Antineoplastics

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Reactions 427 - 14 Nov 1992 S Antineoplastics Myelodysplastic syndrome in children: 2 case reports Pancytopenia developed 19 months after the completion of 2 years’ antineoplastic therapy comprising chlormethine, vincristine, procarbazine and prednisone (MOPP), in a 4-year- old girl with medulloblastoma. In this child, myelodysplastic syndrome (MDS) was diagnosed based on a complete blood count and bone marrow examination. Acute myelomonocytic leukaemia developed 7 months later, and the child eventually died after a brief response to further antineoplastic therapy. A second girl, aged 8 years, was diagnosed with MDS 5 months after the completion of MOPP therapy for medulloblastoma. No treatment was given and she remained moderately pancytopenic 13 months after the completion of MOPP therapy Author comment: ‘The association between MOPP therapy and second malignancies in patients with Hodgkin’s Disease is well recognized. A similar association is not well recognized in children receiving MOPP chemotherapy for brain tumors ... Although we cannot conclude that MOPP therapy caused MDS in our two patients, it is most likely that MOPP played a major role in the pathogenesis of MDS.’ Hayani A, et al. Therapy-related myelodysplastic syndrome in children with medulloblastoma following MOPP chemotherapy. Journal of Neuro-Oncology 14: 57-62, Sep 1992 - 807002343 1 Reactions 14 Nov 1992 No. 427 0114-9954/10/0427-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved

Transcript of Antineoplastics

Page 1: Antineoplastics

Reactions 427 - 14 Nov 1992

SAntineoplastics

Myelodysplastic syndrome in children: 2 casereports

Pancytopenia developed 19 months after the completion of2 years’ antineoplastic therapy comprising chlormethine,vincristine, procarbazine and prednisone (MOPP), in a 4-year-old girl with medulloblastoma. In this child, myelodysplasticsyndrome (MDS) was diagnosed based on a complete bloodcount and bone marrow examination. Acute myelomonocyticleukaemia developed 7 months later, and the child eventuallydied after a brief response to further antineoplastic therapy. Asecond girl, aged 8 years, was diagnosed with MDS 5 monthsafter the completion of MOPP therapy for medulloblastoma.No treatment was given and she remained moderatelypancytopenic 13 months after the completion of MOPPtherapy Author comment: ‘The association between MOPPtherapy and second malignancies in patients with Hodgkin’sDisease is well recognized. A similar association is not wellrecognized in children receiving MOPP chemotherapy forbrain tumors ... Although we cannot conclude that MOPPtherapy caused MDS in our two patients, it is most likely thatMOPP played a major role in the pathogenesis of MDS.’Hayani A, et al. Therapy-related myelodysplastic syndrome in children withmedulloblastoma following MOPP chemotherapy. Journal of Neuro-Oncology 14:57-62, Sep 1992 - 807002343

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Reactions 14 Nov 1992 No. 4270114-9954/10/0427-0001/$14.95 Adis © 2010 Springer International Publishing AG. All rights reserved