Raderer M, Kornek G V, Hejna M H, Weinlaender G, Vorbeck F, Fiebiger W C, Scheithauer W
Department of Internal Medicine, University of Vienna, Austria.
Ann Oncol. 1997 Aug;8(8):797-9. doi: 10.1023/a:1008276004552.
Preclinical data suggest that the levorotatory isomer of leucovorin (1-LV) can augment the cytotoxic effects of 5-fluorouracil (5-FU) more effectively than racemic LV. A phase II study was initiated to evaluate the effect of a combination of the pure L-isomer of LV and 5-FU along with epirubicin in patients with advanced pancreatic cancer.
Twenty-eight consecutive, previously untreated patients with measurable metastatic adenocarcinoma of the pancreas were enrolled in this study. Treatment consisted of epirubicin 50 mg/m2 on day 1 and 5-FU 400 mg/m2 plus 1-LV 100 mg/m2 both administered on days 1 to 5. Treatment cycles were repeated every four weeks for a total of six months unless progressive disease was documented earlier. The study endpoints were survival, toxicity, objective response as well as palliative beneficial effects of the regimen in terms of performance status, body weight and pain.
Six patients had a partial response (21%; 95% CI, 8% to 44%) and 10 (36%) stable disease (35%), while the remaining 12 patients (43%) progressed during treatment. The median time to treatment failure was 2.9 months (range 1.2-13.7 months), and the median survival time was six months (range 1.8-19 months), with three patients (11%) being alive after one year. Beneficial palliative effects in terms of performance status, body weight and/or pain were seen in 12 of 28 patients (43%): an improvement in performance status was recorded in four patients, pain was attenuated and/or analgetic consumption reduced by > or = 50% in eight patients, and five patients had weight gain of > 5% of their pretreatment body weight. Treatment-associated side effects were generally mild to moderate. Severe adverse reactions included (asymptomatic) granulocytopenia in five, mucositis and/or diarrhea WHO grade 3 in four patients.
Our data suggest that epirubicin plus 5-FU and 1-LV is a tolerable regimen that has some positive effects in the treatment of pancreatic cancer. Since this regimen, however, is unlikely to offer any major therapeutic advantage compared to monochemotherapy or other combination regimens, the search for novel and more effective cytotoxic agents must continue.
临床前数据表明,亚叶酸钙的左旋异构体(1-LV)比消旋亚叶酸钙能更有效地增强5-氟尿嘧啶(5-FU)的细胞毒性作用。启动了一项II期研究,以评估左旋亚叶酸钙纯L-异构体与5-FU联合表柔比星治疗晚期胰腺癌患者的效果。
本研究纳入了28例连续的、既往未接受过治疗的可测量胰腺转移性腺癌患者。治疗方案为第1天给予表柔比星50mg/m²,第1至5天给予5-FU 400mg/m²加1-LV 100mg/m²。每四周重复一个治疗周期,共持续六个月,除非更早记录到疾病进展。研究终点包括生存率、毒性、客观缓解率以及该方案在体能状态、体重和疼痛方面的姑息治疗有益效果。
6例患者部分缓解(21%;95%CI,8%至44%),10例(36%)疾病稳定,其余12例患者(43%)在治疗期间病情进展。治疗失败的中位时间为2.9个月(范围1.2 - 13.7个月),中位生存时间为6个月(范围1.8 - 19个月),3例患者(11%)在1年后仍存活。28例患者中有12例(43%)在体能状态、体重和/或疼痛方面出现有益的姑息治疗效果:4例患者体能状态改善,8例患者疼痛减轻和/或镇痛药用量减少≥50%,5例患者体重增加超过预处理体重的5%。与治疗相关的副作用一般为轻至中度。严重不良反应包括5例(无症状)粒细胞减少,4例患者出现WHO 3级黏膜炎和/或腹泻。
我们的数据表明,表柔比星加5-FU和1-LV是一种可耐受的方案,在胰腺癌治疗中具有一些积极作用。然而,由于该方案与单药化疗或其他联合方案相比不太可能提供任何主要的治疗优势,因此必须继续寻找新型且更有效的细胞毒性药物。