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合并症对慢性髓性白血病患者总生存的影响:随机CML研究IV的结果

Impact of comorbidities on overall survival in patients with chronic myeloid leukemia: results of the randomized CML study IV.

作者信息

Saussele Susanne, Krauss Marie-Paloma, Hehlmann Rüdiger, Lauseker Michael, Proetel Ulrike, Kalmanti Lida, Hanfstein Benjamin, Fabarius Alice, Kraemer Doris, Berdel Wolfgang E, Bentz Martin, Staib Peter, de Wit Maike, Wernli Martin, Zettl Florian, Hebart Holger F, Hahn Markus, Heymanns Jochen, Schmidt-Wolf Ingo, Schmitz Norbert, Eckart Michael J, Gassmann Winfried, Bartholomäus Andrea, Pezzutto Antonio, Leibundgut Elisabeth Oppliger, Heim Dominik, Krause Stefan W, Burchert Andreas, Hofmann Wolf-Karsten, Hasford Joerg, Hochhaus Andreas, Pfirrmann Markus, Müller Martin C

机构信息

III Medizinische Klinik, Medizinische Fakultät Mannheim, Universität Heidelberg, Mannheim, Germany;

Institut für Medizinische Informationsverarbeitung, Biometrie und Epidemiologie (IBE), Ludwig-Maximilians-Universität, München, Germany;

出版信息

Blood. 2015 Jul 2;126(1):42-9. doi: 10.1182/blood-2015-01-617993. Epub 2015 Apr 27.

Abstract

We studied the influence of comorbidities on remission rate and overall survival (OS) in patients with chronic myeloid leukemia (CML). Participants of the CML Study IV, a randomized 5-arm trial designed to optimize imatinib therapy, were analyzed for comorbidities at diagnosis using the Charlson Comorbidity Index (CCI); 511 indexed comorbidities were reported in 1519 CML patients. Age was an additional risk factor in 863 patients. Resulting CCI scores were as follows: CCI 2, n = 589; CCI 3 or 4, n = 599; CCI 5 or 6, n = 229; and CCI ≥ 7, n = 102. No differences in cumulative incidences of accelerated phase, blast crisis, or remission rates were observed between patients in the different CCI groups. Higher CCI was significantly associated with lower OS probabilities. The 8-year OS probabilities were 93.6%, 89.4%, 77.6%, and 46.4% for patients with CCI 2, 3 to 4, 5 to 6, and ≥7, respectively. In multivariate analysis, CCI was the most powerful predictor of OS, which was still valid after removal of its age-related components. Comorbidities have no impact on treatment success but do have a negative effect on OS, indicating that survival of patients with CML is determined more by comorbidities than by CML itself. OS may therefore be inappropriate as an outcome measure for specific CML treatments. The trial was registered at www.clinicaltrials.gov as #NCT00055874.

摘要

我们研究了合并症对慢性髓性白血病(CML)患者缓解率和总生存期(OS)的影响。对CML研究IV(一项旨在优化伊马替尼治疗的随机5组试验)的参与者,使用查尔森合并症指数(CCI)在诊断时分析其合并症;1519例CML患者共报告了511项索引合并症。863例患者中年龄是另外一个风险因素。得出的CCI评分如下:CCI 2,n = 589;CCI 3或4,n = 599;CCI 5或6,n = 229;以及CCI≥7,n = 102。不同CCI组患者之间在加速期、急变期的累积发生率或缓解率方面未观察到差异。较高的CCI与较低的OS概率显著相关。CCI 2、3至4、5至6以及≥7的患者8年OS概率分别为93.6%、89.4%、77.6%和46.4%。在多变量分析中,CCI是OS最有力的预测指标,去除其与年龄相关的成分后该指标仍然有效。合并症对治疗成功无影响,但对OS有负面影响,这表明CML患者的生存更多地由合并症而非CML本身决定。因此,OS作为特定CML治疗的结局指标可能并不合适。该试验已在www.clinicaltrials.gov上注册,注册号为#NCT00055874。

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