Minimally invasive interval debulking surgery for advanced ovarian cancer after neoadjuvant chemotherapy.
Interval debulking
Laparoscopic surgery
Minimally invasive surgery
Ovarian cancer
Journal
Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304
Informations de publication
Date de publication:
05 2023
05 2023
Historique:
received:
19
12
2022
revised:
12
01
2023
accepted:
16
01
2023
pmc-release:
01
05
2024
medline:
19
5
2023
pubmed:
29
3
2023
entrez:
28
3
2023
Statut:
ppublish
Résumé
Assess outcomes of interval debulking surgery (IDS) after neoadjuvant chemotherapy via minimally invasive surgery (MIS) compared with laparotomy in patients with advanced epithelial ovarian cancer. Patients diagnosed with stage IIIC or IV epithelial ovarian cancer between 2013 and 2018 who received neoadjuvant chemotherapy and IDS were identified in the National Cancer Database. Primary outcome was overall survival. Secondary outcomes were 5-year survival, 30- and 90-day postoperative mortality, extent of surgery, residual disease, hospitalization duration, surgical conversions, and unplanned readmissions. Propensity score matching was used to compare MIS and laparotomy for IDS. Association of treatment approach with overall survival was assessed using Kaplan-Meier method and Cox regression. Sensitivity analysis was conducted for effect of unmeasured confounders. A total of 7897 patients met inclusion criteria; 2021 (25.6%) underwent MIS. Percentage undergoing MIS increased from 20.3%-29.0% over the study period. After propensity score matching, median overall survival was 46.7 months in the MIS group versus 41.0 months in the laparotomy group [hazard ratio (HR) 0.86 (95%CI 0.79-0.94)]. Five-year survival probability was higher in MIS versus laparotomy (38.3% vs 34.8%, p < 0.01). There was lower 30- and 90-day mortality (0.3% vs 0.7% [p = 0.04] and 1.4% vs 2.5% [p = 0.01], respectively), shorter length of stay (median 3 vs 5 days, p < 0.01), lower residual disease (23.9% vs 26.7%, p < 0.01), and lower additional cytoreductive procedures (59.3% vs 70.8%, p < 0.01) in MIS compared to laparotomy, with similar rates of unplanned readmission (2.7% vs 3.1%, p = 0.39). Patients who undergo IDS by MIS have similar overall survival and decreased morbidity compared with laparotomy.
Identifiants
pubmed: 36977622
pii: S0090-8258(23)00017-3
doi: 10.1016/j.ygyno.2023.01.017
pmc: PMC10192032
mid: NIHMS1873089
pii:
doi:
Types de publication
Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
130-137Subventions
Organisme : NCI NIH HHS
ID : K08 CA234333
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Organisme : NCI NIH HHS
ID : T32 CA101642
Pays : United States
Informations de copyright
Copyright © 2023 Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest In addition to the funding sources listed above, the following authors have additional disclosures: Alexander Melamed: served on AstraZeneca advisory board. J. Alejandro Rauh-Hain: received consulting fees from Schlesinger Group and Guidepoint. John O. Schorge: served on Avenge, Bio, advisory boards and received royalties from McGraw-Hill and UpToDate. Pedro T. Ramirez: received support for travel to the European Society of Gynecologic Oncology (2022), FIGO Regional Meeting (2022), and IGCS Annual Meeting (2022). All other authors report no competing interests.
Références
Pharm Stat. 2011 Mar-Apr;10(2):150-61
pubmed: 20925139
Lancet. 2015 Jul 18;386(9990):249-57
pubmed: 26002111
J Robot Surg. 2018 Jun;12(2):245-250
pubmed: 28631233
N Engl J Med. 2018 Nov 15;379(20):1905-1914
pubmed: 30379613
JAMA. 2017 Mar 28;317(12):1224-1233
pubmed: 28350928
Int J Gynecol Cancer. 2020 Sep;30(9):1450-1454
pubmed: 32690591
J Minim Invasive Gynecol. 2013 Nov-Dec;20(6):754-65
pubmed: 24183269
Int J Gynecol Cancer. 2015 Sep;25(7):1253-7
pubmed: 26111273
Gynecol Oncol. 2016 Nov;143(2):236-240
pubmed: 27612977
Oncology. 2015;89(3):159-66
pubmed: 25968072
Ann Intern Med. 2017 Aug 15;167(4):268-274
pubmed: 28693043
CA Cancer J Clin. 2017 Mar;67(2):93-99
pubmed: 28094848
Gynecol Oncol Rep. 2020 Aug 03;33:100617
pubmed: 32793791
Int J Gynecol Cancer. 2020 Nov;30(11):1657-1664
pubmed: 33028623
Obstet Gynecol. 2017 May;129(5):861-869
pubmed: 28383367
Eur J Cancer. 2016 Sep;64:22-31
pubmed: 27323348
J Clin Oncol. 2002 Mar 1;20(5):1248-59
pubmed: 11870167
J Clin Oncol. 2012 Mar 1;30(7):695-700
pubmed: 22291074
Cancers (Basel). 2021 Feb 05;13(4):
pubmed: 33562443
N Engl J Med. 2010 Sep 2;363(10):943-53
pubmed: 20818904
J Clin Oncol. 2019 Nov 20;37(33):3069-3074
pubmed: 31560581
Obstet Gynecol. 2019 Jan;133(1):6-12
pubmed: 30531569
JAMA Oncol. 2020 Jul 1;6(7):1019-1027
pubmed: 32525511
Am J Obstet Gynecol. 2016 Apr;214(4):503.e1-503.e6
pubmed: 26529370
J Minim Invasive Gynecol. 2020 Jul - Aug;27(5):1167-1177.e2
pubmed: 31518712
Ann Surg Oncol. 2010 Jun;17(6):1471-4
pubmed: 20180029
BMJ. 2018 Jan 3;360:j5463
pubmed: 29298771
Expert Rev Anticancer Ther. 2016 Sep;16(9):899-901
pubmed: 27477495
Int J Gynecol Cancer. 2019 Jan;29(1):5-9
pubmed: 30640676
Ann Surg Oncol. 2012 Mar;19(3):959-65
pubmed: 21994038
J Minim Invasive Gynecol. 2019 Jul - Aug;26(5):902-909
pubmed: 30240899
N Engl J Med. 2018 Nov 15;379(20):1895-1904
pubmed: 30380365
Gynecol Oncol. 2016 Oct;143(1):3-15
pubmed: 27650684