A Pilot Study of Checkpoint Inhibitors in Solid Organ Transplant Recipients with Metastatic Cutaneous Squamous Cell

Irene Tsung1, Francis P Worden1, Robert J Fontana2

  • 1Division of Hematology and Oncology, University of Michigan, Ann Arbor, Michigan, USA.

The Oncologist
|September 24, 2020
PubMed
Abstract

Insights

Immune checkpoint inhibitors (ICIs) show promise for advanced cutaneous squamous cell carcinoma in solid organ transplant (SOT) recipients. Minimizing immunosuppression and using prophylactic steroids may enable safe and effective ICI treatment in this population.

Area of Science:

  • Oncology
  • Transplant Medicine
  • Immunology

Background:

  • Solid organ transplant (SOT) recipients face increased malignancy risk due to long-term immunosuppression.
  • Immune checkpoint inhibitors (ICIs) are effective cancer treatments but SOT recipients are often excluded from trials due to rejection concerns.

Purpose of the Study:

  • To review the safety and efficacy of ICIs in SOT recipients with advanced head and neck cutaneous squamous cell carcinoma (cSCC).

Main Methods:

  • Retrospective review of SOT recipients treated with ICIs between April 2011 and September 2019.
  • Analysis of patient demographics, ICI regimens, immunosuppression modifications, treatment outcomes, and adverse events.

Main Results:

  • Seven SOT recipients with metastatic head and neck cSCC received ICIs (cemiplimab or pembrolizumab) after immunosuppression adjustment.
  • Overall tumor response rate was 57.1%, with one complete and three partial responses.
  • Adverse events included pneumonitis and renal injury; prophylactic steroids in three patients correlated with response and preserved allograft function.

Conclusions:

  • Minimizing calcineurin inhibitors (CNIs) or converting to mTOR inhibitors, alongside prophylactic steroids, may allow safe ICI use in SOT recipients with advanced cSCC.
  • Short-term efficacy is promising, but further prospective studies are needed to standardize protocols and confirm findings.

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