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Early lymphopenia as a risk factor for chemotherapy‐induced febrile neutropenia

医学 内科学 化疗 中性粒细胞减少症 入射(几何) 前瞻性队列研究 发热性中性粒细胞减少症 胃肠病学 癌症 外科 光学 物理
作者
Chul Won Choi,Hwa Jung Sung,Kyong Hwa Park,So Young Yoon,Seok Jin Kim,Sang Cheul Oh,Jae Hong Seo,Byung Soo Kim,Sang Won Shin,Yeul Hong Kim,Jun Suk Kim
出处
期刊:American Journal of Hematology [Wiley]
卷期号:73 (4): 263-266 被引量:40
标识
DOI:10.1002/ajh.10363
摘要

Abstract Febrile neutropenia (FN) is a frequent complication of cancer chemotherapy, which causes death in 4–21% of patients and worsens the quality of life of patients. As a simple and accurate way of identifying patients who are at risk of FN, a lymphocyte count on post‐chemotherapy day 5 was suggested. To confirm the feasibility of this method and to define the incidence of FN among our own patient group, we conducted this prospective study. From September 2001 to February 2002, patients who received cytotoxic chemotherapy at Guro Hospital, Korea University, were enrolled. Blood sampling for a complete blood count was done on the starting day of chemotherapy and on day 3 and day 5 post‐chemotherapy. The prospective results of the CBC were compared between the FN group and non‐FN group. During the study period, 82 patients were enrolled. The male to female ratio was 52:30, and the median age was 56 years old (range: 14–78). Underlying malignancies were non‐Hodgkin's lymphoma (14 patients), stomach cancer (17), breast cancer (11), NSCLC (7), hepatobiliary cancer (10), sarcoma (3), colorectal cancer (3), and others (17). The incidence of FN was 18% (15/82 patients), and ANC at the time of FN was 275 ± 327/μl. Duration of fever was 3.9 ± 3.5 days. The incidence of FN was significantly higher in patients with lymphocyte counts at day 3 ≤ 500/μl ( P = 0.06), day 5 ≤ 500/μl ( P = 0.023), day 3 ≤ 700/μl ( P = 0.01), and day 5 ≤ 700/μl ( P = 0.0001). As a result of a logistic regression test, a day‐5 lymphocyte count ≤ 700/μl was identified as an independent risk factor for FN. In conclusion, a day‐5 lymphocyte count <700/μl was a risk factor for FN. To strengthen our result, we are planning to validate in a larger patient group. Am. J. Hematol. 73:263–266, 2003. © 2003 Wiley‐Liss, Inc.

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