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实体瘤和淋巴瘤患者在接受传统化疗后早期死亡风险的识别。

Identification of patients at risk for early death after conventional chemotherapy in solid tumours and lymphomas.

作者信息

Ray-Coquard I, Ghesquière H, Bachelot T, Borg C, Biron P, Sebban C, LeCesne A, Chauvin F, Blay J Y

机构信息

Centre Léon Bérard, Lyon, France

出版信息

Br J Cancer. 2001 Sep 14;85(6):816-22. doi: 10.1054/bjoc.2001.2011.

Abstract

1-5% of cancer patients treated with cytotoxic chemotherapy die within a month after the administration of chemotherapy. Risk factors for these early deaths (ED) are not well known. The purpose of this study was to establish a risk model for ED after chemotherapy applicable to all tumour types. The model was delineated in a series of 1051 cancer patients receiving a first course of chemotherapy in the Department of Medicine of the Centre Léon Bérard (CLB) in 1996 (CLB-1996 cohort), and then validated in a series of patients treated in the same department in 1997 (CLB-1997), in a prospective cohort of patients with aggressive non-Hodgkin's lymphoma (NHL) (CLB-NHL), and in a prospective cohort of patients with metastatic breast cancer (MBC series) receiving first-line chemotherapy. In the CLB-1996 series, 43 patients (4.1%) experienced early. In univariate analysis, age > 60, PS > 1, lymphocyte (ly) count <or= 700 microl(-1)immediately prior to chemotherapy (d1), d1-platelet count <or= 150 Gl(-1), and the type of chemotherapy were significantly correlated to the risk of early death (P<or= 0.01). Using logistic regression, PS > 1 (hazard ratio 3.9 (95% Cl 2.0-7.5)) and d1-ly count <or= 700 microl(-1) (3.1 (95% Cl 1.6-5.8)) were identified as independent risk factors for ED. The calculated probability of ED was 20% (95% Cl 10-31) in patients with both risk factors, 6% (95% Cl 4-9) for patients with only 1 risk factor, and 1.7% (95% Cl 0.9-3) for patients with none of these 2 risk factors. In the CLB-97, CLB-NHL and MBC validation series, the observed incidences of early death in patients with both risk factors were 19%, 25% and 40% respectively and did not differ significantly from those calculated in the model. In conclusion, poor performance status and lymphopenia identify a subgroup of patients at high risk for early death after chemotherapy.

摘要

接受细胞毒性化疗的癌症患者中有1 - 5%在化疗给药后一个月内死亡。这些早期死亡(ED)的风险因素尚不清楚。本研究的目的是建立一个适用于所有肿瘤类型的化疗后早期死亡风险模型。该模型在1996年于里昂贝拉尔中心(CLB)医学部接受首个化疗疗程的1051例癌症患者系列中进行了描述(CLB - 1996队列),然后在1997年于同一科室治疗的患者系列(CLB - 1997)、侵袭性非霍奇金淋巴瘤(NHL)患者的前瞻性队列(CLB - NHL)以及接受一线化疗的转移性乳腺癌患者前瞻性队列(MBC系列)中进行了验证。在CLB - 1996系列中,43例患者(4.1%)出现早期死亡。单因素分析中,年龄>60岁、体能状态(PS)>1、化疗前即刻(d1)淋巴细胞(ly)计数≤700/μl、d1血小板计数≤150×10⁹/L以及化疗类型与早期死亡风险显著相关(P≤0.01)。使用逻辑回归分析,PS>1(风险比3.9(95%可信区间2.0 - 7.5))和d1 - ly计数≤700/μl(3.1(95%可信区间1.6 - 5.8))被确定为早期死亡的独立风险因素。具有两个风险因素的患者早期死亡的计算概率为20%(95%可信区间10 - 31),仅有一个风险因素的患者为6%(95%可信区间4 - 9),无这两个风险因素的患者为1.7%(95%可信区间0.9 - 3)。在CLB - 97、CLB - NHL和MBC验证系列中,具有两个风险因素的患者观察到的早期死亡发生率分别为19%、25%和40%,与模型计算值无显著差异。总之,体能状态差和淋巴细胞减少可识别出化疗后早期死亡高风险的患者亚组。

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