A phase II, multicenter, open-label study of YM155 plus docetaxel in subjects with stage III (unresectable) or stage IV melanoma.

Authors

null

Joyce Leta Steinberg

Astellas Pharma Global Development, Deerfield, IL

Joyce Leta Steinberg , Agop Y. Bedikian , Bartosz Chmielowski , Bruce Redman , Anne Therese Keating , Fei Jie , Caroline Chen , Jeffrey S. Weber , Ragini Reiney Kudchadkar , D. Scott Ernst

Organizations

Astellas Pharma Global Development, Deerfield, IL, University of Texas M. D. Anderson Cancer Center, Houston, TX, University of California, Los Angeles Translational Oncology Research Laboratory, Los Angeles, CA, University of Michigan, Comprehensive Cancer Center, Ann Arbor, MI, Astellas Pharmaceuticals, Deerfild, IL, Astellas Pharmceuticals, Deerfield, IL, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL, London Regional Cancer Centre, London, ON, Canada

Research Funding

Pharmaceutical/Biotech Company
Background: Survivin is a microtubule-associated protein implicated in both preservation of cell viability and regulation of mitosis in tumor cells. It is over-expressed in melanoma, breast, and non-Hodgkin’s lymphoma. YM155 is a first in class survivin inhibitor. Methods: The study had 2 parts: Part 1 established the dose of docetaxel that was tolerable in combination withYM155 at 5 mg/m2/day continuous infusion over 168 hours q 3 weeks. Part 2 utilized the dose of docetaxel established in Part 1 to further evaluate the tolerability and activity of the combination. The primary endpoint was 6-month progression-free survival (PFS). Secondary endpoints were overall response rate, 1-year overall survival (OS), time from first response to progression, clinical benefit rate, time to response, and safety. Results: 64 patients with metastatic melanoma were treated with docetaxel followed by continuous infusion YM155. 7 patients were treated with 100mg/m2 of docetaxel and 57 patients were treated with 75mg/m2 of docetaxel. Median age was 59, with 44 men and 20 women treated. 6-month PFS per Independent Review Committee (IRC) was 34.8% (95% CI 21.3 – 48.6%). Overall objective response rate per IRC was 12.5%, with no complete responses (CR) and 8 patients with partial responses (PR). The Stable disease (SD) rate was 51.6%, leading to a clinical benefit rate (CR + PR + SD) of 64.1%. Estimated 1-year overall survival is 50.5%. 87.5% of patients experienced a Grade 3 (G3) or Grade 4 (G4) event attributable to either YM155 or docetaxel. The clinically pertinent G3 or 4 toxicities occurring in greater than 5% of patients treated included neutropenia (59.4%), febrile neutropenia (12.5%), mucositis (9.4%), fatigue (7.8%), diarrhea (6.3%), and dehydration (6.3%). There were 3 deaths on study, all attributable to disease progression. Conclusions: YM155 is a novel agent that shows modest activity when combined with docetaxel in patients with melanoma. YM155 was generally well tolerated, but the pre-determined primary endpoint for efficacy was not achieved.

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Abstract Details

Meeting

2012 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Melanoma/Skin Cancers

Track

Melanoma/Skin Cancers

Sub Track

Melanoma

Clinical Trial Registration Number

NCT01009775

Citation

J Clin Oncol 30, 2012 (suppl; abstr 8587)

DOI

10.1200/jco.2012.30.15_suppl.8587

Abstract #

8587

Poster Bd #

37E

Abstract Disclosures