Tom Baker Cancer Centre, 1331 29th St., NW, Calgary, AB T2N 4N2, Canada.
Department of Cardiac Sciences, University of Calgary, Calgary, AB T2N 4N2, Canada.
Curr Oncol. 2024 Sep 18;31(9):5608-5616. doi: 10.3390/curroncol31090415.
Pre-clinical and retrospective data suggest that doxycycline added to treatment regimens has benefit in AL amyloidosis. However, a recent multicenter, open-label, randomized controlled trial in AL amyloidosis patients treated with CyBorD did not demonstrate a progression-free survival (PFS) or cardiac PFS benefit with added doxycycline. The main objective of this study was to explore the role of doxycycline combined with bortezomib-containing regimens (BCRs) for newly diagnosed AL amyloidosis patients with cardiac involvement and to compare them with a cohort of concurrent patients treated with BCR only. AL amyloidosis patients, newly diagnosed between January 2012 and March 2022, who were treated with BCR at the Amyloidosis Program of Calgary (APC) were evaluated. Sixty-four concurrent patients were identified. Thirty-nine patients received doxycycline in addition to BCR (BCR-D) for a median of 8 months. The overall response rate was similar among the groups. No significant differences in VGPR/CR, dFLC at 1 month, time to first response, time to best response, or organ responses were noted between the BCR alone and BCR-D groups. Our retrospective study demonstrated that doxycycline combined with BCR failed to prolong OS, PFS, or cardiac responses compared with BCR alone in patients with cardiac AL amyloidosis.
临床前和回顾性数据表明,在治疗方案中添加多西环素对淀粉样变病有获益。然而,最近一项针对接受 CyBorD 治疗的 AL 淀粉样变病患者的多中心、开放标签、随机对照试验并未显示添加多西环素可带来无进展生存期(PFS)或心脏 PFS 获益。本研究的主要目的是探讨多西环素联合硼替佐米为基础的方案(BCR)在伴有心脏受累的新发 AL 淀粉样变病患者中的作用,并将其与同期仅接受 BCR 治疗的患者队列进行比较。
对 2012 年 1 月至 2022 年 3 月期间在卡尔加里淀粉样变性计划(APC)接受 BCR 治疗的新诊断为 AL 淀粉样变病且伴有心脏受累的患者进行评估。共确定了 64 例同期患者。39 例患者在接受 BCR 治疗的同时还接受了多西环素(BCR-D)治疗,中位数治疗时间为 8 个月。两组间的总体缓解率相似。单独接受 BCR 治疗组和 BCR-D 组在 VGPR/CR、1 个月时 dFLC、首次缓解时间、最佳缓解时间或器官缓解方面无显著差异。
我们的回顾性研究表明,与单独接受 BCR 治疗相比,在伴有心脏 AL 淀粉样变病的患者中,多西环素联合 BCR 并未能延长 OS、PFS 或心脏反应。