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. 2009 Jul 2;114(1):225. doi: 10.1182/blood-2009-03-209015

Incidence of second cancers after allogeneic hematopoietic stem cell transplantation using reduced-dose radiation

Matthew M Hsieh , Courtney D Fitzhugh, John F Tisdale
PMCID: PMC2710951  PMID: 19574484

To the editor:

We read with interest the article by Rizzo et al1 updating their earlier publication2 and describing the largest international retrospective analysis of second cancers after allogeneic hematopoietic stem cell transplantation (HSCT) to date. Their data demonstrate a cumulative incidence of second malignancies of 3.3% at 20 years. The greatest risk of solid tumors, such as melanoma, breast, thyroid, brain, and other tumors, was age younger than 30 at the time of HSCT and total body irradiation (TBI). This higher risk associated with younger age at time of transplantation is similar to the results from atomic bomb survivors,3 and these confirmatory data provide critical information in the counseling of patients considering HSCT. Their current analyses unfortunately grouped those who received doses below 12 Gy, and suggested that TBI doses lower than 12 Gy confer the same second cancer risk as TBI doses above 12 Gy. In contrast, previous analyses in atomic bomb survivors have shown a near-linear relationship between the TBI dose and second cancer risk, especially below 5 Gy.3,4 Further, Curtis et al previously found that lower doses of TBI (< 12 Gy) were associated with a lower risk of second cancer.2 Because a growing number of allogeneic HSCTs employ substantially lower doses of TBI, including doses as low as 2 Gy, this point deserves further clarification. An analysis focusing on the second cancer risk with lower doses of TBI would complement the atomic bomb survivor data and greatly benefit the transplantation community. Additionally, including the incidence of second cancers in patients with nonmalignant disorders, such as hemoglobinopathies or aplastic anemia, would further broaden the applicability of their extensive data analyses.

Authorship

Acknowledgments: This work was supported by the intramural research program of the National Heart, Lung, and Blood Institute and the National Institute of Diabetes and Digestive and Kidney Diseases at the National Institutes of Health (Bethesda, MD).

Conflict-of-interest disclosure: The authors declare no competing financial interests.

Correspondence: Matthew M. Hsieh, National Institutes of Health, 9000 Rockville Pike, Bldg 10, 9N 116, Bethesda, MD 20892; e-mail: matthewhs@mail.nih.gov.

References

  • 1.Rizzo JD, Curtis RE, Socié G, et al. Solid cancers after allogeneic hematopoietic cell transplantation. Blood. 2009;113(5):1175–1183. doi: 10.1182/blood-2008-05-158782. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Curtis RE, Rowlings PA, Deeg HJ, et al. Solid cancers after bone marrow transplantation. N Engl J Med. 1997;336(13):897–904. doi: 10.1056/NEJM199703273361301. [DOI] [PubMed] [Google Scholar]
  • 3.Preston DL, Shimizu Y, Pierce DA, Suyama A, Mabuchi K. Studies of mortality of atomic bomb survivors. Report 13: solid cancer and noncancer disease mortality: 1950-1997. Radiat Res. 2003;160(4):381–407. doi: 10.1667/rr3049. [DOI] [PubMed] [Google Scholar]
  • 4.Pierce DA, Preston DL. Radiation-related cancer risks at low doses among atomic bomb survivors. Radiat Res. 2000;154(2):178–186. doi: 10.1667/0033-7587(2000)154[0178:rrcral]2.0.co;2. [DOI] [PubMed] [Google Scholar]

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