Randomized Multicenter Phase II Trial Comparing Two Schedules of Etirinotecan Pegol (NKTR-102) in Women With Recurrent Platinum-Resistant/Refractory Epithelial Ovarian Cancer
Author(s) -
Ignace Vergote,
Agustin A. García,
John P. Micha,
Charles H. Pippitt,
Johanna C. Bendell,
Daniel L. Spitz,
Nicholas Reed,
G. Dark,
Paula M. Fracasso,
Emad Ibrahim,
Vincent Armenio,
Linda Duska,
Chris Poole,
Christine Gennigens,
Luc Dirix,
Abraham C.F. Leung,
Carol Zhao,
Raoudha SoufiMahjoubi,
Gordon Rustin
Publication year - 2013
Publication title -
journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.482
H-Index - 548
eISSN - 1527-7755
pISSN - 0732-183X
DOI - 10.1200/jco.2012.45.1278
Subject(s) - medicine , neutropenia , nausea , adverse effect , irinotecan , clinical endpoint , tolerability , gastroenterology , ovarian cancer , refractory (planetary science) , randomized controlled trial , oncology , cancer , surgery , chemotherapy , colorectal cancer , physics , astrobiology
Etirinotecan pegol (NKTR-102) is a unique, long-acting topoisomerase-I inhibitor with prolonged systemic exposure to SN38 (7-ethyl-10-hydroxycamptothecin), the active metabolite of irinotecan. This randomized phase II trial investigated two dosing schedules of etirinotecan pegol in patients with platinum-resistant/refractory ovarian carcinoma.
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