Cargando…

Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer

Proton boost of 20 Gy in daily 5 Gy fractions followed by external beam radiotherapy (EBRT) of 50 Gy in daily 2 Gy fractions were given to 278 patients with prostate cancer with T1b to T4N0M0 disease. Fifty-three percent of the patients received neoadjuvant androgen deprivation therapy (N-ADT). The...

Descripción completa

Detalles Bibliográficos
Autores principales: Johansson, Silvia, Åström, Lennart, Sandin, Fredrik, Isacsson, Ulf, Montelius, Anders, Turesson, Ingela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399336/
https://www.ncbi.nlm.nih.gov/pubmed/22848840
http://dx.doi.org/10.1155/2012/654861
_version_ 1782238391585210368
author Johansson, Silvia
Åström, Lennart
Sandin, Fredrik
Isacsson, Ulf
Montelius, Anders
Turesson, Ingela
author_facet Johansson, Silvia
Åström, Lennart
Sandin, Fredrik
Isacsson, Ulf
Montelius, Anders
Turesson, Ingela
author_sort Johansson, Silvia
collection PubMed
description Proton boost of 20 Gy in daily 5 Gy fractions followed by external beam radiotherapy (EBRT) of 50 Gy in daily 2 Gy fractions were given to 278 patients with prostate cancer with T1b to T4N0M0 disease. Fifty-three percent of the patients received neoadjuvant androgen deprivation therapy (N-ADT). The medium followup was 57 months. The 5-year PSA progression-free survival was 100%, 95%, and 74% for low-, intermediate-, and high-risk patients, respectively. The toxicity evaluation was supported by a patient-reported questionnaire before every consultant visit. Cumulative probability and actuarial prevalence of genitourinary (GU) and gastrointestinal (GI) toxicities are presented according to the RTOG classification. N-ADT did not influence curability. Mild pretreatment GU-symptoms were found to be a strong predictive factor for GU-toxicity attributable to treatment. The actuarial prevalence declined over 3 to 5 years for both GU and GI toxicities, indicating slow resolution of epithelial damage to the genitourinary and gastrointestinal tract. Bladder toxicities rather than gastrointestinal toxicities seem to be dose limiting. More than 5-year followup is necessary to reveal any sign of true progressive late side effects of the given treatment. Hypofractionated proton-boost combined with EBRT is associated with excellent curability of localized PC and acceptable frequencies of treatment toxicity.
format Online
Article
Text
id pubmed-3399336
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-33993362012-07-30 Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer Johansson, Silvia Åström, Lennart Sandin, Fredrik Isacsson, Ulf Montelius, Anders Turesson, Ingela Prostate Cancer Clinical Study Proton boost of 20 Gy in daily 5 Gy fractions followed by external beam radiotherapy (EBRT) of 50 Gy in daily 2 Gy fractions were given to 278 patients with prostate cancer with T1b to T4N0M0 disease. Fifty-three percent of the patients received neoadjuvant androgen deprivation therapy (N-ADT). The medium followup was 57 months. The 5-year PSA progression-free survival was 100%, 95%, and 74% for low-, intermediate-, and high-risk patients, respectively. The toxicity evaluation was supported by a patient-reported questionnaire before every consultant visit. Cumulative probability and actuarial prevalence of genitourinary (GU) and gastrointestinal (GI) toxicities are presented according to the RTOG classification. N-ADT did not influence curability. Mild pretreatment GU-symptoms were found to be a strong predictive factor for GU-toxicity attributable to treatment. The actuarial prevalence declined over 3 to 5 years for both GU and GI toxicities, indicating slow resolution of epithelial damage to the genitourinary and gastrointestinal tract. Bladder toxicities rather than gastrointestinal toxicities seem to be dose limiting. More than 5-year followup is necessary to reveal any sign of true progressive late side effects of the given treatment. Hypofractionated proton-boost combined with EBRT is associated with excellent curability of localized PC and acceptable frequencies of treatment toxicity. Hindawi Publishing Corporation 2012 2012-07-08 /pmc/articles/PMC3399336/ /pubmed/22848840 http://dx.doi.org/10.1155/2012/654861 Text en Copyright © 2012 Silvia Johansson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Johansson, Silvia
Åström, Lennart
Sandin, Fredrik
Isacsson, Ulf
Montelius, Anders
Turesson, Ingela
Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer
title Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer
title_full Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer
title_fullStr Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer
title_full_unstemmed Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer
title_short Hypofractionated Proton Boost Combined with External Beam Radiotherapy for Treatment of Localized Prostate Cancer
title_sort hypofractionated proton boost combined with external beam radiotherapy for treatment of localized prostate cancer
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399336/
https://www.ncbi.nlm.nih.gov/pubmed/22848840
http://dx.doi.org/10.1155/2012/654861
work_keys_str_mv AT johanssonsilvia hypofractionatedprotonboostcombinedwithexternalbeamradiotherapyfortreatmentoflocalizedprostatecancer
AT astromlennart hypofractionatedprotonboostcombinedwithexternalbeamradiotherapyfortreatmentoflocalizedprostatecancer
AT sandinfredrik hypofractionatedprotonboostcombinedwithexternalbeamradiotherapyfortreatmentoflocalizedprostatecancer
AT isacssonulf hypofractionatedprotonboostcombinedwithexternalbeamradiotherapyfortreatmentoflocalizedprostatecancer
AT monteliusanders hypofractionatedprotonboostcombinedwithexternalbeamradiotherapyfortreatmentoflocalizedprostatecancer
AT turessoningela hypofractionatedprotonboostcombinedwithexternalbeamradiotherapyfortreatmentoflocalizedprostatecancer