The outcome of patients with serous papillary peritoneal cancer, fallopian tube cancer, and epithelial ovarian cancer by treatment eras: 27 years data from the SEER registry.

Bevacizumab Cancer of unknown primary Epithelial ovarian cancer Novel agents PARP inhibitors Serous papillary peritoneal carcinoma

Journal

Cancer epidemiology
ISSN: 1877-783X
Titre abrégé: Cancer Epidemiol
Pays: Netherlands
ID NLM: 101508793

Informations de publication

Date de publication:
12 2021
Historique:
received: 05 05 2021
revised: 17 08 2021
accepted: 03 10 2021
pubmed: 13 10 2021
medline: 15 12 2021
entrez: 12 10 2021
Statut: ppublish

Résumé

To determine the differential effect of the treatment periods on the survival of patients with stage IV serous papillary peritoneal carcinoma (SPPC), fallopian tube cancers, and epithelial ovarian cancers (EOC). This was an exploratory, population-based observational study of all patients with stage IV SPPC, fallopian tube cancers, and EOC collected from the SEER Research Data 1973-2017. The study period was divided into three time-periods: platinum combinations before the taxane era (1990-1995), platinum plus taxane chemotherapy era (1996-2013), and bevacizumab era (2014-2017). A total of 9828 patients were eligible for analyses: SPPC (3898 patients; 39.7%), fallopian tube cancers (1290 patients; 13.1%) and EOC (4640 patients, 47.2%). In the 1990-1995 era, the 3-year cause-specific survival was 40% for SPPC, 53% for fallopian tube cancers, and 40% for POC. In the following era 1993-2013, the 3-year cause-specific survival increased to 55% for SPPC, 74% for fallopian tube cancers, and 45% for POC. The last era 2014-2017 showed a 3-year cause-specific survival of 64%, 67%, and 45% for patients with SPPC, fallopian tube cancers, and POC, respectively. The differences in cause-specific survival were statistically significant for patients with SPPC (p=0.004). Multivariable analysis showed that the treatment eras and age at diagnosis were associated with cause-specific survival. The results of this study are hypothesis-generating and cannot be considered conclusive given the inherent limitations of registry analysis. Subgroup analyses of the phase III randomized controlled trials, by tumor subset (EOC, fallopian tube cancer, and SPPC) would shed more light on the differential effects of novel therapies.

Identifiants

pubmed: 34638085
pii: S1877-7821(21)00162-4
doi: 10.1016/j.canep.2021.102045
pii:
doi:

Types de publication

Journal Article Observational Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

102045

Subventions

Organisme : NCI NIH HHS
ID : P30 CA042014
Pays : United States

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

Nicholas Pavlidis (N)

University of Ioannina, Stavros Niarchou Avenue, Ioannina 45110, Greece.

Elie Rassy (E)

Gustave Roussy, Département de médecine oncologique, F-94805 Villejuif, France. Electronic address: elie.rassy@hotmail.com.

Jan B Vermorken (JB)

Department of Medical Oncology, Antwerp University Hospital, Edegem, Belgium; Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Tarek Assi (T)

Gustave Roussy, Département de médecine oncologique, F-94805 Villejuif, France.

Joseph Kattan (J)

Department of Hematology-Oncology, Faculty of Medicine, Saint Joseph University, Beirut 166830, Lebanon.

Stergios Boussios (S)

King's College London, Faculty of Life Sciences & Medicine, School of Cancer & Pharmaceutical Sciences, SE1 9RT London, UK; Medway NHS Foundation Trust, Windmill Road, Gillingham, Kent ME7 5NY, UK; AELIA Organization, 9th Km Thessaloniki-Thermi, Thessaloniki 57001, Greece.

Julie Smith-Gagen (J)

School of Community Health Sciences, University of Nevada, Reno, NV, USA.

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