Safety of accelerated hypofractionated whole pelvis radiation therapy prior to high dose rate brachytherapy or stereotactic body radiation therapy prostate boost
Autor: | Christina Phuong, Jason W. Chan, Lisa Ni, Phillip Wall, Osama Mohamad, Anthony C. Wong, I.-Chow Hsu, Albert J. Chang |
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Rok vydání: | 2022 |
Předmět: |
Urologic Diseases
HDR brachytherapy Male Aging Pelvic radiotherapy Clinical Trials and Supportive Activities Oncology and Carcinogenesis Brachytherapy R895-920 Radiosurgery Medical physics. Medical radiology. Nuclear medicine Clinical Research Humans Radiology Nuclear Medicine and imaging Oncology & Carcinogenesis RC254-282 Cancer Aged Retrospective Studies Prostate cancer Research Neoplasms. Tumors. Oncology. Including cancer and carcinogens Evaluation of treatments and therapeutic interventions Prostatic Neoplasms Radiotherapy Dosage 6.5 Radiotherapy and other non-invasive therapies Nodal radiotherapy Oncology Hypofractionation Radiation Dose Hypofractionation Patient Safety Digestive Diseases |
Zdroj: | Radiation Oncology (London, England) Radiation oncology (London, England), vol 17, iss 1 Radiation Oncology, Vol 17, Iss 1, Pp 1-7 (2022) |
ISSN: | 1748-717X |
DOI: | 10.1186/s13014-021-01976-2 |
Popis: | Background To evaluate acute and late genitourinary and gastrointestinal toxicities and patient reported urinary and sexual function following accelerated, hypofractionated external beam radiotherapy to the prostate, seminal vesicles and pelvic lymph nodes and high dose rate (HDR) brachytherapy or stereotactic body radiation therapy (SBRT) prostate boost. Methods Patients at a single institution with NCCN intermediate- and high-risk localized prostate cancer with logistical barriers to completing five weeks of whole pelvic radiotherapy (WPRT) were retrospectively reviewed for toxicity following accelerated, hypofractionated WPRT (41.25 Gy in 15 fractions of 2.75 Gy). Patients also received prostate boost radiotherapy with either HDR brachytherapy (1 fraction of 15 Gy) or SBRT (19 Gy in 2 fractions of 9.5 Gy). The duration of androgen deprivation therapy was at the discretion of the treating radiation oncologist. Toxicity was evaluated by NCI CTCAE v 5.0. Results Between 2015 and 2017, 22 patients with a median age of 71 years completed accelerated, hypofractionated WPRT. Median follow-up from the end of radiotherapy was 32 months (range 2–57). 5%, 73%, and 23% of patients had clinical T1, T2, and T3 disease, respectively. 86% of tumors were Gleason grade 7 and 14% were Gleason grade 9. 68% and 32% of patients had NCCN intermediate- and high-risk disease, respectively. 91% and 9% of patients received HDR brachytherapy and SBRT prostate boost following WPRT, respectively. Crude rates of grade 2 or higher GI and GU toxicities were 23% and 23%, respectively. 3 patients (14%) had late or persistent grade 2 toxicities of urinary frequency and 1 patient (5%) had late or persistent GI toxicity of diarrhea. No patient experienced grade 3 or higher toxicity at any time. No difference in patient-reported urinary or sexual function was noted at 12 months. Conclusions Accelerated, hypofractionated whole pelvis radiotherapy was associated with acceptable GU and GI toxicities and should be further validated for those at risk for harboring occult nodal disease. |
Databáze: | OpenAIRE |
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