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调强放疗联合化-热疗治疗食管癌的疗效 被引量:2

Efficacy of combined IMRT with chemotherapy and thermotherapy for esophageal cancer
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摘要 目的探讨调强放疗(IMRT)联合化-热疗治疗食管癌的近期疗效。方法对78例经病理证实的食管癌患者实施调强放疗,处方剂量PTV为60~66Gy,每次分割量1.8~2.1Gy。化疗方案:5-氟尿嘧啶(5-FU)750mg/d,5d;顺铂(DDP)20mg/d,5d;放疗期热疗每周2次,共6~12次。结果 78例中完全缓解(CR)50例,部分缓解(PR)25例,稳定(NC)3例,近期有效率为96.1%。1年生存率为80.8%。急性毒副反应主要表现骨髓抑制,特别是白细胞减少。结论 IMRT联合化-热疗治疗食管癌近期疗效好,毒副反应可耐受。 Objective To investigate the short-term efficacy of intensive modulated radiation therapy(IMRT) combined with chemotherapy plus thermotherapy for esophageal cancer.MethodsSeventy-eight patients with pathologically confirmed esophageal cancer were received IMRT with a prescribed PTV dose of 60-66 Gy,1.8-2.1 Gy/f,5 f/w. Meanwhile,all patients were administrated one course of chemotherapy,which consisted of fluorouracil 750 mg and cisplatin 20 mg per day for 5 days and a total of 6 to 12 times heat therapy twice a week.Results Of 78 cases,complete remission of the primary tumor was seen in 50 cases,partial remission in 25 cases and no change in 3 cases.The short-term effectiveness rate was 96.1%.The one-year survival rate was 80.8%.The acute toxic effects were manifested primarily as bone marrow suppression,especially as neutropenia.ConclusionIMRT combined with chemotherapy plus thermotherapy has a good short-term efficacy with endurable toxic effects in the patients with esophageal cancer.
出处 《江苏医药》 CAS CSCD 北大核心 2010年第18期2176-2178,共3页 Jiangsu Medical Journal
关键词 食管癌 调强放疗 热疗 Esophageal cancer Intensive modulated radiation therapy thermotherapy
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  • 1Delcamber C, Jacob JH, Dottier D, et al. Localized squamouscell cancer of the esophageal: retrospective analysis of three treatment schedules[J]. Radiother Oncol, 2001, 59 (2) : 195- 201.
  • 2Bedford JL, Vivier.s L, Guzel Z, et al. A quantitative treatment planning study evaluating the potential of dose escalation in eonformal radiotherapy of the oesophagus [J]. Radiother Oncol, 2000,57(2) : 183-193.
  • 3Sawaji Y, Sato T, Takeuchi A, et al. Anti-angiogenic action of hyperthermia by suppressing gene expression and production of turnout-derived vascular endothelial growth factor in vivo and in vitro[J]. Br J Cancer,2002,86(10) : 1597-1603.

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