Multi-institutional study of the angiogenesis inhibitor TNP-470 in metastatic renal carcinoma

Citation
Wm. Stadler et al., Multi-institutional study of the angiogenesis inhibitor TNP-470 in metastatic renal carcinoma, J CL ONCOL, 17(8), 1999, pp. 2541-2545
Citations number
21
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
JOURNAL OF CLINICAL ONCOLOGY
ISSN journal
0732183X → ACNP
Volume
17
Issue
8
Year of publication
1999
Pages
2541 - 2545
Database
ISI
SICI code
0732-183X(199908)17:8<2541:MSOTAI>2.0.ZU;2-T
Abstract
Purpose: Renal cell carcinoma is resistant to most chemotherapy, and only a minority of patients respond to immunotherapy. Its highly vascular nature suggests that antiangiogenesis therapy might be useful. We thus performed a phase II study of the fumigillin analog TNP-470 in previously treated pati ents with metastatic renal cell carcinoma. Patients and Methods: Metastatic renal cell carcinoma patients with good or gan function were entered onto the study through five separate institutions . There were no exclusion criteria for prior therapy All patients were trea ted at a dose of 60 mg/m(2) of TNP-470 infused over 1 hour three times per week. Results: Thirty-three patients were enrolled. Therapy was generally well to lerated, but asthenia, fatigue, vertigo, dizziness, sense of imbalance, and loss of concentration were common and severe enough to lead to therapy dis continuation in five patients. There was only one partial response of short duration (response rate, 3%, 95% confidence interval, 0% to 16%), but six patients (18%) remained on study for 6 or more months without toxicity or d isease progression. Conclusion: Long-term therapy with TNP-470 has manageable toxicities and is feasible in patients with metastatic renal cell carcinoma but does not lea d to any significant objective responses. further studies in this populatio n using TNP-470 schedules that produce mare prolonged drug levels and clini cal trial end points other than objective tumor regression may be indicated . (C) 1999 by American Society of Clinical Oncology.