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Updated: Jun 21, 2025

Murine Full-thickness Skin Transplantation
Published on: January 2, 2017
Use of immune checkpoint inhibitors in solid organ transplant recipients with advanced cutaneous malignancies
Stephanie Ji1, Hao Liu2, Laura Pachella3
1Department of Medicine, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, United States.
Background:
Immune checkpoint inhibitors (ICI) are standard of care therapy for patients with cutaneous malignancies, the most frequently diagnosed cancers in solid organ transplant (SOT) recipients. The activity and rate of allograft rejection in SOT recipients with advanced skin cancers treated with ICI is understudied.
Methods:
We conducted a retrospective analysis of SOT recipients with advanced melanoma, cutaneous squamous cell carcinoma (cSCC), and merkel cell carcinoma (MCC) who were treated with ICI. Unpublished cases from our institution and published cases from the literature were aggregated. Demographics, type of immunosuppressive therapy, type of ICI(s) administered, prior systemic therapies, tumor response to ICI, and evidence of organ rejection and/or failure were recorded. Objective response rates (ORR) and rates of graft rejection and failure are reported.
Results:
Ninety patients were identified; four patients from our institution and 86 unique patients from a literature review. ORR to first-line ICI for the entire cohort was 41.1% (37/90). ORR by tumor type was 31% (18/58), 64.3% (18/28), and 25.0% (1/4) for melanoma, cSCC, and MCC, respectively. The rate of graft rejection was 37.8% (34/90) with 61.8% (21/34) of these cases progressing to graft failure. Number of immunosuppressive agents (0, 1, 2, or 3) was inversely associated with rate of graft failure.
Conclusions:
In this retrospective analysis, ICIs demonstrate clinical activity in SOT recipients with cutaneous malignancies; however, the rate of graft rejection is high. Treatment plans should be individualized through thorough interdisciplinary discussion. Immunosuppressive modifications may be considered prior to starting treatment, but when feasible, enrollment on clinical trials is preferred.
Insights
Immune checkpoint inhibitors (ICI) show activity against skin cancers in organ transplant recipients, but carry a high risk of graft rejection. Individualized treatment and interdisciplinary discussion are crucial for managing these patients.
Area of Science:
- Oncology
- Transplantation Immunology
Background:
- Cutaneous malignancies are common in solid organ transplant (SOT) recipients.
- Immune checkpoint inhibitors (ICI) are standard cancer therapy but their use in SOT recipients is understudied.
- The impact of ICI on allograft rejection in SOT patients with advanced skin cancers requires investigation.
Purpose of the Study:
- To evaluate the efficacy and safety of ICI in SOT recipients with advanced cutaneous malignancies.
- To determine the objective response rates (ORR) of ICI in this patient population.
- To assess the incidence of allograft rejection and graft failure associated with ICI treatment.
Main Methods:
- Retrospective analysis of SOT recipients treated with ICI for advanced melanoma, cutaneous squamous cell carcinoma (cSCC), and merkel cell carcinoma (MCC).
- Inclusion of institutional and published literature cases.
- Data collection included demographics, immunosuppressive therapy, ICI type, prior treatments, tumor response, and graft outcomes.
Main Results:
- Ninety patients were analyzed (4 from institution, 86 from literature).
- Overall ORR to first-line ICI was 41.1%. ORR varied by tumor type: melanoma (31%), cSCC (64.3%), MCC (25%).
- Graft rejection occurred in 37.8% of patients, with 61.8% of these progressing to graft failure. Fewer immunosuppressive agents correlated with lower graft failure rates.
Conclusions:
- ICI demonstrate clinical activity in SOT recipients with cutaneous malignancies.
- However, ICI treatment is associated with a high rate of graft rejection and subsequent failure.
- Individualized treatment strategies, interdisciplinary consultation, and consideration of immunosuppressive modifications or clinical trials are recommended.
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