WR-2721 is phosphorylated aminothiol compound which protects normal tissues selectively (as compared to tumor) in experimental animals. Human toxicology is nearing completion. WR-2721 may be useful in humans to 1) decrease the adverse effects of radiotherapy and alkylating agents on various normal tissues, 2) allow higher doses of radiotherapy and certain chemotherapeutic agents without increasing the toxicity of standard doses of each , 3) decrease the overall time of radiotherapy courses providing lesser patient costs and inconvenience. Although specific assays for WR-2721 are lacking, two promising quantitative methods, are being developed; a) immunoquantitation with monoclonal antibodies, and b) electrochemical detection with high performance liquid chromatography. These may provide information to maximize the difference in WR-2721 concentration in normal tissues vs. tumor, to optimize infusion times and intervals from pretreatment with WR-2721 and treatment with alkylating agents or radiotherapy. Dose modifying factors with WR-2721 pretreatment before cyclophosphamide, nitrogen mustard, cis-platinum and various fractionation schedules of radiotherapy will be determined in human subjects. Reduction in adverse effects by pretreatment with WR-2721 will be investigated in multiple anatomic sites. WR-2721 administration decreases serum calcium and paradoxically parathormone levels. The clinical usefulness of this effect will be explored. Since WR-2721 appears to increase venous blood oxygen content, the mechanisms of this observation and its influence on protection will be investigated.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA030100-05
Application #
3169044
Study Section
Radiation Study Section (RAD)
Project Start
1981-04-01
Project End
1987-12-31
Budget Start
1986-01-01
Budget End
1986-12-31
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
Schools of Medicine
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Glover, D; Grabelsky, S; Fox, K et al. (1989) Clinical trials of WR-2721 and cis-platinum. Int J Radiat Oncol Biol Phys 16:1201-4
Kligerman, M M; Turrisi 3rd, A T; Urtasun, R C et al. (1988) Final report on phase I trial of WR-2721 before protracted fractionated radiation therapy. Int J Radiat Oncol Biol Phys 14:1119-22
Glover, D; Fox, K R; Weiler, C et al. (1988) Clinical trials of WR-2721 prior to alkylating agent chemotherapy and radiotherapy. Pharmacol Ther 39:3-7
Brown, D Q; Graham 3rd, W J; MacKenzie, L J et al. (1988) Can WR-2721 be improved upon? Pharmacol Ther 39:157-68
Shaw, L M; Glover, D; Turrisi, A et al. (1988) Pharmacokinetics of WR-2721. Pharmacol Ther 39:195-201
Nakamura, J; Shaw, L M; Brown, D Q (1987) Hydrolysis of WR2721 by mouse liver cell fractions. Radiat Res 109:143-52
Glover, D; Glick, J H; Weiler, C et al. (1987) WR-2721 and high-dose cisplatin: an active combination in the treatment of metastatic melanoma. J Clin Oncol 5:574-8
Shaw, L M; Turrisi, A T; Glover, D J et al. (1986) Human pharmacokinetics of WR-2721. Int J Radiat Oncol Biol Phys 12:1501-4
Brown, D Q; Shaw, L M; Pittock 3rd, J W et al. (1986) Modification of WR-2721 toxicity and radioprotection by an inhibitor of alkaline phosphatase. Int J Radiat Oncol Biol Phys 12:1491-3
Glover, D; Glick, J H; Weiler, C et al. (1986) WR-2721 protects against the hematologic toxicity of cyclophosphamide: a controlled phase II trial. J Clin Oncol 4:584-8

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