Department of Breast Surgery, An-Nan Hospital, China Medical University, Tainan 709, Taiwan.
Department of Obstetrics and Gynecology, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chia-Yi 600, Taiwan.
Int J Mol Sci. 2024 Oct 6;25(19):10756. doi: 10.3390/ijms251910756.
The routine use of granulocyte colony-stimulating factor (GCSF) is not recommended for the prevention or treatment of chemotherapy-induced neutropenia or febrile neutropenia because risks associated with certain types of cancers, distant organ metastases, and primary tumor growth cannot be excluded. We examined the association between GCSF use and the incidence of brain metastasis (BM), as well as BM-free survival (BMFS). This retrospective cohort study included 121 stage IV breast cancer patients without confirmed BM at the time of diagnosis and who received at least one course of systematic chemotherapy or target therapy at a tertiary teaching hospital between 1 January 2014 and 31 December 2022. The effect of GCSF use on BM was assessed with other confounding factors in Cox regression analyses. In this retrospective cohort, patients who received GCSF treatment had a significantly higher incidence of BM than those who did not (34.9% vs. 13.8%, = 0.011). Univariate Cox regression analysis showed that GCSF use, menopause status, hormone treatment, HER2 treatment, cumulative dosage, dosage density, and neutropenia were independent risk factors for BMFS ( < 0.05). GCSF users had a higher risk of BM (adjusted HR: 2.538; 95% CI: 1.127-5.716, = 0.025) than nonusers. BM risk was significantly associated with those with neutropenia (RR: 1.84, 95% CI: 1.21, 2.80) but not with those without neutropenia (RR: 0.59, 95% CI: 0.41-0.84, Interaction -value 0.05). The higher the dose density of GCSF, the higher the risk compared with those who do not use GCSF ( for trend < 0.01). These preliminary results suggest that GCSF is associated with BM in patients with stage IV breast cancer who did not have BM at initial diagnosis. Further comprehensively designed large-scale observational studies are needed to confirm our preliminary results.
常规使用粒细胞集落刺激因子(GCSF)预防或治疗化疗引起的中性粒细胞减少症或发热性中性粒细胞减少症并不推荐,因为不能排除与某些类型癌症、远处器官转移和原发性肿瘤生长相关的风险。我们研究了 GCSF 使用与脑转移(BM)发生率以及 BM 无进展生存(BMFS)之间的关系。这项回顾性队列研究纳入了 121 例 IV 期乳腺癌患者,这些患者在诊断时没有确诊 BM,并且在 2014 年 1 月 1 日至 2022 年 12 月 31 日期间在一家三级教学医院接受了至少一个疗程的系统化疗或靶向治疗。在 Cox 回归分析中,使用 GCSF 与其他混杂因素评估了 GCSF 使用对 BM 的影响。在这个回顾性队列中,接受 GCSF 治疗的患者发生 BM 的发生率明显高于未接受 GCSF 治疗的患者(34.9% vs. 13.8%,= 0.011)。单变量 Cox 回归分析显示,GCSF 使用、绝经状态、激素治疗、HER2 治疗、累积剂量、剂量密度和中性粒细胞减少症是 BMFS 的独立危险因素(<0.05)。与未使用者相比,GCSF 使用者发生 BM 的风险更高(调整后的 HR:2.538;95%CI:1.127-5.716,= 0.025)。BM 风险与中性粒细胞减少症显著相关(RR:1.84,95%CI:1.21,2.80),但与中性粒细胞正常者无关(RR:0.59,95%CI:0.41-0.84,交互检验值 0.05)。与不使用 GCSF 者相比,GCSF 剂量密度越高,风险越高(趋势检验值 <0.01)。这些初步结果表明,在初始诊断时没有 BM 的 IV 期乳腺癌患者中,GCSF 与 BM 相关。需要进一步进行全面设计的大规模观察性研究来证实我们的初步结果。