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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.
Pavlidis, Nicholas; Rassy, Elie; Vermorken, Jan B; Assi, Tarek; Kattan, Joseph; Boussios, Stergios; Smith-Gagen, Julie.
Afiliação
  • Pavlidis N; University of Ioannina, Stavros Niarchou Avenue, Ioannina 45110, Greece.
  • Rassy E; Gustave Roussy, Département de médecine oncologique, F-94805 Villejuif, France. Electronic address: elie.rassy@hotmail.com.
  • Vermorken JB; Department of Medical Oncology, Antwerp University Hospital, Edegem, Belgium; Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.
  • Assi T; Gustave Roussy, Département de médecine oncologique, F-94805 Villejuif, France.
  • Kattan J; Department of Hematology-Oncology, Faculty of Medicine, Saint Joseph University, Beirut 166830, Lebanon.
  • 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.
  • Smith-Gagen J; School of Community Health Sciences, University of Nevada, Reno, NV, USA.
Cancer Epidemiol ; 75: 102045, 2021 12.
Article em En | MEDLINE | ID: mdl-34638085
ABSTRACT

AIM:

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).

METHODS:

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).

RESULTS:

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.

CONCLUSION:

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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias Peritoneais / Neoplasias das Tubas Uterinas Tipo de estudo: Clinical_trials / Observational_studies Limite: Female / Humans Idioma: En Revista: Cancer Epidemiol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias Peritoneais / Neoplasias das Tubas Uterinas Tipo de estudo: Clinical_trials / Observational_studies Limite: Female / Humans Idioma: En Revista: Cancer Epidemiol Ano de publicação: 2021 Tipo de documento: Article