如何简化骨髓瘤新化疗干预的评估?

Clinical Hematology International Pub Date : 2021-02-08 eCollection Date: 2021-03-01 DOI:10.2991/chi.k.210201.001
Treen Carson Michael Morris, Mary B Drake, Paul J Kettle, Tracey McGuigan, Maeve Leahy, Michael O'Dwyer, Helen Enright, Tanya O'Shea, Rakesh Popat, Heather E Oakervee, Kwee Yong, Jamie D Cavenagh, David A Cairns, Alberto Alvarez-Iglesias, Gordon Cook
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引用次数: 0

摘要

在首次评估硼替佐米[PS341]、阿霉素和地塞米松(PAD)方案时,未经治疗的患者的应答率远远高于传统化疗药物。我们通过比较 53 名接受长春新碱、阿霉素和地塞米松(VAD)或同等方案作为诱导治疗的患者的反应率,证明了 PAD 对复发或难治患者的疗效。25名患者对VAD产生了阳性反应,37名患者对PAD的反应≤部分缓解(PR)(p = 0.023)。如果采用更严格的反应水平,即非常好的 PR (VGPR),结果则非常明显地有利于 PAD 方案(p = 0.006)(麦克尼马斯检验)。使用来自单个患者的配对 M 蛋白水平进行比较也得出了类似的结果。英国血液与骨髓移植学会/英国骨髓瘤论坛骨髓瘤 X(强化)试验现已结束,由于 PAD 方案随后被英国血液与骨髓移植学会/英国骨髓瘤论坛骨髓瘤 X(强化)试验采用为再诱导疗法,我们对这两项研究的结果进行了回顾性分析。将既往接受过自体移植的患者(队列 1)的反应率和不良反应与骨髓瘤 X 的相应数据进行比较,结果显示两者密切相关。这些研究结果证明,在评估新引进的、可能非常有效的抗肿瘤药物时,可以通过直接比较对之前标准方案的反应来快速得出结果,尤其是对相对耐药的肿瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

How to Simplify the Evaluation of Newly Introduced Chemotherapeutic Interventions in Myeloma.

How to Simplify the Evaluation of Newly Introduced Chemotherapeutic Interventions in Myeloma.

How to Simplify the Evaluation of Newly Introduced Chemotherapeutic Interventions in Myeloma.

When the bortezomib [PS341], adriamycin and dexamethasone (PAD) regimen was first evaluated, the response rate in untreated patients was much superior to that elicited by conventional chemotherapeutic agents. We demonstrated the efficacy of PAD in relapsed or refractory patients by comparing the response rate obtained in 53 patients who received vincristine, adriamycin and dexamethasone (VAD) or equivalent regimen as induction therapy, using a comparative design in which each patient acted as their own control. Whereas 25 patients had a positive response to VAD, 37 patients had a response to PAD ≤ partial remission (PR) (p = 0.023). Using the more stringent response level of very good PR (VGPR) the results favored the PAD regimen very significantly (p = 0.006) (McNemars test). Similar results were seen using paired M-protein levels from individual patient comparisons. As the PAD regimen was subsequently adopted as the re-induction therapy in the British Society for Blood and Marrow Transplantation/United Kingdom Myeloma Forum Myeloma X (Intensive) trial, now concluded, we have retrospectively analyzed the findings from both studies. Comparison of response rates and adverse effects of patients having had previous autologous transplantation (Cohort 1) with the corresponding data from Myeloma X showed close correlation. These findings provide evidence that rapid results may be obtained in the evaluation of newly introduced, and potentially highly effective, anti-tumour agents by direct comparison to the response to the immediately preceding standard regimen, particularly in relatively resistant tumours.

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