Long-Term Results of Moderate Hypofractionation to Prostate and Pelvic Nodes Plus Androgen Suppression in High-Risk Prostate Cancer.


Journal

Practical radiation oncology
ISSN: 1879-8519
Titre abrégé: Pract Radiat Oncol
Pays: United States
ID NLM: 101558279

Informations de publication

Date de publication:
Historique:
received: 27 01 2020
revised: 06 05 2020
accepted: 22 06 2020
pubmed: 2 8 2020
medline: 24 8 2021
entrez: 2 8 2020
Statut: ppublish

Résumé

Moderate hypofractionated radiation therapy (HypoRT) is an attractive alternative to conventionally fractionated radiation therapy for prostate cancer. However, most studies using HypoRT only included the prostate as the target volume. We report long-term outcomes of patients with high-risk prostate cancer treated with androgen deprivation therapy (ADT) and HypoRT to the prostate and nodal areas with a simultaneous integrated boost technique. Patients with localized, high-risk prostate cancer entered a prospective phase I/II study with a HypoRT regimen of 60 Gy/20 fractions (4 weeks) to the prostate volume while the nodal areas received 44 Gy in the same 20 fractions delivered with intensity modulated radiation therapy with a simultaneous integrated boost technique. ADT started 2 to 3 months before HypoRT. Toxicity was prospectively assessed according to the Common Terminology Criteria for Adverse Events v3. Outcomes rates were calculated by the actuarial method of Kaplan-Meier from the date of last radiation treatment until date of event. We report on the first 105 patients treated between October 2010 and February 2014. Median follow-up was 74 months, with 97% of patients followed for more than 36 months. Median ADT duration was 18 months. The worst grade 2 or higher late gastrointestinal or genitourinary toxicity was seen in 7% and 9%, respectively. There was no grade 4 or 5 toxicity. At the last follow-up, the rates of grade ≥2 gastrointestinal or genitourinary toxicity were 2% and 3%, respectively, with no residual grade ≥3 toxicity. The 5- and 7-year actuarial overall survival and relapse free survival were 91% and 85% and 87% and 81%, respectively. The longest follow-up report of moderate HypoRT (plus ADT) to the prostate and pelvic nodes shows that this approach is feasible, well tolerated, and effective. It is convenient for patients and the health system. A larger randomized trial using this approach is warranted.

Identifiants

pubmed: 32738465
pii: S1879-8500(20)30196-X
doi: 10.1016/j.prro.2020.06.012
pii:
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0

Types de publication

Clinical Trial, Phase I Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e514-e520

Informations de copyright

Copyright © 2020 American Society for Radiation Oncology. Published by Elsevier Inc. All rights reserved.

Auteurs

Sergio Faria (S)

Department of Radiation Oncology, McGill University, Quebec, Canada. Electronic address: sergio.faria@muhc.mcgill.ca.

Russel Ruo (R)

Department of Medical Physics, McGill University, Quebec, Canada.

Marianna Perna (M)

Department of Radiation Oncology, McGill University, Quebec, Canada.

Fabio Cury (F)

Department of Radiation Oncology, McGill University, Quebec, Canada.

Marie Duclos (M)

Department of Radiation Oncology, McGill University, Quebec, Canada.

Arash Sarshoghi (A)

Student of Health Sciences, Collège Jean de Brébeuf, Montreal, Canada.

Luis Souhami (L)

Department of Radiation Oncology, McGill University, Quebec, Canada.

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Classifications MeSH