TP53 Mutation and Survival in Chronic Lymphocytic Leukemia

Author:

Zenz Thorsten1,Eichhorst Barbara1,Busch Raymonde1,Denzel Tina1,Häbe Sonja1,Winkler Dirk1,Bühler Andreas1,Edelmann Jennifer1,Bergmann Manuela1,Hopfinger Georg1,Hensel Manfred1,Hallek Michael1,Döhner Hartmut1,Stilgenbauer Stephan1

Affiliation:

1. From the University of Ulm, Ulm; University of Cologne, Cologne; Technical University of Munich; Ludwig-Maximilians-University, Munich; University of Heidelberg, Heidelberg, Germany; and Hanusch Hospital, Vienna, Austria.

Abstract

Purpose The precise prognostic impact of TP53 mutation and its incorporation into treatment algorithms in chronic lymphocytic leukemia (CLL) is unclear. We set out to define the impact of TP53 mutations in CLL. Patients and Methods We assessed TP53 mutations by denaturing high-performance liquid chromatography (exons 2 to 11) in a randomized prospective trial (n = 375) with a follow-up of 52.8 months (German CLL Study Group CLL4 trial; fludarabine [F] v F + cyclophosphamide [FC]). Results We found TP53 mutations in 8.5% of patients (28 of 328 patients). None of the patients with TP53 mutation showed a complete response. In patients with TP53 mutation, compared with patients without TP53 mutation, median progression-free survival (PFS; 23.3 v 62.2 months, respectively) and overall survival (OS; 29.2 v 84.6 months, respectively) were significantly decreased (both P < .001). TP53 mutations in the absence of 17p deletions were found in 4.5% of patients. PFS and OS for patients with 17p deletion and patients with TP53 mutation in the absence of 17p deletion were similar. Multivariate analysis identified TP53 mutation as the strongest prognostic marker regarding PFS (hazard ratio [HR] = 3.8; P < .001) and OS (HR = 7.2; P < .001). Other independent predictors of OS were IGHV mutation status (HR = 1.9), 11q deletion (HR = 1.9), 17p deletion (HR = 2.3), and FC treatment arm (HR = 0.6). Conclusion CLL with TP53 mutation carries a poor prognosis regardless of the presence of 17p deletion when treated with F-based chemotherapy. Thus, TP53 mutation analysis should be incorporated into the evaluation of patients with CLL before treatment initiation. Patients with TP53 mutation should be considered for alternative treatment approaches.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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