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Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003

PURPOSE: Our objective was to report the quality of life (QoL) analysis and toxicity in patients with intermediate-risk prostate cancer treated with or without androgen deprivation therapy (ADT) in Proton Collaborative Group (PCG) GU003. METHODS AND MATERIALS: Between 2012 and 2019, patients with in...

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Autores principales: Laughlin, Brady S., Thorpe, Cameron S., DeWees, Todd A., Voss, Molly M., Chang, John H., Hartsell, William F., Sinesi, Christopher C., Rwigema, Jean-Claude M., Keole, Sameer R., Gondi, Vinai, Vargas, Carlos E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991536/
https://www.ncbi.nlm.nih.gov/pubmed/36896215
http://dx.doi.org/10.1016/j.adro.2022.101142
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author Laughlin, Brady S.
Thorpe, Cameron S.
DeWees, Todd A.
Voss, Molly M.
Chang, John H.
Hartsell, William F.
Sinesi, Christopher C.
Rwigema, Jean-Claude M.
Keole, Sameer R.
Gondi, Vinai
Vargas, Carlos E.
author_facet Laughlin, Brady S.
Thorpe, Cameron S.
DeWees, Todd A.
Voss, Molly M.
Chang, John H.
Hartsell, William F.
Sinesi, Christopher C.
Rwigema, Jean-Claude M.
Keole, Sameer R.
Gondi, Vinai
Vargas, Carlos E.
author_sort Laughlin, Brady S.
collection PubMed
description PURPOSE: Our objective was to report the quality of life (QoL) analysis and toxicity in patients with intermediate-risk prostate cancer treated with or without androgen deprivation therapy (ADT) in Proton Collaborative Group (PCG) GU003. METHODS AND MATERIALS: Between 2012 and 2019, patients with intermediate-risk prostate cancer were enrolled. Patients were randomized to receive moderately hypofractionated proton beam therapy (PBT) to 70 Gy relative biologic effectiveness in 28 fractions to the prostate with or without 6 months of ADT. Expanded Prostate Cancer Index Composite, Short-Form 12, and the American Urological Association Symptom Index instruments were given at baseline and 3, 6, 12, 18, and 24 months after PBT. Toxicities were assessed according to Common Terminology Criteria for Adverse Events (version 4). RESULTS: One hundred ten patients were randomized to PBT either with 6 months of ADT (n = 55) or without ADT (n = 55). The median follow-up was 32.4 months (range, 5.5-84.6). On average, 101 out of 110 (92%) patients filled out baseline QoL and patient-reported outcome surveys. The compliance was 84%, 82%, 64%, and 42% at 3, 6, 12, and 24 months, respectively. Baseline median American Urological Association Symptom Index was comparable between arms (6 [11%] ADT vs 5 [9%] no ADT, P = .359). Acute and late grade 2+ genitourinary and gastrointestinal toxicity were similar between arms. The ADT arm experienced a QoL decline of mean scores in the sexual (–16.1, P < .001) and hormonal (–6.3, P < .001) domains, with the largest time-specific hormonal differences at 3 (–13.8, P < .001) and 6 (–11.2, P < .001) months. The hormonal QoL domain returned to baseline 6 months after therapy. There was a trend to baseline in sexual function 6 months after completion of ADT. CONCLUSIONS: After 6 months of ADT, sexual and hormonal domains returned to baseline 6 months after completion of treatment for men with intermediate-risk prostate cancer.
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spelling pubmed-99915362023-03-08 Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003 Laughlin, Brady S. Thorpe, Cameron S. DeWees, Todd A. Voss, Molly M. Chang, John H. Hartsell, William F. Sinesi, Christopher C. Rwigema, Jean-Claude M. Keole, Sameer R. Gondi, Vinai Vargas, Carlos E. Adv Radiat Oncol Scientific Article PURPOSE: Our objective was to report the quality of life (QoL) analysis and toxicity in patients with intermediate-risk prostate cancer treated with or without androgen deprivation therapy (ADT) in Proton Collaborative Group (PCG) GU003. METHODS AND MATERIALS: Between 2012 and 2019, patients with intermediate-risk prostate cancer were enrolled. Patients were randomized to receive moderately hypofractionated proton beam therapy (PBT) to 70 Gy relative biologic effectiveness in 28 fractions to the prostate with or without 6 months of ADT. Expanded Prostate Cancer Index Composite, Short-Form 12, and the American Urological Association Symptom Index instruments were given at baseline and 3, 6, 12, 18, and 24 months after PBT. Toxicities were assessed according to Common Terminology Criteria for Adverse Events (version 4). RESULTS: One hundred ten patients were randomized to PBT either with 6 months of ADT (n = 55) or without ADT (n = 55). The median follow-up was 32.4 months (range, 5.5-84.6). On average, 101 out of 110 (92%) patients filled out baseline QoL and patient-reported outcome surveys. The compliance was 84%, 82%, 64%, and 42% at 3, 6, 12, and 24 months, respectively. Baseline median American Urological Association Symptom Index was comparable between arms (6 [11%] ADT vs 5 [9%] no ADT, P = .359). Acute and late grade 2+ genitourinary and gastrointestinal toxicity were similar between arms. The ADT arm experienced a QoL decline of mean scores in the sexual (–16.1, P < .001) and hormonal (–6.3, P < .001) domains, with the largest time-specific hormonal differences at 3 (–13.8, P < .001) and 6 (–11.2, P < .001) months. The hormonal QoL domain returned to baseline 6 months after therapy. There was a trend to baseline in sexual function 6 months after completion of ADT. CONCLUSIONS: After 6 months of ADT, sexual and hormonal domains returned to baseline 6 months after completion of treatment for men with intermediate-risk prostate cancer. Elsevier 2022-12-09 /pmc/articles/PMC9991536/ /pubmed/36896215 http://dx.doi.org/10.1016/j.adro.2022.101142 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Scientific Article
Laughlin, Brady S.
Thorpe, Cameron S.
DeWees, Todd A.
Voss, Molly M.
Chang, John H.
Hartsell, William F.
Sinesi, Christopher C.
Rwigema, Jean-Claude M.
Keole, Sameer R.
Gondi, Vinai
Vargas, Carlos E.
Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003
title Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003
title_full Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003
title_fullStr Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003
title_full_unstemmed Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003
title_short Initial Quality of Life and Toxicity Analysis of a Randomized Phase 3 Study of Moderately Hypofractionated Radiation Therapy With or Without Androgen Suppression for Intermediate-Risk Adenocarcinoma of the Prostate: PCG GU003
title_sort initial quality of life and toxicity analysis of a randomized phase 3 study of moderately hypofractionated radiation therapy with or without androgen suppression for intermediate-risk adenocarcinoma of the prostate: pcg gu003
topic Scientific Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9991536/
https://www.ncbi.nlm.nih.gov/pubmed/36896215
http://dx.doi.org/10.1016/j.adro.2022.101142
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