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既往未经治疗的骨髓瘤患者的长期预后:纳入风险分层模型中的诱导化疗和大剂量美法仑反应有助于指导新型治疗的应用。

Long-term outcomes of previously untreated myeloma patients: responses to induction chemotherapy and high-dose melphalan incorporated within a risk stratification model can help to direct the use of novel treatments.

作者信息

Alvares Caroline L, Davies Faith E, Horton Clive, Patel Gita, Powles Ray, Sirohi Bhawna, Zuha Roslin, Gatt Alex, Saso Radovan, Treleaven Jennifer G, Dearden Claire E, Potter Michael N, Ethell Mark E, Morgan Gareth J

机构信息

Haemato-oncology Unit, Royal Marsden Hospital, Sutton, Surrey, UK.

出版信息

Br J Haematol. 2005 Jun;129(5):607-14. doi: 10.1111/j.1365-2141.2005.05514.x.

Abstract

Induction chemotherapy followed by high-dose melphalan (HDM) is the standard treatment for fitter patients with myeloma. The place of bortezomib and the thalidomide analogues within this treatment paradigm is yet to be established. We sought to identify patients who may benefit from the introduction of novel agents during their initial management. An intention-to-treat analysis was performed on 383 patients with newly diagnosed myeloma eligible for HDM to determine whether the extent of response to induction therapy and HDM correlated with long-term survival. Early response [complete response (CR) and partial response (PR)] to induction therapy was predictive of overall survival (OS) [median OS, 7.47 years for responders (CR and PR) versus 4.89 years for non-responders; P = 0.035]. The attainment of CR at 3 months post-HDM correlated with a prolonged progression-free survival (PFS) (median PFS, 7.4 years in CR group versus 5.3 years in non-CR group; P = 0.023). This data suggests that, at every stage of treatment, the aim should be to achieve CR. Patients with suboptimal responses could be offered alternative therapy. We propose a multiparametric risk-adapted model that includes response to induction chemotherapy and HDM, for identifying patients who may benefit from novel approaches to treatment.

摘要

诱导化疗后给予大剂量美法仑(HDM)是适合的骨髓瘤患者的标准治疗方法。硼替佐米和沙利度胺类似物在这种治疗模式中的地位尚未确定。我们试图确定在初始治疗期间可能从引入新型药物中获益的患者。对383例符合HDM治疗条件的新诊断骨髓瘤患者进行意向性分析,以确定诱导治疗和HDM的缓解程度是否与长期生存相关。诱导治疗的早期缓解[完全缓解(CR)和部分缓解(PR)]可预测总生存期(OS)[缓解者(CR和PR)的中位OS为7.47年,未缓解者为4.89年;P = 0.035]。HDM后3个月达到CR与无进展生存期(PFS)延长相关(CR组的中位PFS为7.4年,非CR组为5.3年;P = 0.023)。该数据表明,在治疗的每个阶段,目标都应该是实现CR。对缓解欠佳的患者可提供替代治疗。我们提出一种多参数风险适应性模型,该模型包括对诱导化疗和HDM的反应,用于识别可能从新型治疗方法中获益的患者。

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