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1181 例患者在 I 期临床试验中的存活情况:MD 安德森靶向治疗临床中心的经验。

Survival of 1,181 patients in a phase I clinic: the MD Anderson Clinical Center for targeted therapy experience.

机构信息

Department of Investigational Cancer Therapeutics, Phase I Clinical Trials Program, Biostatistics, and Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Clin Cancer Res. 2012 May 15;18(10):2922-9. doi: 10.1158/1078-0432.CCR-11-2217. Epub 2012 Mar 27.

Abstract

PURPOSE

To determine whether the Royal Marsden Hospital (RMH; London, UK) prognostic score for phase I patients can be validated in a large group of individuals seen in a different center and whether other prognostic variables are also relevant, we present an analysis of 1,181 patients treated in the MD Anderson Cancer Center (MDACC; Houston, TX) phase I clinic.

EXPERIMENTAL DESIGN

Medical records of 1,181 consecutive patients who were treated on at least one trial in the phase I clinic were reviewed.

RESULTS

The median age was 58 years and 50% were women. The median number of prior therapies was four and median survival 10 months [95% confidence interval (CI), 9.1-10.9 months]. Independent factors that predicted shorter survival in a multivariate Cox model and could be internally validated included RMH score of >1 (P < 0.0001; albumin <3.5 g/dL; lactate dehydrogenase >upper limit of normal, and >two sites of metastases), gastrointestinal tumor type (P < 0.0001), and Eastern Cooperative Oncology Group performance status ≥ 1 (P = 0.0004). The median survival was 24.0, 15.2, 8.4, 6.2, and 4.1 months for patients with 0, 1, 2, 3, and 4 or 5 of the above risk factors, respectively.

CONCLUSION

The RMH score was validated in a large group of patients at MDACC. Internal validation of the independent prognostic factors for survival led to the development of the MDACC prognostic score, a modification of the RMH score that strengthens it.

摘要

目的

为了确定伦敦皇家马斯登医院(RMH)的 I 期患者预后评分能否在另一个中心的大量患者中得到验证,以及其他预后因素是否也具有相关性,我们对在 MD 安德森癌症中心(MDACC)I 期临床诊所接受治疗的 1181 例患者进行了分析。

实验设计

对至少在 I 期临床诊所的一项试验中接受治疗的 1181 例连续患者的病历进行了回顾。

结果

中位年龄为 58 岁,50%为女性。中位治疗前的疗程数为 4 个,中位生存期为 10 个月(95%置信区间,9.1-10.9 个月)。多变量 Cox 模型预测的独立预后因素,且可进行内部验证,包括 RMH 评分>1(P<0.0001;白蛋白<3.5 g/dL;乳酸脱氢酶>正常值上限,且转移灶>2 个部位)、胃肠道肿瘤类型(P<0.0001)和东部肿瘤协作组表现状态≥1(P=0.0004)。无上述危险因素、有 1、2、3、4 或 5 个危险因素的患者的中位生存期分别为 24.0、15.2、8.4、6.2 和 4.1 个月。

结论

RMH 评分在 MDACC 的大量患者中得到了验证。对生存的独立预后因素进行内部验证后,制定了 MDACC 预后评分,对 RMH 评分进行了修正,增强了其效能。

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