Zaucha J M, Wyrowinska E, Prejzner W, Calbecka M, Hellmann A
Department of Haematology, Medical University of Gdansk, Gdansk, Poland.
Clin Lab Haematol. 2006 Jun;28(3):208-10. doi: 10.1111/j.1365-2257.2006.00772.x.
Imatinib mesylate is a very effective treatment in patients with Philadelphia (Ph)-positive chronic myeloid leukaemia (CML). However, in patients with advanced phase CML, it is still unclear whether, in the presence of myelosuppression, therapy with imatinib should be continued. It has been reported that intermittent filgrastim treatment may overcome imatinib-associated neutropenia and allow improved delivery of imatinib. Such combined sequential treatment is theoretically attractive as it may lead to better disease response. Here, we report a patient with blastic phase CML who developed severe and prolonged myelosuppression during imatinib treatment. Despite cessation of imatinib and 2 months of filgrastim therapy neither recurrence of Ph-positive or Ph-negative cells occurred. We conclude that filgrastim treatment may not always reverse imatinib-associated neutropenia therefore the decision of continued imatinib therapy in patients with advanced CML should be taken with caution.
甲磺酸伊马替尼对费城(Ph)阳性慢性髓性白血病(CML)患者是一种非常有效的治疗方法。然而,对于晚期CML患者,在存在骨髓抑制的情况下,是否应继续使用伊马替尼治疗仍不清楚。据报道,间歇性使用非格司亭治疗可能克服伊马替尼相关的中性粒细胞减少症,并使伊马替尼的给药得以改善。这种联合序贯治疗在理论上具有吸引力,因为它可能导致更好的疾病反应。在此,我们报告1例CML急变期患者,在伊马替尼治疗期间出现严重且持续时间长的骨髓抑制。尽管停用了伊马替尼并进行了2个月的非格司亭治疗,但Ph阳性或Ph阴性细胞均未复发。我们得出结论,非格司亭治疗可能并不总是能逆转伊马替尼相关的中性粒细胞减少症,因此,对于晚期CML患者继续使用伊马替尼治疗的决定应谨慎做出。