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Approximately 20% of children treated with the MACOP-B combination for osteosarcoma will develop acute myeloid leukaemia-like blast proliferation on follow-up. We have developed a system based on image analysis to enable identification of these rare residual leukaemic foci from conventional haematological surface. This new method was used on a first series of 12 bone marrows treated with MACOP-B (methotrexate, cyclophosphamide, doxorubicin and bleomycin) in the context of a retrospective study, with the aim of identifying which patients were likely to develop myeloid leukaemia. We assessed the feasibility of the methodology, reproducibility and repeatability of the analysis, its capacity to define residual bone marrow and prognostic value. The method was shown to be reproducible and repeatable by a second independent observer, with the advantage of identifying discrete areas of haematological enhancement, measuring the amount of residual bone marrow and assessing the presence of bone marrow clumping. The area under the curve of a receiver operating characteristic curve showed that the probability of residual leukaemia was 55% at 2 months, 73% at 3 months, and 84% at 4 months. The sensitivity, specificity and positive predictive value of the method were 89, 83 and 61%, respectively. In conclusion, the area under the curve was high and, as a repeatable method, this methodology has the potential to be used in the follow-up of childhood sarcoma patients treated with MACOP-
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