Ardalan B, Ucar A, Reddy R, Livingstone A S, Markoe A, Schwade J, Richman S P, Donofrio K
Division of Hematology-Oncology, University of Miami, School of Medicine, Florida.
Cancer. 1994 Oct 1;74(7):1869-73. doi: 10.1002/1097-0142(19941001)74:7<1869::aid-cncr2820740707>3.0.co;2-j.
Preclinical and clinical data suggest that N-phosphonacetyl-L-aspartic acid (PALA) can augment the cytotoxic effects of 5-fluorouracil (5-FU). In addition, the combination of 5-FU and radiation therapy has been used with success in prolonging survival and providing palliation of symptoms in patients with advanced unresectable pancreatic carcinoma. This Phase I study was undertaken to determine the feasibility and evaluate the qualitative and quantitative toxicities of PALA and escalating doses of 5-FU administered concomitantly with radiation therapy in patients with locally advanced nonmetastatic pancreatic adenocarcinoma.
Ten previously untreated patients with advanced nonmetastatic adenocarcinoma of the pancreas were treated with 250 mg/m2 of PALA given as an intravenous bolus followed 24 hours later by 5-FU, which was given by continuous 24-hour infusion every week. The 5-FU doses were assigned according to a Phase I drug escalation (1000 mg/m2, 1300 mg/m2, and 1700 mg/m2). Radiation therapy was delivered concurrently with chemotherapy at a dose of 180 cGy per fraction (900 cGy per week) over 6 1/2 weeks. PALA and 5-FU were continued weekly after the end of radiation therapy, with disease assessments made every 8 weeks. Chemotherapy was continued until the disease progressed.
All 10 patients were evaluable. The maximum tolerated dose (MTD) of 5-FU was 1300 mg/m2. Two of the four patients treated at the 1700 mg/m2 dose level experienced dose-limiting toxicities, nausea/vomiting and mucositis, respectively. Toxicities were mild to moderate at the 1000 mg/m2 and 1300 mg/m2 dose levels. Two patients treated with 5-FU at the 1300 mg/m2 dose level had complete responses, and one patient treated at the 1700 mg/m2 dose level had a partial response. The median survival was 12.5 months, and four patients survived more than 1 year.
PALA and 5-FU administered concomitantly with radiation therapy is an active regimen in locally advanced, unresectable pancreatic cancer. Dose-limiting toxicities are nausea/vomiting and mucositis. The MTD of 5-FU is 1300 mg/m2. The regimen is well tolerated and administered in an outpatient setting.
临床前和临床数据表明,N-膦酰乙酰-L-天冬氨酸(PALA)可增强5-氟尿嘧啶(5-FU)的细胞毒性作用。此外,5-FU与放射治疗联合应用已成功用于延长晚期不可切除胰腺癌患者的生存期并缓解症状。本I期研究旨在确定PALA与递增剂量的5-FU与放射治疗同时给药在局部晚期非转移性胰腺腺癌患者中的可行性,并评估其定性和定量毒性。
10例先前未接受过治疗的晚期非转移性胰腺腺癌患者接受250mg/m²的PALA静脉推注,24小时后给予5-FU,每周连续24小时输注。5-FU剂量根据I期药物递增方案(1000mg/m²、1300mg/m²和1700mg/m²)分配。放射治疗与化疗同时进行,剂量为每次180cGy(每周900cGy),持续6.5周。放射治疗结束后每周继续给予PALA和5-FU,每8周进行一次疾病评估。化疗持续至疾病进展。
所有10例患者均可评估。5-FU的最大耐受剂量(MTD)为1300mg/m²。在1700mg/m²剂量水平治疗的4例患者中有2例分别出现剂量限制性毒性,即恶心/呕吐和粘膜炎。在1000mg/m²和1300mg/m²剂量水平,毒性为轻度至中度。在1300mg/m²剂量水平接受5-FU治疗的2例患者获得完全缓解,在1700mg/m²剂量水平治疗的1例患者获得部分缓解。中位生存期为12.5个月,4例患者存活超过1年。
PALA和5-FU与放射治疗同时给药是局部晚期、不可切除胰腺癌的一种有效治疗方案。剂量限制性毒性为恶心/呕吐和粘膜炎。5-FU的MTD为1300mg/m²。该方案耐受性良好,可在门诊环境中给药。