大连医科大学学报
大連醫科大學學報
대련의과대학학보
JOURNAL OF DALIAN MEDICAL UNIVERSITY
2014年
4期
346-350
,共5页
代俊利%李杰%张海峰%许新征%薛润国
代俊利%李傑%張海峰%許新徵%薛潤國
대준리%리걸%장해봉%허신정%설윤국
放化同步治疗%宫颈癌术后%脉管癌栓%疗效%不良反应
放化同步治療%宮頸癌術後%脈管癌栓%療效%不良反應
방화동보치료%궁경암술후%맥관암전%료효%불량반응
chemotherapy combined with radiotherapy%cervical cancer surgery%the vascular cancer embolus%curative efficacy%adverse reaction
目的:观察放化同步治疗宫颈癌术后脉管癌栓阳性患者的近期疗效及不良反应。方法选择宫颈癌术后脉管癌栓阳性患者共118例。按治疗方案的不同分为两组:放化同步治疗组57例,给予术后辅助同步放化疗,同步化疗方案为DDP周疗,于盆腔外照射治疗期间给予,术后病理提示手术切缘阳性、淋巴结阳性和/或宫旁组织阳性的患者予追加192 Ir后装腔内放疗;单纯放疗组61例,放疗方案与放化同步组相同。随访、评估和比较分析,两组患者的3年无病生存率、3年总生存率、1年、2年及3年盆腔复发率及治疗相关不良反应。结果宫颈癌根治术后脉管癌栓阳性的患者,术后放化同步治疗较单纯放疗降低了1年盆腔复发率(放化同步治疗8.77%,单纯放疗22.95%,P<0.05)及2年盆腔复发率(放化同步治疗12.28%,单纯放疗27.87%,P<0.05),3年盆腔复发率放化同步治疗组与单纯放疗组比较,差异无显著性意义(P>0.05),两组3年无病生存率、3年总生存率相似。放化同步组的早期不良反应较单纯放疗组增加,主要体现在骨髓抑制和胃肠道反应,均在可耐受范围内,经积极对症支持处理未影响后续治疗。晚期不良反应两组患者无差别。结论放化同步治疗降低了宫颈癌根治术后脉管癌栓阳性患者近期局部复发率,3年的无进展生存率及总生存率未见明显改善。放化同步治疗的早期不良反应稍有增加。
目的:觀察放化同步治療宮頸癌術後脈管癌栓暘性患者的近期療效及不良反應。方法選擇宮頸癌術後脈管癌栓暘性患者共118例。按治療方案的不同分為兩組:放化同步治療組57例,給予術後輔助同步放化療,同步化療方案為DDP週療,于盆腔外照射治療期間給予,術後病理提示手術切緣暘性、淋巴結暘性和/或宮徬組織暘性的患者予追加192 Ir後裝腔內放療;單純放療組61例,放療方案與放化同步組相同。隨訪、評估和比較分析,兩組患者的3年無病生存率、3年總生存率、1年、2年及3年盆腔複髮率及治療相關不良反應。結果宮頸癌根治術後脈管癌栓暘性的患者,術後放化同步治療較單純放療降低瞭1年盆腔複髮率(放化同步治療8.77%,單純放療22.95%,P<0.05)及2年盆腔複髮率(放化同步治療12.28%,單純放療27.87%,P<0.05),3年盆腔複髮率放化同步治療組與單純放療組比較,差異無顯著性意義(P>0.05),兩組3年無病生存率、3年總生存率相似。放化同步組的早期不良反應較單純放療組增加,主要體現在骨髓抑製和胃腸道反應,均在可耐受範圍內,經積極對癥支持處理未影響後續治療。晚期不良反應兩組患者無差彆。結論放化同步治療降低瞭宮頸癌根治術後脈管癌栓暘性患者近期跼部複髮率,3年的無進展生存率及總生存率未見明顯改善。放化同步治療的早期不良反應稍有增加。
목적:관찰방화동보치료궁경암술후맥관암전양성환자적근기료효급불량반응。방법선택궁경암술후맥관암전양성환자공118례。안치료방안적불동분위량조:방화동보치료조57례,급여술후보조동보방화료,동보화료방안위DDP주료,우분강외조사치료기간급여,술후병리제시수술절연양성、림파결양성화/혹궁방조직양성적환자여추가192 Ir후장강내방료;단순방료조61례,방료방안여방화동보조상동。수방、평고화비교분석,량조환자적3년무병생존솔、3년총생존솔、1년、2년급3년분강복발솔급치료상관불량반응。결과궁경암근치술후맥관암전양성적환자,술후방화동보치료교단순방료강저료1년분강복발솔(방화동보치료8.77%,단순방료22.95%,P<0.05)급2년분강복발솔(방화동보치료12.28%,단순방료27.87%,P<0.05),3년분강복발솔방화동보치료조여단순방료조비교,차이무현저성의의(P>0.05),량조3년무병생존솔、3년총생존솔상사。방화동보조적조기불량반응교단순방료조증가,주요체현재골수억제화위장도반응,균재가내수범위내,경적겁대증지지처리미영향후속치료。만기불량반응량조환자무차별。결론방화동보치료강저료궁경암근치술후맥관암전양성환자근기국부복발솔,3년적무진전생존솔급총생존솔미견명현개선。방화동보치료적조기불량반응초유증가。
Objective To observe the curative efficacy and adverse reaction in vascular cancer embolus (+) patients who received postoperative chemoradiotherapy of the cervical cancer , and to determine whether vascular cancer embolus is the evidence of postoperative chemoradiotherapy .Methods This study included a total of 118 cases of vascular cancer embolus (+) patients.The patients were classified into two groups based on the therapeutic plans .The chemoradiotherapy group included 57 patients who received concurrent DDP chemotherapy in external irradiation stage .192 Ir intracavitary radiothera-py was appended if postoperative pathology was positive in surgical margins , lymph node or parametrial tissue .The radio-therapy group included 61 patients who received radiation therapy only as same as the first group .The patients were fol-lowed up, evaluated and the data were analyzed including 3-year disease -free survival, 3-year overall survival, 1-year, 2-year and 3-year pelvic recurrence rate and adverse reactions .Results Compared to the radiotherapy group , the chemoradiotherapy group had reduced one -year pelvic recurrence rate (8.77% in the chemoradiotherapy group versus 22.95%in the radiotherapy group,P<0.05) and two-year pelvic recurrence rate (12.28% in the chemoradiotherapy group versus 27.87%in the radiotherapy group,P<0.05).However, there was no significant difference in three -year pelvic recurrence rate between the two groups (P>0.05).The 3-year disease-free survival rate and the 3-year overall survival between the two groups were similar (P>0.05).The early adverse reactions in the chemoradiotherapy group were more than the radiotherapy group , mainly in the bone marrow suppression and gastrointestinal reactions which were well tol -erated did not affect the follow -up treatment by active therapy .The late adverse reactions between the two groups were similar.Conclusion Concurrent chemoradiotherapy cuts down the recent local recurrence rate in vascular cancer embolus (+) patients who has received radical hysterectomy , but it makes no significant improvement in 3-year progression-free survival and overall survival .In addition, concurrent chemoradiotherapy induces increased early adverse reaction .