Factors Affecting Early Molecular Response in Chronic Myeloid Leukemia

被引:11
|
作者
Chikkodi, Santosh V. [1 ]
Malhotra, Pankaj [1 ]
Naseem, Shano [1 ]
Khadwal, Alka [1 ]
Prakash, Gaurav [1 ]
Sahu, Kamal Kant [1 ]
Kumari, Savita [1 ]
Suri, Vikas [1 ]
Varma, Neelam [1 ]
Varma, Subhash [1 ]
机构
[1] Postgrad Inst Med Educ & Res, Chandigarh 160012, India
来源
关键词
Complete hematologic response; Developing country; Generic imatinib mesylate; Glivec; Molecular response; BCR-ABL1 TRANSCRIPT LEVELS; CYTOGENETIC RESPONSE; BCR-ABL; IMATINIB; PREDICTS; CML;
D O I
10.1016/j.clml.2015.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In this research study, we looked at the factors affecting BCR ABL(IS) < 10% at 3rd and < 1% at 6 months in 131 newly diagnosed patients of CML chronic phase initiated on Imatinib mesylate therapy. We found patients having peripheral blasts 5 5% and serum LDH < 851 U/L, basophils < 7%, and achievement of complete hematologic response by 6 weeks (CHR velocity) were significantly more likely to achieve BCR ABL (IS) < 10% at 3 months. CHR was also associated with BCR ABL (IS) < 1% at 6 months. Objectives: There is controversy about whether 3- or 6-month molecular assessment predicts progression-free and overall survival in those with chronic myeloid leukemia (CML). The factors predicting molecular response at 3, 6, and 12 months have not been studied extensively. The study objective was to study the factors affecting molecular response at 3 and 6 months in patients with CML who are receiving imatinib mesylate. Methods: We prospectively enrolled patients with newly diagnosed CML who were receiving imatinib mesylate as the initial therapy for CML. The diagnosis of CML was based on clinical examination, bone marrow, and demonstration of BCR ABL(IS) transcripts by polymerase chain reaction. The molecular response's was assessed at 3, 6, and 12 months by GeneXpert (Cepheid, Sunnyvale, CA) and co-related with various baseline characteristics of patients. We also looked at whether early achievement of a complete hematologic response within 6 weeks predicts molecular response at 3 or 6 months. The study took place at a tertiary care hospital in Northwest India catering to patients belonging to low-middle socioeconomic status. Results: We enrolled 131 patients with CML in the chronic phase from July 1, 2013, to August 31, 2014. The median age of the patients was 40 years (range, 13-67) with a male preponderance (61 % were male). Most patients presented with symptoms of low-grade fever (52.7%) and abdominal fullness (26.7%). Spleen was palpable in 84.7% of patients. The median hemoglobin at presentation was 10.8 g/dL (range, 4.8-18.4 g/dL), white cell count was 138.3 x 10(9)/L (4.1-697 x 10(9)/L), and platelet count was 326 x 10(9)/L (85-1819 x 10(9)/L). The median number of peripheral blood basophils was 3% (range, 0%-20%), and blasts were 3% (range, 0%-10%). Myelofibrosis of more than grade 1 was present in 30% of patients. Most patients belonged to intermediate Sokal (45.8%) and Hasford (55%) scores and low EUropean Treatment Outcome Study (78.6%) score. Of 128 evaluable patients at 3 months, 96.9% achieved complete hematologic remission (CHR) and 82.3% achieved BCR ABL(IS) of less than 10%. None of the patients who had BCR ABL(IS) > 10% at 3 months achieved BCR ABL(IS) < 1% at 6 months or < 0.1 % at 12 months. Early achievement of CHR (< 6 weeks), peripheral blood blast count of < 5%, and lactate dehydrogenase < 851 U/L were significantly associated with achievement of BCR ABL(IS) < 10% at 3 months and BCR ABL(IS) < 1% at 6 months. Conclusions: We found that BCR ABL(IS) assessment at 3 months is superior to assessment at 6 months. Patients with CML in the chronic phase who achieve CHR within 6 weeks are more likely to achieve BCR ABL(IS) < 10% at 3 months and < 1% at 6 months than patients who achieve CHR between 7 and 12 weeks. (C) 2015 Elsevier Inc. All rights reserved.
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收藏
页码:S114 / S119
页数:6
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