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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The Korean Society of Nephrology
2012-06-01
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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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