1994
DOI: 10.1200/jco.1994.12.12.2527
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Incidence and characterization of secondary myelodysplastic syndrome and acute myelogenous leukemia following high-dose chemoradiotherapy and autologous stem-cell transplantation for lymphoid malignancies.

Abstract: There is an increased risk of MDS/AML following ABMT/PSCT for lymphoid malignancies. NHL patients age > or = 40 years at the time of transplant and who received TBI are at greatest risk.

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Cited by 306 publications
(160 citation statements)
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“…2,3 However, there are concerns about both late relapses and the development of secondary leukaemia following auto-SCT. [2][3][4][5] Myeloablative therapy and allo-SCT has been employed in patients with advanced FL and is capable of inducing lasting remissions and cure even in patients with advanced disease. [6][7][8] However, this therapeutic modality has been limited in its application due to the high TRM and is generally reserved for younger patients.…”
Section: Introductionmentioning
confidence: 99%
“…2,3 However, there are concerns about both late relapses and the development of secondary leukaemia following auto-SCT. [2][3][4][5] Myeloablative therapy and allo-SCT has been employed in patients with advanced FL and is capable of inducing lasting remissions and cure even in patients with advanced disease. [6][7][8] However, this therapeutic modality has been limited in its application due to the high TRM and is generally reserved for younger patients.…”
Section: Introductionmentioning
confidence: 99%
“…4 Following auto-SCT, tMDS/tAML has been reported to occur in up to 15% of patients. [6][7][8][9][10] One previous study 5 implicated priming with VP-16 as a significant factor for development of tAML following ASCT. A subsequent report detected no increased risk for tMDS/tAML with VP-16 mobilization in the absence of TBI conditioning.…”
Section: Discussionmentioning
confidence: 99%
“…Complications can also occur months to years after HDC. Myelodysplasia and/or acute leukemia has been reported in patients after HDC [62].…”
Section: Nonhematologic Toxicitymentioning
confidence: 99%