在一批符合移植条件的中年多发性骨髓瘤患者中,硼替佐米、环磷酰胺和地塞米松诱导疗法的应答者长期生存率有所提高。

Annals of Saudi medicine Pub Date : 2024-03-01 Epub Date: 2024-04-04 DOI:10.5144/0256-4947.2024.93
Ahmed Kotb Abdrabou, Fahad Al Sharif, Riad El Fakih, Hazaa Al Zahrani, Ruah Al Yamany, Mostafa Saleh, Saud Alhayli, Zakia Al Somali, Ahmad Alotaibi, AlFadel AlShaibani, Farah Deeba, Maryam Asif, Syed Ahmed Osman Ali Ahmed, Feras Al Fraih, Marwan Shaheen, Ali Alahmari, Walid Rasheed, Naeem Arshad Chaudhri, Fahad Al Mohareb, Mahmoud Aljurf, Amr Hanbali
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引用次数: 0

摘要

背景:多发性骨髓瘤(MM多发性骨髓瘤(MM)是第二大最常见的血液系统恶性肿瘤(15%)。硼替佐米、环磷酰胺和地塞米松 VCd(d:低剂量地塞米松)诱导方案因其高效、低毒、耐受性好(尤其是肾功能受损患者)而被广泛使用。目前还缺乏在临床实践中使用 VCD 的实际数据:评估 VCD 方案的实际应用经验:设计:回顾性:患者和方法:2007年7月至2020年7月期间接受VCD诱导并进行自体干细胞移植(ASCT)的新诊断MM患者。主要结局指标:反应评估、无进展生存期(PFS)和总生存期(OS):结果:在102名开始接受VCd诱导的患者中,87名患者出现了部分或更多的反应,总体反应率为85%。)这87名患者确诊时的中位年龄为52岁,其中29.9%的患者伴有肾功能损害,60.3%的患者处于修订版国际分期系统(R-ISS)的2期。与细胞遗传学风险较低的患者相比,细胞遗传学风险达标的患者获得的反应更好(P=0.044)。诱导后的反应率分别为6.9%的严格完全缓解(sCR)、35%的完全缓解(CR)、41.4%的很好部分反应(VGPR)和16.1%的部分反应(PR);移植后第100天,sCR和CR的反应率更高,分别为16.1%的sCR、35.6%的CR、32.2%的VGPR和16.1%的PR。中位 PFS 为 49 个月,5 年 OS 为 84%。获得 sCR 的患者与获得 PR 的患者相比,PFS 更佳(83 个月 vs 35 个月,P=.037)。高LDH、高危细胞遗传学和3期R-ISS患者的中位PFS和OS较差:结论:VCD诱导治疗新诊断的MM是一种高效、方便、可耐受且经济实惠的方案,尤其是在资源有限的中低收入国家,同样具有良好的疗效和生存率:使用登记处数据进行的回顾性分析具有通常的局限性,没有关于生活质量的数据。
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Improved long-term survival rate in the responders to bortezomib, cyclophosphamide, dexamethasone induction therapy in a transplant-eligible cohort of predominantly middle-age multiple myeloma patients.

Background: Multiple myeloma (MM) represents the second most common hematologic malignancy (15%). Induction with bortezomib, cyclophosphamide, and dexamthasone VCd (d: low dose dexamthasone) regimen is widely used due to its high effectiveness, low toxicity and good tolerability, particularly with renal impairment. Real-world data on the use of VCD in clinical practice is lacking.

Objectives: Evaluate the real-world experience of the VCD regimen.

Design: Retrospective.

Setting: Tumor registry database of tertiary cancer care center.

Patients and methods: newly diagnosed MM patients who received VCD induction and underwent autologous stem cell transplant (ASCT) from July 2007 to July 2020.

Main outcome measures: response evaluation, progression-free survival (PFS) and overall survival (OS).

Sample size: 87 patients.

Results: Of 102 patients who started induction with VCd, 87 patients experienced a partial response or more overall response rate of 85%). The median age of these 87 patients at diagnosis was 52 years, of which 29.9% presented with renal impairment and 60.3% of patients had stage 2 by the Revised International Staging System (R-ISS). Patients with a standard cytogenetic risk achieved a better response compared to those with a poor cytogenetic risk (P=.044). The post-induction response rates were 6.9% stringent complete remission (sCR), 35% complete remission (CR); 41.4% very good partial response (VGPR), and 16.1% partial response (PR), respectively; the response rates became greater for sCR and CR post-transplantation at day 100 with 16.1% sCR, 35.6% CR, 32.2% VGPR and 16.1% PR, respectively. The median PFS was 49 months and 5 years OS was 84%. PFS was better in patients who achieved sCR vs PR (83 vs 35 months, P=.037). High LDH, high-risk cytogenetic and stage 3 R-ISS showed a worse median PFS and OS.

Conclusions: VCD induction in newly diagnosed MM is highly effective, convenient, tolerable and affordable regimen, especially in low and middle-income countries with limited resources, also with favorable outcomes and survival. while those who did not respond successfully shifted to VRD or VTD.

Limitations: The usual limitations of a retrospective analysis using registry-level data, no data on quality of life.

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