دورية أكاديمية

Molecular profiling refines minimal residual disease-based prognostic assessment in adults with Philadelphia chromosome-negative B-cell precursor acute lymphoblastic leukemia

التفاصيل البيبلوغرافية
العنوان: Molecular profiling refines minimal residual disease-based prognostic assessment in adults with Philadelphia chromosome-negative B-cell precursor acute lymphoblastic leukemia
المؤلفون: Ribera, Jordi, Zamora, Lurdes, Morgades, Mireia, Vives, Susana, Granada, Isabel, Montesinos, Pau, Gómez‐Seguí, Inés, Mercadal, Santiago, Guàrdia, Ramón, Nomdedéu, Josep F., Pratcorona, Marta, Tormo, Mar, Martínez‐Lopez, Joaquín, Hernández, Jesús M., Ciudad, Juana, Orfao, Alberto, González‐Campos, José, Barba, Pere, Escoda, Lourdes, Esteve, Jordi, Genescà, Eulàlia, Solé, Francesc, Feliu, Evarist, Ribera, Josep-Maria
المساهمون: Josep Carreras Leukemia Foundation, Generalitat de Catalunya, Instituto de Salud Carlos III, European Commission, Fundación "la Caixa", Sociedad Española de Hematología y Hemoterapia
بيانات النشر: Wiley-Liss
سنة النشر: 2019
المجموعة: Digital.CSIC (Consejo Superior de Investigaciones Científicas / Spanish National Research Council)
الوصف: Minimal residual disease (MRD) assessment is an essential tool in contemporary acute lymphoblastic leukemia (ALL) protocols, being used for therapeutic decisions such as hematopoietic stem cell transplantation in high‐risk patients. However, a significant proportion of adult ALL patients with negative MRD still relapse suggesting that other factors (ie, molecular alterations) must be considered in order to identify those patients with high risk of disease progression. We have identified partial IKZF1 gene deletions and CDKN2A/B deletions as markers of disease recurrence and poor survival in a series of uniformly treated adolescent and adult Philadelphia chromosome‐negative B‐cell progenitor ALL patients treated according to the Programa Español de Tratamientos en Hematología protocols. Importantly, CDKN2A/B deletions showed independent significance of MRD at the end of induction, which points out the need for treatment intensification in these patients despite being MRD‐negative after induction therapy. ; Fundació Internacional Josep Carreras; Generalitat de Catalunya, Grant/Award Number: 2017 SGR 288 GRC; Instituto de Salud Carlos III; Ministerio de Salud Carlos III RTICC‐FEDER, Grant/Award Numbers: RD12/0036/0029, RD/0036/044; Obra Social “La Caixa”; Sociedad Española de Hematología y Hemoterapia; Fondo de Investigaciones Sanitarias, Grant/Award Numbers: PI14/01971, PI10/01417
نوع الوثيقة: article in journal/newspaper
اللغة: unknown
تدمد: 1045-2257
1098-2264
العلاقة: http://dx.doi.org/10.1002/gcc.22788Test; Sí; Genes Chromosomes and Cancer 58(11): 815-819 (2019); http://hdl.handle.net/10261/203599Test; http://dx.doi.org/10.13039/501100002809Test; http://dx.doi.org/10.13039/501100000780Test; http://dx.doi.org/10.13039/501100008782Test; http://dx.doi.org/10.13039/501100004587Test; http://dx.doi.org/10.13039/501100005677Test
DOI: 10.1002/gcc.22788
DOI: 10.13039/501100002809
DOI: 10.13039/501100000780
DOI: 10.13039/501100008782
DOI: 10.13039/501100004587
DOI: 10.13039/501100005677
الإتاحة: https://doi.org/10.1002/gcc.22788Test
https://doi.org/10.13039/501100002809Test
https://doi.org/10.13039/501100000780Test
https://doi.org/10.13039/501100008782Test
https://doi.org/10.13039/501100004587Test
https://doi.org/10.13039/501100005677Test
http://hdl.handle.net/10261/203599Test
حقوق: none
رقم الانضمام: edsbas.22D0733D
قاعدة البيانات: BASE
الوصف
تدمد:10452257
10982264
DOI:10.1002/gcc.22788