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Malignancy in patients with sickle cell disease
Author(s) -
Schultz William H.,
Ware Russell E.
Publication year - 2003
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.10427
Subject(s) - malignancy , medicine , disease , intensive care medicine , oncology
Malignancy in patients with sickle cell disease (SCD) has been previously reported, but the types of cancer and its incidence remain undefined. With the advent of hydroxyurea therapy, there is concern about increasing the cancer risk for patients with SCD. The International Association of Sickle Cell Nurses and Physician Assistants identified 52 cases of cancer (49 patients) among 16,613 patients with SCD followed at 52 institutions. The median age at malignancy diagnosis was 34 years (range, 14 months–62 years). Twenty‐one cases (40%) occurred in pediatric patients, primarily leukemia ( n = 7) or Wilms' tumor ( n = 5), with 15 children surviving. Most adults had solid tumors, especially carcinomas, and only nine were known to be alive. Three patients received hydroxyurea before the diagnosis of malignancy. These data provide essential baseline information for the accurate interpretation of future reports of malignancy in patients with SCD, especially those receiving hydroxyurea therapy. Am. J. Hematol. 74:249–253, 2003. © 2003 Wiley‐Liss, Inc.

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