A simple method to distinguish residual elotuzumab from monoclonal paraprotein in immunofixation assays for multiple myeloma patients.


Journal

International journal of hematology
ISSN: 1865-3774
Titre abrégé: Int J Hematol
Pays: Japan
ID NLM: 9111627

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 26 06 2020
accepted: 15 01 2021
revised: 14 01 2021
pubmed: 29 1 2021
medline: 22 6 2021
entrez: 28 1 2021
Statut: ppublish

Résumé

Negative immunofixation electrophoresis (IFE) of serum and/or urine is a diagnostic marker for determining a complete response (CR) after immunotherapy for multiple myeloma (MM). However, residual therapeutic antibodies such as elotuzumab (IgG-κ), can compromise IFE evaluation when the affected immunoglobulins belong to the same IgG-κ subclass. We thus sought to develop a simple and rapid method to treat patient serum before IFE to distinguish the residual elotuzumab. Serum samples from patients receiving elotuzumab were treated with a predetermined amount of soluble signaling lymphocyte activation molecule F7 (SLAMF7) protein and then subjected to conventional IFE testing. We tested our method in samples from 12 patients. The IgG-κ band in IFE disappeared or shifted after elotuzumab treatment in four patients with no bone marrow minimal residual disease and normalized free light chain, whereas seven patients with any sign of residual MM showed a remaining IgG-κ band after treatment. One-hour incubation of samples with 6-9 molar excess soluble SLAMF7 before IFE was sufficient to distinguish residual elotuzumab in 11 of 12 samples. This simple method does not require special reagents, can be performed in most clinical laboratories, and enables differentiation between patients with a CR and those requiring further treatment.

Identifiants

pubmed: 33507526
doi: 10.1007/s12185-021-03088-9
pii: 10.1007/s12185-021-03088-9
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
Biomarkers, Tumor 0
Myeloma Proteins 0
Recombinant Proteins 0
SLAMF7 protein, human 0
Signaling Lymphocytic Activation Molecule Family 0
elotuzumab 1351PE5UGS

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

473-479

Références

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Auteurs

Shurui Chen (S)

Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Toru Kiguchi (T)

Department of Hematology, Chugoku Central Hospital, Fukuyama, Japan.

Yasuyuki Nagata (Y)

Division of Hematology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Yotaro Tamai (Y)

Division of Hematology, Shonan Kamakura General Hospital, Kamakura, Japan.

Takeshi Ikeda (T)

Division of Hematology and Stem Cell Transplantation, Shizuoka Cancer Center, Shizuoka, Japan.

Ryoko Kajiya (R)

Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Takaaki Ono (T)

Division of Hematology, Hamamatsu University School of Medicine, Hamamatsu, Japan.

Daisuke Sugiyama (D)

Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Hiroyoshi Nishikawa (H)

Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan.

Yoshiki Akatsuka (Y)

Department of Immunology, Nagoya University Graduate School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, 466-8550, Japan. yakatsuk@med.nagoya-u.ac.jp.

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