Clinica Ematologica e Centro Trapianti e Terapie Cellulari C. Melzi, Azienda Ospedaliero-Universitaria di Udine, Dipartimento di Ricerche Mediche e Morfologiche, Università di Udine, Udine, Italy.
Leuk Res. 2010 Jul;34(7):942-5. doi: 10.1016/j.leukres.2010.01.008. Epub 2010 Jan 31.
Over-expression of multidrug resistance (MDR) proteins PGP and BCRP has a negative prognostic impact in acute myeloid leukemia (AML) patients. Inclusion of fludarabine in induction chemotherapy increases remission rate in PGP over-expressing cases. We investigated the role of BCRP in 138 adult AML patients receiving induction therapy with fludarabine. None of the MDR-related proteins influenced complete remission attainment. Conversely, high levels of BCRP significantly affected disease-free survival, as higher relapse rates (48.5% vs 28.5%) and earlier relapse occurred in BCRP+ patients. Also overall survival was affected by BCRP positivity, and survival significantly worsened in case of concomitant PGP and BCRP over-expression.
多药耐药(MDR)蛋白 PGP 和 BCRP 的过度表达对急性髓细胞白血病(AML)患者的预后有负面影响。在诱导化疗中加入氟达拉滨可提高 PGP 过表达病例的缓解率。我们研究了 BCRP 在 138 例接受氟达拉滨诱导治疗的成人 AML 患者中的作用。没有一种 MDR 相关蛋白影响完全缓解的获得。相反,BCRP 的高水平显著影响无病生存,BCRP+患者的复发率更高(48.5%比 28.5%),且更早复发。BCRP 阳性也影响总生存,同时过表达 PGP 和 BCRP 时生存显著恶化。