山东大学耳鼻喉眼学报 ›› 2021, Vol. 35 ›› Issue (3): 118-124.doi: 10.6040/j.issn.1673-3770.0.2020.276

• 临床研究 • 上一篇    下一篇

局部晚期头颈部鳞状细胞癌的化疗及靶向进展

卫亚楠综述陈曦审校   

  1. 南京医科大学第一附属医院/江苏省人民医院 耳鼻咽喉科, 江苏 南京 210029
  • 发布日期:2021-05-14
  • 通讯作者: 陈曦. E-mail:jsxycx@sina.com
  • 基金资助:
    江苏省卫生厅面上项目(H2018013)

Progress in chemotherapy and targeted drug therapy for locally advanced head and neck squamous cell carcinoma

WEI Ya'nanOverview,CHEN XiGuidance   

  1. Department of Otorhinolaryngology, The First Affiliated Hospital, Nanjing Medical University/Jiangsu Province Hospital, Nanjing 210029, Jiangsu, China
  • Published:2021-05-14

摘要: 局部晚期头颈部鳞状细胞癌目前主要采用手术、放疗和化疗相结合的综合治疗,但是器官功能保留率和5年生存率没有显著提高。从20世纪70年代末开始,以顺铂为基础的化疗药开始应用于局部晚期头颈部鳞状细胞癌治疗中,研究表明,顺铂联合氟尿嘧啶作为诱导化疗方案提高了喉功能保全率。后来随着紫杉醇的应用,有研究证实在PF方案基础上加用紫杉醇可提高诱导化疗的疗效。与PF方案相比,TPF方案在局部控制率及无进展生存期上有显著的优越性,因此,成为诱导化疗的首选方案。20世纪90年代初期,同步放化疗成为非手术治疗及保喉的新方式,因其在总体生存率、保喉率、局部控制率上有明确的优势,已被列入局部晚期头颈部肿瘤非手术治疗的标准治疗方案。2006年分子靶向治疗药物西妥昔单抗经美国食品和药物管理局批准运用于临床,因其预后的优势及较少的不良反应成为无法耐受化疗药物的新选择。就局部晚期头颈部鳞状细胞癌的化疗药物及靶向药物治疗进展进行综述。

关键词: 局部晚期头颈部鳞癌, 化疗, 放化疗, 诱导, 同步, 靶向

Abstract: Surgery in combination with chemotherapy and radiotherapy is the mainstay of treatment for locally advanced head and neck squamous cell carcinoma(LAHNSCC). However the organ preservation rate and 5-year survival rate have not significantly improved. In the late 1970s, cisplatin-based chemotherapeutic drugs began to be used in the treatment of LAHNSCC. Studies have shown a significant laryngeal preservation benefit of PF. With the application of paclitaxel, studies have confirmed that the TPF regimen has significant advantages in terms of local control and progression-free survival compared with PF. Therefore, it became the first choice for induction chemotherapy. In the early 1990s, concurrent chemoradiotherapy(CCRT)became a new method of non-surgical treatment and laryngeal protection. CCRT has clear advantages in terms of overall survival, laryngeal preservation, and local control and has been the standard non-surgical treatment for LAHNSCC. In 2006, cetuximab(CET)was approved by the US Food and Drug Administration for clinical use. Because of its advantages in terms of prognosis and less side effects, CET offers a new alternative for patients who cannot tolerate chemotherapy. This article reviews the progress in chemotherapy and targeted drug therapy for locally advanced head and neck squamous cell carcinoma.

Key words: Locally advanced head and neck squamous cell carcinoma, Chemotherapy, Induction chemotherapy, Concurrent chemoradiotherapy, Targeted therapy

中图分类号: 

  • R735.1
[1] Gyawali B, Shimokata T, Honda K, et al. Chemotherapy in locally advanced head and neck squamous cell carcinoma[J]. Cancer Treat Rev, 2016, 44: 10-16. doi:10.1016/j.ctrv.2016.01.002.
[2] Cohen EEW, Soulières D, Le Tourneau C, et al. Pembrolizumab versus methotrexate, docetaxel, or cetuximab for recurrent or metastatic head-and-neck squamous cell carcinoma(KEYNOTE-040): a randomised, open-label, phase 3 study[J]. Lancet, 2019, 393(10167): 156-167. doi:10.1016/S0140-6736(18)31999-8.
[3] Wolf GT, Fisher SG, Hong WK, et al. Induction chemotherapy plus radiation compared with surgery plus radiation in patients with advanced laryngeal cancer[J]. N Engl J Med, 1991, 324(24): 1685-1690. doi:10.1056/nejm199106133242402.
[4] Lefebvre JL, Chevalier D, Luboinski B, et al. Larynx preservation in pyriform sinus cancer: preliminary results of a European organization for research and treatment of cancer phase III trial[J]. J Natl Cancer Inst, 1996, 88(13): 890-899. doi:10.1093/jnci/88.13.890.
[5] Pignon JP, Bourhis J, Domenge C, et al. Chemotherapy added to locoregional treatment for head and neck squamous-cell carcinoma: three meta-analyses of updated individual data[J]. Lancet, 2000, 355(9208): 949-955. doi:10.1016/s0140-6736(00)90011-4.
[6] Pignon JP, Maître AL, Maillard E, et al. Meta-analysis of chemotherapy in head and neck cancer(MACH-NC): an update on 93 randomised trials and 17, 346 patients[J]. Radiother Oncol, 2009, 92(1): 4-14. doi:10.1016/j.radonc.2009.04.014.
[7] Vermorken JB, Remenar E, van Herpen C, et al. Cisplatin, fluorouracil, and docetaxel in unresectable head and neck cancer[J]. N Engl J Med, 2007, 357(17): 1695-1704. doi:10.1056/nejmoa071028.
[8] Posner MR, Hershock DM, Blajman CR, et al. Cisplatin and fluorouracil alone or with docetaxel in head and neck cancer[J]. N Engl J Med, 2007, 357(17): 1705-1715. doi:10.1056/nejmoa070956.
[9] Janoray G, Pointreau Y, Garaud P, et al. Long-term results of a multicenter randomized phase III trial of induction chemotherapy with cisplatin, 5-fluorouracil, ±docetaxel for larynx preservation[J]. J Natl Cancer Inst, 2016, 108(4): djv368. doi:10.1093/jnci/djv368.
[10] Blanchard P, Bourhis J, Lacas B, et al. Taxane-cisplatin-fluorouracil as induction chemotherapy in locally advanced head and neck cancers: an individual patient data meta-analysis of the meta-analysis of chemotherapy in head and neck cancer group[J]. J Clin Oncol, 2013, 31(23): 2854-2860. doi:10.1200/jco.2012.47.7802.
[11] Cohen EEW, Karrison TG, Kocherginsky M, et al. Phase III randomized trial of induction chemotherapy in patients with N2 or N3 locally advanced head and neck cancer[J]. J Clin Oncol, 2014, 32(25): 2735-2743. doi:10.1200/JCO.2013.54.6309.
[12] Lee KW, Koh Y, Kim SB, et al. A randomized, multicenter, phase II study of cetuximab with docetaxel and cisplatin as induction chemotherapy in unresectable, locally advanced head and neck cancer[J]. Oncologist, 2015, 20(10): 1119-1120. doi:10.1634/theoncologist.2015-0208.
[13] Zenda S, Ota Y, Kiyota N, et al. A multicenter phase II trial of docetaxel, cisplatin, and cetuximab(TPEx)followed by cetuximab and concurrent radiotherapy for patients with local advanced squamous cell carcinoma of the head and neck(CSPOR HN01: ECRIPS study)[J]. Front Oncol, 2019, 9: 6. doi:10.3389/fonc.2019.00006.
[14] Haddad RI, Massarelli E, Lee JJ, et al. Weekly paclitaxel, carboplatin, cetuximab, and cetuximab, docetaxel, cisplatin, and fluorouracil, followed by local therapy in previously untreated, locally advanced head and neck squamous cell carcinoma[J]. Ann Oncol, 2019, 30(3): 471-477. doi:10.1093/annonc/mdy549.
[15] Wang HM, Lin CY, Hsieh CH, et al. Induction chemotherapy with dose-modified docetaxel, cisplatin, and 5-fluorouracil in Asian patients with borderline resectable or unresectable head and neck cancer[J]. J Formos Med Assoc, 2017, 116(3): 185-192. doi:10.1016/j.jfma.2016.03.005.
[16] Herman LC, Chen L, Garnett A, et al. Comparison of carboplatin-paclitaxel to docetaxel-cisplatin-5-flurouracil induction chemotherapy followed by concurrent chemoradiation for locally advanced head and neck cancer[J]. Oral Oncol, 2014, 50(1): 52-58. doi:10.1016/j.oraloncology.2013.08.007.
[17] Ghi MG, Paccagnella A, Ferrari D, et al. Induction TPF followed by concomitant treatment versus concomitant treatment alone in locally advanced head and neck cancer. A phase Ⅱ-Ⅲ trial[J]. Ann Oncol, 2017, 28(9): 2206-2212. doi:10.1093/annonc/mdx299.
[18] Lefebvre JL, Rolland F, Tesselaar M, et al. Phase 3 randomized trial on larynx preservation comparing sequential vs alternating chemotherapy and radiotherapy[J]. JNCI J Natl Cancer Inst, 2009, 101(3): 142-152. doi:10.1093/jnci/djn460.
[19] Sittitrai P, Reunmarkkaew D, Chaiyasate S. The role of induction chemotherapy followed by surgery in unresectable stage IVb laryngeal and hypopharyngeal cancers: a case series[J]. J Otolaryngol-Head Neck Surg, 2018, 47: 62. doi:10.1186/s40463-018-0310-y.
[20] Forastiere AA, Zhang Q, Weber RS, et al. Long-term results of RTOG 91-11: a comparison of three nonsurgical treatment strategies to preserve the larynx in patients with locally advanced larynx cancer[J]. J Clin Oncol, 2013, 31(7): 845-852. doi:10.1200/JCO.2012.43.6097.
[21] Strojan P, Vermorken JB, Beitler JJ, et al. Cumulative cisplatin dose in concurrent chemoradiotherapy for head and neck cancer: a systematic review[J]. Head Neck, 2016, 38(S1): E2151-E2158. doi:10.1002/hed.24026.
[22] Bourhis J, Sire C, Graff P, et al. Concomitant chemoradiotherapy versus acceleration of radiotherapy with or without concomitant chemotherapy in locally advanced head and neck carcinoma(GORTEC 99-02): an open-label phase 3 randomised trial[J]. Lancet Oncol, 2012, 13(2): 145-153. doi:10.1016/S1470-2045(11)70346-1.
[23] Bonner JA, Harari PM, Giralt J, et al. Radiotherapy plus cetuximab for locoregionally advanced head and neck cancer: 5-year survival data from a phase 3 randomised trial, and relation between cetuximab-induced rash and survival[J]. Lancet Oncol, 2010, 11(1): 21-28. doi:10.1016/S1470-2045(09)70311-0.
[24] Curran D, Giralt J, Harari PM, et al. Quality of life in head and neck cancer patients after treatment with high-dose radiotherapy alone or in combination with cetuximab[J]. J Clin Oncol, 2007, 25(16): 2191-2197. doi:10.1200/jco.2006.08.8005.
[25] Hesketh PJ, Bohlke K, Kris MG. Antiemetics: American society of clinical oncology clinical practice guideline update summary[J]. J Oncol Pract, 2017, 13(12): 825-830. doi:10.1200/jop.2017.026351.
[26] Roila F, Molassiotis A, Molassiotis A, et al. 2016 MASCC and ESMO guideline update for the prevention of chemotherapy-and radiotherapy-induced nausea and vomiting and of nausea and vomiting in advanced cancer patients[J]. Ann Oncol, 2016, 27(suppl 5): v119-v133. doi:10.1093/annonc/mdw270.
[27] Bonner JA, Harari PM, Giralt J, et al. Radiotherapy plus cetuximab for squamous-cell carcinoma of the head and neck[J]. N Engl J Med, 2006, 354(6): 567-578. doi:10.1056/nejmoa053422.
[28] Jonker DJ, O'Callaghan CJ, Karapetis CS, et al. Cetuximab for the treatment of colorectal cancer[J]. N Engl J Med, 2007, 357(20): 2040-2048. doi:10.1056/nejmoa071834.
[29] Magrini SM, Buglione M, Corvò R, et al. Cetuximab and radiotherapy versus cisplatin and radiotherapy for locally advanced head and neck cancer: a randomized phase II trial[J]. J Clin Oncol, 2016, 34(5): 427-435. doi:10.1200/jco.2015.63.1671.
[30] Guigay J, Tahara M, Licitra L, et al. The evolving role of taxanes in combination with cetuximab for the treatment of recurrent and/or metastatic squamous cell carcinoma of the head and neck: evidence, advantages, and future directions[J]. Front Oncol, 2019, 9: 668. doi:10.3389/fonc.2019.00668.
[31] Tao YG, Auperin A, Sire C, et al. Improved outcome by adding concurrent chemotherapy to cetuximab and radiotherapy for locally advanced head and neck carcinomas: results of the GORTEC 2007-01 phase III randomized trial[J]. J Clin Oncol, 2018, 36(31): 3084-3090. doi:10.1200/jco.2017.76.2518.
[32] Patil VM, Noronha V, Joshi A, et al. A randomized phase 3 trial comparing nimotuzumab plus cisplatin chemoradiotherapy versus cisplatin chemoradiotherapy alone in locally advanced head and neck cancer[J]. Cancer, 2019, 125(18): 3184-3197. doi:10.1002/cncr.32179.
[33] Reddy BKM, Lokesh V, Vidyasagar MS, et al. Nimotuzumab provides survival benefit to patients with inoperable advanced squamous cell carcinoma of the head and neck: a randomized, open-label, phase IIb, 5-year study in Indian patients[J]. Oral Oncol, 2014, 50(5): 498-505. doi:10.1016/j.oraloncology.2013.11.008.
[34] 彭月, 向志碧. 尼妥珠单抗在鼻咽癌治疗中的研究进展[J]. 肿瘤预防与治疗, 2020, 33(7): 619-625. doi:10.3969/j.issn.1674-0904.2020.07.013. PENG Yue, XIANG Zhibi. Research progress of nimotuzumab in the treatment of nasopharyngeal carcinoma[J]. Journal of Cancer Control and Treatment, 2020, 33(7): 619-625. doi:10.3969/j.issn.1674-0904.2020.07.013.
[35] Lu Y, Chen D, Liang J, et al. Administration of nimotuzumab combined with cisplatin plus 5-fluorouracil as induction therapy improves treatment response and tolerance in patients with locally advanced nasopharyngeal carcinoma receiving concurrent radiochemotherapy: a multicenter randomized controlled study[J]. BMC Cancer, 2019, 19(1): 1262. doi:10.1186/s12885-019-6459-6.
[36] 阮林, 林小峰, 黄素宁, 等. 头颈鳞状细胞癌靶向治疗现状及进展[J]. 广西医科大学学报, 2020, 37(5): 972-976. doi:10.16190/j.cnki.45-1211/r.2020.05.035. RUAN Lin, LIN Xiaofeng, HUANG Suning, et al. Current status and progress of targeted therapy for head and neck squamous cell carcinoma[J]. Journal of Guangxi Medical University, 2020, 37(5): 972-976. doi:10.16190/j.cnki.45-1211/r.2020.05.035.
[1] 王媚 李志海. 喉癌干细胞:克服多药耐药性的潜在治疗靶点[J]. 山东大学耳鼻喉眼学报, 2022, 36(4): 120-128.
[2] 梁旭,史丽. 慢性鼻窦炎生物靶向药物治疗的研究进展[J]. 山东大学耳鼻喉眼学报, 2022, 36(3): 30-35.
[3] 樊慧娟,张海利. HIF-1α与VEGF在中耳胆脂瘤中的研究进展[J]. 山东大学耳鼻喉眼学报, 2021, 35(5): 93-97.
[4] 范黎,黎越,徐细明. 鼻咽癌同步放化疗前后炎性指标变化及预测价值[J]. 山东大学耳鼻喉眼学报, 2020, 34(6): 36-41.
[5] 青晓艳, 徐义全李超. 甲状腺未分化癌的分子机制研究[J]. 山东大学耳鼻喉眼学报, 2020, 34(3): 26-31.
[6] 崔晓波. 诱导化疗在局部晚期下咽癌治疗中的意义[J]. 山东大学耳鼻喉眼学报, 2019, 33(4): 10-17.
[7] 陆海军,刘霁,丁晓. 鼻咽癌的综合治疗研究进展[J]. 山东大学耳鼻喉眼学报, 2019, 33(2): 26-30.
[8] 宋晓宇,宋西成. 缺氧诱导因子-1α在甲状腺癌中的调节机制[J]. 山东大学耳鼻喉眼学报, 2019, 33(2): 136-138.
[9] 吴静,刘业海. 头颈部鳞状细胞癌的靶向治疗研究进展[J]. 山东大学耳鼻喉眼学报, 2018, 32(5): 97-102.
[10] 李浩,李延忠,王岩. HIF-1α、VEGF在阻塞性睡眠呼吸暂停低通气综合征患者[J]. 山东大学耳鼻喉眼学报, 2018, 32(2): 43-47.
[11] 张彩霞,刘阳云,江文,刘庚勋,曹杭,陈琼,张纪帅. 一氧化氮对鼻咽癌CNE-2细胞株化疗增敏效应的研究[J]. 山东大学耳鼻喉眼学报, 2017, 31(5): 72-78.
[12] 张彦惠, 董频. Argonaute2蛋白及其在人类肿瘤研究中的新进展[J]. 山东大学耳鼻喉眼学报, 2017, 31(3): 95-99.
[13] 陈婷婷,郭其云,刘佳琪,刘丽庭. 探讨同期放化疗对儿童青少年鼻咽癌患者生活质量的影响[J]. 山东大学耳鼻喉眼学报, 2017, 31(2): 55-58.
[14] 董云鹏,许辉杰,高瞻,贾瑞芳,于晖,黄卫红,彭好,黄魏宁. 鼾症患者模拟打鼾与药物诱导睡眠内镜下鼾声来源部位的对比研究[J]. 山东大学耳鼻喉眼学报, 2017, 31(1): 41-44.
[15] 董频,英信江,陈歆维,邓志宏,张少强,於子卫,金斌,孙臻峰,谢晋,祝江才. 新辅助化疗方案尼妥珠单抗联合奈达铂和5-氟尿嘧啶治疗下咽鳞癌初步临床分析[J]. 山东大学耳鼻喉眼学报, 2016, 30(3): 10-14.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
[1] 张晗,黄一飞 . 抗角膜移植排斥的研究进展[J]. 山东大学耳鼻喉眼学报, 2006, 20(1): 84 -87 .
[2] 牛善利,柴茂文,李振秀 . 鼻内镜下鼻甲成形术治疗慢性肥厚性鼻炎60例[J]. 山东大学耳鼻喉眼学报, 2006, 20(1): 16 -18 .
[3] 孟庆国,卢永田,范献良 . 杀伤细胞免疫球蛋白样受体基因多态性与鼻咽癌的关联性[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 196 -199 .
[4] 马玉起,孔祥春 . 先天性双侧下唇窦道1例[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 199 -199 .
[5] 万俐佳,鲁海涛,姜义道,刘 辉,李 琴,佘腊枝 . 改良腭咽成形术治疗阻塞性睡眠呼吸暂停综合征41例[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 204 -205 .
[6] 于青青 ,王跃建 . 硬质耳内镜的临床应用进展[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 222 -224 .
[7] 吉晓滨,邓家德,臧林泉,王 磊,谢 军 . 豚鼠变应性鼻炎模型血清组胺的测定[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 228 -230 .
[8] 向登,卢永田,孙焕吉 . 鼻内镜下修补脑脊液鼻漏19例并文献复习[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 234 -236 .
[9] 邱恩惠,李志春,方文旭 . 嗅觉障碍的中西医治疗[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 253 -257 .
[10] 殷国华,钟 笑 . 激光减容术治疗舌扁桃体肥大的远期疗效[J]. 山东大学耳鼻喉眼学报, 2008, 22(3): 280 -282 .