Prognostic Implications of Rising Serum Monoclonal Protein and Free Light Chains after Autologous Stem Cell Transplantation in Patients with Multiple Myeloma.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
04 2021
Historique:
received: 19 06 2020
revised: 29 11 2020
accepted: 30 11 2020
entrez: 10 4 2021
pubmed: 11 4 2021
medline: 3 7 2021
Statut: ppublish

Résumé

Patients who undergo autologous stem cell transplantation (ASCT) for multiple myeloma (MM) are routinely assessed at day +100 using serum and urine protein electrophoresis/immunofixation and the serum free light chain (sFLC) assay. We evaluated whether an increase in M-spike or FLC from immediately before ASCT to day +100 post-ASCT has any prognostic impact. We retrospectively reviewed 1218 patients with MM at the Mayo Clinic who underwent their first ASCT between 2000 and 2016. We stratified patients into those with a rise in M-spike by at least 0.1 g/dL from immediately before ASCT to day +100 post-ASCT (M-spike cohort 1) and those who did not (M-spike cohort 2). We also stratified patients into those with a rise in the involved FLC by at least 5 mg/dL (FLC cohort 1) and those who did not (FLC cohort 2). Survival analysis for progression-free survival (PFS) and overall survival (OS) was performed using the Kaplan-Meier method. A rise in M-spike by at least 0.1 g/dL from pre-ASCT to day +100 was seen in 53 patients (4.3%). The median PFS and OS were found to be significantly shorter in M-spike cohort 1 compared with their counterparts (median PFS, 10 months versus 26 months [P < .0001]; median OS, 35 months versus 79 months [P < .0001]). An increase in involved FLC by at least 5 mg/dL was observed in 25 patients (2.3%). Similarly, the median PFS and OS were found to be inferior in FLC cohort 1 compared with FLC cohort 2 (median PFS, 4 months versus 28 months [P < .0001]; median OS, 11 months versus 82 months [P < .0001]). An increase of M-spike by at least 0.1 g/dL and an increase in involved FLC by at least 5 mg/dL from pre-ASCT to day +100 increases the likelihood of an early relapse after ASCT, and these patients may benefit from closer surveillance after day +100.

Identifiants

pubmed: 33836869
pii: S2666-6367(20)30049-X
doi: 10.1016/j.jtct.2020.11.022
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

309.e1-309.e5

Informations de copyright

Copyright © 2020 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Harsh Parmar (H)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Abdullah S Al Saleh (AS)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Alissa Visram (A)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Rahma Warsame (R)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Taxiarchis Kourelis (T)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Wilson Gonsalves (W)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

David Dingli (D)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Eli Muchtar (E)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Suzanne Hayman (S)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Prashant Kapoor (P)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Francis Buadi (F)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Angela Dispenzieri (A)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Martha Lacy (M)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Morie Gertz (M)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.

Shaji Kumar (S)

Division of Hematology, Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota. Electronic address: kumar.shaji@mayo.edu.

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Classifications MeSH