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Predictors of progression free survival, overall survival and early cessation of chemotherapy in women with potentially platinum sensitive (PPS) recurrent ovarian cancer (ROC) starting third or subsequent line(≥3) chemotherapy - The GCIG symptom benefit study (SBS).
Roncolato, F T; O'Connell, R L; Joly, F; Lanceley, A; Hilpert, F; Buizen, L; Okamoto, A; Aotani, E; Salutari, V; Donnellan, P; Oza, A; Avall-Lundqvist, E; Berek, J; Fehm, T; Ledermann, J; Roemer-Becuwe, C; Stockler, M R; King, M T; Friedlander, M L.
Afiliación
  • Roncolato FT; NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia; Macarthur Cancer Therapy Centre, Campbelltown, Australia; Australia New Zealand Gynaecological Oncology Group (ANZGOG), Australia. Electronic address: felicia.roncolato@ctc.usyd.edu.au.
  • O'Connell RL; NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
  • Joly F; Centre Francois Baclesse, Caen, GINECO Intergroup, France.
  • Lanceley A; University College London, London, United Kingdom.
  • Hilpert F; AGO Study Group and Onkologisches Therapiezentrum Hamburg am Krankenhaus Jerusalem, GermanyThe Jikei University School of Medicine, Japan.
  • Buizen L; NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
  • Okamoto A; Kitasato Academic Research Organisation, Japan.
  • Aotani E; Kitasato University, Graduate School of Nursing, Tokyo, Japan.
  • Salutari V; Catholic University of the Sacred Heart, Milano, Lombardia, Italy.
  • Donnellan P; Galway University Hospital, Ireland; All-Ireland Oncology Research Group (ICORG), Ireland.
  • Oza A; Princess Margaret Hospital, Canada.
  • Avall-Lundqvist E; Department of Oncology and Department of Clinical and Experimental Medicine, Sweden and Karolinska Institutet, Stockholm, Sweden.
  • Berek J; Stanford Women's Cancer Center, USA.
  • Fehm T; AGO Study Group and University of Duesseldorf, Department of Gynecology and Obstetrics, Duesseldorf, Germany.
  • Ledermann J; UCL Cancer Trials Centre, London, United Kingdom.
  • Roemer-Becuwe C; Cenere d'Oncologie de Gentilly, Nancy, France.
  • Stockler MR; NHMRC Clinical Trials Centre, University of Sydney, Sydney, Australia.
  • King MT; Australia New Zealand Gynaecological Oncology Group (ANZGOG), Australia; Psycho-Oncology Research Group (PoCoG), School of Psychology, Central Clinical School, Sydney Medical School, University of Sydney, Australia.
  • Friedlander ML; Australia New Zealand Gynaecological Oncology Group (ANZGOG), Australia; Department of Medical Oncology, Prince of Wales Hospital, New South Wales, Australia.
Gynecol Oncol ; 156(1): 45-53, 2020 01.
Article en En | MEDLINE | ID: mdl-31836184
ABSTRACT

BACKGROUND:

Potentially platinum sensitive recurrent ovarian cancer (PPS ROC) is defined by a platinum-free interval of >6 months, and usually treated with platinum-based chemotherapy with variable response and benefit in women who have had 3 or more lines of chemotherapy(≥3). We identified baseline characteristics (health-related quality of life[HRQL] and clinicopathological factors), associated with PFS, OS and early progression (within 8 weeks). The goal is to improve patient selection for chemotherapy based on a nomogram predicting PFS.

METHODS:

HRQL was assessed with EORTC QLQ-C30/QLQ-OV28. Associations with PFS and OS were assessed with Cox proportional hazards regression. Variables significant in univariable analysis were included in multivariable analyses using backward elimination to select those significant. Associations with stopping chemotherapy early were assessed with logistic regression.

RESULTS:

378 women were enrolled, with median(m)OS and PFS of 16.6 months and 5.3 months, respectively. The majority had ECOGPS 0-1. Chemotherapy was stopped early in 45/378 participants (12%); with mOS 3.4 months (95% CI 1.7-7.2). Physical function(PF), role function(RF), cognitive function(CF), social function(SF), Global Health Status(GHS) and abdominal/GI symptoms(AGIS) were significant univariable predictors of PFS(p < 0.030). SF remained significant after adjusting for clinicopathological factors; p = 0.03. PF, RF, CF, SF, GHS and AGIS were significant univariable predictors of OS (p < 0.007); PF, RF, SF and GHS remained significant predictors of OS in multivariable models; p < 0.007. Poor baseline PF and GHS were significant univariable predictors of stopping chemotherapy early (p < 0.007) but neither remained significant after adjusting for clinicopathological factors.

CONCLUSION:

Baseline HRQL is simple to measure, is predictive of PFS and OS and when used in conjunction with clinicopathological prognostic factors, can assist with clinical decision making and treatment recommendations for women with PPSROC≥3.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Recurrencia Local de Neoplasia Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Gynecol Oncol Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Recurrencia Local de Neoplasia Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Gynecol Oncol Año: 2020 Tipo del documento: Article