An open-label, multicenter, expanded access study assessing the safety and efficacy of oral ruxolitinib administered to patients with primary myelofibrosis (PMF), post-polycythemia myelofibrosis (PPV MF) or post-essential thrombocythemia myelofibrosis (PET-MF).

Authors

null

Philipp D. le Coutre

University of Medicine Berlin, Charité Campus Virchow, Berlin, Germany

Philipp D. le Coutre , Heinz Gisslinger , Pierre Zachee , Vikas Gupta , Jose Ricardo Perez , Nora Schenk , Suresh Vutukuru , Carmen Garcia-Hernandez , Renato Tavares , Monica Bocchia , Dietger Niederwieser

Organizations

University of Medicine Berlin, Charité Campus Virchow, Berlin, Germany, Medical University of Vienna, Vienna, Austria, ZNA Stuivenberg, Antwerp, Belgium, Princess Margaret Hospital, Toronto, ON, Canada, Novartis Pharmaceuticals, East Hanover, NJ, Novartis Healthcare Pvt. Ltd., Madhapur/Hyderabad, Rangareddy, India, Hospital General Universitario de Alicante, Valencia, Spain, Hospital Universitario de Gojania, Goiânia, Brazil, University of Siena, Siena, Italy, University of Leipzig, Leipzig, Germany

Research Funding

Pharmaceutical/Biotech Company
Background: Myelofibrosis (MF) can be primary in origin or can progress from polycythemia vera (PPV-MF) or essential thrombocythemia (PET-MF). MF is characterized by cytopenias, reactive bone marrow fibrosis, splenomegaly, and constitutional symptoms including weight loss, fever, and night sweats. MF is associated with dysregulation of the Janus kinase pathway, irrespective of JAK2V617F mutation status. Recently, ruxolitinib (INCB018424) was approved for the treatment of MF on the basis of results from 2 phase 3 trials (COMFORT-I and -II). These trials demonstrated marked reductions in splenomegaly and symptom burden, and improvements in health-related quality of life (QoL) measures. Methods: JAK Inhibitor rUxolitinib in Myelofibrosis Patients (JUMP) is a global, phase 3b expanded access trial (NCT01493414) designed to assess the safety and efficacy of ruxolitinib in adult pts with PMF, PPV-MF or PET-MF who are treatment naïve, and are intolerant of, or had progressed on any prior therapy. Inclusion criteria: peripheral blast count of <10%, adequate liver and renal function and intermediate-2 or high risk MF according to IPSS criteria or intermediate-1 risk MF with palpable spleen length ≥ 5 cm. The primary endpoint is to assess the safety of ruxolitinib. Additional endpoints include the proportion of pts with a > 50% reduction in palpable spleen length, % change in white blood cell and platelet counts from baseline (BL), and change in packed red blood cell transfusion requirements. Changes from BL in QoL scores will be assessed using validated ECOG PS, FACT-Lymphoma, and FACIT instruments. Pts with a BL platelet count > 200,000/μL will receive oral ruxolitinib 20 mg BID; pts with a BL platelet count of 100,000/μL to 200,000/μL will receive 15 mg BID; dose modifications are permitted for safety and efficacy. Global enrollment is open and currently includes 277 pts. This is planned to be the largest study ever conducted in pts with MF.
Country # of Pts
Austria 24
Belgium 15
Brazil 24
Germany 173
Spain 28
Argentina 3
Canada 3
Netherlands 3
Italy 4
Total 277

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Abstract Details

Meeting

2012 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Leukemia, Myelodysplasia, and Transplantation

Track

Hematologic Malignancies—Leukemia, Myelodysplastic Syndromes, and Allotransplant

Sub Track

Myeloproliferative Neoplasms (MPN) and Mast Cell Disorders

Clinical Trial Registration Number

NCT01493414

Citation

J Clin Oncol 30, 2012 (suppl; abstr TPS6640)

DOI

10.1200/jco.2012.30.15_suppl.tps6640

Abstract #

TPS6640

Poster Bd #

31A

Abstract Disclosures