Thrombocytopenic myelofibrosis (MF) patients previously treated with a JAK inhibitor in a phase 3 randomized study of momelotinib (MMB) versus danazol (DAN) [MOMENTUM].

Authors

Aaron Gerds

Aaron Thomas Gerds

Cleveland Clinic Taussig Cancer Institute and Case Comprehensive Cancer Center, Cleveland, OH

Aaron Thomas Gerds , Srdan Verstovsek , Alessandro Vannucchi , Haifa Kathrin Al-Ali , David Lavie , Andrew T. Kuykendall , Sebastian Grosicki , Alessandra Iurlo , Yeow Tee Goh , Mihaela Cornelia Lazaroiu , Miklos Egyed , Maria Laura Fox , Donal P. McLornan , Andrew Perkins , Sung-Soo Yoon , Vikas Gupta , Jean-Jacques Kiladjian , Rafe Donahue , Jun Kawashima , Ruben A. Mesa

Organizations

Cleveland Clinic Taussig Cancer Institute and Case Comprehensive Cancer Center, Cleveland, OH, The University of Texas MD Anderson Cancer Center, Houston, TX, University of Florence, Florence, Italy, Krukenberg Cancer Center, University Hospital Halle, Halle, Germany, Hadassah Medical Center, Jerusalem, Israel, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, Department of Hematology, Independent Public Healthcare Facility Municipal Hospitals, Katowice, Poland, Hematology Division, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milano, Italy, Singapore General Hospital, Singapore, Singapore, Policlinica de Diagnostic Rapid Brasov, Brasov, Romania, Somogy County Mór Kaposi General Hospital, Kaposvar, Hungary, Hematology Department, Hospital Universitario Vall d'Hebron, Barcelona, Spain, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom, Australian Centre for Blood Diseases, Monash University, Melbourne, Australia, Seoul National University, Seoul, South Korea, Princess Margaret Cancer Centre, Toronto, ON, Canada, Hôpital Saint-Louis, Université de Paris, Paris, France, Sierra Oncology, Inc., Vancouver, BC, Canada, Gilead Sci Inc., San Ramon, CA, UT Health San Antonio, San Antonio, TX

Research Funding

Pharmaceutical/Biotech Company

Background: MMB, an oral JAK1/2 and ACVR1/ALK2 inhibitor, showed clinical activity on MF symptoms, RBC transfusion requirements (anemia), and spleen volume in the SIMPLIFY trials, including in MF patients (pts) with thrombocytopenia. MOMENTUM is a pivotal phase 3 study of symptomatic and anemic MF pts previously treated with a JAK inhibitor (JAKi) testing MMB vs DAN. This analysis evaluated MOMENTUM pts with baseline (BL) platelet counts (PLT) ≤150 x 109/L. Methods: Eligibility: Primary or post-ET/PV MF; DIPSS high risk, Int-2, or Int-1; MF Symptom Assessment Form Total Symptom Score (MFSAF TSS) ≥10; Hgb <10 g/dL; prior JAKi for ≥90 days, or ≥28 days if RBC transfusions ≥4 units in 8 weeks (wks) or Gr 3/4 thrombocytopenia, anemia, or hematoma; palpable spleen ≥5 cm; PLT ≥25 x 109/L. JAKi taper and washout was ≥21 days. Randomization: 2:1 to MMB 200 mg QD plus DAN placebo or DAN 600 mg QD plus MMB placebo for 24 wks. Primary endpoint: TSS response (≥50% reduction from BL) rate at wk 24. Key secondary endpoints, assessed sequentially at wk 24: RBC transfusion independence (TI) rate, splenic response rate (SRR; ≥25% reduction in volume from BL), change from BL in TSS, SRR (≥35% reduction from BL) and rate of zero transfusions since BL. Results: 60 (74%) of 81 MMB pts and 25 (58%) of 43 DAN pts with BL PLT ≤150 x 109/L completed the 24-week randomized treatment (RT) phase. Median BL TSS were 29 (MMB) and 24 (DAN), Hgb were 7.9 (MMB) and 8.0 (DAN) g/dL, and PLT were 67 x 109/L (MMB) and 64 x 109/L (DAN). Prior JAKi was ruxolitinib in 124 pts (100%) and fedratinib in 6 pts (5%). Efficacy results are in Table. These results are consistent with the overall ITT analysis set (N=195). Most common Gr ≥3 TEAEs in the RT phase were thrombocytopenia (MMB, 31%; DAN, 16%) and anemia (MMB, 7%; DAN, 14%); Gr ≥3 bleeding events occurred in 9% of MMB and 5% of DAN pts. TEAEs led to study drug discontinuation in 15% of MMB and 19% of DAN pts in RT phase. A trend toward improved OS up to wk 24 was seen with MMB vs DAN [HR (95% CI)=0.490 (0.195, 1.235)]. Additional analyses of pts with BL PLT <100 x 109/L (N=100) and BL PLT <50 x 109/L (N=31) show similar treatment effects of MMB vs DAN. Conclusions: In thrombocytopenic MF pts who were symptomatic and anemic, MMB was superior to DAN for symptom responses, transfusion requirements, and spleen responses and showed comparable safety and favorable survival. MMB may address a critical unmet need in thrombocytopenic MF pts. Clinical trial information: NCT04173494.

Wk 24 Endpoint

in Subjects with PLT ≤150x109/L
MMB

(N=81)
DAN

(N=43)
Difference

(95% CI)
TSS response rate, %
29.6
11.6
18.0 (0.7, 31.5)
TI rate, %
32.1
18.6
13.5 (-3.9, 28.5)
SRR ≥25, %
39.5
7.0
32.5 (15.3, 45.4)
TSS change from BL*
-10.7
-3.8
-7.0 (-11.7, -2.2)
SRR ≥35, %
22.2
4.7
17.6 (2.3, 29.1)
Zero transfusion rate, %
30.9
11.6
19.2 (2.3, 32.8)

*Least-squares mean from mixed model for repeated measures.

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Abstract Details

Meeting

2022 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Hematologic Malignancies—Leukemia, Myelodysplastic Syndromes, and Allotransplant

Track

Hematologic Malignancies

Sub Track

Myeloproliferative Neoplasms (MPN) and Mast Cell Disorders

Clinical Trial Registration Number

NCT04173494

Citation

J Clin Oncol 40, 2022 (suppl 16; abstr 7061)

DOI

10.1200/JCO.2022.40.16_suppl.7061

Abstract #

7061

Poster Bd #

292

Abstract Disclosures