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122 Chapter 3: CML<br />

Table 8. Survival of CML after BMT <strong>and</strong> IFN<br />

Proportion surviving<br />

3 years 5 years 10 years<br />

BMT (early) 66-75% 50-75% 50-65%<br />

IFN<br />

Low-risk 95% 75% 45%<br />

Intermediate- <strong>and</strong> high-risk 80% 50% 20%<br />

Data from Hansen et al. 52<br />

; Tura et al. 6<br />

; Appelhaum et al. 53<br />

; van Rhee et al. 54<br />

; German<br />

CML Study Group. 950<br />

expected that the survival curves of IFN-treated <strong>and</strong> transplanted patients will cross<br />

soon. The observation period is still too short for a risk-stratified analysis.<br />

DISCUSSION<br />

In summary, a considerable advance has been made with survival in CML after<br />

both BMT <strong>and</strong> drug treatment. Table 8 gives an overview of the survival rates after<br />

3, 5, <strong>and</strong> 10 years based on published reports. 6<br />

' 9,31,32<br />

The perspectives for the future<br />

include new experimental strategies such as high-dose chemotherapy <strong>and</strong><br />

autografting with early stem cell harvest as outlined above, evaluation of new active<br />

drugs, <strong>and</strong> the optimization of allogeneic BMT procedures. The German CML<br />

Studies III <strong>and</strong> III A are expected to provide contributions to some of these<br />

perspectives. Outcome of CML Study III A will depend on the feasibility of the study<br />

protocol in hematologic practice, on sufficient numbers of recruited <strong>and</strong> autotransplanted<br />

patients within a reasonable time period, <strong>and</strong> on availability <strong>and</strong> success of<br />

alternative treatment approaches. If recruitment proceeds as planned, the required<br />

patient number would be reached in 2003, <strong>and</strong> initial results based on surrogate<br />

markers (hematologic <strong>and</strong> cytogenetic responses) could be available in 2004.<br />

REFERENCES<br />

1. Hehlmann R, Heimpel H, Hasford J, Kolb HJ, Pralle H, Hossfeld DK, Queisser W, Löffler<br />

H, Heinze B, Georgii A, von Wussow P, Bartram C, Griesshammer M, Bergmann L,<br />

Essers U, Falge C, Hochhaus A, Queisser U, Sick C, Meyer P, Schmitz N, Verpoort K,<br />

Eimermacher H, Walther F, Westerhausen M, Kleeberg UR, Heilein A, Käbisch A, Barz<br />

C, Zimmermann R, Meuret G, Tichelli A, Berdel WE, Kanz L, Anger B, Tigges FJ,<br />

Schmid L, Brockhaus W, Zankovich R, Schläfer U, Weissenfeis I, Mainzer K, Tobler A,<br />

Perker M, Hohnloser J, Messerer D, Thiele J, Buhr T, Ansari H, <strong>and</strong> the German CML<br />

Study Group: R<strong>and</strong>omized comparison of busulfan <strong>and</strong> hydroxyurea in chronic myel­<br />

ogenous leukemia: Prolongation of survival by hydroxyurea. Blood 82:398^107, 1993.

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