Stereotactic Body Radiotherapy for Oligoprogression in Castration- Resistant Prostate Cancer: Early Toxicity Analysis of the TRAP Trial

被引:0
作者
Patel, P. H. [1 ]
Dreibe, S. [1 ]
Reid, A. [1 ]
Parker, C. [1 ,2 ]
Murray, J. [1 ,2 ]
Pathmanathan, A. [1 ]
Tirona, A. [1 ]
Guevara, J. [1 ]
Suh, Y. -E. [1 ]
Frew, J. [3 ]
Palaniappan, N. [4 ]
Syndikus, I. [5 ]
Attard, G. [6 ]
Tunariu, N. [1 ,7 ]
Tree, A. C. [1 ,2 ]
机构
[1] Royal Marsden NHS Fdn Trust, London SM2 5PT, England
[2] Inst Canc Res, London SM2 5NG, England
[3] Newcastle Tyne Hosp NHS Fdn Trust, Newcastle Upon Tyne NE7 7DN, England
[4] Velindre Canc Ctr, Cardiff CF14 2TL, Wales
[5] Clatterbridge Canc Ctr NHS Fdn Trust, Wirral CH63 4JY, England
[6] UCL, Canc Inst, London NW1 2BU, England
[7] Univ Coll London Hosp, London NW1 2BU, England
关键词
Abiraterone; androgen receptor targeted agents; enzalutamide; oligoprogression; prostate cancer; stereotactic body radiotherapy;
D O I
10.1016/j.clon.2024.06.047
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: : To assess toxicity and patient quality of life after stereotactic body radiotherapy (SBRT) to oligoprogressive disease (OPD) in patients with metastatic castrate-resistant prostate cancer (CRPC) on androgen receptor targeted agents (ARTA). Material and methods: : This phase II trial enrolled patients with metastatic CRPC with < 2 oligoprogressive lesions in bone, lymph node, lung, or prostate. All patients were receiving systemic treatment with abiraterone or enzalutamide at the time of oligoprogression. All patients received SBRT to the OPD site(s) and continued the current ARTA. Patients received 30 Gy in 5 fractions (alternate days) to the OPD site. The primary endpoint of the trial is to assess if SBRT to OPD sites results in progression free survival of >6 months. The primary endpoint for this toxicity analysis is the rate of grade 3 or higher adverse events at any timepoint up to 6 months after SBRT. Secondary endpoints included comparing pre- and post-SBRT patient-related outcomes reported using visual analogue scale scores and EQ-5D health questionnaire. Results: : Forty enrolled patients had at least 6 months of follow-up at the time of analysis. Grade 3 or higher toxicity from any cause recorded using common terminology criteria for adverse events and radiation therapy oncology group was found in 8/40 (20%) of patients, but only 1/40 (2.5%) was deemed possibly related to SBRT. There was no significant difference in mean EQ5D visual analogue scale score from baseline to each timepoint after SBRT (p = 0.449). Conclusion: : In this prospective phase II clinical trial for OPD whilst on ARTA in the CRPC setting, we report low grade > 3 toxicity after SBRT. There is no discernible change in patient-reported quality of life due to SBRT treatment. The final results of progression-free survival and toxicity of SBRT treatment will be reported once further follow-up is complete. Crown Copyright (c) 2024 Published by Elsevier Ltd on behalf of The Royal College of Radiologists. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页码:585 / 592
页数:8
相关论文
共 5 条
  • [1] [Anonymous], experimental studies/data analysisPriyanka Patel, Alison Tree
  • [2] [Anonymous], literature researchPriyanka Patel, Alison Tree
  • [3] [Anonymous], statistical analysisPriyanka Patel
  • [4] [Anonymous], guarantor of integrity of the entire study - Alison Tree
  • [5] [Anonymous], study concepts and design - Alison Tree