Published October 22, 2013 | Version v1
Journal article

Clinicopathologic features and responses to radiotherapy of myeloid sarcoma

  • 1. Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei, Taiwan (China)
  • 2. Cancer Research Center, National Taiwan University College of Medicine, Taipei, Taiwan (China)
  • 3. Division of Radiation Oncology, Department of Oncology, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan (China)
  • 4. Department of Medical Research, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan (China)
  • 5. National Translational Medicine and Clinical Trial Resource Center, Taipei, Taiwan (China)
  • 6. Department of Internal Medicine, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan (China)
  • 7. Graduate Institute of Oncology, National Taiwan University College of Medicine, Taipei, Taiwan (China)

Description

To evaluate clinicopathological features, radiotherapeutic parameters, and their associations with responses to radiotherapy (RT) in patients with myeloid sarcoma (MS). We reviewed 20 patients receiving RT for MS lesions (in 43 RT courses) and analyzed the patients' clinicopathologic features and radiotherapeutic parameters, and their associations with complete responses (CR) to RT using Fisher's exact test and univariate logistic regression analysis. Generalized Estimating Equation was used to analyze all 43 irradiated lesions and account for the correlations in RT responses among lesions from the same patient. We found that the underlying hematological diseases of the evaluated patients were acute myeloid leukemia (AML) in 14 patients (70%), chronic myeloid leukemia in 4 patients (20%), myelodysplastic syndrome with AML transformation in one patient (5%), and de novo MS in one patient (5%). Most patients (55%) received RT for MS at the time of relapse following bone marrow transplantation (BMT). The most common cytogenetic abnormality was t(8;21)(q22;q22). The median RT dose of 20 Gy (range 6–35 Gy), administered in 1.5-3.5 Gy fractions, provided a 63% CR rate. RT dose, sex, cytogenetics, and bone marrow status at the time of RT had no significant effect on CR. Younger age (<50 y, P = 0.06), BMT prior to RT (P = 0.05), and underlying AML (P = 0.05) were marginally associated with higher CR to RT. Our results indicate that a modest RT dose (20-30 Gy) achieves good local control of MS. Age, previous BMT, and underlying hematologic disease can affect RT response

Availability note (English)

Available from http://dx.doi.org/10.1186/1748-717X-8-245; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4016483

Additional details

Publishing Information

Journal Title
Radiation Oncology (Online)
Journal Volume
8
Journal Page Range
p. 245
ISSN
1748-717X

Optional Information

Copyright
Copyright (c) 2013 Chen et al.
Notes
PMCID: PMC4016483; PUBLISHER-ID: 1748-717X-8-245; PMID: 24148102; OAI: oai:pubmedcentral.nih.gov:4016483; licensee BioMed Central Ltd.