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Biomedical subjects

R P Geĭl

Publications and source records attributed to R P Geĭl.

3 recordsLinked to original sources

[Autotransplants in leukemia: current status and perspectives].

Autotransplants in leukemia are controversial; their rationale and results have been questioned. Here we consider several issues central to this debate: (1) Are there convincing data that more intensive therapy increases cures; (2) Are results post autotransplant a consequence of the transplant or do they reflect subject-selection and time-to-treatment (time censoring) biases; (3) Does leukemia relapse after autotransplant develops from persisting leukemia cells in the subject or the graft; (4) Do autotransplants using hemopoietic stem cells from different sources have distinct outcomes; (5) Are immune mediated anti-leukemia mechanisms likely to prevent relapse after autotransplants; and (6) Can comparably intensive therapy be given without an autotransplant.

Forecasting↗

[Stem cells, clonality and leukemia].

The data we review suggest newer concepts regarding the biology of leukemia. First, all leukemias may originate in a multipotent stem cells. Second, leukemia phenotype may reflect where the leukemia clone expands rather than the site of transformation. Third, preleukemia may always antedate leukemia. And finally, remission and cure may result from re-establishing preleukemia rather than eradicating leukemia cells of favoring their maturation. Also, leukemia and at least some cases of aplastic anemia may represent different ends of a spectrum of one disease.

Clone Cells↗

[Transplantation of the bone marrow after total body irradiation of the victims after the accident at the Chernobyl atomic power plant].

Bone marrow transplantation was carried out in 13 patients. Seven patients (the doses of the total gamma-radiation were from 6.6 to 11.9 Gy; 4 identical, 2 "haplo + I", 1 haploidentical to BMT) died from radiation-induced skin injuries (beta-burns) incompatible with further life, from intestinal and pulmonary lesions from days 17 to 25 after radiation (days +2-+9 after BMT). Four patients (the doses were from 4.4 to 10.2 Gy; 2 identical, 1 "haplo + I", 1 haploidentical to BMT) died from acute secondary disease (ASD) and herpes virus infections within 34 (+27) to 91 (+79) days. Two patients (the doses constituted 5.6 and 8.7 Gy; haploidentical to BMT) are alive. They demonstrated incomplete myelopoietic chimera (up to +32-+36 days), non-grave ASD (from day +13 to day +57), the onset of the own myelopoiesis on days 27-28 and its final recovery by the termination of the 3d-4th month following radiation.

Accidents↗