Patients' and clinicians' preferences in adjuvant treatment for high-risk endometrial cancer: Implications for shared decision making.


Journal

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

Informations de publication

Date de publication:
06 2021
Historique:
received: 25 01 2021
accepted: 02 03 2021
pubmed: 14 3 2021
medline: 4 1 2022
entrez: 13 3 2021
Statut: ppublish

Résumé

Decision making regarding adjuvant therapy for high-risk endometrial cancer is complex. The aim of this study was to determine patients' and clinicians' minimally desired survival benefit to choose chemoradiotherapy over radiotherapy alone. Moreover, influencing factors and importance of positive and negative treatment effects (i.e. attribute) were investigated. Patients with high-risk endometrial cancer treated with adjuvant pelvic radiotherapy with or without chemotherapy and multidisciplinary gynaecologic oncology clinicians completed a trade-off questionnaire based on PORTEC-3 trial data. In total, 171 patients and 63 clinicians completed the questionnaire. Median minimally desired benefit to make chemoradiotherapy worthwhile was significantly higher for patients versus clinicians (10% vs 5%, p = 0.02). Both patients and clinicians rated survival benefit most important during decision making, followed by long-term symptoms. Older patients (OR 0.92 [95%CI 0.87-0.97]; p = 0.003) with comorbidity (OR 0.34 [95% CI 0.12-0.89]; p = 0.035) had lower preference for chemoradiotherapy, while patients with better numeracy skills (OR 1.2 [95%CI 1.05-1.36], p = 0.011) and chemoradiotherapy history (OR 25.0 [95%CI 8.8-91.7]; p < 0.001) had higher preference for chemoradiotherapy. There is a considerable difference in minimally desired survival benefit of chemoradiotherapy in high-risk endometrial cancer among and between patients and clinicians. Overall, endometrial cancer patients needed higher benefits than clinicians before preferring chemoradiotherapy.

Sections du résumé

BACKGROUND
Decision making regarding adjuvant therapy for high-risk endometrial cancer is complex. The aim of this study was to determine patients' and clinicians' minimally desired survival benefit to choose chemoradiotherapy over radiotherapy alone. Moreover, influencing factors and importance of positive and negative treatment effects (i.e. attribute) were investigated.
METHODS
Patients with high-risk endometrial cancer treated with adjuvant pelvic radiotherapy with or without chemotherapy and multidisciplinary gynaecologic oncology clinicians completed a trade-off questionnaire based on PORTEC-3 trial data.
RESULTS
In total, 171 patients and 63 clinicians completed the questionnaire. Median minimally desired benefit to make chemoradiotherapy worthwhile was significantly higher for patients versus clinicians (10% vs 5%, p = 0.02). Both patients and clinicians rated survival benefit most important during decision making, followed by long-term symptoms. Older patients (OR 0.92 [95%CI 0.87-0.97]; p = 0.003) with comorbidity (OR 0.34 [95% CI 0.12-0.89]; p = 0.035) had lower preference for chemoradiotherapy, while patients with better numeracy skills (OR 1.2 [95%CI 1.05-1.36], p = 0.011) and chemoradiotherapy history (OR 25.0 [95%CI 8.8-91.7]; p < 0.001) had higher preference for chemoradiotherapy.
CONCLUSIONS
There is a considerable difference in minimally desired survival benefit of chemoradiotherapy in high-risk endometrial cancer among and between patients and clinicians. Overall, endometrial cancer patients needed higher benefits than clinicians before preferring chemoradiotherapy.

Identifiants

pubmed: 33712276
pii: S0090-8258(21)00198-0
doi: 10.1016/j.ygyno.2021.03.004
pii:
doi:

Substances chimiques

Adjuvants, Immunologic 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

727-733

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Cathalijne C B Post (CCB)

Department of radiation oncology, Leiden University Medical Centre, Leiden, the Netherlands. Electronic address: c.c.b.post@lumc.nl.

Jan Willem M Mens (JWM)

Department of radiation oncology, Erasmus MC, Rotterdam, the Netherlands.

Marie A D Haverkort (MAD)

Department of radiation oncology, Radiotherapiegroep, Arnhem, the Netherlands.

Friederike Koppe (F)

Department of radiation oncology, Institute Verbeeten, Tilburg, the Netherlands.

Ina M Jürgenliemk-Schulz (IM)

Department of radiation oncology, University Medical Centre Utrecht, Utrecht, the Netherlands.

An Snyers (A)

Department of radiation oncology, Radboud University Medical Centre, Nijmegen, the Netherlands.

Ellen M A Roeloffzen (EMA)

Department of radiation oncology, Isala, Zwolle, the Netherlands.

Eva E Schaake (EE)

Department of radiation oncology, National Cancer Institute, Amsterdam, the Netherlands.

Annerie Slot (A)

Department of radiation oncology, Radiotherapeutic Institute Friesland, Leeuwarden, the Netherlands.

Tanja C Stam (TC)

Department of radiation oncology, Haaglanden Medical Centre, the Hague, the Netherlands.

Jannet C Beukema (JC)

Department of radiation oncology, University Medical Centre Groningen, Groningen, the Netherlands.

Hetty A van den Berg (HA)

Department of radiation oncology, Catharina Hospital, Eindhoven, the Netherlands.

Ludy C H W Lutgens (LCHW)

Department of radiation oncology, Maastro, Maastricht, the Netherlands.

Hans W Nijman (HW)

Department of obstetrics and gynaecology, University Medical Centre Groningen, Groningen, the Netherlands.

Cornelis D de Kroon (CD)

Department of obstetrics and gynaecology, Leiden University Medical Centre, Leiden, the Netherlands.

Judith R Kroep (JR)

Department of medical oncology, Leiden University Medical Centre, Leiden, the Netherlands.

Anne M Stiggelbout (AM)

Department of biomedical data sciences, Leiden University Medical Centre, Leiden, the Netherlands.

Carien L Creutzberg (CL)

Department of radiation oncology, Leiden University Medical Centre, Leiden, the Netherlands.

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