Department of Medical Oncology, Dana-Farber Cancer Institute, Dana 1220, Boston, MA, 02115, USA.
Cancer Chemother Pharmacol. 2010 Oct;66(5):961-8. doi: 10.1007/s00280-010-1248-6. Epub 2010 Feb 4.
In some reports, 5-fluorouracil has been associated with modest activity in patients with neuroendocrine tumors. Pemetrexed is a multitargeted antifolate with activity in tumor types not significantly responsive to other antifolates. We evaluated the efficacy of pemetrexed in a phase II study of patients with advanced neuroendocrine tumors.
Patients with metastatic neuroendocrine tumors (excluding small-cell carcinoma) were treated with pemetrexed administered intravenously at a dose of 500 mg/m(2) every 21 days. To reduce potential toxicity, patients also received folic acid, vitamin B12 supplementation, and peri-infusional treatment with dexamethasone. Patients were followed for response, toxicity, and survival.
The study was designed with a total accrual goal of 32 patients. Due to lack of radiographic responses in patients during the study period, accrual was terminated at 17. However, one patient achieved a delayed partial response following discontinuation of pemetrexed. Ten patients were evaluable for biochemical response; five (50%) experienced >50% decrease in plasma chromogranin A. Among the 17 patients, 5 (29%) discontinued therapy due to treatment-related toxicity. The median overall survival was 12.1 months.
Pemetrexed does not appear to have significant antitumor activity in patients with advanced neuroendocrine tumors. The limited antitumor activity and potential toxicity associated with pemetrexed mirrors experience with the majority of other cytotoxic agents in patients with neuroendocrine tumors. Investigation of novel, molecularly targeted agents may offer more promise in this disease.
在一些报告中,5-氟尿嘧啶在神经内分泌肿瘤患者中表现出一定的活性。培美曲塞是一种多靶点抗叶酸剂,对其他抗叶酸剂无明显反应的肿瘤类型具有活性。我们评估了培美曲塞在晚期神经内分泌肿瘤患者的 II 期研究中的疗效。
转移性神经内分泌肿瘤(不包括小细胞癌)患者接受培美曲塞静脉滴注治疗,剂量为 500mg/m²,每 21 天一次。为降低潜在毒性,患者还接受叶酸、维生素 B12 补充和地塞米松围输注治疗。对患者的反应、毒性和生存情况进行随访。
该研究的总入组目标为 32 例患者。由于研究期间患者的影像学反应缺乏,入组在 17 例时终止。然而,1 例患者在停止培美曲塞治疗后出现延迟部分缓解。10 例患者可评估生化反应;5 例(50%)患者血浆嗜铬粒蛋白 A 下降>50%。在 17 例患者中,有 5 例(29%)因治疗相关毒性而停止治疗。总生存期中位数为 12.1 个月。
培美曲塞似乎对晚期神经内分泌肿瘤患者没有明显的抗肿瘤活性。培美曲塞的有限抗肿瘤活性和潜在毒性与大多数神经内分泌肿瘤患者的其他细胞毒性药物的经验相符。对新型、分子靶向药物的研究可能为该疾病带来更多希望。