TY - JOUR
T1 - AL patients don't dare go without dara
AU - Dispenzieri, Angela
N1 - Funding Information:
Conflict-of-interest disclosure: A.D. receives research funding from Celgene, Takeda, Pfizer, and Alnylam and serves on the advisory boards to Janssen, Intellia, and Akcea. n
Publisher Copyright:
© 2020 by The American Society of Hematology
PY - 2020/4
Y1 - 2020/4
N2 - In this issue of Blood, 3 papers by the teams of Roussel et al, Sanchorawala et al, and Kimmich et al demonstrate high rates of efficacy and low rates of toxicity of single-agent daratumumab (dara) in patients with previously treated immunoglobulin light-chain (AL) amyloidosis.1-3 These 3 reports include 2 small phase 2 prospective trials employing single-agent dara1,2 and a compilation of 168 consecutive patients treated with either daratumumab and dexamethasone (DD) or bortezomib and DD (DVD).3 Among previously treated AL patients, dara with low-intensity corticosteroid yielded partial hematologic response (PR) or better and very good partial response (VGPR) or better in 64% to 90% and in 56% to 86% of patients, respectively.1-3 Progression-free survival (PFS) ranged from 12 to 28 months. Renal and cardiac responses were observed in 24% to 67% and 22% to 50% of patients, respectively. The vast majority of hematologic responses occurred after the first 4 doses of dara.
AB - In this issue of Blood, 3 papers by the teams of Roussel et al, Sanchorawala et al, and Kimmich et al demonstrate high rates of efficacy and low rates of toxicity of single-agent daratumumab (dara) in patients with previously treated immunoglobulin light-chain (AL) amyloidosis.1-3 These 3 reports include 2 small phase 2 prospective trials employing single-agent dara1,2 and a compilation of 168 consecutive patients treated with either daratumumab and dexamethasone (DD) or bortezomib and DD (DVD).3 Among previously treated AL patients, dara with low-intensity corticosteroid yielded partial hematologic response (PR) or better and very good partial response (VGPR) or better in 64% to 90% and in 56% to 86% of patients, respectively.1-3 Progression-free survival (PFS) ranged from 12 to 28 months. Renal and cardiac responses were observed in 24% to 67% and 22% to 50% of patients, respectively. The vast majority of hematologic responses occurred after the first 4 doses of dara.
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U2 - 10.1182/BLOOD.2020005436
DO - 10.1182/BLOOD.2020005436
M3 - Review article
C2 - 32353125
AN - SCOPUS:85089984068
SN - 0006-4971
VL - 135
SP - 1509
EP - 1510
JO - Blood
JF - Blood
IS - 18
ER -