TY - JOUR
T1 - Wound healing adverse events in kidney transplant recipients receiving everolimus with reduced calcineurin inhibitor exposure or current standard-of-care
T2 - Insights from the 24 month TRANSFORM study
AU - Citterio, Franco
AU - Henry, Mitchell
AU - Kim, Dean Y.
AU - Kim, Myoung Soo
AU - Han, Duck Jong
AU - Kenmochi, Takashi
AU - Mor, Eytan
AU - Tisone, Giuseppe
AU - Bernhardt, Peter
AU - Hernandez Gutierrez, Maria Pilar
AU - Watarai, Yoshihiko
N1 - Funding Information:
F Citterio has received consulting honoraria and travel grants from Novartis, Astellas, Pfizer and Bristol Myers Squibb. M Henry has received consulting honoraria from Novartis. MP Hernandez Gutierrez and P Bernhardt are employees of Novartis. Y Watarai has received consulting honoraria and travel grants from Novartis, Astellas and Chugai Pharma. The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript. This includes employment, consultancies, honoraria, stock ownership or options, expert testimony, grants or patents received or pending, or royalties.
Funding Information:
The TRANSFORM study was funded by Novartis Pharma AG, Basel, Switzerland. Medical writing support was funded by Novartis. The manuscript was prepared with assistance from a professional medical writer (Edgar A. Mueller, 3P Consulting), funded by Novartis.
Publisher Copyright:
© 2020, © 2020 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/7/20
Y1 - 2020/7/20
N2 - Objectives: In TRANSFORM, de novo kidney transplant recipients received either everolimus in combination with reduced-exposure calcineurin inhibitor (EVR+rCNI) at standard EVR pre-dose concentrations of 3-8 ng/mL or mycophenolic acid plus standard-exposure CNI (MPA+sCNI). The authors analyzed the incidence of wound healing adverse events (WHAEs) over the 2-year study period. Methods: Patients were randomized to either EVR+rCNI or MPA+sCNI, both combined with induction therapy and steroids. Results: The safety population consisted of 2,026 patients (EVR+rCNI: 1,014, MPA+sCNI: 1,012). The proportion of patients with at least 1 WHAE was comparable between EVR+rCNI and MPA+sCNI treatment groups [20.6% vs. 17.3%; risk ratio (RR): 1.19; 95% confidence interval (CI): 0.99, 1.43] at month 24. The numerical difference between EVR+rCNI and MPA+sCNI was mainly caused by an increased proportion of EVR patients with lymphocele and wound dehiscence [7.5% vs. 5.1% (RR: 1.46; 95% CI: 1.04, 2.05) and 3.9 vs. 1.8% (RR: 2.22; 95%CI: 1.28, 3.84), respectively]. Conclusion: The immediate introduction of EVR+rCNI after kidney transplantation was associated with an overall comparable incidence of WHAEs versus current standard-of-care over the 24-month study period. There was an increased relative risk of experiencing lymphocele and wound dehiscence but the absolute risks were rather low in both groups. CT.gov identifier: NCT01950819.
AB - Objectives: In TRANSFORM, de novo kidney transplant recipients received either everolimus in combination with reduced-exposure calcineurin inhibitor (EVR+rCNI) at standard EVR pre-dose concentrations of 3-8 ng/mL or mycophenolic acid plus standard-exposure CNI (MPA+sCNI). The authors analyzed the incidence of wound healing adverse events (WHAEs) over the 2-year study period. Methods: Patients were randomized to either EVR+rCNI or MPA+sCNI, both combined with induction therapy and steroids. Results: The safety population consisted of 2,026 patients (EVR+rCNI: 1,014, MPA+sCNI: 1,012). The proportion of patients with at least 1 WHAE was comparable between EVR+rCNI and MPA+sCNI treatment groups [20.6% vs. 17.3%; risk ratio (RR): 1.19; 95% confidence interval (CI): 0.99, 1.43] at month 24. The numerical difference between EVR+rCNI and MPA+sCNI was mainly caused by an increased proportion of EVR patients with lymphocele and wound dehiscence [7.5% vs. 5.1% (RR: 1.46; 95% CI: 1.04, 2.05) and 3.9 vs. 1.8% (RR: 2.22; 95%CI: 1.28, 3.84), respectively]. Conclusion: The immediate introduction of EVR+rCNI after kidney transplantation was associated with an overall comparable incidence of WHAEs versus current standard-of-care over the 24-month study period. There was an increased relative risk of experiencing lymphocele and wound dehiscence but the absolute risks were rather low in both groups. CT.gov identifier: NCT01950819.
KW - calcineurin inhibitor
KW - everolimus
KW - kidney transplantation
KW - randomized
KW - safety
KW - wound healing
UR - https://www.scopus.com/pages/publications/85087752065
U2 - 10.1080/14740338.2020.1792441
DO - 10.1080/14740338.2020.1792441
M3 - Article
C2 - 32633157
AN - SCOPUS:85087752065
SN - 1474-0338
SP - 1339
EP - 1348
JO - Expert Opinion on Drug Safety
JF - Expert Opinion on Drug Safety
ER -