Nucl Med Mol Imaging.  2020 Oct;54(5):256-260. 10.1007/s13139-020-00652-9.

Acute Promyelocytic Leukemia After Radium-223 Exposure for Prostate Cancer in a Chemotherapy-Naïve Patient

Affiliations
  • 1Hematology, Polo Universitario Pontino, “Sapienza”, Via A. Canova S.M. Goretti Hospital, Latina, Italy
  • 2Department of Biomedicine and Prevention, University of Rome “Tor Vergata”, Rome, Italy
  • 3Department of Medical Oncology, Medical and Surgical Sciences and Biotechnology, “Sapienza University”, Rome, Italy
  • 4Department of Nuclear Medicine, Santa Maria Goretti Hospital, Latina, Italy

Abstract

223Ra-dichloride is a bone-seeking targeted alpha (α)-emitting approved for bone metastases in prostate cancer. Here, we report a case of therapy-related acute promyelocytic leukemia (t-APL) following administration of 223Ra, showing some evidence of a causative relationship. A patient with metastatic prostate cancer received therapy with 223Ra, with 6 injections of the radiopharmaceutical at a standard dose of 55 kBq/kg at 4-week intervals for a cumulative administered activity of 26.3 MBq. PET/CT with 18F-methylcholine repeated 1 month after the conclusion of 223Ra was negative. After 8 months, he developed pancytopenia and we made a diagnosis of therapy-related acute promyelocytic leukemia (t-APL). We then studied the genomic locations of the breakpoints in the PML and RARA genes, which were at nucleotide positions 1708-09 of PML intron 3, respectively, outside the previously reported Topo II-associated hotspot region. t-APL was cured with all-trans-retinoic acid (ATRA) and arsenic trioxide. The type of PML/RARA rearrangement we identified, in absence of other myelotoxic treatments, is suggestive of a possible direct causal relationship with exposure to 223Ra and warrants further investigations.

Keyword

Acute promyelocytic leukemia; Prostate cancer. radium-223; Therapy-related acute myeloid leukemia
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