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宫颈癌新辅助化疗临床疗效评价 被引量:4

Efficacy Evaluation of Neoadjuvant Chemotherapy for Cervical Cancer
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摘要 目的:探讨早期宫颈癌新辅助化疗的疗效和安全性。方法:选择Ib1期至IIb期宫颈癌39例,采用DBM方案动脉灌注化疗1-2个疗程后,行腹腔镜下广泛性子宫切除术及盆腔淋巴结清扫术;观察化疗前后癌灶的变化、化疗副反应及术后病理结果等指标。结果:全部病例化疗后宫颈局部肿瘤直径均不同程度缩小,化疗有效率100%;3例IIb期宫旁病灶改善不满意直接行放疗,其余36例行腹腔镜下宫颈癌根治术;手术成功率100%;有12例(12/36)术后病理结果未发现癌灶。主要毒副反应为消化道症状及I-II度白细胞减少,用药后可缓解。结论:宫颈癌新辅助化疗近期疗效好,副反应轻。 Objective:To evaluate the response and security to neoadjuvant chemotherapy ( NACT) in patients of Ib1-IIb cervical cancer .Method:A retrospective study were made on 39 cervical cancer patients ( FIGO stage Ib1-IIb) underwent this DBM therapy by arterial infusion chemotherapy for 1 or 2 courses and followed by radical hysterectomy .The observation indexes included the change of the local lesion , side effect and pathological outcomes after the surgery .Result: All the patients indicated reduction of the lesions .the effective rate was 100%.Except 3 patients in IIb stage took radiotherapy , the rest take laparoscopic radical operation.The success rate of operation was 100%.There’re 12 (12/36) pathological reports showed that no cancer residue were detected .The main side effects were symptom of digestive tract like nausea and vomiting and I-II degree leucocytopenia .All these symptoms could be remittent after the symptomatic treatment .Con-clusion:Neoadjuvant chemotherapy ( NACT) is effective in short-term efficacy and the side effect is tolera-ble.
出处 《河北医学》 CAS 2014年第4期611-614,共4页 Hebei Medicine
关键词 宫颈癌 新辅助化疗 DBM方案 动脉灌注化疗 Cervical cancer Neoadjuvant chemotherapy DBM therapy Arterial infusion chemotherapy
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  • 1Benedetti-Panici P, Greggi S, Colombo A,et al. Neoadju- vant chemotherapy and radical surgery versus exclusive ia- diotherapy in locally advanced squamous cell cervical canc- er: results from the Italian multicenter randomized study[ J]. Clin Oncol,2002,20( 1 ) :179-188.
  • 2Hu T, Li S, Chen Y, et al. Matched-ease comparison of neoadjuvant chemotherapy in patients with FIGO stage IBI- IIB cervical cancer to establish selection criteria [ J ]. Eur Cancer,2012,48(15) :2353-2360.
  • 3Sardi JE, Boixadera MA, Sardi JJ. Neoadjuvant chemothera- py in cervical cancer: a new trend[ J] .Curt Opin Obstet Gy- necol, 2005,17: 43 -47.
  • 4Yamaguchi S, Nishimura R, Yaegashi N, et al. Phase 1I study of neoadjuvant chemotherapy with irinotecan hydro- chloride and nedaplatin followed by radical hysterectomy for bulky stage Ib2 to IIb, cervical squamous cell carcinoma: Japanese Gynecologic Oncology Group study (JGOG 1065) [J].Oneol Rep,2012,28(2) :487-493.
  • 5Shen Y, Yang L, Wang Z. Treatment of early bulky cervical cancer with neoadjuvant paclitaxel, carboplatin and cisplatin prior to laparoscopical radical hysterectomy and pelvic lymphadenectomy [ J] .Oncol Lett ,2012,3 (3) : 641-645.
  • 6Katsumata N, Yoshikawa H, Kobayashi H, et al.Phase Ill randomised controlled trial of neoadjuvant chemotherapy plus radical surgery vs radical surgery alone for stages IB2, llA2, and liB cervical cancer: a Japan Clinical Oncology Group trial (JCOG 0102)[ J] .Br Cancer,2013,2.

同被引文献28

  • 1Seebacher V,Polterauer S,Grimm C,et al. The prognostic valueof plasma fibrinogen levels in patients with endometrial cancer:a multi-centre trial[J]. British journal of cancer, 2010,102(6):952-956.
  • 2Palumbo JS,Talmage KE,Massari JV,et al. Platelets and fibrin(ogen) increase metastatic potential by impeding natural killercell - mediated elimination of tumor cells[J]. Blood, 2005,105Cl): 178-185.
  • 3Polterauer S,Seebacher V, Hefler-Frischmuth K, et al. Fibrino-gen plasma levels are an independent prognostic parameter inpatients with cervical cancer[J]. American journal of obstetricsand gynecology, 2009,200(6) ; 647. el-7.
  • 4Jensen T, Kierulf P, Sandset PM, et al. Fibrinogen and fibrininduce synthesis of proinflammatory cytokines from isolated pe-ripheral blood mononuclear cells[J]. Thromb Haemost,2007,97(5) : 822.
  • 5Koh SC, Khalil R, Lim FK,et al. The association between fi-brinogen, von Willebrand Factor, antithrombin III,and I>di-mer levels and survival outcome by 36 months from ovariancancer [J]. Clinical and applied thrombosis/hemostasis,2006,12(1) : 3-8.
  • 6Wang X,Wang E,Kavanagh JJ,et al. Ovarian cancer,the coag-ulation pathway . and inflammation[J]. Journal of translationalmedicine,2005 ,3(1) : 25.
  • 7JUSTIN O, PARKHURST, MADHULIKA V, et ah Cervical can- cer and the global health agenda:lnsighB from multiple poli- cy-analysis frameworks[J]. Global Public Health, 2013, 8(10) 1093-1108.
  • 8LEE J, GOLLAHON L. Nek2-targeted ASO or siRNA pre-treat- ment enhances anticancer dnag sensitivity in triple negative breast cancer cells[J],Int J Oncol, 2013, 42(3): 839-847.
  • 9FRY A M. The Nek2 protein kinase:a novel regulator of centro- some-structure[J]. Oncogene, 2002, 21(40): 6184-6194.
  • 10DAS T K, DANA D, PAROI,Y S S, et ah Centrosomal kinase Nek2 cooperates with oncogenic pathways to promote melastasis[J]. Oncogenesis, 2013, 2(9), DOI: 10.1038/oncsis.2013.34.

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