Bone marrow plasma cell infiltration in light chain amyloidosis: impact on organ involvement and outcome

Natalia Tovar1, Luis Gerardo Rodríguez-Lobato1, Maria Teresa Cibeira1

  • 1a Amyloidosis and Myeloma Unit, Department of Hematology , Hospital Clínic of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona , Barcelona , Spain.

Insights

Higher bone marrow plasma cell (BMPC) infiltration in immunoglobulin light-chain (AL) amyloidosis correlates with worse outcomes. However, newer therapies may mitigate the negative prognostic impact of increased BMPC burden.

Area of Science:

  • Hematology
  • Oncology
  • Internal Medicine

Background:

  • Prognosis in immunoglobulin light-chain (AL) amyloidosis is influenced by cardiac involvement and disease burden.
  • Elevated bone marrow plasma cell (BMPC) burden is an established adverse prognostic factor in AL amyloidosis.

Purpose of the Study:

  • To investigate the relationship between BMPC infiltration, clinical characteristics, and patient outcomes in AL amyloidosis.

Main Methods:

  • Retrospective analysis of clinical records from 79 AL amyloidosis patients treated at a single institution.

Main Results:

  • Median BMPC infiltration was 11%, correlating with serum free light-chain difference (p < .001).
  • Patients with >10% BMPC infiltration showed higher rates of cardiac involvement (86% vs 63%, p = .015), a trend towards increased early mortality (27% vs 11%, p = .08), and significantly shorter progression-free survival (PFS) (18 vs 48 months, p = .02) and overall survival (33 months vs. not reached, p = .046).
  • Multivariate analysis confirmed BMPC infiltration >10% as an adverse prognostic factor for PFS (HR = 2.26, p = .038).

Conclusions:

  • Increased BMPC infiltration in AL amyloidosis is linked to greater systemic organ damage, especially cardiac involvement.
  • Myeloma features are rarely associated with high BMPC infiltration in AL amyloidosis.
  • Emerging therapeutic agents may counteract the adverse prognostic effects of elevated BMPC levels.
Abstract

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