Serum insulinlike growth factor is not elevated in patients with multiple myeloma but is still a prognostic factor

Author:

Standal Therese1,Borset Magne1,Lenhoff Stig1,Wisloff Finn1,Stordal Berit1,Sundan Anders1,Waage Anders1,Seidel Carina1

Affiliation:

1. From the Institute of Cancer Research and Molecular Biology, Faculty of Medicine, Norwegian University of Science and Technology, Trondheim, Norway; Department of Haematology, Lund University Hospital, Lund, Sweden; Department of Hematology, Ullevål University Hospital, Oslo, Norway; and Division of Pathology, Institute of Microbiology, Pathology and Immunology, Karolinska Institute, Huddinge University Hospital, Stockholm, Sweden.

Abstract

Insulinlike growth factor 1 (IGF-1) has growth-promoting effects on myeloma cells in vitro as well as in vivo. In this study, we measured the concentration of IGF-1 and its major binding protein, IGF- binding protein 3 (IGFBP-3), in serum from 127 patients with multiple myeloma. Serum had been drawn at the time of diagnosis, before treatment with high-dose melphalan. IGFBP-3 in myeloma patients (1.6 ± 0.73 μg/mL; mean ± SD) was significantly decreased compared to healthy age- and sex-matched controls (2.2 ± 0.42 μg/mL). However, IGFBP-3 had no prognostic value in this study. The mean IGF-1 level did not differ between myeloma patients (17.8 ± 7.7 nM) and controls (17.3 ± 5.6 nM). Nevertheless, IGF-1 was a strong indicator of prognosis. After 80 months of follow-up, myeloma patients with low levels (< 13 nM) of serum IGF-1 had not reached median survival. In the patient group with IGF-1 levels above 13 nM, median survival was 62 months (P = .006). These findings support the hypothesis of a role for IGF-1 in myeloma disease progression.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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