TY - JOUR
T1 - Clinical outcomes of solid organ transplant recipients with metastatic cancers who are treated with immune checkpoint inhibitors
T2 - A single-center analysis
AU - Owoyemi, Itunu
AU - Vaughan, Lisa E.
AU - Costello, Collin M.
AU - Thongprayoon, Charat
AU - Markovic, Svetomir N.
AU - Herrmann, Joerg
AU - Otley, Clark C.
AU - Taner, Timucin
AU - Mangold, Aaron R.
AU - Leung, Nelson
AU - Herrmann, Sandra M.
AU - Kukla, Aleksandra
N1 - Funding Information:
Aaron R. Mangold has acted as a clinical investigator for Eli Lilly, Novartis, Sun Pharmaceutical, Pfizer, Actelion, Incyte, Corbus Pharmaceuticals Holdings, miRagen Therapeutics, Soligenix Inc, and Regeneron and is a current member of the scientific advisory board for Kirin. Sandra M. Herrmann is supported by National Institute of Health grant K08 DK118120 from the National Institute of Diabetes and Digestive and Kidney Diseases and by the Mary Kathryn and Michael B. Panitch Career Development Award. The other authors made no disclosures.
Publisher Copyright:
© 2020 American Cancer Society
PY - 2020/11/1
Y1 - 2020/11/1
N2 - Background: Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy, but to the authors' knowledge, limited data exist regarding the safety and efficacy of these agents in transplant recipients. Herein, the authors have reported their experience with 17 patients who were treated with ICIs for metastatic malignancies after undergoing solid organ transplantation. Methods: Data were abstracted for solid organ transplant recipients who received ICIs for the treatment of malignancy between January 1, 2016, and September 30, 2019. The authors identified 7 kidney, 8 liver, and 2 heart transplant recipients. Outcomes of interest were adverse drug reactions, cancer progression, and patient survival. Results: The most common malignancies treated with ICIs were metastatic squamous cell carcinoma (5 patients; 29%) and hepatocellular carcinoma (5 patients; 29%), which were noted exclusively among liver transplant recipients. The median duration on ICIs was 1.7 months (interquartile range, 0.4-7.6 months). Five patients (29%) developed adverse reactions, including 4 patients (24%) with immune-related adverse events(irAEs), 3 patients (18%) with acute allograft rejections, 1 patient (6%) with autoimmune colitis, and 1 patient (6%) with ICI-induced cardiotoxicity (the patient was a heart transplant recipient). The cumulative incidence of cancer progression was 50% and 69%, respectively, at 6 months and 12 months. Eleven patients (65%) died over the median follow-up period of 4.6 months (interquartile range, 1.5-13.2 months) from the time of ICI initiation, with cancer progression being the most common cause of death. Conclusions: ICIs can be used as individualized therapy in selected patients who have undergone solid organ transplantation but more studies are needed to determine how best to use these agents to improve outcomes further.
AB - Background: Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy, but to the authors' knowledge, limited data exist regarding the safety and efficacy of these agents in transplant recipients. Herein, the authors have reported their experience with 17 patients who were treated with ICIs for metastatic malignancies after undergoing solid organ transplantation. Methods: Data were abstracted for solid organ transplant recipients who received ICIs for the treatment of malignancy between January 1, 2016, and September 30, 2019. The authors identified 7 kidney, 8 liver, and 2 heart transplant recipients. Outcomes of interest were adverse drug reactions, cancer progression, and patient survival. Results: The most common malignancies treated with ICIs were metastatic squamous cell carcinoma (5 patients; 29%) and hepatocellular carcinoma (5 patients; 29%), which were noted exclusively among liver transplant recipients. The median duration on ICIs was 1.7 months (interquartile range, 0.4-7.6 months). Five patients (29%) developed adverse reactions, including 4 patients (24%) with immune-related adverse events(irAEs), 3 patients (18%) with acute allograft rejections, 1 patient (6%) with autoimmune colitis, and 1 patient (6%) with ICI-induced cardiotoxicity (the patient was a heart transplant recipient). The cumulative incidence of cancer progression was 50% and 69%, respectively, at 6 months and 12 months. Eleven patients (65%) died over the median follow-up period of 4.6 months (interquartile range, 1.5-13.2 months) from the time of ICI initiation, with cancer progression being the most common cause of death. Conclusions: ICIs can be used as individualized therapy in selected patients who have undergone solid organ transplantation but more studies are needed to determine how best to use these agents to improve outcomes further.
KW - advanced metastatic cancers
KW - allograft rejection
KW - cytotoxic T-lymphocyte antigen 4 (CTLA-4) inhibitors
KW - immune checkpoint inhibitors
KW - programmed cell death protein 1 (PD-1) inhibitors
KW - programmed death–ligand 1 (PD-L1) inhibitors
KW - solid organ transplant recipients
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U2 - 10.1002/cncr.33134
DO - 10.1002/cncr.33134
M3 - Article
C2 - 32786022
AN - SCOPUS:85089312334
SN - 0008-543X
VL - 126
SP - 4780
EP - 4787
JO - Cancer
JF - Cancer
IS - 21
ER -