中华肿瘤杂志
中華腫瘤雜誌
중화종류잡지
CHINESE JOURNAL OF ONCOLOGY
2011年
8期
629-631
,共3页
柯庆华%周世琼%苏小岩%刘珍%张文涛%杨继元
柯慶華%週世瓊%囌小巖%劉珍%張文濤%楊繼元
가경화%주세경%소소암%류진%장문도%양계원
宫颈肿瘤%综合疗法%药物疗法%放射疗法%奈达铂
宮頸腫瘤%綜閤療法%藥物療法%放射療法%奈達鉑
궁경종류%종합요법%약물요법%방사요법%내체박
Uterine cervical neoplasms%Combined modality therapy%Drug therapy%Radiotherapy%Nedaplatin
目的 探讨奈达铂联合甲地孕酮同步放化疗治疗中晚期宫颈癌的近期疗效.方法 42例中晚期(Ⅱb~Ⅳa期)宫颈癌患者随机分为单纯放疗组(RT组,21例),奈达铂联合甲地孕酮同步放疗组(RT+C组,21例),两组放疗方法相同.RT+C组在放疗开始后,每周1次奈达铂30 mg/m2,静脉滴注,第1天,共4~5周,并常规给予止吐药物及适当水化,患者从治疗开始均每天服用甲地孕酮160mg至治疗结束.结果 RT+C组患者中,完全缓解(CR)17例(81.0%),部分缓解(PR)4例(19.0%),有效率为100%;RT组患者中,CR 8例(38.1%),PR 9例(42.9%),有效率81.0%.RT+C组的CR及有效率均高于RT组,差异有统计学意义.RT+C组患者的1年生存率为100%(21/21),RT组患者的1年生存率为81.0%(17/21),差异有统计学意义(x2=4.42,P<0.05).结论 奈达铂联合甲地孕酮同步放化疗可提高中晚期宫颈癌的近期疗效,虽毒性反应有所增加,但患者可以耐受.
目的 探討奈達鉑聯閤甲地孕酮同步放化療治療中晚期宮頸癌的近期療效.方法 42例中晚期(Ⅱb~Ⅳa期)宮頸癌患者隨機分為單純放療組(RT組,21例),奈達鉑聯閤甲地孕酮同步放療組(RT+C組,21例),兩組放療方法相同.RT+C組在放療開始後,每週1次奈達鉑30 mg/m2,靜脈滴註,第1天,共4~5週,併常規給予止吐藥物及適噹水化,患者從治療開始均每天服用甲地孕酮160mg至治療結束.結果 RT+C組患者中,完全緩解(CR)17例(81.0%),部分緩解(PR)4例(19.0%),有效率為100%;RT組患者中,CR 8例(38.1%),PR 9例(42.9%),有效率81.0%.RT+C組的CR及有效率均高于RT組,差異有統計學意義.RT+C組患者的1年生存率為100%(21/21),RT組患者的1年生存率為81.0%(17/21),差異有統計學意義(x2=4.42,P<0.05).結論 奈達鉑聯閤甲地孕酮同步放化療可提高中晚期宮頸癌的近期療效,雖毒性反應有所增加,但患者可以耐受.
목적 탐토내체박연합갑지잉동동보방화료치료중만기궁경암적근기료효.방법 42례중만기(Ⅱb~Ⅳa기)궁경암환자수궤분위단순방료조(RT조,21례),내체박연합갑지잉동동보방료조(RT+C조,21례),량조방료방법상동.RT+C조재방료개시후,매주1차내체박30 mg/m2,정맥적주,제1천,공4~5주,병상규급여지토약물급괄당수화,환자종치료개시균매천복용갑지잉동160mg지치료결속.결과 RT+C조환자중,완전완해(CR)17례(81.0%),부분완해(PR)4례(19.0%),유효솔위100%;RT조환자중,CR 8례(38.1%),PR 9례(42.9%),유효솔81.0%.RT+C조적CR급유효솔균고우RT조,차이유통계학의의.RT+C조환자적1년생존솔위100%(21/21),RT조환자적1년생존솔위81.0%(17/21),차이유통계학의의(x2=4.42,P<0.05).결론 내체박연합갑지잉동동보방화료가제고중만기궁경암적근기료효,수독성반응유소증가,단환자가이내수.
Objective To investigate the early efficacy of nedaplatin combined with megestrol in concurrent chemoradiotherapy for advanced cervical cancer. Methods Forty-two cases of cervical cancer (FIGO Ⅱb to Ⅳa) were divided randomly into two groups: radiotherapy alone (21 cases) and radiation plus chemotherapy (Nedaplatin) group. The same radiotherapy was given to the two groups. Patients of the RT + C group received nedaplatin 30 mg/m2 in intravenous drip infusion once weekly on day 1, for 4 to 5 weeks, and megestrol 160 mg orally every day during the radiation therapy. Results The early outcome:the complete remission rate was 81.0% and partial remission rate was 19.0% in the RT + C group,significantly better than the CR (38.1%) and PR (42.9%) in the RT group. The 1-year survival rates in the two groups were 100% (21/21) and 81.0% ( 17/21 ), respectively, with a significant difference between the two groups ( P < 0.05 ). Conclusions The combination of nedaplatin and megestrol with concurrent chemoradiotherapy can improve the early outcome of advanced cervical cancer, with somewhat increased but tolerable adverse effects.