Improvement in long-term outcomes with successive Total Therapy trials for multiple myeloma: are patients now being cured?

被引:86
作者
Usmani, S. Z. [1 ]
Crowley, J. [2 ]
Hoering, A. [2 ]
Mitchell, A. [2 ]
Waheed, S. [1 ]
Nair, B. [1 ]
AlSayed, Y. [1 ]
vanRhee, F. [1 ]
Barlogie, B. [1 ]
机构
[1] Univ Arkansas Med Sci, Myeloma Inst Res & Therapy, Little Rock, AR 72205 USA
[2] Canc Res & Biostat, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
multiple myeloma; transplant; survival; MOLECULAR CLASSIFICATION; CELL TRANSPLANTATION; REGRESSION-MODELS; EXPRESSION; ABNORMALITIES; CYTOGENETICS; BORTEZOMIB; LEUKEMIA; IMPACT; GENES;
D O I
10.1038/leu.2012.160
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The concept of applying all active therapeutic agents in Total Therapy (TT) clinical trials for newly diagnosed multiple myeloma was pursued with the intent of developing curative treatment. The results of TT1 (n = 231), TT2 (n = 668) without or with thalidomide and TT3 with added bortezomib (n = 303) have been reported. An update with median follow-up times of 17.1, 8.7 and 5.5 years, respectively, is provided. Conditional overall survival (OS) analysis from a 4-year landmark was applied to account for earlier protocol failure owing to disease aggressiveness and toxicities. Cumulative relative survival was computed in the context of age-and gender-matched US population, and interval-specific relative survival ratios were estimated to determine times to normal survival expectation. Based on Cox model-adjusted statistics, OS, progression-free survival and complete-response duration all improved with the transitions from TT1 to TT2 to TT3; improvement was also evident from time-to-progression estimates, 4-year conditional survival data and cumulative relative survival. Interval-specific relative survival normalized progressively sooner, reaching near-normal levels with TT3 in patients who attained complete response. Thus, a strategy using all myeloma-effective agents up-front seems effective at preventing, in progressively larger patient cohorts over time, the outgrowth of resistant tumor cells that account for ongoing relapses. Leukemia (2013) 27, 226-232; doi: 10.1038/leu.2012.160
引用
收藏
页码:226 / 232
页数:7
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