1999
DOI: 10.1002/(sici)1097-0142(19990201)85:3<608::aid-cncr11>3.0.co;2-5
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Extramedullary tumors of myeloid blasts in adults as a pattern of relapse following allogeneic bone marrow transplantation

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Cited by 80 publications
(72 citation statements)
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“…1 However, other studies have reported an incidence of up to 20% among long-term survivors. [1][2][3][4][5][6] There are no established guidelines for clinical decision making pertaining to the treatment of extramedullary relapse after HSCT. 7 Common practice entails a combination of localized radiation, systemic chemotherapy, immunotherapy with donor lymphocyte infusions (DLI), and repeated transplantation if possible.…”
mentioning
confidence: 99%
“…1 However, other studies have reported an incidence of up to 20% among long-term survivors. [1][2][3][4][5][6] There are no established guidelines for clinical decision making pertaining to the treatment of extramedullary relapse after HSCT. 7 Common practice entails a combination of localized radiation, systemic chemotherapy, immunotherapy with donor lymphocyte infusions (DLI), and repeated transplantation if possible.…”
mentioning
confidence: 99%
“…2 Among long-term survivors the incidence has been reported to be over 20%. [2][3][4][5][6][7] Recently, Shimoni et al reported on 356 consecutive patients with acute myeloblastic leukemia/myelodysplastic syndrome (n=277) and acute lymphoblastic leukemia (n=79). 8 Incidence of extramedullary relapse among the acute myeloblastic leukemia/myelodysplastic syndrome cohort was 8% with a median follow-up of 30 months.…”
mentioning
confidence: 99%
“…The prognosis is poor, but prolonged survival has been observed in some of these patients, with 13 out of 52 evaluable patients alive having a median survival time of 49 months (range, 11-121). The most effective treatment appeared to be a combined modality of HDCHT and RT, as 7 (54%) out of 13 living patients have been treated with this combined modality [4][5][6][7][8][9][10][11][12][13][14][15][16][17][18][19]. The patient in this report showed two factors associated to IEMR, namely, M4 FAB phenotype and intermediate cytogenetic risk group, including aberration of chromosome 8.…”
Section: Resultsmentioning
confidence: 95%