Division of Radiation Oncology, Department of Oncology, London Health Sciences Centre, 790 Commissioners Rd. E, London, Ontario, N6C 1K1, Canada.
Department of Medical Biophysics, London Health Sciences Centre, London, Ontario, Canada.
BMC Cancer. 2021 Apr 14;21(1):405. doi: 10.1186/s12885-021-08020-2.
Patients with polymetastatic cancer are most often treated with systemic therapy to improve overall survival and/or delay progression, with palliative radiotherapy reserved for sites of symptomatic disease. Stereotactic ablative radiotherapy (SABR) has shown promise in the treatment of oligometastatic disease, but the utility of SABR in treating all sites of polymetastatic disease has yet to be evaluated. This study aims to evaluate the maximally tolerated dose (MTD) of SABR in patients with polymetastatic disease.
Up to 48 patients with polymetastatic cancer (> 10 sites) will be enrolled on this phase I, modified 3 + 3 design trial. Eligible patients will have exhausted (or refused) standard systemic therapy options. SABR will be delivered as an escalating number of weekly fractions of 6 Gy, starting at 6 Gy × 2 weekly fractions (dose level 1). The highest dose level (dose level 4) will be 6 Gy × 5 weekly fractions. Feasibility and safety of SABR will be evaluated 6 weeks following treatment using a composite endpoint of successfully completing treatment as well as toxicity outcomes.
This study will be the first to explore delivering SABR in patients with polymetastatic disease. SABR will be planned using the guiding principles of: strict adherence to dose constraints, minimization of treatment burden, and minimization of toxicity. As this represents a novel use of radiotherapy, our phase I study will allow for careful selection of the MTD for exploration in future studies.
This trial was prospectively registered in ClinicalTrials.gov as NCT04530513 on August 28, 2020.
患有广泛转移癌的患者通常接受全身治疗以提高总生存率和/或延迟进展,姑息性放疗保留给有症状疾病的部位。立体定向消融放疗 (SABR) 在治疗寡转移疾病方面显示出前景,但 SABR 在治疗广泛转移疾病的所有部位的效用尚未得到评估。本研究旨在评估 SABR 在广泛转移疾病患者中的最大耐受剂量 (MTD)。
多达 48 名患有广泛转移癌 (>10 个部位) 的患者将参加这项 I 期、改良的 3+3 设计试验。符合条件的患者将已经用尽 (或拒绝) 标准全身治疗选择。SABR 将作为每周 6Gy 的递增分数进行,从 6Gy×2 周分数开始 (剂量水平 1)。最高剂量水平 (剂量水平 4) 将是 6Gy×5 周分数。治疗后 6 周将使用成功完成治疗和毒性结果的综合终点来评估 SABR 的可行性和安全性。
这项研究将是首次探索在广泛转移疾病患者中使用 SABR。SABR 将按照以下指导原则进行计划:严格遵守剂量限制、最大限度地减少治疗负担和最大限度地减少毒性。由于这代表了放疗的新用途,我们的 I 期研究将允许仔细选择 MTD,以便在未来的研究中进行探索。
该试验于 2020 年 8 月 28 日前瞻性地在 ClinicalTrials.gov 注册为 NCT04530513。