Citation
Tracy, S I., et al. "Vitamin D Insufficiency Is Associated With an Increased Risk of Early Clinical Failure in Follicular Lymphoma." Blood Cancer Journal, vol. 7, no. 8, 2017, pp. e595.
Tracy SI, Maurer MJ, Witzig TE, et al. Vitamin D insufficiency is associated with an increased risk of early clinical failure in follicular lymphoma. Blood Cancer J. 2017;7(8):e595.
Tracy, S. I., Maurer, M. J., Witzig, T. E., Drake, M. T., Ansell, S. M., Nowakowski, G. S., Thompson, C. A., Inwards, D. J., Johnston, P. B., Micallef, I. N., Allmer, C., Macon, W. R., Weiner, G. J., Slager, S. L., Habermann, T. M., Link, B. K., & Cerhan, J. R. (2017). Vitamin D insufficiency is associated with an increased risk of early clinical failure in follicular lymphoma. Blood Cancer Journal, 7(8), e595. https://doi.org/10.1038/bcj.2017.70
Tracy SI, et al. Vitamin D Insufficiency Is Associated With an Increased Risk of Early Clinical Failure in Follicular Lymphoma. Blood Cancer J. 2017 08 25;7(8):e595. PubMed PMID: 28841207.
TY - JOUR
T1 - Vitamin D insufficiency is associated with an increased risk of early clinical failure in follicular lymphoma.
AU - Tracy,S I,
AU - Maurer,M J,
AU - Witzig,T E,
AU - Drake,M T,
AU - Ansell,S M,
AU - Nowakowski,G S,
AU - Thompson,C A,
AU - Inwards,D J,
AU - Johnston,P B,
AU - Micallef,I N,
AU - Allmer,C,
AU - Macon,W R,
AU - Weiner,G J,
AU - Slager,S L,
AU - Habermann,T M,
AU - Link,B K,
AU - Cerhan,J R,
Y1 - 2017/08/25/
PY - 2016/12/22/received
PY - 2017/05/02/revised
PY - 2017/05/08/accepted
PY - 2017/8/26/entrez
PY - 2017/8/26/pubmed
PY - 2018/8/30/medline
SP - e595
EP - e595
JF - Blood cancer journal
JO - Blood Cancer J
VL - 7
IS - 8
N2 - We evaluated whether vitamin D insufficiency (VDI; 25(OH)D <20 ng/ml) was associated with adverse outcomes among follicular lymphoma (FL) patients using an observational prospective cohort study of 642 FL patients enrolled from 2002-2012. The median age at diagnosis was 60 years. At a median follow-up of 59 months, 297 patients (46%) had an event (progression, treatment failure), 78 had died and 42 (6.5%) had a lymphoma-related death. VDI was associated with inferior event-free survival (EFS) at 12 months (EFS12, odds ratio (OR)=2.05; 95% confidence interval (CI) 1.18-3.54), overall survival (OS, hazards ratio (HR)=2.35; 95%CI 1.37-4.02), and lymphoma-specific survival (LSS, HR=2.97; 95% CI 1.52-5.80) for the full cohort. Among patients treated with immunochemotherapy (IC), VDI was associated with inferior EFS12 (OR=3.00; 95% CI 1.26-7.13), OS (HR=2.86; 95% CI 1.39-5.85), and LSS (HR=2.96; 95% CI 1.29-6.79). For observed patients, VDI was associated with inferior OS (HR=2.85; 95% CI 1.20-6.76). For other therapies, VDI was associated with inferior OS (HR=3.06; 95% CI 1.01-9.24). Our work is the first to reveal an association of VDI with early clinical failure, and to demonstrate an association of VDI with adverse outcomes among patients who are observed or treated with therapies other than IC. Our findings suggest a potentially modifiable prognostic factor to address in patients with FL.
SN - 2044-5385
UR - https://www.unboundmedicine.com/medline/citation/28841207/full_citation
DB - PRIME
DP - Unbound Medicine
ER -