Surgical complexity score and role of laparoscopy in women with advanced ovarian cancer treated with neoadjuvant chemotherapy.


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
03 2019
Historique:
received: 01 10 2018
revised: 10 12 2018
accepted: 10 12 2018
pubmed: 19 12 2018
medline: 18 4 2019
entrez: 19 12 2018
Statut: ppublish

Résumé

To evaluate surgical complexity scores (SCS) and minimally invasive surgery (MIS) at interval debulking surgery (IDS) in advanced epithelial ovarian cancer (EOC) patients receiving neoadjuvant chemotherapy (NACT). A multi-institutional study of NACT with IDS for advanced EOC was conducted. Demographic data were abstracted and SCS assigned based on IDS findings. Disease-specific overall survival (DSS) was defined as the time from completion of adjuvant chemotherapy to death due to disease. Cox proportional hazards regression models were used for univariate and multivariate survival analyses. 282 patients were identified; 80.5% had high-grade serous histology and 54.6% were <75 (median 63.9; range 34.1-84.8). Approximately 84% were optimally cytoreduced (61% R0; 23% <1 cm). In multivariate analyses, age 75+ (p ≤ 0.001), residual disease (>1 cm; p = 0.03), and SCS ≥ 3 (p = 0.04) were significantly predictive of worse DSS when morbidity and ASA score were also in the model. When optimally debulked was defined as R0, only age 75+ (<0.001) was significantly associated with decreased DSS. In the R0 cohort, SCS did not significantly predict DSS. However, subset analysis defining optimal ≤1 cm, revealed higher SCS was associated with a 1.6-fold increased risk of death (p = 0.02). Fifty-one patients underwent laparoscopic IDS. Twenty-four (47%) were converted to laparotomy to achieve optimal debulking in 21 patients (87.5%); while 25 had laparoscopic optimal cytoreduction (19/25 [76%] R0). In women with advanced EOC treated with NACT, older age, SCS ≥ 3, and residual disease >1 cm at IDS were predictors of worse survival. MIS appears safe and feasible with acceptable optimal cytoreduction rates.

Identifiants

pubmed: 30558972
pii: S0090-8258(18)31475-6
doi: 10.1016/j.ygyno.2018.12.011
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

554-559

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Brittany A Davidson (BA)

Division of Gynecologic Oncology, Duke Cancer Institute, Durham, NC, United States of America. Electronic address: brittany.davidson@duke.edu.

Gloria Broadwater (G)

Department of Biostatistics and Bioinformatics, Duke Cancer Institute, Durham, NC, United States of America.

Aleia Crim (A)

Division of Gynecologic Oncology, University of Oklahoma, Oklahoma City, OK, United States of America.

Robert Boccacio (R)

Department of OB/GYN, University of Oklahoma, Oklahoma City, OK, United States of America.

Kristin Bixel (K)

Division of Gynecologic Oncology, The Ohio State University, Columbus, OH, United States of America.

Floor Backes (F)

Division of Gynecologic Oncology, The Ohio State University, Columbus, OH, United States of America.

Rebecca A Previs (RA)

Division of Gynecologic Oncology, Duke Cancer Institute, Durham, NC, United States of America.

Julia Salinaro (J)

Duke University School of Medicine, Durham, NC, United States of America.

Ritu Salani (R)

Division of Gynecologic Oncology, The Ohio State University, Columbus, OH, United States of America.

Katherine Moore (K)

Division of Gynecologic Oncology, University of Oklahoma, Oklahoma City, OK, United States of America.

Angeles Alvarez Secord (AA)

Division of Gynecologic Oncology, Duke Cancer Institute, Durham, NC, United States of America.

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