国际肿瘤学杂志
國際腫瘤學雜誌
국제종류학잡지
JOURNAL OF INTERNATIONAL ONCOLOGY
2014年
5期
390-393
,共4页
朱亚杰%苏晓妹%刘桢%程朋%陈滔%张涛
硃亞傑%囌曉妹%劉楨%程朋%陳滔%張濤
주아걸%소효매%류정%정붕%진도%장도
白细胞介素11%血小板减少%肿瘤
白細胞介素11%血小闆減少%腫瘤
백세포개소11%혈소판감소%종류
Interleukin-11%Thrombocytopenia%Neoplasms
目的 观察重组人白细胞介素-11(Ⅰ) [rhIL-11(Ⅰ)]对恶性实体瘤患者放化疗所致血小板减少的疗效及不良反应.方法 选择成都军区总医院2010年12月至2012年12月收治的放化疗后血小板计数(PLT)< 50×109/L的恶性实体瘤患者96例,采用随机数字表法将患者随机分为两组,观察组给予rhIL-11(Ⅰ)25 g·kg-1·d-1皮下注射,对照组给予常规治疗,当血小板升至正常(PLT≥100×109/L)或血小板升高绝对值>50×109/L时停药.观察两组患者用药周期中患者生命体征、肝肾功能、凝血功能、心肺功能变化.结果 观察组患者放化疗后血小板最低值平均为(27.4±7.6)×109/L,与对照组平均值(28.1±7.9)×109/L相比,差异无统计学意义(t=1.083,P>0.05);但治疗后观察组血小板升高最高值平均为(116.3±22.8)×109/L,显著高于对照组的(76.2±21.3)×109/L,差异有统计学意义(t =21.092,P<0.05).观察组患者血小板<50×109/L持续天数平均值为(4.3±1.7)d,血小板从最低值升至绝对值大于5万的平均时间为(6.8±2.4)d,均短于对照组,差异具有统计学意义(t=11.347,P<0.05; t=15.196,P<0.05);且两组患者不良反应可耐受,未出现Ⅲ、Ⅳ度不良反应.结论 rhIL-11(Ⅰ)对于治疗恶性实体瘤患者放化疗后血小板减少疗效确切,不良反应耐受性好.
目的 觀察重組人白細胞介素-11(Ⅰ) [rhIL-11(Ⅰ)]對噁性實體瘤患者放化療所緻血小闆減少的療效及不良反應.方法 選擇成都軍區總醫院2010年12月至2012年12月收治的放化療後血小闆計數(PLT)< 50×109/L的噁性實體瘤患者96例,採用隨機數字錶法將患者隨機分為兩組,觀察組給予rhIL-11(Ⅰ)25 g·kg-1·d-1皮下註射,對照組給予常規治療,噹血小闆升至正常(PLT≥100×109/L)或血小闆升高絕對值>50×109/L時停藥.觀察兩組患者用藥週期中患者生命體徵、肝腎功能、凝血功能、心肺功能變化.結果 觀察組患者放化療後血小闆最低值平均為(27.4±7.6)×109/L,與對照組平均值(28.1±7.9)×109/L相比,差異無統計學意義(t=1.083,P>0.05);但治療後觀察組血小闆升高最高值平均為(116.3±22.8)×109/L,顯著高于對照組的(76.2±21.3)×109/L,差異有統計學意義(t =21.092,P<0.05).觀察組患者血小闆<50×109/L持續天數平均值為(4.3±1.7)d,血小闆從最低值升至絕對值大于5萬的平均時間為(6.8±2.4)d,均短于對照組,差異具有統計學意義(t=11.347,P<0.05; t=15.196,P<0.05);且兩組患者不良反應可耐受,未齣現Ⅲ、Ⅳ度不良反應.結論 rhIL-11(Ⅰ)對于治療噁性實體瘤患者放化療後血小闆減少療效確切,不良反應耐受性好.
목적 관찰중조인백세포개소-11(Ⅰ) [rhIL-11(Ⅰ)]대악성실체류환자방화료소치혈소판감소적료효급불량반응.방법 선택성도군구총의원2010년12월지2012년12월수치적방화료후혈소판계수(PLT)< 50×109/L적악성실체류환자96례,채용수궤수자표법장환자수궤분위량조,관찰조급여rhIL-11(Ⅰ)25 g·kg-1·d-1피하주사,대조조급여상규치료,당혈소판승지정상(PLT≥100×109/L)혹혈소판승고절대치>50×109/L시정약.관찰량조환자용약주기중환자생명체정、간신공능、응혈공능、심폐공능변화.결과 관찰조환자방화료후혈소판최저치평균위(27.4±7.6)×109/L,여대조조평균치(28.1±7.9)×109/L상비,차이무통계학의의(t=1.083,P>0.05);단치료후관찰조혈소판승고최고치평균위(116.3±22.8)×109/L,현저고우대조조적(76.2±21.3)×109/L,차이유통계학의의(t =21.092,P<0.05).관찰조환자혈소판<50×109/L지속천수평균치위(4.3±1.7)d,혈소판종최저치승지절대치대우5만적평균시간위(6.8±2.4)d,균단우대조조,차이구유통계학의의(t=11.347,P<0.05; t=15.196,P<0.05);차량조환자불량반응가내수,미출현Ⅲ、Ⅳ도불량반응.결론 rhIL-11(Ⅰ)대우치료악성실체류환자방화료후혈소판감소료효학절,불량반응내수성호.
Objective To observe the efficacy and safety of recombinant human interleukin-11 (rnIL-11) in the treatment of thrombocytopenia induced by chemoradiotherapy in patients with solid tumor.Methods Solid tumor patients whose PLT count was lower than 50 × 109/L from December 2010 to December 2012 in PLA general hospital of Chengdu Commond were studied.They were divided into two groups randomly.The observed group was given subcutaneous injection of recombinant human interleukin-11 (Ⅰ) at the dose of 25 g · kg-1 · d-1,until the PLT rising subsolute value was more than 50 × 109/L.The control group was given usual treatment.The vital signs,hepatorenal function,coagulation function and cardio-pulmonary function of the patients were recorded during the whole process of treatment.Results The patients after chemotherapy had the platelet lowest average of (27.4 ± 7.6) × 109/L,and the average of the control group was (28.1 ± 7.9) × 109/L.The difference was not statistically significant (t =1.083,P > 0.05),but treatment after the observation of elevated had the platelet highest average of (116.3 ± 22.8) × 109/L,which was significantly higher than that of (76.2 ± 21.3) × 109/L; the difference was significant (t =21.092,P < 0.05).Platelets of patients in the observation group were <50 × 109/L for several days with an average of (4.3 ± 1.7) d,while platelets rose from the lowest value of the average absolute value greater than 50 000 hours (6.8 ± 2.4) d,shorter than the control group.By comparing the two groups,the differences were significant (t =11.347,P < 0.05 ; t =15.196,P < 0.05).Two groups of patients can tolerate adverse reactions.Ⅲ,Ⅳ degree of adverse reaction was not observed.Conclusion This study shows that rhIL-11 is well tolerated and has thrombopoietic activity in the treatment of thrombocytopenia.