Your browser doesn't support javascript.
loading
TGF-α and IL-6 plasma levels selectively identify CML patients who fail to achieve an early molecular response or progress in the first year of therapy.
Nievergall, E; Reynolds, J; Kok, C H; Watkins, D B; Biondo, M; Busfield, S J; Vairo, G; Fuller, K; Erber, W N; Sadras, T; Grose, R; Yeung, D T; Lopez, A F; Hiwase, D K; Hughes, T P; White, D L.
Afiliação
  • Nievergall E; Cancer Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
  • Reynolds J; School of Medicine, University of Adelaide, Adelaide, SA, Australia.
  • Kok CH; Biostatistics Platform, Faculty of Medicine, Nursing and Health Sciences, Monash University, The Alfred Centre, Melbourne, VIC, Australia.
  • Watkins DB; Cancer Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
  • Biondo M; School of Medicine, University of Adelaide, Adelaide, SA, Australia.
  • Busfield SJ; Cancer Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
  • Vairo G; School of Medicine, University of Adelaide, Adelaide, SA, Australia.
  • Fuller K; CSL Limited, Parkville, VIC, Australia.
  • Erber WN; CSL Limited, Parkville, VIC, Australia.
  • Sadras T; CSL Limited, Parkville, VIC, Australia.
  • Grose R; School of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia.
  • Yeung DT; School of Pathology and Laboratory Medicine, The University of Western Australia, Perth, WA, Australia.
  • Lopez AF; Cancer Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
  • Hiwase DK; School of Medicine, University of Adelaide, Adelaide, SA, Australia.
  • Hughes TP; Cancer Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
  • White DL; School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Leukemia ; 30(6): 1263-72, 2016 06.
Article em En | MEDLINE | ID: mdl-26898188
ABSTRACT
Early molecular response (EMR, BCR-ABL1 (IS)⩽10% at 3 months) is a strong predictor of outcome in imatinib-treated chronic phase chronic myeloid leukemia (CP-CML) patients, but for patients who transform early, 3 months may be too late for effective therapeutic intervention. Here, we employed multiplex cytokine profiling of plasma samples to test newly diagnosed CP-CML patients who subsequently received imatinib treatment. A wide range of pro-inflammatory and angiogenesis-promoting cytokines, chemokines and growth factors were elevated in the plasma of CML patients compared with that of healthy donors. Most of these normalized after tyrosine kinase inhibitor treatment while others remained high in remission samples. Importantly, we identified TGF-α and IL-6 as novel biomarkers with high diagnostic plasma levels strongly predictive of subsequent failure to achieve EMR and deep molecular response, as well as transformation to blast crisis and event-free survival. Interestingly, high TGF-α alone can also delineate a poor response group raising the possibility of a pathogenic role. This suggests that the incorporation of these simple measurements to the diagnostic work-up of CP-CML patients may enable therapy intensity to be individualized early according to the cytokine-risk profile of the patient.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Indução de Remissão / Leucemia Mielogênica Crônica BCR-ABL Positiva / Fator de Crescimento Transformador alfa / Interleucina-6 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Indução de Remissão / Leucemia Mielogênica Crônica BCR-ABL Positiva / Fator de Crescimento Transformador alfa / Interleucina-6 Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article