Santorsola Domenico, Abruzzese Elisabetta
Domenico Santorsola; MD, Servizio Dipartimentale di Ematologia ed Oncologia San Nicola Pellegrino Trani, Italy.
Elisabetta Abruzzese, MD, PhD, Hematology, S. Eugenio Hospital, Tor Vergata University, Rome, Italy.
Mediterr J Hematol Infect Dis. 2015 Feb 15;7(1):e2015020. doi: 10.4084/MJHID.2015.020. eCollection 2015.
We report a case of a young patient with chronic viral hepatitis HBV infection, diagnosed with CML in March 2006 and treated with imatinib 400mg/die as first line therapy with concomitant Lamivudine. Patient obtained a complete hematologic response (CHR) in 2 months, complete cytogenetic response (CCyR) in six months and major molecular response (MMR) at 24 months. After three years of treatment, she became imatinib intolerant and resistant. In November 2009 patient started nilotinib 400mg/BID. Patient tolerated well the new molecule never experiencing hepatic impairment. After switching to nilotinib, she reached in 12 months transcript reduction more than 3 log (MMR). Even if patient had been informed of the need of continuous therapy and to use effective methods of contraception during tyrosine kinase inhibitor (TKI) treatment, in 2012 she decided to plan a pregnancy. In August 2012 a MR4 was documented, and treatment discontinued before starting pregnancy. She was placed on interferon and observed throughout her pregnancy. The disease remained stable achieving an undetectable transcript level; she delivered a healthy boy in September 2013. Treatment with nilotinib was re-started three months after delivery, and she is still in molecular remission (MR5). A complete discussion of the case and the available literature is presented.
我们报告了一例年轻患者,该患者患有慢性乙型肝炎病毒(HBV)感染,于2006年3月被诊断为慢性粒细胞白血病(CML),并接受伊马替尼400mg/日作为一线治疗,同时服用拉米夫定。患者在2个月时获得完全血液学缓解(CHR),6个月时获得完全细胞遗传学缓解(CCyR),24个月时获得主要分子学缓解(MMR)。经过三年的治疗,她对伊马替尼不耐受且产生耐药。2009年11月,患者开始服用尼洛替尼400mg,每日两次。患者对新药物耐受性良好,从未出现肝损伤。换用尼洛替尼后,她在12个月内转录本降低超过3 log(MMR)。尽管患者已被告知在酪氨酸激酶抑制剂(TKI)治疗期间需要持续治疗并采用有效的避孕方法,但在2012年她决定计划怀孕。2012年8月记录到达到MR4,在开始怀孕前停止治疗。她在整个孕期接受干扰素治疗并接受观察。疾病保持稳定,转录本水平检测不到;她于2013年9月产下一名健康男婴。产后三个月重新开始使用尼洛替尼治疗,她目前仍处于分子学缓解状态(MR5)。本文对该病例及现有文献进行了全面讨论。