Phase II evaluation of VP-16-213 (NSC-141540) in patients with advanced ovarian carcinoma resistant to alkylating agents

Author:

Edmonson J.H.,Decker D.G.,Malkasian G.D.,Webb M.J.,Jorgensen E.O.

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Oncology

Reference5 articles.

1. Clinical trial of the oral form of 4′-demethyl-epipodophyllotoxin-β-d ethylidene gluocoside (NSC 141540) VP-16-213;Falkson,1974

2. Second trial drugs in ovarian cancer;Stanhope;Gynecol. Oncol.,1977

3. Phase I clinical trial of a new antitumor agent, 4′-demethylepipodophyllotoxin 9-(4,6-0 ethylidene-β-d-glucopyranoside) (NSC-141540; VP-16-213);Nissen;Cancer Chemother. Rep.,1972

4. Evaluation of VP-16 and the combination of adriamycin and vincristine in advanced breast cancer;Eagan;Oncology,1976

5. Phase II evaluation of VP-16-213 (NSC-141540) and cytembena (NSC-104801) in patients with advanced breast cancer;Ahmann;Cncer Treat. Rep.,1976

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