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4252 No Risk of Arterial or Venous Thrombosis in Monoclonal Gammopathy of Undetermined Significance: Results from a Population-Based Study

Myeloma: Therapy, excluding Transplantation
Program: Oral and Poster Abstracts
Session: 653. Myeloma: Therapy, excluding Transplantation: Poster III
Monday, December 7, 2015, 6:00 PM-8:00 PM
Hall A, Level 2 (Orange County Convention Center)

Ebba K Lindqvist, MD1*, Sigrún H. Lund, PhD2*, Rene Costello3*, Debra Burton3*, Neha S Korde, MD4,5, Sham Mailankody, MBBS3*, Vilmundur Gudnason, MD, PhD6,7*, Gudny Eiriksdottir7*, Leonore Launer, PhD8*, Tamara B Harris, MD8*, Malin Hultcrantz, MD PhD1, Ola Landgren, MD, PhD1,5, Sigurdur Y Kristinsson, MD, PhD1,9 and Magnus Bjorkholm, MD, PhD1

1Department of Medicine, Division of Hematology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden
2Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland
3Center for Cancer Research, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD
4Department of Medicine, Myeloma Service, National Cancer Institute, National Institutes of Health, Bethesda, MD
5Department of Medicine, Myeloma Service, Memorial Sloan Kettering Cancer Center, New York, NY
6Faculty of Medicine, University of Iceland, Reykjavik, Iceland
7Icelandic Heart Association, Kopavogur, Iceland
8National Institute on Aging, National Institutes of Health (NIH), Bethesda, MD
9University of Iceland, Faculty of Medicine, Reykjavik, Iceland

Background

Monoclonal gammopathy of undetermined significance (MGUS) is a precursor condition to multiple myeloma (MM) and other lymphoproliferative disorders. Patients with MM have an increased risk of venous and arterial thrombosis. Results from previous studies have also shown an increased risk of thrombosis in MGUS. However, these studies have been performed on clinically established cohorts, and no previous study has examined the risk of thrombosis in light chain MGUS (LC-MGUS).

Methods

We performed a population-based study on the longitudinal cohort of the AGES-Reykjavik Study, consisting of 5,764 elderly Icelandic men and women. Through screening all participants with free light chain analysis and serum protein electrophoresis, MGUS and LC-MGUS were identified in 299 and 52 individuals, respectively. The outcome was first incidence/occurrence of venous or arterial thrombosis, as diagnosis or as cause of death. Information on outcomes was supplemented by health care records, available from nine years prior to study baseline and for a median follow-up time of 8.8 years. Through logistic regression, odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate history of arterial and venous thrombosis, respectively, at study baseline. A Cox proportional hazards model was used to estimate hazard ratios (HRs) and 95% CIs for the risk of first incidence of thrombosis during follow-up.

Results

A history of any thrombosis during the nine years prior to diagnosis was present in 30 (10.0%) of individuals with MGUS, 13 (25.0%) of individuals with LC-MGUS, and 643 (12.0%) of individuals without MGUS. In a model adjusting for age, sex, smoking, serum cholesterol levels, diabetes, hypertension, and family history of thrombosis, the odds of having had a thrombosis was not significantly different for neither MGUS (OR = 0.75, 95% CI 0.50-1.12) nor LC-MGUS (OR = 1.81, 0.92-3.58), compared to those without MGUS.

During a median follow-up time of 8.8 years, 80 (26.8%) of individuals with MGUS, 14 (26.9%) of individuals with LC-MGUS, and 1,344 (25.0%) of individuals without MGUS were diagnosed with thrombosis. Individuals with MGUS and with LC-MGUS had no increased risk of arterial thrombosis, when adjusted for age, sex, cholesterol, diabetes, hypertension, smoking, and family history of thrombosis (HR 1.04, 0.82-1.32). Similarly, no increased risk was found in MGUS or LC-MGUS for venous thrombosis, in a model adjusted for age, sex, body mass index, and previous or current cancer (HR 0.89, 0.41-1.89). Excluding individuals with a diagnosis of thrombosis occurring before baseline, or adjusting for a personal history of thrombosis, did not affect the results.

Summary and conclusions

In this large, population-based, screening cohort study, we found no increased risk of arterial or venous thrombosis in MGUS. A history of thrombosis was more common in individuals with LC-MGUS, which might be an effect of higher age in LC-MGUS individuals. To our knowledge, this is the first study to investigate risk of thrombosis in LC-MGUS. The results from our screened study contradict previous findings from clinically established cohorts. Future work is needed to better understand observed differences between studies and across populations. For example, potential underlying factors may include aggregation of underlying comorbidities in clinically diagnosed MGUS patients, and biological variations (shared germline genetic susceptibility) by ethnic groups.

Table. Risk of thrombosis in individuals with MGUS and LC-MGUS, compared to individuals without MGUS.

 

MGUS

LC-MGUS

No MGUS

 

 

No.

HR (95% CI)

No.

HR (95% CI)

No.

HR (95% CI)

 

 

 

 

 

 

 

Any thrombosis*

80 (26.76%)

1.01 (0.80-1.26)

14 (26.92%)

1.13 (0.80-1.26)

1,344 (25.02%)

1.00 (Reference)

Arterial thrombosis

76 (25.42%)

1.04 (0.82-1.32)

14 (26.92%)

1.16 (0.67-2.01)

1,240 (23.08%)

1.00 (Reference)

Venous thrombosis††

7 (2.34%)

0.89 (0.41-1.89)

0 (0.0%)

-

151 (2.81%)

1.00 (Reference)

 

*Results adjusted for age and sex.

Results adjusted for age, sex, smoking, hypertension, cholesterol, diabetes, and family history of arterial thrombosis.

††Results adjusted for age, sex, body mass index, and previous or current cancer.

 

MGUS: monoclonal gammopathy of undetermined significance, LC-MGUS: light-chain monoclonal gammopathy of undetermined significance. HR: hazard ratio, CI: confidence interval.

 

Disclosures: Landgren: Celgene: Consultancy ; BMJ Publishing: Consultancy ; Onyx: Research Funding ; International Myeloma Foundation: Research Funding ; Bristol-Myers Squibb: Consultancy ; Onyx: Honoraria ; Celgene: Honoraria ; Bristol-Myers Squibb: Honoraria ; Medscape: Honoraria ; BMJ Publishing: Honoraria ; Onyx: Consultancy ; Medscape: Consultancy .

*signifies non-member of ASH