Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy

Post-transplant malignancy (PTM) is a limiting factor for both patient and allograft survival in kidney transplant recipients (KTRs). We hypothesized that active vitamin D compounds (AVDs) could reduce the development of PTM in KTRs and evaluated the effects of AVD therapy in a prospective cohort of...

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Main Authors: Yoshitsugu Obi, Naotsugu Ichimaru, Isao Matsui, Takayuki Hamano, Shiro Takahara, Yoshitaka Isaka
Format: Article
Language:English
Published: The Korean Society of Nephrology 2012-06-01
Series:Kidney Research and Clinical Practice
Online Access:http://www.sciencedirect.com/science/article/pii/S2211913212005359
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spelling doaj-05e701d94c2d4354a37abaedaf00fa9e2020-11-24T23:43:31ZengThe Korean Society of NephrologyKidney Research and Clinical Practice2211-91322012-06-01312A6110.1016/j.krcp.2012.04.502Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancyYoshitsugu ObiNaotsugu IchimaruIsao MatsuiTakayuki HamanoShiro TakaharaYoshitaka IsakaPost-transplant malignancy (PTM) is a limiting factor for both patient and allograft survival in kidney transplant recipients (KTRs). We hypothesized that active vitamin D compounds (AVDs) could reduce the development of PTM in KTRs and evaluated the effects of AVD therapy in a prospective cohort of ambulatory KTRs in a Japanese single center. We used a propensity score (PS) of having received AVDs estimated by 25 clinically relevant factors to adjust for these confounders. Among 218 participants, the mean age was 49.4 (SD, 12.1) years, 63.3% were male, the median time since transplantation was 11.2 (interquartile range [IQR], 5.2–17.1) years, and 42.2% had been treated with AVDs at baseline. The AVDs consisted of calcitriol (58.7%) and alfacalcidol (41.3%), and their median doses were 0.5 (IQR, 0.5–0.5) μg and 0.5 (IQR, 0.25–1.0) μg, respectively. During a median follow-up of 2.9 (IQR, 2.1–3.0) years, PTM was observed to have developed in 5 (5.4%) of 92 AVD users and in 11 (8.7%) of 126 non-users. Cox regression analysis with stratification by the PS tertiles showed that AVDs were significantly associated with a lower risk of PTM (hazard ratio, 0.25 [95% confidence interval, 0.07–0.82], P=0.022). The level of serum 25-hydroxyvitamin D was generally low (median, 16.6 ng/ml), and not significantly associated with PTM. Sensitivity analyses with stratification by PS quartiles, PS matching, or inverse probability weighting yielded similar results. Our results suggest a novel potential strategy to prevent PTM by using a normal dose of AVDs with a well-known safety profile. A randomized controlled trial should be performed to confirm our findings.http://www.sciencedirect.com/science/article/pii/S2211913212005359
collection DOAJ
language English
format Article
sources DOAJ
author Yoshitsugu Obi
Naotsugu Ichimaru
Isao Matsui
Takayuki Hamano
Shiro Takahara
Yoshitaka Isaka
spellingShingle Yoshitsugu Obi
Naotsugu Ichimaru
Isao Matsui
Takayuki Hamano
Shiro Takahara
Yoshitaka Isaka
Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
Kidney Research and Clinical Practice
author_facet Yoshitsugu Obi
Naotsugu Ichimaru
Isao Matsui
Takayuki Hamano
Shiro Takahara
Yoshitaka Isaka
author_sort Yoshitsugu Obi
title Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
title_short Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
title_full Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
title_fullStr Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
title_full_unstemmed Oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
title_sort oral active vitamin d therapy as a potential chemoprevention against post-transplant malignancy
publisher The Korean Society of Nephrology
series Kidney Research and Clinical Practice
issn 2211-9132
publishDate 2012-06-01
description Post-transplant malignancy (PTM) is a limiting factor for both patient and allograft survival in kidney transplant recipients (KTRs). We hypothesized that active vitamin D compounds (AVDs) could reduce the development of PTM in KTRs and evaluated the effects of AVD therapy in a prospective cohort of ambulatory KTRs in a Japanese single center. We used a propensity score (PS) of having received AVDs estimated by 25 clinically relevant factors to adjust for these confounders. Among 218 participants, the mean age was 49.4 (SD, 12.1) years, 63.3% were male, the median time since transplantation was 11.2 (interquartile range [IQR], 5.2–17.1) years, and 42.2% had been treated with AVDs at baseline. The AVDs consisted of calcitriol (58.7%) and alfacalcidol (41.3%), and their median doses were 0.5 (IQR, 0.5–0.5) μg and 0.5 (IQR, 0.25–1.0) μg, respectively. During a median follow-up of 2.9 (IQR, 2.1–3.0) years, PTM was observed to have developed in 5 (5.4%) of 92 AVD users and in 11 (8.7%) of 126 non-users. Cox regression analysis with stratification by the PS tertiles showed that AVDs were significantly associated with a lower risk of PTM (hazard ratio, 0.25 [95% confidence interval, 0.07–0.82], P=0.022). The level of serum 25-hydroxyvitamin D was generally low (median, 16.6 ng/ml), and not significantly associated with PTM. Sensitivity analyses with stratification by PS quartiles, PS matching, or inverse probability weighting yielded similar results. Our results suggest a novel potential strategy to prevent PTM by using a normal dose of AVDs with a well-known safety profile. A randomized controlled trial should be performed to confirm our findings.
url http://www.sciencedirect.com/science/article/pii/S2211913212005359
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