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晚期霍奇金淋巴瘤患者的治疗相关性死亡率:德国霍奇金研究组的分析。

Treatment-related mortality in patients with advanced-stage hodgkin lymphoma: an analysis of the german hodgkin study group.

机构信息

University Hospital of Cologne, Cologne, Germany.

出版信息

J Clin Oncol. 2013 Aug 1;31(22):2819-24. doi: 10.1200/JCO.2012.47.9774. Epub 2013 Jun 24.

Abstract

PURPOSE

The introduction of BEACOPP(escalated) (escalated-dose bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone) has significantly improved tumor control and overall survival in patients with advanced-stage Hodgkin lymphoma. However, this regimen has also been associated with higher treatment-related mortality (TRM). Thus, we analyzed clinical course and risk factors associated with TRM during treatment with BEACOPP(escalated).

PATIENTS AND METHODS

In this retrospective analysis, we investigated incidence, clinical features, and risk factors for BEACOPP(escalated)-associated TRM in the German Hodgkin Study Group trials HD9, HD12, and HD15.

RESULTS

Among a total of 3,402 patients, TRM of 1.9% (64 of 3,402) was mainly related to neutropenic infections (n = 56; 87.5%). Twenty of 64 events occurred during the first course of BEACOPP(escalated) (31.3%). Higher risk of TRM was seen in patients age ≥ 40 years with poor performance status (PS) and in patients age ≥ 50 years. PS and age were then used to construct a new risk score; those with a score ≥ 2 had TRM of 7.1%, whereas patients who scored 0 or 1 had TRM of 0.9%.

CONCLUSION

The individual risk of TRM associated with BEACOPP(escalated) can be predicted by a simple algorithm based on age and PS. High-risk patients should receive special clinical attention.

摘要

目的

采用 BEACOPP(强化)方案(博来霉素、依托泊苷、多柔比星、环磷酰胺、长春新碱、丙卡巴肼和泼尼松)治疗晚期霍奇金淋巴瘤,显著提高了肿瘤控制率和总生存率。然而,该方案也与更高的治疗相关死亡率(TRM)相关。因此,我们分析了 BEACOPP(强化)治疗期间与 TRM 相关的临床过程和危险因素。

患者和方法

在这项回顾性分析中,我们调查了德国霍奇金研究组试验 HD9、HD12 和 HD15 中 BEACOPP(强化)相关 TRM 的发生率、临床特征和危险因素。

结果

在总共 3402 例患者中,TRM 为 1.9%(3402 例中的 64 例),主要与中性粒细胞减少性感染有关(n=56;87.5%)。64 例事件中的 20 例发生在 BEACOPP(强化)的第一个疗程期间(31.3%)。年龄≥40 岁、表现状态(PS)差和年龄≥50 岁的患者发生 TRM 的风险更高。然后,PS 和年龄被用于构建一个新的风险评分;评分≥2 的患者 TRM 为 7.1%,而评分 0 或 1 的患者 TRM 为 0.9%。

结论

基于年龄和 PS 的简单算法可以预测与 BEACOPP(强化)相关的 TRM 的个体风险。高危患者应接受特别的临床关注。

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