Health-related quality of life after interval cytoreductive surgery with or without hyperthermic intraperitoneal chemotherapy (HIPEC) in patients with stage III ovarian cancer.


Journal

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
ISSN: 1532-2157
Titre abrégé: Eur J Surg Oncol
Pays: England
ID NLM: 8504356

Informations de publication

Date de publication:
01 2021
Historique:
received: 13 02 2019
accepted: 08 05 2019
pubmed: 28 5 2019
medline: 21 4 2021
entrez: 27 5 2019
Statut: ppublish

Résumé

The addition of hyperthermic intraperitoneal chemotherapy (HIPEC) to interval cytoreductive surgery (CRS) improves recurrence-free (RFS) and overall survival (OS) in patients with FIGO stage III ovarian cancer. We evaluated the effect of HIPEC on patient's health-related quality of life (HRQoL) in the OVHIPEC trial. OVHIPEC was a multicentre, open-label, randomized phase III trial for patients with stage III ovarian cancer. Patients were randomly assigned (1:1) to receive interval CRS with or without HIPEC with cisplatin. HRQoL was assessed using the EORTC QLQ-C30, and the ovarian (QLQ-OV28) and colorectal cancer (QLQ-CR38) modules. HRQoL questionnaires were administered at baseline, after surgery, after end of treatment, and every three months thereafter. HRQoL was a secondary endpoint, with the prespecified focus on the QLQ-C30 summary score and symptom scores on fatigue, neuropathy and gastro-intestinal symptoms. HRQoL was analysed using linear and non-linear mixed effect models. In total, 245 patients were randomized. One-hundred-ninety-seven patients (80%) completed at least one questionnaire. No significant difference over time in the QLQ-C30 summary scores was observed between the study arms (p-values for linear and non-linear growth: p > 0.133). The pattern over time for fatigue, neuropathy and gastro-intestinal symptoms did not significantly differ between treatment arms. The addition of HIPEC to interval CRS does not negatively impact HRQoL in patients with stage III ovarian cancer who are treated with interval CRS due to the extent of disease. These HRQoL results, together with the improvement in RFS and OS, support the viability of HIPEC as an important treatment option in this patient population. CLINICALTRIALS. NCT00426257. 2006-003466-34.

Identifiants

pubmed: 31128948
pii: S0748-7983(19)30444-5
doi: 10.1016/j.ejso.2019.05.006
pii:
doi:

Substances chimiques

Carboplatin BG3F62OND5
Paclitaxel P88XT4IS4D

Banques de données

ClinicalTrials.gov
['NCT00426257']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

101-107

Informations de copyright

Copyright © 2019 Elsevier Ltd, BASO ~ The Association for Cancer Surgery, and the European Society of Surgical Oncology. All rights reserved.

Auteurs

S N Koole (SN)

Department of Gynecology, The Netherlands Cancer Institute, Amsterdam, the Netherlands; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands; Center for Gynecologic Oncology Amsterdam, Amsterdam, the Netherlands.

J M Kieffer (JM)

Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Department of Biometrics, The Netherlands Cancer Institute, Amsterdam, the Netherlands.

J H Schagen van Leeuwen (JH)

Department of Obstetrics & Gynecology, Sint Antonius Hospital, Nieuwegein, the Netherlands.

H W R Schreuder (HWR)

Department of Gynecological Oncology, UMC Utrecht Cancer Center, Utrecht, the Netherlands.

R H Hermans (RH)

Department of Gynecology and Obstetrics, Catharina Hospital, Eindhoven, the Netherlands.

I H de Hingh (IH)

Department of Surgery, Catharina Hospital, Eindhoven, the Netherlands; The Dutch Peritoneal Oncology Group, the Netherlands.

J van der Velden (J)

Center for Gynecologic Oncology Amsterdam, Amsterdam, the Netherlands; Department of Obstetrics and Gynecology, Amsterdam University Medical Center, Amsterdam, the Netherlands.

H J Arts (HJ)

Department of Gynecological Oncology, University Medical Center Groningen, Groningen, the Netherlands.

M A P C van Ham (MAPC)

Department of Gynecological Oncology, Radboud University Medical Center, Nijmegen, the Netherlands.

A G Aalbers (AG)

The Dutch Peritoneal Oncology Group, the Netherlands; Department of Surgical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.

V J Verwaal (VJ)

Department of Surgery, Aarhus University Hospital, Aarhus, Denmark.

K K Van de Vijver (KK)

Department of Pathology, University Hospital Ghent, Ghent, Belgium.

G S Sonke (GS)

Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands; Center for Gynecologic Oncology Amsterdam, Amsterdam, the Netherlands.

W J van Driel (WJ)

Department of Gynecology, The Netherlands Cancer Institute, Amsterdam, the Netherlands; Center for Gynecologic Oncology Amsterdam, Amsterdam, the Netherlands; Dutch Gynecological Oncology Group, the Netherlands.

N K Aaronson (NK)

Division of Psychosocial Research and Epidemiology, The Netherlands Cancer Institute, Amsterdam, the Netherlands. Electronic address: n.aaronson@nki.nl.

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Classifications MeSH