Prostate Stereotactic Body Radiation Therapy With a Focal Simultaneous Integrated Boost: 5-Year Toxicity and Biochemical Recurrence Results From a Prospective Trial

被引:3
|
作者
Maas, Jared A. [1 ]
Dobelbower, Michael C. [1 ]
Yang, Eddy S. [1 ]
Clark, Grant M. [2 ]
Jacob, Rojymon [1 ]
Kim, Robert Y. [1 ]
Cardan, Rex A. [1 ]
Popple, Richard [1 ]
Nix, Jeffrey W. [3 ]
Rais-Bahrami, Soroush [3 ,4 ]
Fiveash, John B. [1 ]
Mcdonald, Andrew M. [1 ]
机构
[1] Univ Alabama Birmingham, Dept Radiat Oncol, Birmingham, AL 35294 USA
[2] East Tennessee Radiat Oncol Grp, Dept Radiat Oncol, Knoxville, TN USA
[3] Univ Alabama Birmingham, Dept Urol, Birmingham, AL USA
[4] Univ Alabama Birmingham, Dept Radiol, Birmingham, AL USA
关键词
DOSE-ESCALATION; CANCER; RADIOTHERAPY; BIOPSY; MRI;
D O I
10.1016/j.prro.2023.05.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Stereotactic body radiation therapy (SBRT) is increasingly used as a definitive treatment option for patients with prostate adenocarcinoma. The aim of this study was to assess the late toxicity, patient-reported quality of life outcomes, and biochemical recurrence rates after prostate SBRT with simultaneous integrated boost (SIB) targeting lesions defined by magnetic resonance imaging (MRI). Methods and Materials: Patients were eligible if they had biopsy-proven low-or intermediate-risk prostate adenocarcinoma, one or more focal lesions on MRI, and an MRI-defined total prostate volume of <120 mL. All patients received SBRT delivered to the entire prostate to a dose of 36.25 Gy in 5 fractions with an SIB to the lesions seen on MRI to 40 Gy in 5 fractions. Late toxicity was defined as any possible treatment-related adverse event occurring after 3 months from the completion of SBRT. Patient-reported quality of life was ascertained using standardized patient surveys. Results: A total of 26 patients were enrolled. Six patients (23.1%) had low-risk disease and 20 patients had intermediate-risk disease (76.9%). Seven patients (26.9%) received androgen deprivation therapy. Median follow-up was 59.5 months. No biochemical failures were observed. Three patients (11.5%) experienced late grade 2 genitourinary (GU) toxicity requiring cystoscopy, and 7 patients (26.9%) had late grade 2 GU toxicity requiring oral medications. Three patients (11.5%) had late grade 2 gastrointestinal toxicity characterized by hematochezia requiring colonoscopy and steroids per rectum. There were no grade 3 or higher toxicity events observed. The patient-reported quality-of-life metrics at the time of last follow-up were not significantly different than the pre-treatment baseline. Conclusions: The results of this study support that SBRT to the entire prostate to a dose of 36.25 Gy in 5 fractions with focal SIB to 40 Gy in 5 fractions has excellent biochemical control and is not associated with undue late gastrointestinal or GU toxicity or long-term quality of life decrement. Focal dose escalation with an SIB planning approach may be an opportunity to improve biochemical control while limiting dose to nearby organs at risk. (c) 2023 American Society for Radiation Oncology. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:466 / 474
页数:9
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