临床和实验医学杂志
臨床和實驗醫學雜誌
림상화실험의학잡지
JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE
2014年
15期
1232-1235
,共4页
沈晶%杨凌志%付丽%魏娜%黄达永%王昭
瀋晶%楊凌誌%付麗%魏娜%黃達永%王昭
침정%양릉지%부려%위나%황체영%왕소
慢性粒细胞白血病%伊马替尼%干扰素%羟基脲%生存率
慢性粒細胞白血病%伊馬替尼%榦擾素%羥基脲%生存率
만성립세포백혈병%이마체니%간우소%간기뇨%생존솔
Chronic myeloid leukemia%Imatinib%Interferon-alpha%Hydroxyurea%Survival rate
目的分析70例慢性粒细胞白血病( CML)的治疗现状。方法回顾分析1998年4月至2014年3月起病的70例患者的临床资料及治疗反应。结果全部为Ph染色体阳性CML,男女性各35例,中位年龄50岁。70例患者中,使用酪氨酸激酶抑制剂( TKI)伊马替尼、干扰素和羟基脲的患者分别占35.7%、35.7%和52.9%,接受异基因造血干细胞移植( allo-HSCT)的患者占11.4%。随访时间从4月至16年,中位随访27个月。TKI治疗组3年总生存(OS)率是85.7%,而羟基脲(和/或)干扰素组及异基因造血干细胞移植病人3年OS率分别是46.4%和75.0%,与TKI 治疗组比较的P值分别是0.04和0.19。结论 CML是一种骨髓增殖性疾病,随着TKI作为一线治疗用药的越来越广泛的临床应用,使得CML患者的治疗效果和生存质量均得到明显改善。
目的分析70例慢性粒細胞白血病( CML)的治療現狀。方法迴顧分析1998年4月至2014年3月起病的70例患者的臨床資料及治療反應。結果全部為Ph染色體暘性CML,男女性各35例,中位年齡50歲。70例患者中,使用酪氨痠激酶抑製劑( TKI)伊馬替尼、榦擾素和羥基脲的患者分彆佔35.7%、35.7%和52.9%,接受異基因造血榦細胞移植( allo-HSCT)的患者佔11.4%。隨訪時間從4月至16年,中位隨訪27箇月。TKI治療組3年總生存(OS)率是85.7%,而羥基脲(和/或)榦擾素組及異基因造血榦細胞移植病人3年OS率分彆是46.4%和75.0%,與TKI 治療組比較的P值分彆是0.04和0.19。結論 CML是一種骨髓增殖性疾病,隨著TKI作為一線治療用藥的越來越廣汎的臨床應用,使得CML患者的治療效果和生存質量均得到明顯改善。
목적분석70례만성립세포백혈병( CML)적치료현상。방법회고분석1998년4월지2014년3월기병적70례환자적림상자료급치료반응。결과전부위Ph염색체양성CML,남녀성각35례,중위년령50세。70례환자중,사용락안산격매억제제( TKI)이마체니、간우소화간기뇨적환자분별점35.7%、35.7%화52.9%,접수이기인조혈간세포이식( allo-HSCT)적환자점11.4%。수방시간종4월지16년,중위수방27개월。TKI치료조3년총생존(OS)솔시85.7%,이간기뇨(화/혹)간우소조급이기인조혈간세포이식병인3년OS솔분별시46.4%화75.0%,여TKI 치료조비교적P치분별시0.04화0.19。결론 CML시일충골수증식성질병,수착TKI작위일선치료용약적월래월엄범적림상응용,사득CML환자적치료효과화생존질량균득도명현개선。
Objective To investigate the clinical characteristics and treatment response of 70 patients with chronic myeloid leukemia ( CML). Methods Clinical data,treatment efficacy and outcomes of 70 cases of CML enrolled from April 1998 to March 2014 were retrospective-ly analyzed. Results All the patients were Ph chromosome positive. Median age of onset were 50 years old. Male and female were 35 patients re-spectively. Of all 70 patients with the treatment of tyrosine-kinase inhibitor,interferon-alpha and hydroxyurea treatment account for 35. 7%, 35. 7% and 52. 9%,respectively. The allogeneic hematopoietic stem cell transplantation(allo-HSCT)account for 11. 4%. The time of follow up is from 4 months to 16 years. The median follow up time is 27 months. 3 year overall survival rate(OS)was 85. 7% in TKI treatment group. 3 years OS rates in hydroxyurea and interferon group were 46. 4% and 75%,respectively. Compared with TKI group,p value were 0. 04 and 0. 19 in the interferon and hydroxyurea group. Conclusion CML is a myeloproliferative disorder of hematopoietic stem cells. TKIs are now the first line of treatment for CML. Therefore,the treatment for CML changed significantly.