Secondary Acute Myelogenous Leukemia in Patients with Retinoblastoma. Is Chemotherapy a Factor?

Dan S. Gombos, John Hungerford, David H. Abramson, Judith Kingston, Guillermo Chantada, Ira J. Dunkel, Celia B G Antoneli, Mark Greenwald, Barret G. Haik, Carlos A. Leal, Aurora Medina-Sanson, Amy C. Schefler, Gavivann Veerakul, Regina Wieland, Norbert Bornfeld, Mathew W. Wilson, Christopher Bing On Yu

Research output: Contribution to journalArticlepeer-review

183 Scopus citations


Purpose: To describe a series of patients with secondary acute myelogenous leukemia (sAML) and retinoblastoma (RB). Design: Retrospective observational cases series. Participants: Ocular and pediatric oncologists at referral centers in Europe and the Americas and the RB databases at the National Institutes of Health and the Ophthalmic Oncology Service at Memorial Sloan-Kettering Cancer Center. Methods: Physician survey, retrospective database review, and literature search. Main Outcome Measures: History of RB and development of sAML, management of RB (surgery, radiotherapy, chemotherapy), age at diagnosis of RB and leukemia, French-American-British (FAB) subtype, and current status of patient (alive or dead). Results: Fifteen patients with sAML were identified; 13 occurred in childhood. Mean latent period from RB to AML diagnosis was 9.8 years (median, 42 months). Nine cases were of the M2 or M5 FAB subtypes. Twelve patients (79 %) had received chemotherapy with a topoisomerase II inhibitor, 8 (43%) had received chemotherapy with an epipodophyllotoxin. Ten children died of their leukemia. Conclusions: Acute myelogenous leukemia is a rare secondary malignancy among retinoblastoma patients, many of whom were treated with primary or adjuvant chemotherapy. Additional studies are needed to assess potential risk factors contributing to sAML development in this cohort.

Original languageEnglish (US)
Pages (from-to)1378-1383
Number of pages6
Issue number7
StatePublished - Jul 2007

ASJC Scopus subject areas

  • Ophthalmology


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