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Survival impact of achieving minimal residual negativity by multi-parametric flow cytometry in AL amyloidosis.

Eli MuchtarAngela DispenzieriDragan JevremovicDavid DingliFrancis K BuadiMartha Q LacyWilson GonsalvesRahma WarsameTaxiarchis V KourelisSuzanne R HaymanPrashant KapoorNelson R LeungStephen RussellJohn A LustYi LinRonald S GoSteven ZeldenrustRobert A KyleS Vincent RajkumarShaji K KumarMorie A Gertz
Published in: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis (2019)
Response assessment in light chain (AL) amyloidosis is challenging given the low level of circulating free light chains usually seen. Multi-parametric flow cytometry (MFC) from a marrow aspirate was demonstrated to retain a prognostic significance in several recent studies. In this work, 82 AL patients who had MFC study at end of therapy were analysed based on whether clonal plasma cells were detected or not. Among patients who achieved deep response (i.e. very good partial response or complete response) to first-line therapy, lack of clonal marrow plasma cells as measured by MFC was associated with improved progression-free survival (PFS) compared to patients with residual clonal plasma cells (3-year PFS 88% vs. 46%, p = .003), particularly among patients who achieved a complete response (3-year PFS 100% vs. 33%, p = .001). Absence of clonal plasma cells by MFC compared with patients with detectable clonal plasma cells among deep responders was associated with lower level of involved light chain (involved free light chain (iFLC), median 1.1 vs. 1.7 mg/dL; p = .02) and higher frequency of renal response (100% vs. 68%; p = .005). Further studies are needed to determine if MFC should be incorporated into response criteria in AL amyloidosis.
Keyphrases
  • induced apoptosis
  • cell cycle arrest
  • flow cytometry
  • free survival
  • endoplasmic reticulum stress
  • stem cells
  • signaling pathway
  • cell death
  • oxidative stress
  • pi k akt
  • cell proliferation
  • bone marrow
  • case control