Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38821
Title: The risk of cancer in kidney transplant recipients may be reduced in those maintained on everolimus and reduced cyclosporine.
Authors: Kanellis J.;Chadban S.J.;Lim W.H.;Russ G.R.;Wong G.;Pilmore H.
Institution: (Lim) Department of Renal Medicine, Sir Charles Gairdner Hospital, Perth, Australia (Lim) University of Western Australia, Perth, Australia (Russ) Central and Northern Adelaide Renal and Transplantation Services, South Australia, Australia (Wong) Centre for Transplant and Renal Research, Westmead Hospital, New South Wales, Australia (Wong) Centre for Kidney Research, The Children's Hospital at Westmead, New South Wales, Australia (Pilmore) Renal Unit, Auckland Hospital, Auckland, New Zealand (Pilmore) Department of Medicine, Auckland University, Auckland, New Zealand (Kanellis) Department of Nephrology and Transplant Services, Monash Medical Centre, Melbourne, Australia (Chadban) Department of Renal Medicine, Royal Prince Alfred Hospital, Sydney, Australia (Chadban) Kidney Node, Charles Perkins Centre, University of Sydney, Australia
Issue Date: 8-Apr-2017
Copyright year: 2017
Publisher: Elsevier B.V.
Place of publication: Netherlands
Publication information: Kidney International. 91 (4) (pp 954-963), 2017. Date of Publication: 01 Apr 2017.
Journal: Kidney International
Abstract: Kidney transplant recipients are at a high risk of developing cancers after transplantation. Switching from calcineurin inhibitors to sirolimus has been shown to prevent secondary nonmelanoma skin cancer but whether everolimus with reduced exposure to calcineurin inhibitors has similar anti-cancer effects remains unknown. Therefore, we compared the risk of incident cancer over seven years of follow-up among kidney transplant recipients randomized to everolimus plus reduced exposure cyclosporine versus mycophenolate sodium and standard exposure cyclosporine. Using the Australian and New Zealand Dialysis and Transplant Registry (ANZDATA), we assessed the seven-year risk of incident cancer and other graft outcomes among a subgroup of recipients who had participated in the A2309 study using adjusted Cox proportional hazard models. Of 95 recipients, 66 were randomized to everolimus (1.5 mg or 3 mg) with reduced cyclosporine and 29 received mycophenolate sodium and standard exposure cyclosporine. Compared to mycophenolate sodium and standard exposure cyclosporine, everolimus treatment was associated with unadjusted hazard ratios of 0.28 (95% confidence interval 0.11-0.74), 0.39 (0.16-0.98) and 0.41 (0.23-0.71), respectively for nonmelanoma skin cancer, non-skin cancers and any cancers. Interestingly, the adjusted hazard ratios were 0.34 (0.13-0.91), 0.35 (0.09-1.25) and 0.32 (0.15-0.71), respectively. There was no association between treatment groups and rejection, graft loss or death. Compared to standard-exposure cyclosporine, everolimus with reduced exposure to cyclosporine may be associated with a reduced risk of cancer, particularly for non-melanoma skin cancer. Thus, if confirmed in larger patient cohorts, de novo use of everolimus with reduced exposure to calcineurin inhibitors may enable a reduction in cancer burden after transplantation.Copyright © 2017 International Society of Nephrology
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.kint.2016.11.008
Link to associated publication: Click here for full text options
PubMed URL: 28109543 [http://www.ncbi.nlm.nih.gov/pubmed/?term=28109543]
ISSN: 0085-2538
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/38821
Type: Article
Subjects: article
bk virus infection/si [Side Effect]
cancer chemotherapy
cancer risk
clinical effectiveness
controlled study
cytomegalovirus infection/si [Side Effect]
drug efficacy
drug exposure
drug withdrawal
edema/si [Side Effect]
female
follow up
graft recipient
human
hyperlipidemia/si [Side Effect]
kidney graft
kidney graft rejection/co [Complication]
kidney graft rejection/dt [Drug Therapy]
kidney graft rejection/pc [Prevention]
major clinical study
male
*malignant neoplasm/dt [Drug Therapy]
malignant neoplasm/dt [Drug Therapy]
non melanoma skin cancer/dt [Drug Therapy]
outcome assessment
randomized controlled trial
risk assessment
viremia/si [Side Effect]
wound complication/si [Side Effect]
*cyclosporin/ct [Clinical Trial]
*cyclosporin/dt [Drug Therapy]
*everolimus/ae [Adverse Drug Reaction]
*everolimus/dt [Drug Therapy]
mycophenolic acid/ae [Adverse Drug Reaction]
mycophenolic acid/ct [Clinical Trial]
mycophenolic acid/dt [Drug Therapy]
*everolimus/ct [Clinical Trial]
adult
drug withdrawal
edema / side effect
female
follow up
graft recipient
human
hyperlipidemia / side effect
kidney graft
kidney graft rejection / complication / drug therapy / prevention
major clinical study
male
*malignant neoplasm / *drug therapy
malignant neoplasm / drug therapy
non melanoma skin cancer / drug therapy
outcome assessment
randomized controlled trial
risk assessment
wound complication / side effect
viremia / side effect
adult
cancer chemotherapy
cancer risk
clinical effectiveness
controlled study
cytomegalovirus infection / side effect
drug efficacy
drug exposure
Article
bk virus infection / side effect
Type of Clinical Study or Trial: Randomised controlled trial
Appears in Collections:Articles

Show full item record

Page view(s)

10
checked on Aug 18, 2024

Google ScholarTM

Check


Items in Monash Health Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.