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
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
63Informations de copyright
© 2023. The Author(s).
Références
J Natl Cancer Inst. 2020 Aug 1;112(8):829-838
pubmed: 31742639
Int J Epidemiol. 2017 Jun 1;46(3):924-938
pubmed: 27789668
Dig Liver Dis. 2017 Aug;49(8):831-840
pubmed: 28610905
Clin Cancer Res. 2019 Apr 1;25(7):2109-2115
pubmed: 30504426
J Clin Oncol. 2020 Aug 1;38(22):2510-2518
pubmed: 32530769
Ther Adv Med Oncol. 2020 Dec 04;12:1758835920975356
pubmed: 33329760
Ann Oncol. 2013 Dec;24(12):3045-50
pubmed: 24114858
JAMA. 2015 Oct 20;314(15):1637-8
pubmed: 26501539
Lancet Oncol. 2018 Aug;19(8):1094-1106
pubmed: 30042063
Eur J Cancer. 2022 Feb;162:138-147
pubmed: 34995900