Takagi Yusuke, Hosomi Yukio, Sunami Kuniko, Nakahara Yoshiro, Okuma Yusuke, Yomota Makiko, Shimokawa Tsuneo, Nagamata Makoto, Iguchi Mari, Okamoto Hiroaki, Okamura Tatsuru, Shibuya Masahiko
Department of Thoracic Oncology and Respiratory Medicine, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan; Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan; Department of Respiratory Medicine and Medical Oncology, Yokohama Municipal Citizen's Hospital, Yokohama, Japan; Department of Internal Medicine, Tokyo Metropolitan Matsuzawa Hospital, Tokyo, Japan
Department of Thoracic Oncology and Respiratory Medicine, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, Tokyo, Japan; Department of Thoracic Oncology, National Cancer Center Hospital, Tokyo, Japan; Department of Respiratory Medicine and Medical Oncology, Yokohama Municipal Citizen's Hospital, Yokohama, Japan; Department of Internal Medicine, Tokyo Metropolitan Matsuzawa Hospital, Tokyo, Japan.
Oncologist. 2014 Nov;19(11):1194-9. doi: 10.1634/theoncologist.2014-0221. Epub 2014 Sep 26.
Prior supplementation with folic acid and vitamin B12 is required to reduce pemetrexed therapy toxicity; the recommended lead-in time is at least 7 days. On the basis of previous pharmacokinetic and clinical studies, we hypothesized that the lead-in time could be shortened to 24 hours, enabling earlier commencement of standard chemotherapy; thus, we planned the first prospective trial of this regimen.
Patients with advanced nonsquamous non-small cell lung cancer who had not previously received cytotoxic chemotherapy were enrolled. After measurement of homocysteine concentrations, the patients received 1,000 μg of vitamin B12 by intramuscular injection and began taking 350-500 μg of oral folic acid daily. Starting 24-48 hours after the vitamin B12 injection, the patients received intravenous 500 mg/m(2) pemetrexed and 75 mg/m(2) cisplatin for 4 cycles at 3 weekly intervals. The primary endpoint was the proportion of patients who developed neutropenia grade ≥3.
Thirty patients received chemotherapy starting within 48 hours of the vitamin B12 injection. No treatment-related deaths or grade 4 toxicity occurred. Neutropenia grade ≥3, other laboratory toxicities grade ≥3, and nonlaboratory toxicities grade ≥3 occurred in 6.7%, 13%, and 13% of patients, respectively. The baseline homocysteine concentrations were not higher in patients with grade ≥3 toxicities than in the remainder of the cohort (mean values, 8.6 and 10.7 μmol/L, respectively). The response rate to chemotherapy was 43%.
The shortened vitamin supplementation was well tolerated and retained antitumor efficacy. Analysis of baseline homocysteine concentrations confirmed the efficacy of short-term vitamin supplementation.
先前需要补充叶酸和维生素B12以降低培美曲塞治疗的毒性;推荐的导入期至少为7天。基于先前的药代动力学和临床研究,我们推测导入期可缩短至24小时,从而能够更早开始标准化疗;因此,我们计划了该方案的首个前瞻性试验。
纳入先前未接受过细胞毒性化疗的晚期非鳞状非小细胞肺癌患者。在测定同型半胱氨酸浓度后,患者接受1000μg维生素B12肌肉注射,并开始每日口服350 - 500μg叶酸。在维生素B12注射后24 - 48小时开始,患者接受静脉注射500mg/m²培美曲塞和75mg/m²顺铂,每3周为1个周期,共4个周期。主要终点是发生≥3级中性粒细胞减少的患者比例。
30例患者在维生素B12注射后48小时内开始化疗。未发生与治疗相关的死亡或4级毒性反应。≥3级中性粒细胞减少、其他≥3级实验室毒性反应和≥3级非实验室毒性反应分别发生在6.7%、13%和13%的患者中。≥3级毒性反应患者的基线同型半胱氨酸浓度并不高于队列中的其余患者(平均值分别为8.6和10.7μmol/L)。化疗的缓解率为43%。
缩短维生素补充时间耐受性良好且保留了抗肿瘤疗效。对基线同型半胱氨酸浓度的分析证实了短期维生素补充的有效性。