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autologous blood and marrow transplantation - Blog Science ...

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58 Chapter 2: ALL<br />

Table 1. Comparison of disease-free survival in alloBMT <strong>and</strong> chemotherapy for AML<br />

<strong>and</strong> ALL<br />

Allogeneic BMT<br />

CR1 (%) CR2 (early first relapse) (%) >CR2(%)<br />

AML 40-65 15-40 5-20<br />

ALL 40-65 2540 10-20<br />

Chemotherapy<br />

AML 20-40 0-5 0<br />

ALL 20-40 0-5 0<br />

Several studies have been reported on patients with ALL who are beyond first<br />

remission or in relapse. 23<br />

Over the past decade, several studies have reported on<br />

allogeneic bone <strong>marrow</strong> <strong>transplantation</strong> (alloBMT) in first remission, with the<br />

cumulative data suggesting a disease-free survival of 40-65% <strong>and</strong> a relapse rate of<br />

10-40%, mostly during the first 2 years. 14,5<br />

A retrospective study from the International Bone Marrow Transplant Registry<br />

(IBMTR) with selected published data of chemotherapy using matched patients<br />

showed no significant difference between allogeneic transplants for patients in first<br />

remission when compared with st<strong>and</strong>ard chemotherapy. Treatment-related<br />

mortality was significantly higher in patients undergoing allotransplant but was<br />

offset by a far greater relapse among those receiving chemotherapy. 6<br />

Prognostic factors that impact favorably on the outcome of allogeneic <strong>transplantation</strong><br />

in ALL are first complete remission, low tumor burden, absence of resistant<br />

disease, <strong>and</strong> the presence of mild (grade 1-2) posttransplant graft-vs.-host disease. 7<br />

The majority of patients do not have a suitable HLA-compatible donor. While<br />

recent reports on the use of allogeneic matched unrelated donors show promise,<br />

such a procedure cannot be justified for ALL in first remission except for those<br />

with the presence of the Philadelphia chromosome. For all other patients who do<br />

not have a histocompatible sibling, the only transplant alternative to be considered<br />

is <strong>autologous</strong> stem cell <strong>transplantation</strong>.<br />

Unlike AML, the st<strong>and</strong>ard postremission therapy for ALL includes protracted<br />

consolidation/maintenance chemotherapy for up to 2 years, <strong>and</strong> a single course of<br />

<strong>autologous</strong> stem cell <strong>transplantation</strong> early in the course of disease may significantly<br />

improve the quality of life of patients in first remission, even if the long-term<br />

outcome is not superior to st<strong>and</strong>ard therapy but is at least as good. Obviously, the<br />

ultimate aim would be to develop a stem cell regimen that would improve on<br />

st<strong>and</strong>ard therapy, but the consideration for stem cell transplant must take into<br />

account the difficult period that patients undergo during their protracted st<strong>and</strong>ard<br />

therapy with chemotherapy.<br />

In reviewing the data, rather surprisingly, a considerable number of <strong>autologous</strong><br />

transplants have been performed in ALL <strong>and</strong> there is no shortage of published

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