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Major Route Additional Chromosomal Aberrations (ACA) Precede Increase of Blasts in CML: An Analysis of the German CML-Studies III and IIIA
Journal article

Major Route Additional Chromosomal Aberrations (ACA) Precede Increase of Blasts in CML: An Analysis of the German CML-Studies III and IIIA

  • Dietz, Christian T. III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Fabarius, Alice Charlotte III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Lauseker, Michael Institut für medizinische Informationsverarbeitung, Biometrie und Epidemiologie, Ludwig-Maximilians-Universität, München, Germany
  • Saussele, Susanne III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Kalmanti, Lida III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Rinaldetti, Sébastien III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Haferlach, Claudia MLL Münchner Leukämielabor, München, Germany
  • Schlegelberger, Brigitte Institut für Humangenetik, Medizinische Hochschule, Hannover, Germany
  • Jotterand, Martine Service de génétique médicale, Centre Hospitalier Universitaire Vaudois (CHUV),, Lausanne, Switzerland
  • Gratwohl, Alois Behandlungszentrum Stammzelltransplantation, Universitätsspital, Basel, Switzerland
  • Zander, Axel R. Interdisziplinäre Klinik und Poliklinik für Stammzelltransplantation, Universitätsklinikum Eppendorf, Hamburg, Germany
  • Kröger, Nicolaus Interdisziplinäre Klinik und Poliklinik für Stammzelltransplantation, Universitätsklinikum Eppendorf, Hamburg, Germany
  • Beelen, Dietrich W. Klinik für Knochenmarktransplantation, Universitästsklinikum, Essen, Germany
  • Novotny, Jürgen Klinik für Hämatologie, Universitätsklinikum, Essen, Germany
  • Nerl, Christoph Klinik für Hämatologie, Onkologie, Immunologie, Palliativmedizin, Infektiologie und Tropenmedizin, Klinikum Schwabing, München, Germany
  • Scheid, Christof Klinik I für Innere Medizin, Universitätsklinikum, Köln, Germany
  • Spiekermann, Karsten Medizinische Klinik und Poliklinik III, Klinikum der Ludwig-Maximilians-Universität, München, Germany
  • Mayer, Jiri Interní hematologická a onkologická klinika, Masarykova univerzita, Brno, Czech Republic
  • Sayer, Herbert G. Klinik für Innere Medizin II, Universitätsklinikum, Jena, Germany
  • Falge, Christiane Medizinische Klinik 5, Klinikum Nürnberg-Nord, Nürnberg, Germany
  • Bunjes, Donald Department of Internal Medicine III, University of Ulm, Ulm, Germany
  • Döhner, Hartmut Klinik für Innere Medizin III, Universitätsklinikum, Ulm, Germany
  • Ganser, Arnold Klinik für Hämatologie, Hämostaseologie, Onkologie und Stammzelltransplantation, Medizinische Hochschule, Hannover, Germany
  • Brossart, Peter Medizinische Klinik III für Hämatologie und Onkologie, Universitätsklinikum, Bonn, Germany
  • Schwerdtfeger, Rainer KMT-Zentrum, Deutsche Klinik für Diagnostik, Wiesbaden, Germany
  • Baumann, Herrad KMT-Zentrum, Deutsche Klinik für Diagnostik, Wiesbaden, Germany
  • Kuse, Rolf Abteilung für Hämatologie und Stammzelltransplantation, Asklepios Klinik St. Georg, Hamburg, Germany
  • Lindemann, Hans Walter Klinik für Hämatologie und Onkologie, St.-Marien-Hospital, Hagen, Germany
  • Bormann, Matthias I. Medizinische Klinik, Klinikum Bremen-Mitte, Bremen, Germany
  • Hertenstein, Bernd I. Medizinische Klinik, Klinikum Bremen-Mitte, Bremen, Germany
  • Baerlocher, Gabriela M. Universitätsklinik für Hämatologie und hämatologisches Zentrallabor, Inselspital, Bern, Switzerland
  • Aul, Carlo Klinik für Onkologie und Hämatologie, HELIOS St. Johannes Klinik, Duisburg, Germany
  • Staib, Peter Klinik für Hämatologie und Onkologie, St. Antonius Hospital, Eschweiler, Germany
  • Edinger, Matthias Abteilung Hämatologie und Internistische Onkologie, Universitätsklinikum, Regensburg, Germany
  • Schatz, Michael II. Medizinische Klinik, St. Vincentius Kliniken, Karlsruhe, Germany
  • Fauser, Axel A Klinik für Knochenmarktransplantation und Hämatologie/Onkologie, Idar-Oberstein, Germany
  • Arnold, Renate Medizinische Klinik mit Schwerpunkt Hämatologie, Onkologie und Tumorimmunologie, Campus Virchow-Klinikum, Charité - Universitätsmedizin, Berlin, Germany
  • Hossfeld, Dieter K. II. Medizinische Klinik, Universitätsklinikum Eppendorf, Hamburg, Germany
  • Kolb, Hans-Jochem Medizinische Klinik und Poliklinik III, Klinikum der Ludwig-Maximilians-Universität, München, Germany
  • Schnittger, Susanne MLL Münchner Leukämielabor, München, Germany
  • Müller, Martin C. III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Reiter, Andreas III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
  • Hochhaus, Andreas Universitätsklinikum Jena, Jena, Germany
  • Pfirrmann, Markus Institut für medizinische Informationsverarbeitung, Biometrie und Epidemiologie, Ludwig-Maximilians-Universität, München, Germany
  • Hasford, Joerg Institut für medizinische Informationsverarbeitung, Biometrie und Epidemiologie, Ludwig-Maximilians-Universität, München, Germany
  • Baccarani, Michele Istituto di Ematologia, Universita di, Bologna, Italy
  • Hehlmann, Ruediger III. Medizinische Klinik, Medizinische Fakultät Mannheim der Uni Heidelberg, Mannheim, Germany
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Published in:
  • Blood. - American Society of Hematology. - 2015, vol. 126, no. 23, p. 1581-1581
Immunology
Cell Biology
Biochemistry
Hematology
English Abstract

During the course of chronic myeloid leukemia (CML) progression to blast crisis (BC) is thought to be caused by genetic instability such as cytogenetic aberrations in addition to the translocation t(9;22)(q34;q11). We have shown previously that major route ACA indicate an unfavorable outcome (Fabarius et al., Blood 2011). We now investigate whether there is a correlation in time between appearance of major route ACA and increase in blast count.
Methods: Cytogenetic data and blast count in the peripheral blood were available from 1,290 CML patients recruited to the German CML-studies III (621 patients) and IIIa (669 patients) from January 1995 to January 2004. Treatments were interferon-alpha-based or related allogeneic stem cell transplantation (HSCT). Presence of ACA and major route ACA was considered as a time-dependent covariate. Multivariate proportional hazards models were estimated taking Euro CML score, study III vs. IIIa and stem cell transplantability into account. Cumulative incidences of blast increases were calculated starting at the date of the first ACA or major route ACA, respectively, regarding death as a competing risk. Patients were censored at the date of HSCT with an unrelated donor.
Results: 1,287 patients were evaluable with median observation times of 13 and 12 years and a 10-year survival of 48% and 61% in CML studies III and IIIa, respectively. 258 patients progressed to BC with a cumulative 10-year incidence of 20%. 195 patients displayed ACA during the course of disease. 45 patients (15.7%) showed ACA already at diagnosis. 44 patients showed unbalanced minor route, 29 balanced minor route aberrations, 23 -Y. 109 patients showed major route aberrations including 10 with other prior ACA.
In a multivariate analysis on 1,257 patients, patients with ACA had a hazard ratio (HR) for a blast increase of between 2.0-2.2 (p<0.001) for blast increases to ≥1%, ≥5%, ≥10%, ≥15%, ≥ 20% and ≥30% compared with patients without ACA (Table). When the same model was performed for major route ACA only at any time during disease, HRs of 2.2-2.7 (p<0.001) were found. For ACA without major route ACA HRs were 1.6-2.1 (p<0.001). In the multivariate analyses of major route ACA vs. no major route ACA a blast increase of 1-5% after diagnosis of major route ACA seems already indicative of progression.
5 years after the diagnosis of any ACA the cumulative incidence for a blast increase was 30% (95%- confidence interval (CI): 23-38%), of a major route ACA 40% (95%- CI: 28-49%). The 6-year probability of death without blast increase was 10%. 14 additional patients received an unrelated transplant of which 6 died.
We conclude that ACA, particularly major route ACA, precede an increase of blasts. Major route ACA have to be considered as a prognostic indicator for disease progression at any time.
Table 1. Blast increase to HR (univariate): ACA vs. no ACA HR(multivariate)*: ACA vs. no ACA HR (univariate): major route ACA vs. no major route ACA HR (multivariate)*: major route ACA vs. no major route ACA ≥30% 2.409 2.139 2.646 2.203 ≥20% 2.413 2.144 2.656 2.211 ≥15% 2.415 2.161 2.868 2.426 ≥10% 2.416 2.160 2.799 2.357 ≥5% 2.286 2.047 2.719 2.278 ≥1% 2.209 1.999 3.171 2.684
*adjusted to Euro-Score, study (III vs. IIIa) and transplantability

Disclosures
Saussele: ARIAD: Honoraria; BMS: Honoraria, Other: Travel grant, Research Funding; Pfizer: Honoraria, Other: Travel grant; Novartis Pharma: Honoraria, Other: Travel grant, Research Funding. Haferlach:MLL Munich Leukemia Laboratory: Employment, Equity Ownership. Scheid:Janssen-Cilag: Honoraria, Membership on an entity's Board of Directors or advisory committees; Celgene: Honoraria, Membership on an entity's Board of Directors or advisory committees. Baerlocher:Geron Corporation: Research Funding; Novartis: Research Funding. Schnittger:MLL Munich Leukemia Laboratory: Employment, Equity Ownership. Müller:BMS: Consultancy, Honoraria, Research Funding; Ariad: Consultancy, Honoraria, Research Funding; Novartis: Consultancy, Honoraria, Research Funding. Hochhaus:ARIAD: Honoraria, Research Funding; Pfizer: Honoraria, Research Funding; Bristol-Myers Squibb: Honoraria, Research Funding; Novartis: Honoraria, Research Funding. Pfirrmann:BMS: Consultancy, Honoraria; Novartis Pharma: Consultancy, Honoraria. Baccarani:Bristol-Myers Squibb: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; NOVARTIS: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; ARIAD Pharmaceuticals, Inc.: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau; PFIZER: Honoraria, Membership on an entity's Board of Directors or advisory committees, Speakers Bureau. Hehlmann:BMS: Consultancy; Novartis Pharma: Research Funding.
Language
  • English
Open access status
bronze
Identifiers
Persistent URL
https://sonar.ch/global/documents/336
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