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最大日剂量 G-CSF 对预防妇科癌症患者发热性中性粒细胞减少症复发至关重要:一项病例对照研究。

Maximum daily dose of G-CSF is critical for preventing recurrence of febrile neutropenia in patients with gynecologic cancer: A case-control study.

机构信息

Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, Seongnam, Korea.

Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul, Korea.

出版信息

Medicine (Baltimore). 2022 Aug 26;101(34):e30155. doi: 10.1097/MD.0000000000030155.

Abstract

No study has evaluated the effect of therapeutic granulocyte colony-stimulating factor (G-CSF) in preventing recurrence of febrile neutropenia (FN) and survival outcomes in gynecologic cancer patients. Objective of this study is to optimize and to identify the use of G-CSF and identify the critical factors for preventing the recurrence of FN in women undergoing chemotherapy for the treatment of gynecologic cancer. The medical records of consecutive patients who underwent chemotherapy for the treatment of gynecologic cancer and experienced FN at least once were retrospectively reviewed. Clinico-laboratory variables were compared between those with and without recurrence of FN to identify risk factors for the recurrence and the most optimal usage of G-CSF that can prevent FN. Student t test, χ2 test, and multivariate Cox regression analysis were used. A total of 157 patients who met the inclusion criteria were included. Of 157, 49 (31.2%) experienced recurrence of FN. Age ≥55 years (P = .043), previous lines of chemotherapy ≤1 (P = .002), thrombocytopenia (P = .025), total dose (P = .003), and maximum daily dose (P = .009) of G-CSF were significantly associated with recurrence of FN. Multiple regression analysis showed that age ≥55 years (HR, 2.42; 95% CI, 1.14-5.14; P = .022), previous chemotherapy ≤1 (HR, 4.01; 95% CI, 1.40-11.55; P = .010), and maximum daily dose of G-CSF ≤600 μg (HR, 5.18; 95% CI, 1.12-24.02; P = .036) were independent risk factors for recurrent FN. Multivariate Cox regression analysis showed that a maximum daily dose of G-CSF ≤600 μg was the only independent risk factor for short recurrence-free survival of FN (HR, 4.75; 95% CI, 1.15-19.56; P = .031). Dose-dense administration of G-CSF >600 μg/day could prevent recurrence of FN in women who undergo chemotherapy for the treatment of gynecologic cancer and FN. Old age and FN at early lines of chemotherapy seem to be associated with FN recurrence.

摘要

尚无研究评估治疗性粒细胞集落刺激因子(G-CSF)在预防妇科癌症患者发热性中性粒细胞减少症(FN)复发和生存结局中的作用。本研究的目的是优化并确定 G-CSF 的使用方法,并确定预防女性在接受化疗治疗妇科癌症期间 FN 复发的关键因素。对至少经历过一次 FN 的连续接受化疗治疗妇科癌症的患者的病历进行回顾性分析。比较有和无 FN 复发患者的临床-实验室变量,以确定复发的危险因素和预防 FN 最优化的 G-CSF 使用方法。使用学生 t 检验、卡方检验和多变量 Cox 回归分析。符合纳入标准的患者共 157 例,其中 49 例(31.2%)发生 FN 复发。年龄≥55 岁(P=.043)、化疗线数≤1(P=.002)、血小板减少症(P=.025)、G-CSF 总剂量(P=.003)和最大日剂量(P=.009)与 FN 复发显著相关。多变量回归分析显示,年龄≥55 岁(HR,2.42;95%CI,1.14-5.14;P=.022)、化疗线数≤1(HR,4.01;95%CI,1.40-11.55;P=.010)和 G-CSF 最大日剂量≤600μg(HR,5.18;95%CI,1.12-24.02;P=.036)是 FN 复发的独立危险因素。多变量 Cox 回归分析显示,G-CSF 最大日剂量≤600μg 是 FN 复发无复发生存时间较短的唯一独立危险因素(HR,4.75;95%CI,1.15-19.56;P=.031)。G-CSF 剂量密集给药>600μg/天可预防妇科癌症患者化疗期间 FN 复发和 FN。早期化疗线 FN 和老年似乎与 FN 复发有关。

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