Phase I trial of low dose N-phosphonacetyl-L-aspartic acid and high dose 5-fluorouracil administered concomitantly with radiation therapy for unresectable localized adenocarcinoma of the pancreas
- PMID: 8082092
- DOI: 10.1002/1097-0142(19941001)74:7<1869::aid-cncr2820740707>3.0.co;2-j
Phase I trial of low dose N-phosphonacetyl-L-aspartic acid and high dose 5-fluorouracil administered concomitantly with radiation therapy for unresectable localized adenocarcinoma of the pancreas
Abstract
Background: 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.
Methods: 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.
Results: 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.
Conclusions: 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.
Similar articles
-
A randomized phase I and II study of short-term infusion of high-dose fluorouracil with or without N-(phosphonacetyl)-L-aspartic acid in patients with advanced pancreatic and colorectal cancers.J Clin Oncol. 1988 Jun;6(6):1053-8. doi: 10.1200/JCO.1988.6.6.1053. J Clin Oncol. 1988. PMID: 3373260 Clinical Trial.
-
A phase I study of continuous infusion 5-fluorouracil plus calcium leucovorin in combination with N-(phosphonacetyl)-L-aspartate in metastatic gastrointestinal adenocarcinoma.Cancer Res. 1993 Oct 15;53(20):4828-36. Cancer Res. 1993. PMID: 8402669 Clinical Trial.
-
Phase I study of high dose 5-fluorouracil and high dose Leucovorin with low dose phosphonacetyl-L-aspartic acid in patients with advanced malignancies.Int J Radiat Oncol Biol Phys. 1992;22(3):511-4. doi: 10.1016/0360-3016(92)90864-e. Int J Radiat Oncol Biol Phys. 1992. PMID: 1735689
-
Preclinical and clinical aspects of biomodulation of 5-fluorouracil.Cancer Treat Rev. 1994 Jan;20(1):11-49. doi: 10.1016/0305-7372(94)90009-4. Cancer Treat Rev. 1994. PMID: 7507404 Review.
-
The role of low-dose PALA in biochemical modulation.Pharmacol Ther. 1990;48(3):371-80. doi: 10.1016/0163-7258(90)90055-7. Pharmacol Ther. 1990. PMID: 2084707 Review.
Cited by
-
[Therapy of pancreatic adenocarcinoma].Med Klin (Munich). 1999 Nov 15;94(11):614-25. doi: 10.1007/BF03045002. Med Klin (Munich). 1999. PMID: 10603733 Review. German.
-
Genetic instability as a consequence of inappropriate entry into and progression through S-phase.Cancer Metastasis Rev. 1995 Mar;14(1):59-73. doi: 10.1007/BF00690212. Cancer Metastasis Rev. 1995. PMID: 7606822 Review.
-
A phase II trial of FUdR in patients with advanced pancreatic cancer.J Cancer Res Clin Oncol. 2004 Oct;130(10):561-6. doi: 10.1007/s00432-004-0584-5. Epub 2004 Jul 29. J Cancer Res Clin Oncol. 2004. PMID: 15449185 Free PMC article. Clinical Trial.
-
Pancreaticoduodenectomy for pancreatic adenocarcinoma: postoperative adjuvant chemoradiation improves survival. A prospective, single-institution experience.Ann Surg. 1997 May;225(5):621-33; discussion 633-6. doi: 10.1097/00000658-199705000-00018. Ann Surg. 1997. PMID: 9193189 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical