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Phase II prospective trial "Give Me Five" short-term high precision radiotherapy for early prostate cancer with simultaneous boost to the dominant intraprostatic lesion: the impact of toxicity on quality of life (AIRC IG-13218).

Authors :
Marvaso, Giulia
Gugliandolo, Simone Giovanni
Bellerba, Federica
Gandini, Sara
Corrao, Giulia
Volpe, Stefania
Rojas, Damaris Patricia
Riva, Giulia
Zerini, Dario
Pepa, Matteo
Fodor, Cristiana Iuliana
La Rocca, Eliana
Pricolo, Paola
Alessi, Sarah
Petralia, Giuseppe
Mistretta, Francesco Alessandro
Cambria, Raffaella
Cattani, Federica
De Cobelli, Ottavio
Orecchia, Roberto
Source :
Medical Oncology; Aug2020, Vol. 37 Issue 8, pN.PAG-N.PAG, 1p
Publication Year :
2020

Abstract

As part of the AIRC IG-13218 (NCT01913717), we analyzed data from patients with low- and intermediate-risk prostate cancer treated with extreme hypofractionated radiotherapy (RT) and simultaneous boost to the intraprostatic lesion. The aim of the study is to identify clinically meaningful information through the analysis of validated questionnaires testing gastrointestinal (GI) and genitourinary (GU) RT-related toxicity and their impact on quality of life (QoL). At the end of RT treatment, clinical assessment and prostate-specific antigen (PSA) measurements were performed every 3 months for at least 2 years and GI and GU toxicities were evaluated contextually. QoL of enrolled patients was assessed by International Prostate Symptoms score (IPSS), European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30), EORTC QLQ prostate specific (QLQ-PR25), and sexual activity by International Index of Erectile Function (IIEF-5). Patients' score changes were calculated at the end of RT, at one month after RT and at 12 and 24 months. Sixty-five prospectively enrolled patients were analyzed. Extensive analysis of different QoL assessments showed that patients' tolerance was satisfactory across all the considered time points, with no statistically significant change of QoL from baseline compared to that before RT. Overall survival and biochemical progression-free survival at 2-years were of 98% and 97%, respectively. Despite the toxicity of extreme hypofractionation was low and tumor control was encouraging, a longer follow-up is necessary to confirm our findings. The increasing dose to the dominant intraprostatic lesion does not worsen the RT toxicity and consequently does not affect patients' QoL, thus questioning the possibility of an even more escalated treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13570560
Volume :
37
Issue :
8
Database :
Complementary Index
Journal :
Medical Oncology
Publication Type :
Academic Journal
Accession number :
145492662
Full Text :
https://doi.org/10.1007/s12032-020-01397-3