Toxicity at 1 Year After Stereotactic Body Radiation Therapy in 3 Fractions for Localized Prostate Cancer.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
01 09 2021
Historique:
received: 18 11 2020
revised: 20 02 2021
accepted: 14 03 2021
pubmed: 23 3 2021
medline: 5 10 2021
entrez: 22 3 2021
Statut: ppublish

Résumé

To assess the toxicity profile of prostate cancer stereotactic body radiation therapy (SBRT) in 3 fractions. This was a prospective, multicenter phase 2 toxicity study enrolling patients with low to favorable intermediate-risk prostate cancer. Before simulation, 3 to 4 fiducial markers along with a rectal spacer were placed. The target (prostate only) was prescribed 40 Gy, whereas the maximum dose to the urethra was limited to 33 Gy with the highest priority at planning; less stringent objectives were placed on the bladder, the filling of which was controlled via a Foley catheter. Treatment was delivered every other day. Toxicity was prospectively scored with Common Terminology Criteria for Adverse Events, and several patient-reported outcomes were collected. The maximum allowed prevalence rate of grade 2+ genitourinary (GU) toxicity at 1 year was set at 15%, and the study was sized accordingly. Between November 2015 and May 2019, 59 patients were enrolled by 3 participating institutions. Acute gastrointestinal toxicity was occasional and mild, whereas 11.9% of patients developed acute grade 2 GU toxicity and 1.7% developed acute grade 3 GU toxicity. No patient had persistent treatment-related grade 2+ GU toxicity at 12 months after SBRT; thus, the null hypothesis was rejected. We observed a clinically relevant worsening of both International Prostate Symptom Score (IPSS) and International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF) scores at 12 months compared with baseline. Moreover, we found a strong association between all selected bladder dose/volume metrics at planning and ICIQ-SF worsening at 12 months, whereas for the IPSS, the correlation with bladder dose metrics was marginal. The results suggest that at 12 months after treatment, the toxicity profile of SBRT in 3 fractions is acceptable.

Identifiants

pubmed: 33745951
pii: S0360-3016(21)00287-X
doi: 10.1016/j.ijrobp.2021.03.027
pii:
doi:

Types de publication

Clinical Trial, Phase II Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

93-100

Informations de copyright

Copyright © 2021 Elsevier Inc. All rights reserved.

Auteurs

Alessandro Magli (A)

Radiation Oncology, Azienda Sanitaria-Universitaria Friuli Centrale, Udine, Italy.

Alessia Farneti (A)

Radiation Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Adriana Faiella (A)

Radiation Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Mariaconsiglia Ferriero (M)

Urology, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Valeria Landoni (V)

Physics, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Diana Giannarelli (D)

Biostatistics, IRCCS Regina Elena National Cancer Institute, Rome, Italy.

Eugenia Moretti (E)

Physics, Azienda Sanitaria-Universitaria Friuli Centrale, Udine, Italy.

Ugo de Paula (U)

Radiation Oncology, San Giovanni-Addolorata Hospital, Rome, Italy.

Sara Gomellini (S)

Radiation Oncology, San Giovanni-Addolorata Hospital, Rome, Italy.

Giuseppe Sanguineti (G)

Radiation Oncology, IRCCS Regina Elena National Cancer Institute, Rome, Italy. Electronic address: giuseppe.sanguineti@ifo.gov.it.

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Classifications MeSH