期刊文献+

宫颈癌新辅助化疗近期疗效及病理学改变

Clinical Effects and Histopathological Changes of Cervical Cancer Following Neoadjuvant Chemotherapy
下载PDF
导出
摘要 [目的]观察子宫颈癌单疗程新辅助化疗后的近期疗效及病理学改变。[方法]40例ⅠIb2~Ⅱb期宫颈癌病例,给予单疗程新辅助化疗(NACT),化疗前后作B超、病理学检查及c-erbB-2、p53、nm23、VEGF免疫组化检测。[结果]有效率(RR)52.5%(21/40),其中完全缓解(CR)3例(7.5%),部分缓解(PR)18例(45.0%),无变化(NC)19例,无进展(PD)病例。化疗后手术切除率92.5%(37/40)。化疗后瘤体缩小或消失,瘤细胞变性、坏死、出血。淋巴结内转移肿瘤亦呈上述改变。化疗后VEGF表达降低,c-erbB-2、p53、nm23表达无变化。[结论]宫颈癌单疗程NACT近期临床疗效明显,能引起原发灶及转移灶肿瘤细胞坏死,肿瘤生长受抑制。 [Purpose]To investigate clinical effects and histopathological changes in cervical cancer following a single course of neoadjuvant chemotherapy (NACT). [Methods] B-uhrosound, histopathological and immunohistochemical examination including markers c-erbB-2,p53,nm23,VEGF were carried out in 40 cases with cervical cancer stage Ⅰb2-Ⅱb bcfore and 1 course NACT.[Results] Response rate (RR) was 52.5%(21/40), with CR, 7.5%(3/dO);PR, 45.0%(18/40); NC,19/dO;and PD, O. After NACT, resection rate of 92.5%(37/40) was achieved and cancer volum decreased or disppeared, degeneration, necrosis, and hemorrhage in tumor tissue, and metastatic lymph nodes were found. The expression of VEGF decreased significantly, but the other markers such as c-erbB-2, p53, nm23 had no significant change after chemotherapy. [Conclusion] One course of NACT is effective to cervical cancer, and can cause necrosis both in primary cancer and metastatic lymph nodes, and inhibits the growth of tumor.
出处 《肿瘤学杂志》 CAS 2006年第2期114-116,共3页 Journal of Chinese Oncology
关键词 宫颈肿瘤 肿瘤辅助疗法 病理学 免疫组织化学 cervix neoplasms neoadjuvant chemotherapy pathology immunohistochemistry
  • 相关文献

参考文献9

  • 1Patricia JE,Levenback C.Cancer of the female lower genital tract[M].London:BC Decker Inc.Hamilton,2001.272-273.
  • 2Nagata Y,Okajiama K,Kokubo M,et al.Clinical results of transcatheter arterial infusion for uterine cervical cancer[J].Am J Clin Oncol Cancer Clin Trials,1999,22 (1):97-102.
  • 3Benedetti-Panici P,Geogi S,Colombo A,et al.Neoadjuvant Intraarterial Chemotherapy and radical surgery versus exclusive radiotherapy in locally advanced squamous cell cervical cancer:results from the Italian multicenter randomized study[J].J Clin Oncol,2002,20(1):179-188.
  • 4高永良.化疗在子宫颈癌综合治疗中的地位[J].中国实用妇科与产科杂志,2004,20(3):135-137. 被引量:11
  • 5Zanetta G,Fei G,Mangioni C.Chemotheropy with paclitaxel,ifosfamide,and cisplatin for the treatment of squamous cell cervical cancer:the experience of Monza[J].Semin Oncol,2000,27 (Suppl 1):23-27.
  • 6Hanahan D,Folkman J.Patients and emerging mechanisms of the angiogenic during tumorigenesis[J].Cell,1996,86:353-364.
  • 7O'Reilly MS,Boehm T,Shing Y,et al.Endostantin:an endogenus inhibitor of angiogenesis and tumor growth[J].Cell,1997,88:277-285.
  • 8Yamazaki K,Abe S,Takekawa H,et al.Tumor angiogenesis in human lung adenocarcinoma[J].Cancer,1994,74:2245-2250.
  • 9令狐华,徐小蓉,梅耀宇,唐均英,唐良萏,孙彤.早期巨块型宫颈癌术前静脉化疗临床观察[J].中国肿瘤,2003,12(11):679-681. 被引量:14

二级参考文献6

  • 1Micheletti E, La Face B, Bianchi E.Continuous infusion of carboplatin during conventional radiotherapy treatment in advanced squamous carcinoma of the cervix uteri Ⅱb-Ⅲb (UICC).A phase Ⅰ/Ⅱ and pharmacokinetic study[J].Am J Clin Oncol, 1997,20(6):613-620.
  • 2Horn LC, Fischer U, Bilek K. Histopathological prognostic factors in primary surgically treated cervix carcinoma[J].Zentralbl Gynakol,2001,123(5):266-274.
  • 3Scheungraber C, Muller B, Kohler C,et al. Detection of disseminated tumor cells in patients with cervical cancer[J].J Cancer Res Clin 0ncol,2002,128(6):329-335.
  • 4Perez CA, Grigsby PW, Chao KS, et all Tumor size, irradiation dose, and long-term outcome of carcinoma of uterine cervix [J].Int J Radiat Oncol Biol Phys,1998,41(2):307-317.
  • 5Chen CA, Cheng WF, Wei LH,et al.Radical hysterectomy alone or combined with neoadjuvant chemotherapy in the treatment of early stage bulky cervical carcinoma [J]. J Formos Med Assoc,2002,101(3):195-202.
  • 6吕育纯,辛培玲,陈丽光,郭冰冰.中、晚期宫颈癌43例同步放疗、化疗的临床疗效观察[J].实用癌症杂志,2003,18(5):533-535. 被引量:14

共引文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部