Jalal Shadia, Ansari Rafat, Govindan Ramaswamy, Bhatia Sumeet, Bruetman Daniel, Fisher William, Masters Gregory, White Angela, Stover Daniel, Yu Menggang, Hanna Nasser
Indiana University Melvin and Bren Simon Cancer Center, Indianapolis, Indianapolis, USA.
J Thorac Oncol. 2009 Jan;4(1):93-6. doi: 10.1097/JTO.0b013e31818de1e6.
: Small cell lung cancer (SCLC) is initially a chemotherapy-sensitive disease. Nevertheless, drug-resistance results in disease recurrence in most patients. Many drugs, including antimetabolites, are active, but only minimal progress has been made in improving survival times for those with advanced disease. Based on the need to discover better systemic therapies, we conducted a phase II study of pemetrexed in patients with relapsed SCLC.
: Eligible patients had SCLC or poorly differentiated neuroendocrine cancers of the lung, Eastern Cooperative Oncology Group performance status of 0 to 2, and had received less than or equal to two prior chemotherapy regimens (additional targeted agents were allowed). Both chemotherapy-sensitive (relapse >/=90 days from completion of first line therapy) and chemotherapy-resistant (progressive disease during or within 90 days from completion of first line treatment) patients were eligible and analyzed separately. Pemetrexed was administered at 500 mg/m intravenously every 21 days for up to six cycles. All patients received folic acid, vitamin B12, and steroid prophylaxis. The primary objective of the trial was to estimate the clinical benefit rate (complete plus partial response plus stable disease) in each group.
: From January 2005 to September 2005, 20 patients were enrolled in the chemotherapy-sensitive arm and 23 patients in the chemotherapy-resistant arm. The majority of patients were men, the median age of the two groups were 62.5 and 65, respectively; 75% had a performance status of 0 or 1, and more than 50% had received more than one prior regimen. Grade 3/4 toxicities were as expected for pemetrexed. Progressive disease was the best response in 16 patients (80%) in the chemo-sensitive group and 19 patients (83%) in the chemo-refractory group. One patient had a partial response and three had stable disease in each group.
: Pemetrexed has minimal single agent activity in relapsed SCLC.
小细胞肺癌(SCLC)最初是一种对化疗敏感的疾病。然而,耐药性导致大多数患者疾病复发。许多药物,包括抗代谢物,都具有活性,但在改善晚期患者的生存时间方面仅取得了微小进展。基于发现更好的全身治疗方法的需求,我们对培美曲塞治疗复发性小细胞肺癌患者进行了一项II期研究。
符合条件的患者患有小细胞肺癌或肺低分化神经内分泌癌,东部肿瘤协作组体能状态为0至2,且之前接受的化疗方案少于或等于两个(允许使用额外的靶向药物)。化疗敏感(自一线治疗完成后复发≥90天)和化疗耐药(在一线治疗期间或完成后90天内疾病进展)的患者均符合条件并分别进行分析。培美曲塞以500mg/m²静脉注射,每21天一次,最多六个周期。所有患者均接受叶酸、维生素B12和类固醇预防用药。该试验的主要目的是估计每组的临床获益率(完全缓解加部分缓解加疾病稳定)。
从2005年1月至2005年9月,化疗敏感组纳入20例患者,化疗耐药组纳入23例患者。大多数患者为男性,两组的中位年龄分别为62.5岁和65岁;75%的患者体能状态为0或1,超过50%的患者之前接受过不止一个疗程的治疗。培美曲塞的3/4级毒性反应如预期。疾病进展是化疗敏感组16例患者(80%)和化疗难治组19例患者(83%)的最佳反应。每组各有1例患者部分缓解,3例患者疾病稳定。
培美曲塞在复发性小细胞肺癌中的单药活性极小。