Quality of Life in Patients With Low-Risk Prostate Cancer Treated With Hypofractionated vs Conventional Radiotherapy: A Phase 3 Randomized Clinical Trial.


Journal

JAMA oncology
ISSN: 2374-2445
Titre abrégé: JAMA Oncol
Pays: United States
ID NLM: 101652861

Informations de publication

Date de publication:
01 May 2019
Historique:
pubmed: 15 2 2019
medline: 11 2 2020
entrez: 15 2 2019
Statut: ppublish

Résumé

Hypofractionated radiotherapy (HRT) would be more convenient for men with low-risk prostate cancer and cost less than conventional radiotherapy (CRT) as long as HRT is noninferior to CRT in terms of survival and quality of life (QOL) is not found to be worse. To assess differences in QOL between men with low-risk prostate cancer who are treated with HRT vs CRT. In this phase 3 randomized clinical trial, men with low-risk prostate cancer were enrolled from sites within the National Cancer Institute's National Clinical Trials Network in the United States, Canada, and Switzerland. Random assignment to CRT (73.8 Gy in 41 fractions over 8.2 weeks) or to HRT (70 Gy in 28 fractions over 5.6 weeks). Quality of life was assessed using the Expanded Prostate Index Composite questionnaire measuring bowel, urinary, sexual, and hormonal domains; the 25-item Hopkins Symptom Checklist measuring anxiety and depression; and the EuroQol-5 Dimension questionnaire measuring global QOL. All data were collected at baseline and 6, 12, 24, and 60 months. Change scores were compared between treatment arms using the Wilcoxon signed rank test. A significance level of .0125 to adjust for multiple comparisons was used for an overall 2-sided type 1 error of .05. Clinical significance was determined for the Expanded Prostate Index Composite change scores by an effect size of 0.5. Of 1092 patients analyzable for the primary end point, 962 (mean [SD] age, 66.6 [7.4] years) consented to the QOL component. No statistically significant differences with regard to baseline characteristics nor any of the QOL baseline domains were measured between arms. There were no differences in change score between arms with respect to any of the Expanded Prostate Index Composite questionnaire domain scores except at 12 months when the HRT arm had a larger decline than the CRT arm in the bowel domain (mean score, -7.5 vs -3.7, respectively; P<.001), but it did not reach clinical significance (effect size = 0.29). There were no differences between arms at any time point for the Hopkins Symptom Checklist nor EuroQol-5 Dimension questionnaire. Treatment with HRT is noninferior to CRT in men with low-risk prostate cancer in terms of disease-free survival and, as shown in the present study, in prostate cancer-specific (eg, bowel, bladder, sexual) and general QOL, as well as in anxiety and depression. This study provides evidence to affirm that HRT is a practice standard for men with low-risk prostate cancer. ClinicalTrials.gov identifier: NCT00331773.

Identifiants

pubmed: 30763425
pii: 2724800
doi: 10.1001/jamaoncol.2018.6752
pmc: PMC6459051
doi:

Banques de données

ClinicalTrials.gov
['NCT00331773']

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

664-670

Subventions

Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189867
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180868
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180822
Pays : United States
Organisme : NCI NIH HHS
ID : U10 CA180822
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014236
Pays : United States
Organisme : NCI NIH HHS
ID : UG1 CA189867
Pays : United States

Commentaires et corrections

Type : ErratumIn
Type : CommentIn

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Auteurs

Deborah W Bruner (DW)

Winship Cancer Institute, Emory University, Atlanta, Georgia.

Stephanie L Pugh (SL)

NRG Oncology Statistics and Data Management Center, University of Pittsburgh, Pittsburgh, Pennsylvania.

W Robert Lee (WR)

Duke University Medical Center, Durham, North Carolina.

William A Hall (WA)

Medical College of Wisconsin, Milwaukee.

James J Dignam (JJ)

NRG Oncology Statistics and Data Management Center, University of Pittsburgh, Pittsburgh, Pennsylvania.
University of Chicago, Chicago, Illinois.

Daniel Low (D)

Washington University in St Louis, St Louis, Missouri.

Gregory P Swanson (GP)

University of Texas Health Science Center at San Antonio, San Antonio.

Amit B Shah (AB)

WellSpan York Cancer Center, York, Pennsylvania.

Shawn Malone (S)

London Regional Cancer Program, London, Ontario, Canada.

Jeff M Michalski (JM)

Washington University in St Louis, St Louis, Missouri.

Ian S Dayes (IS)

Juravinski Cancer Centre, McMaster University, Hamilton, Ontario, Canada.

Samantha A Seaward (SA)

Kaiser Permanente Northern California, Santa Clara.

Paul L Nguyen (PL)

Dana-Farber Cancer Institute, Boston, Massachusetts.

Thomas M Pisansky (TM)

Mayo Clinic, Rochester, Minnesota.

Yuhchyau Chen (Y)

University of Rochester, Rochester, New York.

Howard M Sandler (HM)

Cedars-Sinai Medical Center, Los Angeles, California.

Benjamin Movsas (B)

Henry Ford Hospital, Detroit, Michigan.

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Classifications MeSH