中华放射医学与防护杂志
中華放射醫學與防護雜誌
중화방사의학여방호잡지
Chinese Journal of Radiological Medicine and Protection
2014年
1期
30-33
,共4页
易福梅%王皓%袁慧书%李金娜%姜玉良%田素青%王俊杰
易福梅%王皓%袁慧書%李金娜%薑玉良%田素青%王俊傑
역복매%왕호%원혜서%리금나%강옥량%전소청%왕준걸
直肠癌%局部复发%放射性粒子%疗效
直腸癌%跼部複髮%放射性粒子%療效
직장암%국부복발%방사성입자%료효
Rectal cancer%Local recurrence%Radioactive seed%Efficacy
目的 观察CT引导125I放射性粒子植入治疗局部复发性直肠癌(LRRC)的疗效和不良反应.方法 回顾性分析2003年9月至2011年10月本院收治的30例接受CT引导125I放射性粒子植入治疗的LRRC患者的临床疗效.术前利用三维放射性粒子治疗计划系统计算肿瘤靶区需要粒子数目、活度和剂量.每颗粒子活度14.8 ~29.6 MBq(中位25.9 MBq),植入粒子数目33 ~ 137颗(中位74.5颗).术后即行CT扫描进行剂量验证,处方剂量120~160 Gy,实际剂量D9075.91~159.32 Gy(中位119.77 Gy).对患者进行疗效及不良反应分析.结果 中位随访时间15.2个月(4.2 ~35.0个月).肿瘤控制总有效率50.0%,其中完全缓解率13.3%,部分缓解率36.7%.1和2年局部控制率分别为30.0%和8.0%.1和2年生存率分别为66.5%和32.9%,中位生存期21.5个月.疼痛缓解率95.2%,并发症发生率20.0%,主要为1、2级皮肤和泌尿系统不良反应(尿频、尿急和排尿困难).结论 CT引导125I放射性粒子植入治疗局部复发性直肠癌创伤小、疗效好、不良反应少,可作为局部复发性直肠癌患者的治疗新选择.
目的 觀察CT引導125I放射性粒子植入治療跼部複髮性直腸癌(LRRC)的療效和不良反應.方法 迴顧性分析2003年9月至2011年10月本院收治的30例接受CT引導125I放射性粒子植入治療的LRRC患者的臨床療效.術前利用三維放射性粒子治療計劃繫統計算腫瘤靶區需要粒子數目、活度和劑量.每顆粒子活度14.8 ~29.6 MBq(中位25.9 MBq),植入粒子數目33 ~ 137顆(中位74.5顆).術後即行CT掃描進行劑量驗證,處方劑量120~160 Gy,實際劑量D9075.91~159.32 Gy(中位119.77 Gy).對患者進行療效及不良反應分析.結果 中位隨訪時間15.2箇月(4.2 ~35.0箇月).腫瘤控製總有效率50.0%,其中完全緩解率13.3%,部分緩解率36.7%.1和2年跼部控製率分彆為30.0%和8.0%.1和2年生存率分彆為66.5%和32.9%,中位生存期21.5箇月.疼痛緩解率95.2%,併髮癥髮生率20.0%,主要為1、2級皮膚和泌尿繫統不良反應(尿頻、尿急和排尿睏難).結論 CT引導125I放射性粒子植入治療跼部複髮性直腸癌創傷小、療效好、不良反應少,可作為跼部複髮性直腸癌患者的治療新選擇.
목적 관찰CT인도125I방사성입자식입치료국부복발성직장암(LRRC)적료효화불량반응.방법 회고성분석2003년9월지2011년10월본원수치적30례접수CT인도125I방사성입자식입치료적LRRC환자적림상료효.술전이용삼유방사성입자치료계화계통계산종류파구수요입자수목、활도화제량.매과입자활도14.8 ~29.6 MBq(중위25.9 MBq),식입입자수목33 ~ 137과(중위74.5과).술후즉행CT소묘진행제량험증,처방제량120~160 Gy,실제제량D9075.91~159.32 Gy(중위119.77 Gy).대환자진행료효급불량반응분석.결과 중위수방시간15.2개월(4.2 ~35.0개월).종류공제총유효솔50.0%,기중완전완해솔13.3%,부분완해솔36.7%.1화2년국부공제솔분별위30.0%화8.0%.1화2년생존솔분별위66.5%화32.9%,중위생존기21.5개월.동통완해솔95.2%,병발증발생솔20.0%,주요위1、2급피부화비뇨계통불량반응(뇨빈、뇨급화배뇨곤난).결론 CT인도125I방사성입자식입치료국부복발성직장암창상소、료효호、불량반응소,가작위국부복발성직장암환자적치료신선택.
Objective To evaluate the efficacy and adverse reactions of CT-guided 125I radioactive seed implantation in treatment of locally recurrent rectal cancer (LRRC).Methods Thirty patients with LRRC who refused operation or were unable to endure pelvic radiotherapy received 125I seed implantation under CT guidance.Three-dimensional treatment planning system was used to calculate the number,activity,and dose of the seeds needed.The activity of seeds ranged from 14.8 to 29.6 MBq with a median of 25.9 MBq,the seed numbers ranged from 33 to 137 with a median of 74.5,the prescription doses ranged from120-160 Gy,and the actual verification dose D90 ranged from 75.91 to 159.32 Gy with a median of 119.77 Gy.Dosimetric verification by CT scanning was conducted immediately after the treatment.Follow-up was conducted for 15.2 months(4.2-35.0 months).Results The follow-up rate was 93.3%.The pain relief rate was 95.2%.The overall response rate was 50.0%,including a complete response rate of 13.3% and a partial response rate of 36.7%.The 1-and 2-year local control rates were 30.0% and 8.0% respectively.The median local control survival time was 7.8 month.The 1-and 2-year survival rates were 66.5% and 32.9% respectively.The median overall survival time was 21.5 months.Complications,mainly adverse effects of skin and urinary system (frequent urination,urgent urination,and dysuria) occurred in 6 patients with a rate of 20.0%.Conclusions Minimally invasive and with satisfying efficacy and tolerable complications,CT-guided 125I radioactive seed implantation is a favorable option for treatment of LRRC,especially for the patients who have undergone previous pelvic radiation.