[同时使用二甲双胍对接受培美曲塞化疗的非小细胞肺癌患者血液学不良事件的影响:一项使用日本索赔数据库的研究]。

IF 0.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan Pub Date : 2025-01-01 DOI:10.1248/yakushi.24-00172
Masahiro Hayafune, Shungo Imai, Hayato Kizaki, Masami Tsuchiya, Satoko Hori
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引用次数: 0

摘要

培美曲塞是一种叶酸类似物抑制剂,用于治疗非小细胞肺癌(NSCLC)。预防性补充维生素B12和叶酸可减少培美曲塞相关的血液毒性。抗糖尿病药物二甲双胍与维生素B12缺乏的潜在副作用有关。这项回顾性观察性研究旨在利用医学数据视觉数据库评估同时使用二甲双胍对接受培美曲塞化疗的非小细胞肺癌患者血液学不良事件的影响。2008年4月至2021年5月期间接受培美曲塞治疗的III期及以上NSCLC患者被分为二甲双胍治疗组(MTF)和非二甲双胍治疗组(non-MTF)。主要终点是培美曲塞治疗周期(C) 1至C2或C2至C3期间粒细胞集落刺激因子(G-CSF)给药的比例。使用倾向评分匹配(PSM)来平衡各组之间的基线特征。共有1174例患者符合纳入标准(54例MTF, 1120例非MTF)。经PSM治疗后,每组52例。MTF组的中位二甲双胍剂量为PSM前500 mg/d, PSM后625 mg/d。MTF组与非MTF组在G-CSF给药方面差异无统计学意义(15.4% vs. 21.2%, p=0.446)。多因素logistic回归分析也显示,二甲双胍的使用对血液毒性没有显著影响(优势比:1.208,95% CI: 0.554-2.634)。这表明,在接受培美曲塞化疗的日本非小细胞肺癌患者中,同时使用相对低剂量的二甲双胍不太可能显著增加血液毒性的风险。
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[Effect of Concomitant Metformin Use on Hematologic Adverse Events in Non-Small-Cell Lung Cancer Patients Undergoing Pemetrexed-Based Chemotherapy: A Study Using a Japanese Claims Database].

Pemetrexed is a folate analog inhibitor for the treatment of non-small-cell lung cancer (NSCLC). Prophylactic supplementation with vitamin B12 and folic acid reduces hematotoxicity associated with pemetrexed. Metformin, the antidiabetic agent, has been associated with the potential side effect of vitamin B12 deficiency. This retrospective observational study aimed to evaluate the effect of concomitant metformin use on hematologic adverse events in patients with NSCLC undergoing pemetrexed-based chemotherapy using the Medical Data Vision Database. Patients with stage III or higher NSCLC who received pemetrexed from April 2008 to May 2021 were categorized into metformin-treated (MTF) and non-metformin-treated (non-MTF) groups. The primary outcome was the proportion of granulocyte colony-stimulating factor (G-CSF) administration during cycle (C) 1 to C2 or C2 to C3 of pemetrexed therapy. Propensity score matching (PSM) was used to balance the baseline characteristics between the groups. A total of 1174 patients met the inclusion criteria (54 in MTF and 1120 in non-MTF). After PSM, 52 patients were included in each group. The median metformin dosage in the MTF group was 500 mg/d before and 625 mg/d after PSM. There were no significant differences between the MTF and non-MTF groups in G-CSF administration (15.4 vs. 21.2%, p=0.446). Multivariate logistic regression analysis also showed that metformin use did not significantly affect hematologic toxicity (odds ratio: 1.208, 95% CI: 0.554-2.634). This suggests that the concomitant use of a relatively low dose of metformin is unlikely to significantly increase the risk of hematotoxicity in Japanese patients with NSCLC receiving pemetrexed-based chemotherapy.

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