Assiduous surveillance for genetic aberrations is necessary in patients on cytotoxic therapies to detect therapy-related myeloid neoplasms (t-MN). Current modalities include metaphase cytogenetics and FISH. Since t-MN may develop abruptly in cytogenetically normal patients, a discussion exploring additional methods such as SNP-array and targeted-deep-sequencing to detect subchromosomal abnormalities is needed.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4377252PMC
http://dx.doi.org/10.1002/ccr3.180DOI Listing

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