Thrombotic microangiopathy in metastatic melanoma patients treated with adoptive cell therapy and total body irradiation

Jennifer Tseng, Deborah E. Citrin, Meryl Waldman, Donald E. White, Steven A. Rosenberg, James C. Yang

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND Thrombotic microangiopathy (TMA) is a complication that developed in some patients receiving 12 Gy total body irradiation (TBI) in addition to lymphodepleting preparative chemotherapy prior to infusion of autologous tumor-infiltrating lymphocytes (TIL) with high-dose aldesleukin (IL-2). This article describes the incidence, presentation, and course of radiation-associated TMA. METHODS The data for patients with metastatic melanoma who received ACT with TIL plus aldesleukin following myeloablative chemotherapy and 12-Gy TBI was examined, in order to look at patient characteristics and the natural history of TMA. RESULTS The median time to presentation was approximately 8 months after completing TBI. The estimated cumulative incidence of TMA was 31.2% (median follow-up of 24 months). Noninvasive criteria for diagnosis included newly elevated creatinine levels, new-onset hypertension, new-onset anemia, microscopic hematuria, thrombocytopenia, low haptoglobin, and elevated lactate dehydrogenase values. Once diagnosed, patients were managed with control of their hypertension with multiple agents and supportive red blood cell transfusions. TMA typically stabilized or improved and no patient progressed to dialysis. TMA was associated with a higher probability of an antitumor response. CONCLUSIONS TMA occurs in approximately a third of patients treated with a lymphodepleting preparative chemotherapy regimen with TBI prior to autologous T cell therapy. The disease has a variable natural history, however, no patient developed end-stage renal failure. Successful management with supportive care and aggressive hypertension control is vital to the safe application of a systemic therapy that has shown curative potential for patients with disseminated melanoma. Cancer 2014;120:1426-1432. Published 2014. This article is a U.S. Government work and is in the public domain in the USA. T-cell transfer therapy for patients with melanoma which incorporates preparative total body irradiation induces thrombotic microangiopathy in approximately a third of patients. Diagnosis and treatment of this entity can prevent renal failure and allow the safe administration of a potentially curative regimen for metastatic melanoma.

Original languageEnglish (US)
Pages (from-to)1426-1432
Number of pages7
JournalCancer
Volume120
Issue number9
DOIs
StatePublished - May 1 2014

Keywords

  • adopted cell therapy
  • autologous T cell therapy
  • immunotherapy
  • metastatic melanoma
  • thrombotic microangiopathy
  • total body irradiation
  • tumor infiltrating lymphocytes

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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