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局部中晚期直肠癌术前同期加量调强放疗前瞻性临床研究的初步结果 被引量:18

Preliminary results of the prospective clinical trial of preoperative concomitant boost intensity-modulated radiotherapy in locally advanced rectal cancer
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摘要 目的 评估对Ⅱ~Ⅲ期可手术切除的直肠癌患者行术前同期加量调强放疗(SIB-IMRT)并同步口服卡培他滨化疗的可行性、安全性及近期疗效.方法 2012年8月至2013年5月间共13例Ⅱ~Ⅲ期可手术切除的直肠癌患者接受术前调强放疗,给予肿瘤原发病灶及转移淋巴结56.25 Gy/25次(2.25 Gy/次),高危复发区域和区域淋巴引流区50 Gy/25次(2.0 Gy/次),同时口服卡培他滨同步化疗(825 mg/m2,2次/d,5 d/周×5周).放化疗结束后4~8周患者接受全直肠系膜切除术(TME).研究主要终点为病理完全缓解率(ypCR率)、TNM降期率、急性期不良反应及术后并发症发生率,次要终点为保肛手术率.结果 所有患者顺利完成术前同步放化疗并接受TME,TNM降期率为10/13,其中T降期率为9/13,N降期率为4/6,ypCR率为3/13.放化疗期间不良反应全部为1~2级,包括2级骨髓抑制5例,1级骨髓抑制4例,1级腹泻2例.1例患者术后出现膀胱瘘.保肛手术率为10/13.结论 局部中晚期直肠癌患者行SIB-IMRT并口服卡培他滨的术前同步放化疗方案的初步结果表明其疗效好、安全可行、不良反应发生率低. Objective To evaluate the feasibility,safety,and short-term efficacy of preoperative capecitabine and simultaneous integrated boost(SIB)intensity-modulated radiotherapy(IMRT)in patients with locally advanced rectal cancer.Methods Between August 2012 and May 2013,a total of 13 patients with resectable stage Ⅱ or Ⅲ rectal cancer received capecitabine(825 mg/m2 P.O,twice a day,5 d/week for 5 weeks)and SIB-IMRT delivering 56.25 Gy(2.25 Gy/fraction)to the gross tumor while simultaneously delivering 50 Gy(2.0 Gy/fraction)to the regional lymph nodes and areas at risk for harboring microscopic disease.Total mesorectal excision was scheduled 4 to 8 weeks after the completion of chemoradiation.The primary endpoints included pathological complete response rate(ypCR),tumor downstaging,toxicity and postoperative complications.The secondary endpoint included the rate of sphincter-sparing surgery.Results All patients completed chemoradiation with strict compliance to the protocol schedule and then went on to surgical resection.Three patients had no residual tumor in the surgical specimen.Downstaging of the primary tumor and lymph nodes was observed in 9 and 4 patients,respectively.Grade 1 or 2 toxicities included leucopenia,thrombocytopenia and diarrhea.One patient developed vesical fistula after surgery.Ten patients underwent sphincter-sparing procedures.Conclusions Preoperative chemoradiation with capecitabine and SIB-IMRT can be safe and well tolerated for patients with locally advanced rectal cancer and the short term outcomes could be promising.
出处 《中华放射医学与防护杂志》 CAS CSCD 北大核心 2013年第5期512-515,共4页 Chinese Journal of Radiological Medicine and Protection
关键词 直肠癌 调强放疗 卡培他滨 Rectal cancer Intensity-modulated radiation therapy Capecitabine
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  • 1Wiltshire KL, Ward IG, Swallow C, et al. Preoperative radiation with concurrent chemotherapy for resectable rectal cancer: effect of dose escalation on pathologic complete response, local recurrence-free survival, disease-free survival, and overall survival. Int J Radiat Oncol Biol Phys, 2006, 64 (3) :709-716. 被引量:1
  • 2Mohiuddin M, Regine WF, John W J, et al. Preoperative chemoradiation in fixed distal rectal cancer: dose time factors for pathological complete response. Int J Radiat Oncol Biol Phys, 2000, 46 (4) :883-888. 被引量:1
  • 3Capirci C, Valentini V, Cionini L, et al. Prognostic value of pathologic complete response after neoadjuvant therapy in locally advanced rectal cancer: long-term analysis of 566 pCR patients. Int J Radiat Oncol Biol Phys, 2008, 72 (1) :99-107. 被引量:1
  • 4Zorcolo L, Rosman AS, Restivo A, et al. Complete pathologic response after combined modality treatment for rectal cancer and long-term survival: a meta-analysis. Ann Surg Oncol, 2012, 19 (9) : 2822-2832. 被引量:1
  • 5Rodel C, Liersch T, Becker H, et al. Preoperative chemoradiotherapy and postoperative chemotherapy with fluorouracil and oxaliplatin versus fluorouracil alone in locally advanced rectal cancer: initial results of the German CAO/ARO/ AIO-04 randomised phase 3 trial. Lancet Oneol, 2012, 13 (7) : 679-687. 被引量:1
  • 6Asehele C, Cionini L, Lonardi S, et al. Primary tumor response to preoperative chemoradiation with or without oxallplatin in locally advanced rectal cancer: pathologic results of the STAR-01 randomized phase III trial. J Clin Oneol, 2011,29 (20) :2773- 2780. 被引量:1
  • 7Gorard JP, Azria D, Geurgou-Bourgade S, et al. Comparison of two neoadjuvant chemoradlotherapy regimens for locally advanced reetal cancer: results of the phase III trial ACCORD 12/0405- Prodige 2. J Clin Oneol, 2010, 28 (10): 1638-1644. 被引量:1
  • 8Hofheinz RD, Wenz F, Post S, et al. Chemoradiotherapy with eapeeitabine versus fluorouraeil for locally advanced reetal cancer: a randomised, muhieentre, non-inferiority, phase Ⅲ trial. Lancet Oneol, 2012, 13 (6):579-588. 被引量:1
  • 9Mok H, Crane CH, Palmer MB, et al. Intensity modulated radiation therapy (IMRT)': differences in target volumes and improvement in clinically relevant doses to small bowel in rectal carcinoma. Radiat Oncol, 2011, 6: 63. 被引量:1
  • 10Samuelian JM, Callister MD, Ashman JB, et al. Reduced acute bowel toxicity in patients treated with intensity-modulated radiotherapy for rectal cancer. Int J Radiat Oncol Biol Phys, 2012, 82 (5) :1981-1987. 被引量:1

同被引文献164

  • 1綦晓龙,傅仲学,邓靖宇.血管内皮生长因子C及其受体3在直肠癌组织中的表达及其临床意义[J].中华胃肠外科杂志,2004,7(5):407-410. 被引量:7
  • 2AndrewsDW ScottCB SperdutoPW FlandersAE GasparLE SchellMC Werner-WasikM DemasW RyuJ BaharyJP SouhamiL RotmanM MehtaMP CurranWJJr.Whole brain radiation therapy with or without stereotactic radiosurgery boost for patients with one to three brain metastases: phase Ⅲ resuIts of the RTOG 9508 randomised trial[J].中国神经肿瘤杂志,2004,2(3):192-192. 被引量:214
  • 3Tveit KM, Wiig JN, Olsen DR, Storaas A, Poulsen JP, Giercksky KE. Combined modality treatment including intraoperative radiotherapy in locally ad- vanced and recurrent rectal cancer. Radiothcr Oncol 1997; 44:277-282 [PM I D: 9380828 DOI: 10.1016/ S0167-8140(97)00070-4]. 被引量:1
  • 4Francois Y, Nemoz CJ, Baulieux J, Vignal J, Grand- jean JP, Partensky C, Souquet JC, Adeleine P, Ge- rard JP. Influence of the interval between preopera- tive radiation therapy and surgery on downstaging and on the rate of sphincter-sparing surgery for rectal cancer: the Lyon R90-01 randomized trial. J Clin Onco11999; 17:2396 [PMID: 10561302]. 被引量:1
  • 5Tulchinsky H, Shmueli E, Figer A, Klausner JM, Rabau M. An interval & gt; 7 weeks between neo- adjuvant therapy and surgery improves pathologic complete response and disease-free survival in pa- tients with locally advanced rectal cancer. Ann SuG, Oncol 2008; 15:2661-2667 IPM1D: 18389322 DOI: 10.1245 / s10434-008 -9892-31]. 被引量:1
  • 6Wolthuis AM, Penninckx F, Haustermans K, De Hertogh G, Fieuws S, Van Cutsem E, D'Hoore A. Impact of interval between neoadjuvant chemo- radiotherapy and TME for locally advanced rectal cancer on pathologic response and oncologic out- come. Ann Surg Oncol 2012; 19:2833-2841 [PMID: 22451236 DOI: 10.1245/s10434-012-2327-1]. 被引量:1
  • 7金晶,任骅,李哗雄,王淑莲.王维虎,宋永文,刘跃平,房辉,刘新帆,余子豪.Ⅱ/Ⅲ期直肠癌术前同步放化疗加根治术的毒性和疗效分析.第七届江珠江区域放射肿瘤学学术大会,2012. 被引量:1
  • 8Greene FL, Page DL, Fleming ID, Fritz A, Balch CM, Hailer DG, Morrow M, eds. American Joint Com- mittee on Cancer: AJCC Cancer Staging Manual. 6th ed, New York, NY, USA: Springer, 2002:157-164. 被引量:1
  • 9孙燕,万德森,李进,蔡三军,徐瑞华.NCCN直肠癌临床实践指南(中国版).第1版.2010:REC-3. 被引量:1
  • 10Saner R, Becker H, Hohenberger W, ROdel C, Witte- kind C, Fietkau R, Martus P, Tschmelitsch J, Hager E, Hess CF, Karstens JH, Liersch T, Schmidberger H, Raab R. Preoperative versus postoperative chemo- radiotherapy for rectal cancer. N Engl J Med 2004; 351:1731-1740 [PMID: 15496622 DOI: 10.1056/NEJ- Moa040694]. 被引量:1

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