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autologous blood and marrow transplantation - Blog Science ...

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Autografring for Chronic Myeloid Leukemia<br />

in Chronic Phase:<br />

EBMT Retrospective Analysis <strong>and</strong> Proposals<br />

for a Prospective Study<br />

J.M. Goldman, J. Reiffers, J.E Apperley, AM. Carella<br />

ICSM Haematology Department, Hammersmith Hospital, London, U.K.;<br />

Université Victor Segalen, Bordeaux, France; <strong>and</strong><br />

Ospedale San Martino, Genoa, Italy<br />

In the late 1970s, selected patients with CML in transformation were treated by<br />

high-dose chemotherapy <strong>and</strong> autografted with <strong>marrow</strong> <strong>and</strong> later with <strong>blood</strong>-derived<br />

stem cells. The majority of patients were restored to chronic phase hematopoiesis,<br />

but there was no convincing evidence that their survival was prolonged. In the early<br />

1980s, various groups performed autografts for patients in chronic phase using<br />

unmanipulated <strong>marrow</strong> or <strong>blood</strong> stem cells. The collected data for EBMT collaborating<br />

centers has been analyzed on a number of occasions. The toxicity of the<br />

procedure was low. Patients who achieved some degree of Ph-negativity survived<br />

longer than those who recovered exclusively Ph-positive hematopoiesis. Some<br />

patients achieved durable Ph-negativity. Again, there was no formal proof that<br />

survival was prolonged in comparison with conventional treatment with cytotoxic<br />

drugs or interferon-alpha. Against this background, the EBMT has designed <strong>and</strong><br />

activated a prospective study whereby patients at diagnosis will be r<strong>and</strong>omly<br />

allocated to receive either treatment with interferon-alpha (± cytarabine) or an<br />

autograft with stem cells collected at diagnosis or after mobilization with cytotoxic<br />

drugs <strong>and</strong> G-CSF. This study addresses the issue of whether the addition of an<br />

autograft procedure early after diagnosis contributes to prolongation of survival for<br />

patients not eligible for an allograft procedure.<br />

Ill

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