Narang Neha Chopra, Rusia Usha, Sikka Meera, Kotru Mrinalini
Senior Resident, Department of Pathology, University College of Medical Sciences & Guru Teg Bahadur Hospital, Dilshad Garden, Shahadra, Delhi, India.
Professor, Department of Pathology, University College of Medical Sciences & Guru Teg Bahadur Hospital, Dilshad Garden, Shahadra, Delhi, India.
J Clin Diagn Res. 2017 Apr;11(4):EC25-EC29. doi: 10.7860/JCDR/2017/25173.9650. Epub 2017 Apr 1.
Imatinib mesylate is used extensively for first line treatment of Chronic Myeloid Leukemia (CML). However, not many studies have documented morphological changes in bone marrow biopsies produced during Imatinib therapy with reference to myelofibrosis.
To document the morphological changes produced in the bone marrow during Imatinib therapy.
This longitudinal study followed up 75 Philadelphia Chromosome Positive Chronic Myeloid Leukemia with chronic phase(Ph+ CML- CP) patients sequentially, receiving 400-600mg Imatinib over a period of 12 or more months. Haematologic parameters were measured at admission, 2 weeks, 1 month, 3 months, 6 months and 12 or more months. Morphologic changes in bone marrow aspirate and biopsy were evaluated at admission, 6 months and ≥12 months of treatment in accordance with National Comprehensive Cancer Network(NCCN) guidelines.
Complete Haematologic Response (CHR) was seen in 47.1%, 80%, 85.4%, 90.4% at ≥1 month, 3 months, 6 months and 12 months respectively after therapy. It was noted that patients not showing CHR by 3 months were less likely to show CHR at 6 months and beyond. Bone marrow aspirates and biopsies showed reduction in cellularity and myeloid precursors with regeneration of erythroid precursors in 70-83% at ≥12 months. A significant decrease in myelofibrosis (p-value< 0.04) was noted as early as 6 months. Mild to moderate hypoplasia was noted in 31.8% of biopsies within 6 months. Pseudo gaucher cells and benign lymphoid nodules were also seen.
Sequential analysis showed that Imatinib reduced the grade of myelofibrosis significantly (p-value< 0.04). It also prevented development of myelofibrosis in patients who did not have it at presentation. Hence Imatinib is effective when used early in the course of CML-CP.
甲磺酸伊马替尼被广泛用于慢性髓性白血病(CML)的一线治疗。然而,关于伊马替尼治疗期间骨髓活检中与骨髓纤维化相关的形态学变化,相关研究并不多。
记录伊马替尼治疗期间骨髓产生的形态学变化。
这项纵向研究对75例慢性期费城染色体阳性慢性髓性白血病(Ph+CML-CP)患者进行了连续随访,这些患者在12个月或更长时间内接受400-600mg伊马替尼治疗。在入院时、2周、1个月、3个月、6个月以及12个月或更长时间测量血液学参数。根据美国国立综合癌症网络(NCCN)指南,在入院时、治疗6个月和≥12个月时评估骨髓穿刺和活检的形态学变化。
治疗后≥1个月、3个月、6个月和12个月时,完全血液学缓解(CHR)率分别为47.1%、80%、85.4%、90.4%。值得注意的是,3个月时未显示CHR的患者在6个月及以后显示CHR的可能性较小。≥12个月时,70-83%的骨髓穿刺和活检显示细胞成分和髓系前体细胞减少,红系前体细胞再生。早在6个月时就注意到骨髓纤维化显著降低(p值<0.04)。6个月内31.8%的活检显示轻度至中度发育不全。还可见假戈谢细胞和良性淋巴结节。
序贯分析表明,伊马替尼显著降低了骨髓纤维化程度(p值<0.04)。它还预防了初诊时没有骨髓纤维化的患者发生骨髓纤维化。因此,伊马替尼在CML-CP病程早期使用时是有效的。