H. Link et al., 10 YEARS TRANSPLANTATION OF BONE-MARROW A ND OF HEMATOPOIETIC STEM-CELLS AT THE MEDICAL-SCHOOL HANOVER, Medizinische Klinik, 91, 1996, pp. 3-17
Patients and methods: From January 1986 until August 1995 230 adult pa
tients received an allogeneic or autologous transplantation of bone ma
rrow or hematopoietic blood stem cells. The conditioning and myeloabla
tive treatment regimens were chosen according to the underlying diseas
e and type: of transplant. Results: The observation period comprises 1
to 115 months after transplantation. After allogeneic transplantation
from HLA-identical family donors, the probabilities of disease-free s
urvival were for acute myeloid leukemia in first complete remission (C
R) (n = 35) 77%, for acute lymphoid leukemia in Ise CR (n = 7) 72% and
in 2nd CR (n = 10) 40%, in first chronic phase of chronic myeloid leu
kemia (n = 34) 50% and in severe aplastic anemia (n = 7) 100%. Followi
ng myeloablative therapy and autologous transplantation the probabilit
ies oi disease-free survival were 47% in relapsed Hodgkin's disease (n
= 22) and 42% for relapsed high-grade non-Hodgkin's lymphoma (n = 12)
. Eight of 10 patients with acute myeloid and 7 of 8 with acute lympho
id leukemia suffered a leukemic relapse after autologous bone marrow t
ransplantation. Three of 8 patients with relapsed testicular cancer su
rvived relapse-free. Treatment failures were due to more advanced acut
e graft versus host disease alter allogeneic transplantation and cause
d by relapse after autologous transplantation. Current protocols evalu
ate the allogeneic transplantation of enriched CD34(+) blood seem cell
s. In chronic myeloid leukemia the autologous transplantation of blood
stem cells after myeloablative therapy is being studied.