Influence of Induction Therapy Using Basiliximab With Delayed Tacrolimus Administration in Heart Transplant Recipients - Comparison With Standard Tacrolimus-Based Triple Immunosuppression.


Journal

Circulation journal : official journal of the Japanese Circulation Society
ISSN: 1347-4820
Titre abrégé: Circ J
Pays: Japan
ID NLM: 101137683

Informations de publication

Date de publication:
25 11 2020
Historique:
pubmed: 6 11 2020
medline: 15 12 2021
entrez: 5 11 2020
Statut: ppublish

Résumé

Appropriate indications and protocols for induction therapy using basiliximab have not been fully established in heart transplant (HTx) recipients. This study elucidated the influence of induction therapy using basiliximab along with delayed tacrolimus (Tac) initiation on the outcomes of high-risk HTx recipients.Methods and Results:A total of 86 HTx recipients treated with Tac-based immunosuppression were retrospectively reviewed. Induction therapy was administered to 46 recipients (53.5%) with impaired renal function, pre-transplant sensitization, and recipient- and donor-related risk factors (Induction group). Tac administration was delayed in the Induction group. Induction group subjects showed a lower cumulative incidence of acute cellular rejection grade ≥1R after propensity score adjustment, but this was not significantly different (hazard ratio [HR]: 0.63, 95% confidence interval [CI]: 0.37-1.08, P=0.093). Renal dysfunction in the Induction group significantly improved 6 months post-transplantation (P=0.029). The cumulative incidence of bacterial or fungal infections was significantly higher in the Induction group (HR: 10.6, 95% CI: 1.28-88.2, P=0.029). These results suggest that basiliximab-based induction therapy with delayed Tac initiation may suppress mild acute cellular rejection and improve renal function in recipients with renal dysfunction, resulting in its non-inferior outcome, even in high-risk patients, when applied to the appropriate recipients. However, it should be carefully considered in recipients at a high risk of bacterial and fungal infections.

Sections du résumé

BACKGROUND
Appropriate indications and protocols for induction therapy using basiliximab have not been fully established in heart transplant (HTx) recipients. This study elucidated the influence of induction therapy using basiliximab along with delayed tacrolimus (Tac) initiation on the outcomes of high-risk HTx recipients.Methods and Results:A total of 86 HTx recipients treated with Tac-based immunosuppression were retrospectively reviewed. Induction therapy was administered to 46 recipients (53.5%) with impaired renal function, pre-transplant sensitization, and recipient- and donor-related risk factors (Induction group). Tac administration was delayed in the Induction group. Induction group subjects showed a lower cumulative incidence of acute cellular rejection grade ≥1R after propensity score adjustment, but this was not significantly different (hazard ratio [HR]: 0.63, 95% confidence interval [CI]: 0.37-1.08, P=0.093). Renal dysfunction in the Induction group significantly improved 6 months post-transplantation (P=0.029). The cumulative incidence of bacterial or fungal infections was significantly higher in the Induction group (HR: 10.6, 95% CI: 1.28-88.2, P=0.029).
CONCLUSIONS
These results suggest that basiliximab-based induction therapy with delayed Tac initiation may suppress mild acute cellular rejection and improve renal function in recipients with renal dysfunction, resulting in its non-inferior outcome, even in high-risk patients, when applied to the appropriate recipients. However, it should be carefully considered in recipients at a high risk of bacterial and fungal infections.

Identifiants

pubmed: 33148937
doi: 10.1253/circj.CJ-20-0164
doi:

Substances chimiques

Immunosuppressive Agents 0
Basiliximab 9927MT646M
Tacrolimus WM0HAQ4WNM

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2212-2223

Auteurs

Takuya Watanabe (T)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Masanobu Yanase (M)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Osamu Seguchi (O)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Tomoyuki Fujita (T)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Toshimitsu Hamasaki (T)

Department of Data Science, National Cerebral and Cardiovascular Center.

Seiko Nakajima (S)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Kensuke Kuroda (K)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Yuto Kumai (Y)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Koichi Toda (K)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Keiichiro Iwasaki (K)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Yuki Kimura (Y)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Hiroki Mochizuki (H)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Eiji Anegawa (E)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Yasumori Sujino (Y)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Nobuichiro Yagi (N)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Koichi Yoshitake (K)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Kyoichi Wada (K)

Department of Pharmacy, National Cerebral and Cardiovascular Center.

Sachi Matsuda (S)

Department of Pharmacy, National Cerebral and Cardiovascular Center.

Hiromi Takenaka (H)

Department of Pharmacy, National Cerebral and Cardiovascular Center.

Megumi Ikura (M)

Department of Pharmacy, National Cerebral and Cardiovascular Center.

Kazuki Nakagita (K)

Department of Pharmacy, National Cerebral and Cardiovascular Center.

Shin Yajima (S)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Yorihiko Matsumoto (Y)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Naoki Tadokoro (N)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Takashi Kakuta (T)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Satsuki Fukushima (S)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Hatsue Ishibashi-Ueda (H)

Department of Pathology, National Cerebral and Cardiovascular Center.

Junjiro Kobayashi (J)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center.

Norihide Fukushima (N)

Department of Transplant Medicine, National Cerebral and Cardiovascular Center.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH