AI Article Synopsis

  • Isolated myeloid sarcoma (MS) is a rare form of acute myeloid leukemia (AML) that occurs outside the bone marrow, and its outcomes are not well understood due to its rarity.
  • A study analyzed data from the SEER database, identifying 345 patients diagnosed with isolated MS between 1973 and 2010 to compare survival rates between MS and non-MS AML patients.
  • Results showed that the 3-year survival rate for MS was 31.9%, significantly higher than the 17.2% for non-MS AML, with survival rates varying based on the disease's primary site, with certain locations showing better outcomes than others.

Article Abstract

Isolated myeloid sarcoma (MS) is a rare extramedullary presentation of acute myeloid leukemia (AML). Little is known about MS outcomes due to its rarity. A population-based analysis of MS using the Survival, Epidemiology, and End Results (SEER) database was performed. We identified 345 patients, aged 15 or older, diagnosed with isolated MS between 1973 and 2010. Overall survival (OS) was calculated and compared between MS and non-MS AML using the log-rank test. Survival was also evaluated based upon the primary site of disease presentation. The 3-year survival rate for MS (0.319; 95% confidence interval [CI]: 0.267-0.371) was greater than for non-MS AML (0.172; 95% CI: 0.168-0.175). There was variation in survival based on the site of involvement. The survival rates for isolated MS involving the pelvis/genitourinary organs, eyes/gonads and gastrointestinal mucosa appeared to be slightly improved when compared to primary sites of soft tissues, lymphatic/hematopoietic tissues or nervous system.

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http://dx.doi.org/10.3109/10428194.2014.963080DOI Listing

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