Adverse Prognostic Impact of Bone Marrow Microvessel Density in Multiple Myeloma.
10.3343/alm.2015.35.6.563
- Author:
Nuri LEE
1
;
Hyewon LEE
;
Soo Young MOON
;
Ji Yeon SOHN
;
Sang Mee HWANG
;
Ok Jin YOON
;
Hye Sun YOUN
;
Hyeon Seok EOM
;
Sun Young KONG
Author Information
1. Department of Laboratory Medicine, Center for Diagnostic Oncology, Hospital and Research Institute, National Cancer Center, Goyang, Korea. ksy@ncc.re.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Multiple myeloma;
Bone marrow;
Angiogenesis;
Microvessel;
Immunohistochemistry;
CD34;
Progression-free survival
- MeSH:
Aged;
Antigens, CD34/metabolism;
Bone Marrow/metabolism/*pathology;
Disease-Free Survival;
Female;
Humans;
Immunohistochemistry;
Kaplan-Meier Estimate;
Male;
Microvessels/*physiopathology;
Middle Aged;
Multiple Myeloma/*diagnosis/mortality;
Neoplasm Staging;
Neovascularization, Pathologic;
Plasma Cells/cytology;
Prognosis;
Proportional Hazards Models;
Regression Analysis;
Risk Factors
- From:Annals of Laboratory Medicine
2015;35(6):563-569
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Angiogenesis is important for the proliferation and survival of multiple myeloma (MM) cells. Bone marrow (BM) microvessel density (MVD) is a useful marker of angiogenesis and is determined by immunohistochemical staining with anti-CD34 antibody. This study investigated the prognostic impact of MVD and demonstrated the relationship between MVD and previously mentioned prognostic factors in patients with MM. METHODS: The study included 107 patients with MM. MVD was assessed at initial diagnosis in a blinded manner by two hematopathologists who examined three CD34-positive hot spots per patient and counted the number of vessels in BM samples. Patients were divided into three groups according to MVD tertiles. Cumulative progression-free survival (PFS) and overall survival (OS) curves, calculated by using Kaplan-Meier method, were compared among the three groups. Prognostic impact of MVD was assessed by calculating Cox proportional hazard ratio (HR). RESULTS: Median MVDs in the three groups were 16.8, 33.9, and 54.7. MVDs were correlated with other prognostic factors, including beta2-microglobulin concentration, plasma cell percentage in the BM, and cancer stage according to the International Staging System. Multivariate Cox regression analysis showed that high MVD was an independent predictor of PFS (HR=2.57; 95% confidence interval, 1.22-5.42; P=0.013). PFS was significantly lower in the high MVD group than in the low MVD group (P=0.025). However, no difference was observed in the OS (P=0.428). CONCLUSIONS: Increased BM MVD is a marker of poor prognosis in patients newly diagnosed with MM. BM MVD should be assessed at the initial diagnosis of MM.
