| Literature DB >> 31758090 |
Eli Muchtar1, Morie A Gertz2, Taxiarchis V Kourelis2, Surbhi Sidana3, Ronald S Go2, Martha Q Lacy2, Francis K Buadi2, David Dingli2, Suzanne R Hayman2, Prashant Kapoor2, Nelson Leung2,4, Amie Fonder2, Miriam Hobbs2, Yi Lisa Hwa2, Wilson Gonsalves2, Rahma Warsame2, Stephen Russell2, John A Lust2, Yi Lin2, Steven Zeldenrust2, S Vincent Rajkumar2, Robert A Kyle2, Shaji K Kumar2, Angela Dispenzieri2.
Abstract
We explored the association between bone marrow plasma cells (BMPCs) and disease presentation and outcome among 1574 AL patients. Three BMPC groups were formulated: <5% (n = 231, 15% of study population), 5-19% (n = 1045, 66%), and ≥20% (n = 298, 19%). Heart and renal involvement were more and less prevalent, respectively, with increasing BMPCs. Patients with ≥20% BMPCs had higher likelihood for classic myeloma phenotype with less skewed lambda restriction, a higher rate of intact immunoglobulin secretion, a lower hemoglobin and higher rates of hypercalcemia and bone lytic lesions. High-risk cytogenetic abnormalities were more common in ≥20% BMPCs. Complete hematological response was less frequent with rising BMPCs. The median survival was inversely associated with the BMPC groups (81, 33, 12 months for <5%, 5-19%, and ≥20% BMPCs, respectively; P < 0.001). Survival discrimination was maintained at 1-year landmark and in those who achieved a complete response. Multivariate analysis accounting for known prognostic markers yielded an independent prognostic role for ≥20% BMPCs, but not for the other BMPC groups. AL patients with 20% or greater BMPCs have poorer outcome independent of their cardiac risk category and stem cell transplant eligibility. Distinct interventions in these patients should be explored to improve outcome.Entities:
Mesh:
Year: 2019 PMID: 31758090 DOI: 10.1038/s41375-019-0655-x
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528