[an error occurred while processing this directive] | [an error occurred while processing this directive]
IMRT combined with Iressa for patients with locally advanced non-small cell lung cancer unsuitable for surgery or concurrent chemoradiotherapy:the preliminary results of a phase Ⅱ clinical trial
Fu Zhixue, Yang Xu, Wang Wenqing, Deng Lei, Zhang Tao, Bi Nan, Wang Xiaozhen, Chen Dongfu, Zhou Zongmei, Wang Luhua, Liang Jun
Department of Radiation Oncology,National Cancer Center/Cancer Hospital,Chinese Academy of Medical Sciences and Peking Union Medical College,Beijing 10021,China
AbstractObjective To observe the objective response rate,survival and safety of radiotherapy combined with Iressa for patients with locally advanced non-small cell lung cancer (NSCLC) unsuitable for surgery or concurrent chemoradiotherapy. Methods The patients with locally advanced NSCLC unsuitable for surgery or concurrent chemoradiotherapy were recruited and received thoracic intensity-modulated radiotherapy (IMRT) combined with Iressa 250 mg daily. Results A total of 30 patients were enrolled between July 2014 and March 2017. Twenty-nine patients were analyzed. At 1 month after radiotherapy,the complete response (CR) was 0,partial response (PR) was 21(72%),stable disease (SD) was 6(21%),progressive disease (PD) was 2(7%),the disease control rate (CR+PR+SD) was 93%,and the objective response rate was 72%. The median follow-up time was 25 months. Fourteen (48%) patients died,and 15(52%) survived. Twenty-three (79%) patients obtained PD including local progression in 18(62%) and distant metastasis in 14(48%). The median survival time (MST) was 26 months and the median PFS was 11 months. The 1-year OS and PFS were 79% and 44%,and the 2-year OS and PFS were 55% and 18%. Univariate analysis demonstrated that smoking history and disease stage were influencing factors for OS (P=0.035,0.031). Moreover,disease stage,the primary tumor diameter,the volume of GTV and PTV were influencing factors for PFS (P=0.000,0.016,0.039,0.030). Multivariable analysis revealed that disease stage and the volume of PTV were independent prognostic factors for PFS (P=0.000,0.012).Two patients (7%) developed grade 3 acute adverse events and 7(24%) experienced grade 2 acute irradiation pneumonitis. Conclusions For patients with locally advanced NSCLC unsuitable for surgery or concurrent chemoradiotherapy,IMRT combined with Iressa yields high objective response rate and well tolerance. The long-term clinical efficacy remains to be validated.
Fund:Chinese Geriatric Oncology Society (CGOS-02-2014-1-1-01500)
Corresponding Authors:
Jun Liang,Email:liang23400@63.com
Cite this article:
Fu Zhixue,Yang Xu,Wang Wenqing et al. IMRT combined with Iressa for patients with locally advanced non-small cell lung cancer unsuitable for surgery or concurrent chemoradiotherapy:the preliminary results of a phase Ⅱ clinical trial[J]. Chinese Journal of Radiation Oncology, 2018, 27(6): 559-563.
Fu Zhixue,Yang Xu,Wang Wenqing et al. IMRT combined with Iressa for patients with locally advanced non-small cell lung cancer unsuitable for surgery or concurrent chemoradiotherapy:the preliminary results of a phase Ⅱ clinical trial[J]. Chinese Journal of Radiation Oncology, 2018, 27(6): 559-563.
[1] American Cancer Society. Cancer facts and figures[M].Atlanta:American Cancer Society,2007. [2] Schaake-Koning C,van den Bogaert W,Dalesio O,et al. Effects of concomitant cisplatin and radiotherapy on inoperable non-small-cell lung cancer[J].N Engl J Med,1992,326(8):524-530. [3] Furuse K,Fukuoka M,Kawahara M,et al. Phase Ⅲ study of concurrent versus sequential thoracic radiotherapy in combination with mitomycin,vindesine,and cisplatin in unresectable stage Ⅲ non-small-cell lung cancer[J].J Clin Oncol,1999,17(9):2692-2699. [4] Curran Jr WJ,Paulus R,Langer CJ,et al. Sequential vs. Concurrent chemoradia-tion for stage Ⅲ non-small cell lung cancer:randomized phase Ⅲ trial RTOG 9410[J].J Natl Cancer Inst 2011,103(19):1452-1460. [5] Zatloukal P,Petruzelka L,Zemanova M,et al. Concurrent versus sequential chemorad-iotherapy with cisplatin and vinorelbine in locally advanced non-small cell lung cancer:a randomized study. Lung Cancer[J].2004,46(1):87-98. [6] Huber RM,FlentjeM,SchmidtM,etal:Simultaneous chemoradiotherapy compared with radiotherapy alone after induction chemotherapy in inoperable stage ⅢA or ⅢB non small-cell lung cancer:Study CTRT99/97by the Bronchial Carcinoma Therapy Group[J].J Clin Oncol, 2006,24(27):4397-4404. [7] Clamon G,Herndon J,Cooper R,et al. Radiosensitization with carboplatin for patients with unresectable stage Ⅲ non-small-cell lung cancer:a phase Ⅲ trial of the Cancer and Leukemia Group B and the Eastern Cooperative Oncology Group[J].J Clin Oncol,1999,17(1):4-11. [8] Belderbos J,Uitterhoeve L,van Zandwijk N,et al. Randomised trial of sequential versus concurrent chemo-radiotherapy in patients with inoperable non-small cell lung cancer (EORTC 08972-22973)[J].Eur J Cancer,2007,43(1):114-121. [9] Groen HJ,van der Leest AH,Fokkema E,et al. Continuously infused carboplatin used as radiosensitizer in locally unresectable non-small-cell lung cancer:A multicenter phase Ⅲ study[J].Ann Oncol,2004,15(1):427-432. [10] Fournel P,Robinet G,Thomas P,et al. Randomized phase Ⅲ trial of sequential chemoradiotherapy compared with concurrent chemoradiotherapy in locally advanced non-small-cell lung cancer:groupe Lyon-Saint-Etienne d′Oncologie Thoracique-Groupe Francais de Pneumo-Cancerologie NPC 95-01 Study[J].J Clin Oncol,2005,23(25):5910-5917. [11] Gervais R,Ducolone A,Lechevalier T,et al. Conventional radiation (RT) with daily carboplatin (Cb) compared to RT alone after induction chemotherapy (ICT)[vinorelbine (Vr)-cisplatine (P)]:final results of a randomized phase Ⅲ trial in stage Ⅲ unresectable non small cell lung (NSCLC) cancer. Study CRG/BMS/NPC/96 of the French Lung Cancer Study Group FNCLCC and IFCT[J].J Clin Oncol,2005,23:7016. [12] Ready N,Janne PA,Bogart J,et al. Chemoradiotherapy andgefitinib in stage Ⅲ non-small cell lung cancer withepidermal growth factor receptor and KRAS mutationanalysis:Cancer and leukemia group B (CALEB)30106,aCALGB-stratified phase Ⅱ trial[J].J Thorac Oncol,2010,5(9):1382-1390. [13] Lilenbaum R,Samuels M,Wang X,et al. A phaseⅡstudy of induction chemotherapy followed by thoracic radiotherapy and erlotinib in poor-risk stage Ⅲ non-small-cell lung cancer:results of CALGB 30605(Alliance)/RTOG 0972(NRG)[J].J Thorac Oncol,2015,10(1):143-147. [14] Shinji A,Masaaki K,Akira Y,et al. Thoracic radiotherapy with or without daily low-dose carboplatin in elderly patients with non-small cell lung cancer:a randomized controlled,phase 3 trial by the Japan Clinical Oncology Group (JCOG 0301)[J].Lancet Oncol,2012,13(7):671-678. [15] Martínez,Maite Martínez,Mikel rico,et al. Feasibility,tolerability,and effcacy of the concurrent addition of erlotinib to thoracic radiotherapy in locally advanced unresectable non-small-cell lung cancer:a Phase Ⅱ trial[J].Onco Targets and Therapy,2016:9:1057-1066. [16] Ciardiello F,Tortora G.EGFR antagonists in cancer treatment[J].N Engl J Med,2008,358(11):1160-1174. [17] Dacic S,Flanagan M,Cieply K,et al. Significance of EGFR protein expression and gene amplification in non-small cell lung carcinoma[J].Am J Clin Pathol,2006,125(6):860-865. [18] Ang KK,Bonner JA,Curran WJ,et al. The expanding role of EGFR-targeted therapies in NSCLC and head and neck cancer[M].NY:Skillman,American Academy of CME,2006. [19] Meert AP,Martin B,Delmotte P,Berghmans T,et al. The role of EGF-R expression on patient survival in lung cancer:a review with meta-analysis[J]. Eur Respir J,2002,20(4):75-81. [20] Hongqing zhuang,Zhiyong Yuan. Radiation pneumonitis in patients with non-small-cell lung cancer treated with erlotinib concurrent with thoracic radiotherapy[J].J Thorac Oncol,2014,9(6):882-885. [21] Ren S,Li Y,Li W,et al. Fatal asymmetric interstitial lung disease after erlotinib for lung cancer[J].Respiration,2012,84(5):431-435. [22] Tsubata Y,Hamada A,Sutani A,et al. Erlotinib-induced acute interstitial lung disease associated with extreme elevation of the plasma concentration in an elderly non-small-cell lung cancer patient[J].J Cancer Res Ther,2012,8(1):154-156. [23] Nanda A,Dias-Santagata DC,Stubbs H,et al. Unusual tumor response and toxicity from radiation and concurrent erlotinib for non-small-cell lung cancer[J].Clin Lung Cancer,2008,9(5):285-287. [24] Chang CC,Chi KH,Kao SJ,et al. Upfront geftinib/erlotinib treatment followed by concomitant radiotherapy for advanced lung cancer:a mono-institutional experience[J]. Lung Cancer,2011,73(2):189-194. [25] Niho S,Ohe Y,Ishikura S,et al. Induction chemotherapy followed by gefitinib and concurrent thoracic radiotherapy for unresectable locally advanced adenocarcinoma of the lung:a multicenter feasibility study (JCOG 0402)[J].Ann Oncol,2012,23(9):2253-2258. [26] Mok TS,Wu YL,Thongprasert S,et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma[J].N Engl J Med,2009,361(10):947-957.