Survival impact of histological response to neoadjuvant chemotherapy according to number of cycles in patients with advanced ovarian cancer.

Ovarian Cancer Pathology Surgical Oncology

Journal

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
ISSN: 1525-1438
Titre abrégé: Int J Gynecol Cancer
Pays: England
ID NLM: 9111626

Informations de publication

Date de publication:
20 Jul 2022
Historique:
entrez: 20 7 2022
pubmed: 21 7 2022
medline: 21 7 2022
Statut: aheadofprint

Résumé

We sought to evaluate the impact of chemotherapy response score according to the number of cycles of neoadjuvant chemotherapy, on disease-free survival and overall survival, in patients with advanced epithelial ovarian cancer ineligible for primary debulking surgery. This multicenter retrospective study included patients with International Federation of Gynecology and Obstetrics (FIGO) stage IIIC-IV epithelial ovarian cancer who underwent 3-4 or 6 cycles of a platinum and taxane-based neoadjuvant chemotherapy, followed by complete cytoreduction surgery (CC-0) or cytoreduction to minimal residual disease (CC-1), between January 2008 and December 2015, in four institutions. Disease-free survival and overall survival were assessed according to the histological response to chemotherapy defined by the validated chemotherapy response score. A total of 365 patients were included: 219 (60.0%) received 3-4 cycles of neoadjuvant chemotherapy, and 146 (40.0%) had 6 cycles of neoadjuvant chemotherapy before cytoreductive surgery. There were no significant differences in early relapses, disease-free survival, and overall survival according to the number of neoadjuvant chemotherapy cycles. However, regardless of the number cycles of neoadjuvant chemotherapy, persistent extensive histological disease (chemotherapy response score 1-2) was significantly associated with a higher peritoneal cancer index, minimal residual disease (CC-1), and early relapses. Median disease-free survival in patients with complete or near-complete response (score 3) was 28.3 months (95% CI 21.6 to 36.8), whereas it was 16.3 months in patients with chemotherapy response score 1-2 (95% CI 14.7 to 18.0, p<0.001). In our cohort, the number of neoadjuvant chemotherapy cycles was not associated with disease-free survival or overall survival. Chemotherapy response score 3 improved oncological outcome regardless of the number of neoadjuvant chemotherapy cycles.

Identifiants

pubmed: 35858711
pii: ijgc-2021-003313
doi: 10.1136/ijgc-2021-003313
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© IGCS and ESGO 2022. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Sarah Betrian (S)

Department of Medical Oncology, Institut Universitaire du Cancer de Toulouse, Toulouse, France betrian.sarah@iuct-oncopole.fr.

Martina Aida Angeles (MA)

Surgical Oncology, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.

Antonio Gil Moreno (A)

Gynecology, Vall d'Hebron Hospital, Barcelona, Spain.
Universitat Autònoma de Barcelona, Barcelona, Spain.

Bastien Cabarrou (B)

Biostatistics Unit, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.

Marion Deslandres (M)

Department of Medical Oncology, Institut Universitaire du Cancer de Toulouse, Toulouse, France.

Gwenael Ferron (G)

Surgical Oncology, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.

Eliane Mery (E)

Pathology, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.

Anne Floquet (A)

Medical Oncology Department, Institut Bergonié, Bordeaux, France.

Frederic Guyon (F)

Surgical oncology, Institut Bergonié, Bordeaux, France.

Assumpció Pérez-Benavente (A)

Gynecology, Vall d'Hebron Hospital, Barcelona, Spain.

Emanuela Spagnolo (E)

Gynecologic Oncology Unit, La Paz University Hospital, Madrid, Spain.

Agnieszka Rychlik (A)

Maria Sklodowska-Curie National Research Institute of Oncology in Warsaw, Warszawa, Poland.

Laurence Gladieff (L)

Department of Medical Oncology, Institut Universitaire du Cancer de Toulouse, Toulouse, France.

Alicia Hernández Gutiérrez (A)

Gynecologic Oncology Unit, La Paz University Hospital, Madrid, Spain.

Alejandra Martinez (A)

Surgical Oncology, Institut Universitaire du Cancer Toulouse Oncopole, Toulouse, France.

Classifications MeSH