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Journal of Clinical Oncology, Vol 17, Issue 1 (January), 1999: 277
© 1999 American Society for Clinical Oncology

Prognostic Significance of Magnetic Resonance Imaging of Femoral Marrow in Patients With Myelodysplastic Syndromes

Shojiro Takagi, Osamu Tanaka, Hideki Origasa, Yasusada Miura

From the Division of Hematology and Department of Radiology, Omiya Medical Center, Jichi Medical School, Omiya, Saitama; Division of Biostatistics, Toyama Med-Pharm University, Toyama; and Division of Hematology, Jichi Medical School, Tochigi, Japan.

Address reprint requests to Shojiro Takagi, MD, Division of Hematology, Omiya Medical Center, Jichi Medical School, 1–847 Amanuma-cho, Omiya, Saitama 330, Japan.

PURPOSE: To investigate whether the abnormalities observed on femoral marrow magnetic resonance images are related to the development of leukemia and survival of patients with myelodysplastic syndromes (MDS).

PATIENTS AND METHODS: The findings on magnetic resonance images of the femoral marrow were evaluated over periods of 1 to 92 months (median, 18 months) in 42 consecutive adult patients with newly diagnosed MDS. Magnetic resonance images were obtained by the T1-weighted spin echo method and the short TI inversion recovery technique.

RESULTS: Magnetic resonance images showed that the femoral marrow patterns changed from fatty, faint, or nodular to scattered or uniform as the disease progressed. Development of acute myeloid leukemia was observed in only 13 patients whose marrow exhibited a scattered or uniform pattern. The overall survival of the 29 patients with a scattered or uniform marrow pattern was significantly shorter than that of the 13 patients with a fatty, faint, or nodular marrow pattern (10.7% v 73.3% at 7 years; P < .01). The period of leukemia-free survival was also significantly shorter in the patients with a scattered or uniform marrow pattern versus a fatty, faint, or nodular pattern (37.7% v 100% at 7 years; P < .01).

CONCLUSION: Magnetic resonance images of the femoral marrow can provide valuable information for assessing the prognosis and determining the most appropriate management of patients with MDS.




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M. L. Heaney and D. W. Golde
Myelodysplasia
N. Engl. J. Med., May 27, 1999; 340(21): 1649 - 1660.
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