中国组织工程研究
中國組織工程研究
중국조직공정연구
Journal of Clinical Rehabilitative Tissue Engineering Research
2013年
49期
8551-8556
,共6页
万鼎铭%李丽%谢新生%孙玲%孙慧%姜中兴%张毅%曹伟杰%边志磊%周雪芳
萬鼎銘%李麗%謝新生%孫玲%孫慧%薑中興%張毅%曹偉傑%邊誌磊%週雪芳
만정명%리려%사신생%손령%손혜%강중흥%장의%조위걸%변지뢰%주설방
干细胞%干细胞移植%急性髓系白血病M2%自体外周血造血干细胞移植%细胞因子诱导的杀伤细胞%无病生存率%总生存率%白血病复发
榦細胞%榦細胞移植%急性髓繫白血病M2%自體外週血造血榦細胞移植%細胞因子誘導的殺傷細胞%無病生存率%總生存率%白血病複髮
간세포%간세포이식%급성수계백혈병M2%자체외주혈조혈간세포이식%세포인자유도적살상세포%무병생존솔%총생존솔%백혈병복발
背景:细胞因子诱导的杀伤细胞作为一种有效的过继免疫治疗方法,成为治疗急性髓系白血病的一种新的手段,目前关于急性髓系白血病自体移植后序贯细胞因子诱导的杀伤细胞治疗的报道尚少,值得进一步研究。<br> 目的:观察急性髓系白血病 M2患者自体外周血造血干细胞移植后序贯细胞因子诱导的杀伤细胞治疗的临床疗效和不良反应。<br> 方法:入选45例低、中危急性髓系白血病M2患者,其中19例在自体外周血造血干细胞移植后序贯了细胞因子诱导的杀伤细胞治疗,另26例未序贯细胞因子诱导的杀伤细胞治疗,比较两组患者的复发率、无病生存率、总生存率,观察细胞因子诱导的杀伤细胞治疗的安全性。<br> 结果与结论:①序贯细胞因子诱导的杀伤细胞治疗组的复发率低于未序贯细胞因子诱导的杀伤细胞治疗组(21.05%,38.46%,P<0.05);序贯细胞因子诱导的杀伤细胞治疗组患者的2年无病生存率和2年总生存率均高于未序贯细胞因子诱导的杀伤细胞治疗组,差异均有显著性意义(P<0.05)。②19例接受细胞因子诱导的杀伤细胞治疗的患者均顺利完成治疗方案,治疗过程中除4例出现寒战、发热外,无其他不良反应。结果显示低、中危急性髓系白血病 M2患者自体外周血造血干细胞移植后序贯细胞因子诱导的杀伤细胞治疗可降低原发病的复发率,提高患者的无病生存率及总生存率,且无明显不良反应,是一种安全、有效、可行的治疗方法。
揹景:細胞因子誘導的殺傷細胞作為一種有效的過繼免疫治療方法,成為治療急性髓繫白血病的一種新的手段,目前關于急性髓繫白血病自體移植後序貫細胞因子誘導的殺傷細胞治療的報道尚少,值得進一步研究。<br> 目的:觀察急性髓繫白血病 M2患者自體外週血造血榦細胞移植後序貫細胞因子誘導的殺傷細胞治療的臨床療效和不良反應。<br> 方法:入選45例低、中危急性髓繫白血病M2患者,其中19例在自體外週血造血榦細胞移植後序貫瞭細胞因子誘導的殺傷細胞治療,另26例未序貫細胞因子誘導的殺傷細胞治療,比較兩組患者的複髮率、無病生存率、總生存率,觀察細胞因子誘導的殺傷細胞治療的安全性。<br> 結果與結論:①序貫細胞因子誘導的殺傷細胞治療組的複髮率低于未序貫細胞因子誘導的殺傷細胞治療組(21.05%,38.46%,P<0.05);序貫細胞因子誘導的殺傷細胞治療組患者的2年無病生存率和2年總生存率均高于未序貫細胞因子誘導的殺傷細胞治療組,差異均有顯著性意義(P<0.05)。②19例接受細胞因子誘導的殺傷細胞治療的患者均順利完成治療方案,治療過程中除4例齣現寒戰、髮熱外,無其他不良反應。結果顯示低、中危急性髓繫白血病 M2患者自體外週血造血榦細胞移植後序貫細胞因子誘導的殺傷細胞治療可降低原髮病的複髮率,提高患者的無病生存率及總生存率,且無明顯不良反應,是一種安全、有效、可行的治療方法。
배경:세포인자유도적살상세포작위일충유효적과계면역치료방법,성위치료급성수계백혈병적일충신적수단,목전관우급성수계백혈병자체이식후서관세포인자유도적살상세포치료적보도상소,치득진일보연구。<br> 목적:관찰급성수계백혈병 M2환자자체외주혈조혈간세포이식후서관세포인자유도적살상세포치료적림상료효화불량반응。<br> 방법:입선45례저、중위급성수계백혈병M2환자,기중19례재자체외주혈조혈간세포이식후서관료세포인자유도적살상세포치료,령26례미서관세포인자유도적살상세포치료,비교량조환자적복발솔、무병생존솔、총생존솔,관찰세포인자유도적살상세포치료적안전성。<br> 결과여결론:①서관세포인자유도적살상세포치료조적복발솔저우미서관세포인자유도적살상세포치료조(21.05%,38.46%,P<0.05);서관세포인자유도적살상세포치료조환자적2년무병생존솔화2년총생존솔균고우미서관세포인자유도적살상세포치료조,차이균유현저성의의(P<0.05)。②19례접수세포인자유도적살상세포치료적환자균순리완성치료방안,치료과정중제4례출현한전、발열외,무기타불량반응。결과현시저、중위급성수계백혈병 M2환자자체외주혈조혈간세포이식후서관세포인자유도적살상세포치료가강저원발병적복발솔,제고환자적무병생존솔급총생존솔,차무명현불량반응,시일충안전、유효、가행적치료방법。
BACKGROUND:Cytokine induced kil er cells therapy as an effective means of adoptive immunotherapy, becomes a new way to treat acute myeloid leukemia. But, the researches about sequential cytokine induced kil er cells therapy after autologous peripheral blood stem celltransplantation in acute myeloid leukemia patients are stil less, which deserve further research. <br> OBJECTIVE:To observe the clinical efficiency and safety of sequential cytokine induced kil er cells therapy after autologous peripheral blood stem celltransplantation in acute myeloid leukemia M2 patients. <br> METHODS:Total y 45 patients with low-or intermediate-risk acute myeloid leukemia M2 were recruited in this study. Among them, 19 patients received sequential cytokine induced kil er cells therapy after autologous peripheral blood stem celltransplantation and 26 patients only received autologous peripheral blood stem celltransplantation. The relapse rate, disease-free survival, and overal survival were compared between two groups, and safety of cytokine induced kil er cells therapy was observed. <br> RESULTS AND CONCLUSION:(1) Compared with the patients only receiving autologous peripheral blood stem celltransplantation, the relapse rate was lower (21.05%vs. 38.46%;P<0.05), and elevated percentages of the disease-free survival and overal survival were observed in the patients receiving sequential cytokine induced kil er cells therapy after autologous peripheral blood stem celltransplantation (P<0.05). (2) The 19 patients who received sequential cytokine induced kil er cells therapy after autologous peripheral blood stem celltransplantation al completed the treatment scheme successful y. Only four patients appeared to have chil s and fever, and no more side effects were observed. These findings suggested that the sequential cytokine induced kil er cells therapy after autologous peripheral blood stem celltransplantation can improve the disease-free survival and overal survival of low-or intermediate-risk acute myeloid leukemia M2 patients without remarkable side effects, which is a safe, effective and feasible way for the treatment of acute myeloid leukemia M2.