Περίληψη:
Patients with Waldenström macroglobulinemia (WM) lacking activating mutations in the MYD88 gene (MYD88WT) have demonstrated relatively poor outcomes to ibrutinib monotherapy, with no major responses reported in a phase 2 pivotal study. Zanubrutinib is a novel, selective Bruton tyrosine kinase (BTK) inhibitor designed to maximize BTK occupancy and minimize off-target activity. The ASPEN study consisted of a randomized comparison of zanubrutinib and ibrutinib efficacy and safety in patients with WM who have the MYD88 mutation, as well as a separate cohort of patients without MYD88 mutation (MYD88WT) or with unknown mutational status who received zanubrutinib. Results from the latter single-arm cohort are reported herein. Efficacy endpoints included overall, major and complete (CR) or very good partial response (VGPR) rates, progression-free survival (PFS), duration of response (DOR), and overall survival (OS). Twenty-eight patients (23 relapsed/ refractory; 5 treatment-naïve) were enrolled, including 26 with centrally confirmed MYD88WT disease and 2 with unknown MYD88 mutational status. At a median follow-up of 17.9 months, 7 of 26 MYD88WT patients (27%) had achieved a VGPR and 50% a major response (partial response or better); there were no CRs. At 18 months, the estimated PFS and OS rates were 68% and 88%, respectively, while the median DOR had not been reached. Two patients discontinued zanubrutinib due to adverse events. Treatment-emergent hypertension, atrial fibrillation, and major hemorrhages were reported in 3, 1 and 2 patients (including 1 concurrent with enoxaparin therapy), respectively. Results of this substudy demonstrate that zanubrutinib monotherapy can induce high quality responses in patients with MYD88WT WM. This trial is registered on www.clinicaltrials.gov as NCT #03053440. © 2020 by The American Society of Hematology
Συγγραφείς:
Dimopoulos, M.
Sanz, R.G.
Lee, H.-P.
Trneny, M.
Varettoni, M.
Opat, S.
D'Sa, S.
Owen, R.G.
Cull, G.
Mulligan, S.
Czyz, J.
Castillo, J.J.
Motta, M.
Siddiqi, T.
Mesa, M.G.
Gorrochategui, M.G.
Talaulikar, D.
Zinzani, P.L.
Askari, E.
Grosicki, S.
Oriol, A.
Rule, S.
Kloczko, J.
Tedeschi, A.
Buske, C.
Leblond, V.
Trotman, J.
Chan, W.Y.
Michel, J.
Schneider, J.
Tan, Z.
Cohen, A.
Huang, J.
Tam, C.S.
ASPEN investigators
Λέξεις-κλειδιά:
bendamustine; chlorambucil; cisplatin; cyclophosphamide; dexamethasone; enoxaparin; hemoglobin; hydrocortisone; ifosfamide; immunoglobulin M; lomustine; melphalan; methylprednisolone; myeloid differentiation factor 88; ofatumumab; prednisolone; prednisone; rituximab; zanubrutinib, adult; aged; anemia; arthralgia; Article; atrial fibrillation; backache; basal cell carcinoma; bleeding; cellulitis; clinical article; constipation; contusion; coughing; decreased appetite; diarrhea; drug dose reduction; drug efficacy; drug safety; drug withdrawal; fatigue; female; fever; gene mutation; headache; hemoptysis; herpes zoster; human; hypertension; hyponatremia; infection; laceration; lymphadenopathy; male; monotherapy; multicenter study (topic); muscle spasm; MYD88 gene; neutropenia; opportunistic infection; overall survival; peripheral edema; phase 3 clinical trial (topic); pneumonia; priority journal; progression free survival; pruritus; randomized controlled trial (topic); rash; respiratory tract infection; second cancer; skin cancer; splenomegaly; subdural hematoma; thrombocytopenia; upper respiratory tract infection; urinary tract infection; very elderly; Waldenstroem macroglobulinemia
