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化疗引起的中性粒细胞减少作为一线多西他赛-吉西他滨化疗的晚期非小细胞肺癌患者的一个预后因素。

Chemotherapy-induced neutropenia as a prognostic factor in patients with advanced non-small cell lung cancer treated with front-line docetaxel-gemcitabine chemotherapy.

作者信息

Pallis A G, Agelaki S, Kakolyris S, Kotsakis A, Kalykaki A, Vardakis N, Papakotoulas P, Agelidou A, Geroyianni A, Agelidou M, Hatzidaki D, Mavroudis D, Georgoulias V

机构信息

Department of Medical Oncology, University General Hospital of Heraklion, P.O. Box 1352, 71110 Heraklion, Crete, Greece.

出版信息

Lung Cancer. 2008 Dec;62(3):356-63. doi: 10.1016/j.lungcan.2008.03.030. Epub 2008 May 22.

Abstract

BACKGROUND

Front-line docetaxel-gemcitabine (DG) combination represents an alternative to platinum-based chemotherapy in patients with advanced NSCLC. One of its more common side effects is neutropenia. The association between the grade of DG-induced neutropenia and the clinical outcome was analyzed.

PATIENTS AND METHODS

Eight hundred fifty-eight patients with locally advanced/metastatic NSCLC, treated with front-line DG were retrospectively analyzed. Patients were categorized into three groups according to the presented worst neutropenia grade: absent (grade 0), mild (grades I/II) and severe (grades III/IV).

RESULTS

Response rate, median time to tumor progression (TTP) and median overall survival (OS) were significantly better in patients developing any grade of neutropenia compared with those without neutropenia. The median TTPs were 3.0, 5.4 and 5.6 months for the groups with absent, mild and severe neutropenia, respectively; the median OSs were 7.9, 12.5 and 11.2 months for the same groups, respectively. Multivariate analysis revealed that both mild and severe chemotherapy-induced neutropenia were independent factors associated with a better TTP and OS survival.

CONCLUSION

Although DG-induced neutropenia was emerged as an independent prognostic factor, it remains to be demonstrated in prospective studies that dose escalation of chemotherapy drugs in patients who do not develop neutropenia may improve the clinical efficacy.

摘要

背景

对于晚期非小细胞肺癌(NSCLC)患者,一线多西他赛-吉西他滨(DG)联合方案是铂类化疗的一种替代方案。其较常见的副作用之一是中性粒细胞减少。分析了DG诱导的中性粒细胞减少分级与临床结局之间的关联。

患者与方法

对858例接受一线DG治疗的局部晚期/转移性NSCLC患者进行回顾性分析。根据出现的最严重中性粒细胞减少分级将患者分为三组:无(0级)、轻度(I/II级)和重度(III/IV级)。

结果

与未出现中性粒细胞减少的患者相比,出现任何级别的中性粒细胞减少的患者的缓解率、肿瘤进展中位时间(TTP)和总生存中位时间(OS)均显著更好。中性粒细胞减少无、轻度和重度组的中位TTP分别为3.0、5.4和5.6个月;相同组别的中位OS分别为7.9、12.5和11.2个月。多因素分析显示,轻度和重度化疗诱导的中性粒细胞减少均是与更好的TTP和OS生存相关的独立因素。

结论

虽然DG诱导的中性粒细胞减少已成为独立的预后因素,但对于未出现中性粒细胞减少的患者增加化疗药物剂量是否可提高临床疗效,仍有待前瞻性研究证实。

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