) regimens were prospectively evaluated in advanced squamous anal cell carcinoma (SCCA), and validated as standard treatments. Even though the high efficacy and good tolerance of DCF regimen were confirmed in 3 independent prospective trials, doublet CP regimen is still recommended in several guidelines based in its better safety profile with similar efficacy compared to CF regimen. We performed a propensity score-adjusted method with inverse probability of treatment weighted (IPTW) and matched case control (MCC) comparison among patients with metastatic or non-resectable locally advanced recurrent SCCA, treated with chemotherapy as first line regimen. The primary endpoint was the overall survival (OS), and the secondary endpoint was the progression-free survival (PFS). 247 patients were included for analysis. 154 patients received DCF and 93 patients received a doublet regimen. The median OS was 32.3 months with DCF and 18.3 months with doublet regimens (HR 0.53, 95%CI 0.38-0.74; p = 0.0001), and the median PFS was 11.2 months with DCF versus 7.6 months with doublet regimens (HR 0.53, 95%CI 0.39-0.73; p < 0.0001). The hazard ratios by IPTW and MCC analyses were 0.411 (95% CI, 0.324-0.521; p < 0.0001) and 0.406 (95% CI, 0.261-0.632; p < 0.0001) for OS, and 0.466 (95% CI, 0.376-0.576; p < 0.0001) and 0.438 (95% CI, 0.298-0.644; P < 0.0001) for PFS. The triplet DCF regimen provides a high and significant benefit in OS and PFS over doublet regimens, and should be considered as upfront treatment for eligible patients with advanced SCCA.

Identifiants

pubmed: 37480095
doi: 10.1186/s40164-023-00413-2
pii: 10.1186/s40164-023-00413-2
pmc: PMC10362607
doi:

Types de publication

Letter

Langues

eng

Pagination

63

Informations de copyright

© 2023. The Author(s).

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Auteurs

Stefano Kim (S)

Clinical Investigational Center, INSERM CIC-1431, Centre Hospitalier Universitaire de Besançon, Besançon, France. stefano.kim@univ-fcomte.fr.
INSERM Unit 1098, University of Bourgogne Franche-Comté, Besançon, France. stefano.kim@univ-fcomte.fr.
Department of Oncology, Sanatorio Allende, Cordoba, Argentina. stefano.kim@univ-fcomte.fr.

Véronique Vendrely (V)

Department of Radiation Oncology, Bordeaux University Hospital, Pessac, France.

Angélique Saint (A)

Department of Oncology, Centre Antoine Lacassagne, Nice, France.

Thierry André (T)

Sorbonne Université and Hôpital Saint Antoine, Paris, France.

Pauline Vaflard (P)

Department of Oncology, Institut Curie, Paris, France.

Emmanuelle Samalin (E)

Department of Oncology, Institut du Cancer de Montpellier, Montpellier, France.

Simon Pernot (S)

Department of Oncology, Institut Bergonié, Bordeaux, France.

Oliver Bouché (O)

Department of Digestive Oncology, Université de Reims Champagne Ardenne, CHU Reims, Reims, France.

Mustapha Zubir (M)

Department of Oncology, Hôpital Privé des Peupliers, Paris, France.

Jérôme Desrame (J)

Department of Oncology, Hôpital Privé Jean Mermoz, Lyon, France.

Christelle de la Fouchardière (C)

Department of Oncology, Centre Léon Bérard, Lyon, France.

Denis Smith (D)

Department of Oncology, Bordeaux University Hospital, Bordeaux, France.

François Ghiringhelli (F)

Department of Oncology, Centre Georges-François Leclerc, Dijon, France.

Angélique Vienot (A)

Clinical Investigational Center, INSERM CIC-1431, Centre Hospitalier Universitaire de Besançon, Besançon, France.
INSERM Unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Department of Oncology, University Hospital of Besançon, Besançon, France.

Marion Jacquin (M)

Clinical Investigational Center, INSERM CIC-1431, Centre Hospitalier Universitaire de Besançon, Besançon, France.
Cancéropôle Grand-Est, Strasbourg, France.

Elodie Klajer (E)

Department of Oncology, University Hospital of Besançon, Besançon, France.

Thierry Nguyen (T)

Department of Oncology, University Hospital of Besançon, Besançon, France.
Hôpital Nord Franche Comté, Montbéliard, France.

Éric François (É)

Department of Oncology, Centre Antoine Lacassagne, Nice, France.

Julien Taieb (J)

Department of Gastroenterology and Digestive Oncology, Université Paris-Cité, Georges Pompidou European Hospital, SIRIC CARPEM, Paris, France.

Karine Le Malicot (K)

Fédération Francophone de Cancérologie Digestive (FFCD), EPICAD INSERM LNC-UMR 1231, University of Burgundy and Franche Comté, Dijon, France.

Dewi Vernerey (D)

INSERM Unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Methodology and Quality of Life in Oncology Unit, University Hospital of Besançon, Besançon, France.

Aurélia Meurisse (A)

INSERM Unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Methodology and Quality of Life in Oncology Unit, University Hospital of Besançon, Besançon, France.

Christophe Borg (C)

Clinical Investigational Center, INSERM CIC-1431, Centre Hospitalier Universitaire de Besançon, Besançon, France.
INSERM Unit 1098, University of Bourgogne Franche-Comté, Besançon, France.
Department of Oncology, University Hospital of Besançon, Besançon, France.

Classifications MeSH