Morbidity after secondary cytoreductive surgery with or without hyperthermic intraperitoneal chemotherapy for ovarian cancer: An analysis of a randomized phase II trial.
Humans
Female
Hyperthermic Intraperitoneal Chemotherapy
/ adverse effects
Cytoreduction Surgical Procedures
/ adverse effects
Combined Modality Therapy
Hyperthermia, Induced
/ adverse effects
Ovarian Neoplasms
/ drug therapy
Carcinoma, Ovarian Epithelial
/ surgery
Morbidity
Postoperative Complications
/ epidemiology
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Hyperthermic intraperitoneal chemotherapy
Morbidity
Postoperative complications
Recurrent ovarian cancer
Secondary cytoreductive surgery
Survival
Journal
Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304
Informations de publication
Date de publication:
04 2023
04 2023
Historique:
received:
08
12
2022
revised:
31
01
2023
accepted:
02
02
2023
pmc-release:
01
04
2024
medline:
28
3
2023
pubmed:
23
2
2023
entrez:
22
2
2023
Statut:
ppublish
Résumé
To assess postoperative complications after secondary cytoreductive surgery (SCS) with or without hyperthermic intraperitoneal chemotherapy (HIPEC), we conducted an exploratory analysis of patients with platinum-sensitive recurrent ovarian cancer enrolled in a randomized phase II trial. Complications occurring within 30 days of surgery were graded using Common Terminology Criteria for Adverse Events (CTCAE) version 5.0; only hemoglobin and platelet levels were assessed. Patients were grouped by CTCAE grade ≥ 3 and < 3 complications. Among 83 eligible patients, 33 (40%) had grade ≥ 3 complications and 50 (60%) had grade < 3 complications; anemia and abdominal infections were the most common. There were no perioperative mortalities. Time to initiation of postoperative chemotherapy for patients with grade ≥ 3 and grade < 3 events was 34 days (range, 18-60) and 31 days (range, 21-43), respectively (P = .017). Median progression-free survival (PFS) did not significantly differ between patients with grade ≥ 3 and grade < 3 complications (11.2 months [95% CI: 9.3-14.4] vs 14.9 months [95% CI: 11.3-16.5], respectively; P = .186), nor did median overall survival (OS) (46.9 months [95% CI: 34-NE] vs 68.2 months [95% CI: 52.1-NE], respectively; P = .053). Postoperative complications following SCS with or without HIPEC were associated with slight delays in chemotherapy initiation but did not significantly impact oncologic outcomes.
Identifiants
pubmed: 36804618
pii: S0090-8258(23)00057-4
doi: 10.1016/j.ygyno.2023.02.003
pmc: PMC10206782
mid: NIHMS1881258
pii:
doi:
Types de publication
Clinical Trial, Phase II
Randomized Controlled Trial
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
23-30Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Informations de copyright
Copyright © 2023 Elsevier Inc. All rights reserved.
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