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Improved survival modeling in cancer research using a reduced piecewise exponential approach.使用简化的分段指数方法改进癌症研究中的生存模型。
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Superior results of Total Therapy 3 (2003-33) in gene expression profiling-defined low-risk multiple myeloma confirmed in subsequent trial 2006-66 with VRD maintenance.在后续的 2006-66 试验中,使用 VRD 维持治疗,在基因表达谱定义的低危多发性骨髓瘤中,证实了 Total Therapy 3(2003-33)的优异疗效。
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Long-term follow-up of autotransplantation trials for multiple myeloma: update of protocols conducted by the intergroupe francophone du myelome, southwest oncology group, and university of arkansas for medical sciences.自体移植治疗多发性骨髓瘤的长期随访:法国骨髓瘤协作组、西南肿瘤协作组和阿肯色大学医学科学中心进行的方案更新。
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Lenalidomide plus high-dose dexamethasone versus lenalidomide plus low-dose dexamethasone as initial therapy for newly diagnosed multiple myeloma: an open-label randomised controlled trial.来那度胺联合高剂量地塞米松与来那度胺联合低剂量地塞米松作为初治多发性骨髓瘤的初始治疗:一项开放标签随机对照试验。
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Bortezomib plus melphalan and prednisone for initial treatment of multiple myeloma.硼替佐米联合美法仑和泼尼松用于多发性骨髓瘤的初始治疗。
N Engl J Med. 2008 Aug 28;359(9):906-17. doi: 10.1056/NEJMoa0801479.
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Oral melphalan, prednisone, and thalidomide in elderly patients with multiple myeloma: updated results of a randomized controlled trial.口服美法仑、泼尼松和沙利度胺用于老年多发性骨髓瘤患者:一项随机对照试验的更新结果
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Prospective, randomized study of single compared with double autologous stem-cell transplantation for multiple myeloma: Bologna 96 clinical study.多发性骨髓瘤单倍体与双倍体自体干细胞移植的前瞻性随机研究:博洛尼亚96临床研究
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A randomized phase 2 study of lenalidomide therapy for patients with relapsed or relapsed and refractory multiple myeloma.来那度胺治疗复发或复发难治性多发性骨髓瘤患者的随机2期研究。
Blood. 2006 Nov 15;108(10):3458-64. doi: 10.1182/blood-2006-04-015909. Epub 2006 Jul 13.
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Thalidomide and hematopoietic-cell transplantation for multiple myeloma.沙利度胺与造血干细胞移植治疗多发性骨髓瘤
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Standard chemotherapy compared with high-dose chemoradiotherapy for multiple myeloma: final results of phase III US Intergroup Trial S9321.标准化疗与大剂量放化疗治疗多发性骨髓瘤的比较:美国国际协作组III期试验S9321的最终结果
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多发性骨髓瘤生存的预后因素分析,采用 S9321 国际试验(INT 0141):检验不同变量是否控制不同的生存时间阶段。

Prognostic factor analyses of myeloma survival with intergroup trial S9321 (INT 0141): examining whether different variables govern different time segments of survival.

机构信息

Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, 4301 West Markham #816, Little Rock, AR 72205, USA.

出版信息

Ann Hematol. 2011 Apr;90(4):423-8. doi: 10.1007/s00277-010-1130-y. Epub 2010 Dec 14.

DOI:10.1007/s00277-010-1130-y
PMID:21153898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3053415/
Abstract

Multiple myeloma (MM) survival plots usually display steeper initial and shallower subsequent slopes reflecting differences in disease biology and likely prognostic factors (PF). S9321 trial was selected to determine PF operative at baseline and subsequent 3, 4, 5, and 7-year landmarks (LM-0, LM-3, LM-4, LM-5, and LM-7). With a median follow-up of 8.2 years, survival was similar in transplant and standard therapy arms, justifying data pooling. Median survival for 775 eligible patients is 48 months. According to proportional hazards models, seven of 12 investigated baseline variables retained independent significance for LM-0, of which only two (beta-2-microglobulin and age) extended out to LM-7; the remaining five comprised features of disease aggressiveness (lactate dehydrogenase, calcium, platelet count, C-reactive protein) and host co-morbidity (performance status). Our observations of LM dependency of PF can be exploited toward advancing myeloma therapy by stratifying patients according to whether early or late portions of the survival history are being targeted.

摘要

多发性骨髓瘤(MM)生存曲线通常显示初始斜率较陡,后续斜率较浅,反映了疾病生物学和可能的预后因素(PF)的差异。选择 S9321 试验来确定基线和随后的 3、4、5 和 7 年里程碑(LM-0、LM-3、LM-4、LM-5 和 LM-7)时的 PF 操作。中位随访 8.2 年后,移植组和标准治疗组的生存情况相似,因此可以对数据进行汇总。775 名合格患者的中位生存时间为 48 个月。根据比例风险模型,12 个基线变量中有 7 个在 LM-0 时具有独立意义,其中只有 2 个(β-2-微球蛋白和年龄)扩展到 LM-7;其余 5 个包括疾病侵袭性(乳酸脱氢酶、钙、血小板计数、C 反应蛋白)和宿主合并症(表现状态)的特征。我们观察到 PF 对 LM 的依赖性可以通过根据生存史的早期或晚期部分是否作为目标来分层患者,从而推进骨髓瘤治疗。