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Table 1. Outcome after relapse in MRC AML 10<br />

AutoBMT NoBMT<br />

Burnett 13<br />

% in CR2 % Survival at 2 years<br />

(n) (n) AutoBMT NoBMT AutoBMT NoBMT<br />

All 60 101 34 59 15 18<br />

Risk group<br />

Good 12 20 67 90 38 38<br />

St<strong>and</strong>ard 35 59 31 54 12 9<br />

Poor 11 11 10 45 0 15<br />

Unknown 6 11 33 45 17 9<br />

Age group (years)<br />

0-14 15 26 27 65 18 35<br />

15-34 18 25 56 48 7 16<br />

>35 31 50 26 62 17 12<br />

From Burnett et al. 9<br />

to be sure they are cured, it does seem a reasonably secure strategy to delay transplant<br />

in these groups. The trial data demonstrate that 40% will become long-term survivors<br />

with chemotherapy only, <strong>and</strong> about a third of those who relapse can be rescued.<br />

These data preceded the introduction of all frans-retinoic acid for patients with<br />

acute promyelocytic leukemia. This development improves the prospect of cure<br />

without <strong>transplantation</strong> <strong>and</strong> further endorses the strategy of delaying transplant in<br />

this subgroup (Burnett AK, Grimwade D, Solomon E, Wheatley K, Goldstone AH,<br />

manuscript submitted). 13,14<br />

For patients in other risk groups, e.g., poor- or st<strong>and</strong>ard-risk or patients >15 years<br />

old, the prospects of salvage after relapse are much less reliable (Table 1). While there<br />

remains uncertainty about the best approach to consolidation, it is probably unwise to<br />

rely on rescuing patients who relapse. In contrast, it remains a priority to optimize firstline<br />

treatment. The relapse risk can be reduced in these patients by more treatment than<br />

the four intensive courses given in MRC AML 10, but it is important to harness this<br />

effect with minimal toxicity. In st<strong>and</strong>ard risk, or patients >35 years old, the mortality<br />

in the autograft patients was 16 <strong>and</strong> 18%, respectively, so there is an opportunity to<br />

reduce treatment-related risk <strong>and</strong> thereby harness the antileukemic effect of autograft.<br />

While the MRC trial provides important evidence that more is better, it remains to be<br />

tested whether this is best achieved with a transplant or further chemotherapy. This is<br />

the central question on the ongoing MRC12 trial.<br />

REFERENCES<br />

1. Mayer RJ, Davis RB, Schiffer CA, Berg DT, Powell BL, Schulman P, Omura GA, Moore<br />

JO, Mcintyre OR, Frei E: Intensive postremission chemotherapy in adults with acute<br />

myeloid leukemia. N Engl J Med 331:896-942, 1994.

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