期刊文献+

TP方案诱导化疗后同期TP与DDP治疗局部晚期鼻咽癌的对照研究 被引量:14

Induction chemotherapy with docetaxel plus cisplatin(TP regimen) followed by concurrent chemoradiotherapy with TP regimen versus cisplatin in treating locally advanced nasopharyngeal carcinoma
下载PDF
导出
摘要 背景与目的:以往多西紫杉醇(docetaxel)联合顺铂(cisplatin,DDP)(TP方案)治疗鼻咽癌的临床试验的样本量小,得出的结果不一。本研究比较TP方案诱导化疗后TP与DDP同期放化疗在局部晚期鼻咽癌治疗中的近期疗效、不良反应。方法:57例初治鼻咽癌患者随机分为两组:同期TP方案放化疗组(TP组)30例;同期DDP放化疗组(DDP组)27例。两组诱导化疗采用TP方案(Docetaxel 70mg/m2第11天,DDP 80mg/m2d1),每3周1次,共2周期。同期化疗(每3周1次,共2周期):TP组采用TP方案(Docetaxel 60mg/m2d1,DDP 80mg/m2d2);DDP组采用DDP 80mg/m2d1。照射野采用CT-Sim设计,常规分割放疗。结果:57例患者完成诱导化疗111周期;53例患者完成同期化疗103周期。诱导化疗终止4例,同期化疗终止3例。所有入组患者都完成放疗。诱导化疗不良反应主要为血液毒性,同期放化疗不良反应主要为血液毒性和口腔粘膜反应。TP组3~4度白细胞减少、3~4度中性粒细胞减少的发生率明显高于DDP组,差异有统计学意义(P<0.005)。同期放化疗中,TP组患者100%使用G-CSF,明显高于DDP组(72.0%),两组比较差异有统计学意义(P<0.005)。同期放化疗后鼻咽部病灶完全缓解率:TP组93.3%,DDP组96.3%;区域淋巴结完全缓解率:TP组92.9%,DDP组91.3%。两组肿瘤反应比较差异无统计学意义。结论:TP方案诱导化疗后,TP同期放化疗的肿瘤缓解率与DDP同期放化疗相似。TP同期放化疗的不良反应发生比DDP同期放化疗高,但在G-CSF支持下,患者能耐受。TP方案的远期疗效值得进一步临床探讨。 Background and Objective. Clinical trials on docetaxel plus cisplatin (DDP) (TP regimen) in treating nasopharyngeal carcinoma (NPC) are still uncertain due to limited samples. This study was to compare the short-term efficacy and toxicity of induction chemotherapy with TP regimen followed by concurrent chemoradiotherapy with TP regimen versus DDP in treating locally advanced NPC. Methods: Fifty-seven patients with stage T3-4N2-3M0 NPC diagnosed pathologically from December 2005 to December 2006 were randomized into TP group (30 patients) and DDP group (27 patients). Both groups received TP regimen as induction chemotherapy with docetaxel (70 mg/m^2) on Day 1 and DDP (80 mg/m^2) on Day 2, repeating every 21 days for 2 cycles. For concurrent chemotherapy, TP group were administered docetaxel (60 mg/m^2) on Day 1 and DDP (80 mg/m^2) on Day 2; DDP group were administered DDP (80 mg/m^2) on Day 1. Both schedules were repeated every 21 days for 2 cycles. Linear accelerator was used as radioactive source. Irradiation field was designed with CT-simulation and conventional fractions. Results. The 57 patients received 111 cycles of induction chemotherapy, and 53 of them received 103 cycles of concurrent chemotherapy; four patients ceased induction chemotherapy and three ceased concurrent chemotherapy. All patients completed radiotherapy. The major toxicity of induction chemotherapy was hematologic toxicity; the main toxicities of concurrent chemoradiotherapy were hematologic toxicity and mucositis. The occurrence rates of Grade 3-4 leucopenia and Grade 3-4 neutropenia were significantly higher in TP group than in DDP groups (P 〈0.05). In concurrent chemoradiotherapy, the application rate of granulocyte colony stimulating factor (G-CSF) was significantly higher in TP group than in DDP group (100% vs. 72.0%, P〈0.05). After concurrent chemoradiotherapy, the complete remission (CR) rates of the nasopharynx and regional lymph nodes were 93.3% and 92.9% in TP group, a
出处 《癌症》 SCIE CAS CSCD 北大核心 2009年第3期279-285,共7页 Chinese Journal of Cancer
基金 广东省科技计划项目(No.2006B36001009)~~
关键词 鼻咽肿瘤 放射疗法 诱导化疗 泰素帝 顺铂 疗效 对照研究 nasopharyngeal neoplasm, radiotherapy, induction chemotherapy, docetaxel, cisplatin, efficacy, comparative study
  • 相关文献

参考文献18

  • 1Kwong DL, Pow EH, Sham JS, et al. Intensity-modulated radiotherapy for early-stage nasopharyngeal carcinoma: a prospective study on disease control and preservation of Cancer, 2004,101(7):1584-1593 被引量:1
  • 2Kam MK, Teo PM, Chau RM, et al. Treatment of nasopharyngeal carcinoma with intensity-modulated radiotherapy: the Hong Kong experience [J]. Int J Radiat Oncol Biol Phys, 2004,60(5) : 1440-1450. 被引量:1
  • 3Oh JL, Vokes EE, Kies MS, et al. Induction chemotherapy followed by concomitant chemoradiotherapy in tne treatment of locoregionally advanced nasopharyngeal cancer [J]. Ann Oncol, 2003,14(4):564-569. 被引量:1
  • 4Chan AT, Ma BB, Lo D, et al. Phase II study of neoadjuvant carboplatin and paclitaxel followed by radiotherapy and concurrent cisplatin in patients with locoregionally advanced nasopharyngeal carcinoma: therapeutic monitoring with plasma Epstein-Barr virus DNA [J]. J Clin Oncol, 2004,22 ( 15 ) : 3053-3060. 被引量:1
  • 5Abdullah AA, Nasser AR, Yasser K, et al. Neoadjuvant chemotherapy followed by concurrent chemo-radiation therapy in locally advanced nasopharyngeal carcinoma [J]. Int J Radiat Oncol Biol Phys, 2005,62(2):508-513. 被引量:1
  • 6Yau TK, Lee AW, Wong DH, et al. Induction chemotherapy with cisplatin and gemcitabine followed by accelerated radiotherapy and concurrent cisplatin in patients with IV (A-B) nasopharyngeal carcinoma [J]. Head Neck, 2006,28(10) : 880- 887. 被引量:1
  • 7McCarthy JS, Tannock IF, Degendorfer P, et al. A phase II trial of docetaxel and cisplatin in patients with recurrent or metastatic nasopharyngeal carcinoma [J]. Oral Oncol, 2002,38 (7):686-90. 被引量:1
  • 8Chua DT, Sham JS, Au GK. A phase Ⅱstudy of docetaxel and cisplatin as first-line chemotherapy in patients with metastatic nasopharyngeal carcinoma [J]. Oral Oncol, 2005,41 (6) :589- 595. 被引量:1
  • 9Jonson FM, Grden A, Palmer JL, et al. A phase II study of docetaxel and carboplatin as neoadjuvant therapy for nasopharyngeal carcinoma with early status and advanced N status [J]. Cancer, 2003,100(5) :991-998. 被引量:1
  • 10Yamouni M, Benhadji K, Lahfa I, et al. A phase Ⅱ trial of docetaxel and cisplatin combination in patients with locally advanced undifferentiated carcinoma of nasopharyngeal type (UCNT) [abstract 5599] [J]. Proc Am Soc Clin Oncol, 2004, 23:511. 被引量:1

二级参考文献13

  • 1Pignon JP, Bourhis J, Deoinne C, et al. chemotherapy added to locoregional treatment for head and neck squeamou-cell carcinoma: three meta--anaalyyses of updated individual date[J]. Lancet Vol, 2000, 355(3): 949-955. 被引量:1
  • 2Bourhis J, Amand C, Pignom JP. Update of MACH-NC Meat-Analysis of Chemotherapy in HeadgoNeck Cancer database focused on concomitant chemomdiothempy. 2004 Annual Meeting Proceedings ASCO, 2004. 488 Abstract No:5505. 被引量:1
  • 3Budach VG, Stuschke M, Budach W, et al. Accelerated hyperfractionated chemoradiation (C-HAART)plus 5-FU/MMC is superior to to HART for inoperable Iocally advanced head and neck cancer. Final results of the German ARO 95--06 Multicentre Trial. 2004 Annual Meeting Proceedings ASCO, 2004. 487 Abstract No:5503. 被引量:1
  • 4管忠震 黄慧强.鼻咽癌肿瘤化学预防和药物治疗[A].韩锐 主编.肿瘤化学预防及药物治疗[C].北京:北京医科大学协和医科大学联合出版社,1991.527-535. 被引量:1
  • 5Lee AW, Lau WH, Tung SY, et al. Prospective randomized study on therapeutic gain achieved by addition of chemotherapy for T1---4N2-3M0 Nasopharyngeal Carcinoma (NPC). 2004 Annual Meeting Proceedings ASCO, 2004. 487 Abstract No:5506. 被引量:1
  • 6Jean-Pierre Pignon, Nathalie Syz, Marshall Posner, et al. Adjiusting for patient selection suggests the addition of docetaxel to 5-fluorouracil-cisplatin induction therapy may offer survival benefit in squamous cell cancer of the head and neck []]. Anti-cancer Drugs, 2004,(15):331~340. 被引量:1
  • 7Katori H, Tsukuda M, Mochimatu I, et al. Phase I trial of concurrent chemoradiotherapy with docetaxel, cisplafin and 5-fluorouracll (TPF) in patients with locally advanced squamous cell carcinoma of the head and neck (SCCHN)[J]. Br J Cancer, 2004,90(2) :348 -352. 被引量:1
  • 8Johnson FM, Garden A, Palmer JL, et al. A Phase Ⅱ study of docetaxel and carboplatin as neoadjuvant therapy for nasopharyngeal carcinoma with early T status and advanced N status [J].Cancer, 2004, 100(5): 991-998. 被引量:1
  • 9MccarthyJS, Tannock IF, Degendorfer P. A Phase Ⅱ trial of docetaxel and cisplatin in patients with recurrent or metastaic nasopharyngeal carcinoma[J]. Oral Oncal, 2002, 38(7):686-690. 被引量:1
  • 10徐兵河 孙燕.紫杉特尔[A].见:孙燕 周际昌 主编.临床肿瘤内科手册 第3版[C].北京:人民卫生出版社,1987.381-384. 被引量:1

共引文献14

同被引文献128

引证文献14

二级引证文献78

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