Kantarjian Hagop, Talpaz Moshe, O'Brien Susan, Giles Francis, Rios Mary Beth, White Kevin, Garcia-Manero Guillermo, Ferrajoli Alessandra, Verstovsek Srdan, Wierda William, Kornblau Steven, Cortes Jorge
Department of Leukemia, University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
Cancer. 2003 May 1;97(9):2225-8. doi: 10.1002/cncr.11381.
Obtaining a major (Philadelphia chromosome [Ph] of < 35%) or a complete cytogenetic response (Ph of 0%) has been associated with excellent long-term survival. Cytogenetic response may continue to improve with therapy. Because early allogeneic stem cell transplantation (SCT) may be associated with a better outcome, early parameters predicting for subsequent cytogenetic responses would optimize the treatment decision-making.
The current study was performed to analyze whether early cytogenetic responses may be predictive of later major or complete cytogenetic responses to imatinib mesylate therapy in patients with Ph-positive chronic myelogenous leukemia (CML).
Two hundred sixty-one patients with Ph-positive, chronic-phase CML after failure with interferon therapy who were treated with imatinib mesylate therapy were analyzed. A persistence of 100% Ph-positive cells after > or = 6 months of imatinib mesylate therapy was associated with a major cytogenetic response rate of 9-13% and a complete cytogenetic response rate of 0-4%. However, a minor cytogenetic response after 3-12 months of therapy still was associated with high rates of major (68-83%) or complete (35-54%) cytogenetic response rates.
Patients with Ph-positive, chronic-phase CML who have persistent 100% Ph-positive disease after > or = 6 months of imatinib mesylate therapy may be offered allogeneic SCT or considered for alternative investigational therapies.
获得主要细胞遗传学反应(费城染色体[Ph]<35%)或完全细胞遗传学反应(Ph为0%)与长期生存率高相关。细胞遗传学反应可能会随着治疗持续改善。由于早期异基因干细胞移植(SCT)可能与更好的结果相关,预测后续细胞遗传学反应的早期参数将优化治疗决策。
进行本研究以分析早期细胞遗传学反应是否可预测甲磺酸伊马替尼治疗的Ph阳性慢性髓性白血病(CML)患者随后的主要或完全细胞遗传学反应。
分析了261例接受干扰素治疗失败后接受甲磺酸伊马替尼治疗的Ph阳性慢性期CML患者。甲磺酸伊马替尼治疗≥6个月后100%Ph阳性细胞持续存在与9% - 13%的主要细胞遗传学反应率和0% - 4%的完全细胞遗传学反应率相关。然而,治疗3 - 12个月后的微小细胞遗传学反应仍与高比例的主要(68% - 83%)或完全(35% - 54%)细胞遗传学反应率相关。
甲磺酸伊马替尼治疗≥6个月后Ph阳性慢性期CML患者仍存在持续100%Ph阳性疾病,可考虑进行异基因SCT或考虑替代研究性治疗。