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Testing for minimal residual disease in adults with acute lymphoblastic leukemia in Europe: a clinician survey

Authors :
Pau Montesinos
J McKendrick
Arnaud Pigneux
Heather Wieffer
Monika Brüggemann
Anja K. Pownell
Ze Cong
Xinke Zhang
Biothérapies des maladies génétiques et cancers
Université Bordeaux Segalen - Bordeaux 2-Institut National de la Santé et de la Recherche Médicale (INSERM)
Service d'Hématologie Clinique et Thérapie Cellulaire [CHU Bordeaux]
Université de Bordeaux (UB)-CHU Bordeaux [Bordeaux]
Hospital Universitari i Politècnic La Fe = University and Polytechnic Hospital La Fe
Instituto de Salud Carlos III [Madrid] (ISC)
Amgen Inc
PRMA Consulting [Hampshire, UK] (Linea House)
University of Technology Sydney (UTS)
Universitätsklinikum Schleswig-Holstein
Amgen Inc.
Bodescot, Myriam
Hospital Universitario La Fe, Valencia
Source :
BMC Cancer, BMC Cancer, BioMed Central, 2018, 18 (1), pp.1100. ⟨10.1186/s12885-018-5002-5⟩, BMC Cancer, Vol 18, Iss 1, Pp 1-8 (2018), Bmc Cancer, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe, instname
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

Background In acute lymphoblastic leukemia (ALL), the presence of minimal residual disease (MRD) after induction/consolidation chemotherapy is a strong prognostic factor for subsequent relapse and mortality. Accordingly, European clinical guidelines and protocols recommend testing patients who achieve a complete hematological remission (CR) for MRD for the purpose of risk stratification. The aim of this study was to provide quantitative information regarding real-world clinical practice for MRD testing in five European countries. Methods A web-based survey was conducted in March/April 2017 in France, Germany, Italy, Spain, and the UK. The survey was developed after consultation with specialist clinicians and a review of published literature. Eligible clinicians (20 per country; 23 in Spain) were board-certified in hemato-oncology or hematology, had at least five years’ experience in their current role after training, had treated at least two patients with B-cell precursor ALL in the 12 months before the survey or at least five patients in the last five years, and had experience of testing for MRD in clinical practice. Results MRD testing is now standard practice in the treatment of adult ALL across the five European countries, with common use of recent treatment protocols which specify testing. Respondents estimated that, among clinicians in their country who conduct MRD testing, 73% of patients in first CR (CR1) and 63% of patients in second or later CR (CR2+) are tested for MRD. The median time point reported as most commonly used for the first MRD test, to establish risk status and to determine a treatment plan was four weeks after the start of induction therapy. The timing and frequency of tests is similar across countries. An average of four or five post-CR1 tests per patient in the 12 months after the first MRD test were reported across countries. Conclusions This comprehensive study of MRD testing patterns shows consistent practice across France, Germany, Italy, Spain, and the UK with respect to the timing and frequency of MRD testing, aligning with use of national protocols. MRD testing is used in clinical practice also in patients who reach CR2 + . Electronic supplementary material The online version of this article (10.1186/s12885-018-5002-5) contains supplementary material, which is available to authorized users.

Details

Language :
English
ISSN :
14712407
Database :
OpenAIRE
Journal :
BMC Cancer, BMC Cancer, BioMed Central, 2018, 18 (1), pp.1100. ⟨10.1186/s12885-018-5002-5⟩, BMC Cancer, Vol 18, Iss 1, Pp 1-8 (2018), Bmc Cancer, r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe, instname
Accession number :
edsair.doi.dedup.....e03f846615828a350adb84177af8db1b