Chinese Medical Sciences Journal ›› 2019, Vol. 34 ›› Issue (4): 292-296.doi: 10.24920/003487
• Case Report • Previous Articles Next Articles
Zhang Ling1, Sun Lei1, Mu Xiaoyan2, Ji Youxin2, *()
Received:
2018-07-05
Accepted:
2018-12-13
Published:
2019-12-31
Online:
2019-11-12
Contact:
Ji Youxin
E-mail:123456789ji@gmail.com
Zhang Ling, Sun Lei, Mu Xiaoyan, Ji Youxin. Bevacizumab Combined with Icotinib Overcomes Osimertinib Resistance in a Patient of Non-Small Cell Lung Cancer[J].Chinese Medical Sciences Journal, 2019, 34(4): 292-296.
Add to citation manager EndNote|Reference Manager|ProCite|BibTeX|RefWorks
Figure 1.
CT and pathological images showing the therapeutic responses of a 61-year-old woman with left pulmonary adenocarcinoma. (A) A 10.1 cm X 6.1cm mass in the superior lobe of left lung, with multiple metastatic nodules in bilateral lungs. (B) Microscopically nests of adenocarcinoma cells in the fibrous connective tissue arranged in an alveolar pattern (arrow) demonstrate pulmonary adenocarcinoma (HE, X10), EGFR 19 del mutation positive. (C) After 2.5 months treatment of icotinib, the primary tumor decreased to 3.2 cm X 2.2 cm, partial response (PR). (D) After 6 months remission, the primary tumor enlarged to 3.1cm X 3.0cm. (E) A new soft-tissue nodule found in the inferior lobe of left lung. (F) Biopsy of the new nodule revealed intrapulmonary metastasis pathologically (HE, X40), disease progressed. EGFR T790M mutation was found. After 2 months of osimertinib treatment, the primary tumor (G) and the metastatic lesion (H) enlarged. After 2 months of icotinib re-challenged treatment, the primary tumor (I) and the metastatic lesion (J) enlarged continuously; re-biopsy for the lesion in left inferior lobe showed EGFR 19 del mutation positive, but EGFR T790M mutation was lost. After 2-cycle of icotinib plus bevacizumab therapy, the primary tumor (K) and intrapulmonary metastatic lesion (L) shrank significantly."
1. | Ou SI, Cui J, Schrock AB , et al. Emergence of novel and dominant acquired EGFR solvent-front mutations at Gly796 (G796S/R) together with C797S/R and L792F/H mutations in one EGFR (L858R/T790M) NSCLC patient who progressed on osimertinib. Lung Cancer 2017; 108(12):228-31. doi: 10.1016/j.lungcan.2017.04.003. |
2. | Choo JR, Tan CS, Soo RA . Treatment of EGFR T790M-positive non-small cell lung cancer. Targeted oncology 2018; 13(2):141-56. doi: 10.1007/s11523-018-0554-5. |
3. | Wang S, Song Y, Liu D . EAI045: the fourth-generation EGFR inhibitor overcoming T790M and C797S resistance. Cancer Letters 2017; 385:51-4. doi: 10.1016/j.canlet.2016.11.008. |
4. | Uchibori K, Inase N, Araki M , et al. Brigatinib combined with anti-EGFR antibody overcomes osimertinib resistance in EGFR-mutated non-small-cell lung cancer. Nature Communi 2017; 8:14768. doi: 10.1038/ncomms14768. |
5. | Suda K, Onozato R, Yatabe Y , et al. EGFR T790M mutation: a double role in lung cancer cell survival? J Thorac Oncol 2009; 4(1):1-4. doi: 10.1097/JTO.0b013e3181913c9f. |
6. | Mok TS, Wu YL, Thongprasert S , et al. Gefitinib or carboplatin-paclitaxel in pulmonary adenocarcinoma. N Engl J Med 2009; 361(10):947-57. doi: 10.1056/NEJMoa0810699. |
7. | Zhou C, Wu YL, Chen G , et al. BEYOND: A randomized, double-blind, placebo-controlled, multicenter, phase III study of first-line Carboplatin/Paclitaxel plus Bevacizumab or placebo in Chinese patients with advanced or recurrent nonsquamous non-small-cell lung cancer. J Clin Oncol 2015; 33(19):2197-204. doi: 10.1200/JCO.2014.59.4424. |
8. | Goss G, Tsai CM, Shepherd FA , et al. Osimertinib for pretreated EGFR Thr790Met-positive advanced non-small-cell lung cancer (AURA2): a multicentre, open-label, single-arm, phase 2 study. Lancet Oncol 2016; 17(12):1643-52. doi: 10.1016/S1470-2045(16)30508-3. |
9. | Ercan D, Choi HG, Yun CH , et al. EGFR mutations and resistance to irreversible pyrimidine-based EGFR inhibitors. Clin Cancer Res 2015; 21(17):3913-23. doi: 10.1158/1078-0432.CCR-14-2789. |
10. | Wang S, Song Y, Yan F , et al. Mechanisms of resistance to third-generation EGFR tyrosine kinase inhibitors. Fronti Med 2016; 10(4):383-8. doi: 10.1007/s11684-016-0488-1. |
11. | Russo A, Franchina T, Ricciardi GRR , et al. Third generation EGFR TKIs in EGFR-mutated NSCLC: Where are we now and where are we going. Crit Rev Oncol Hematol 2017; 117:38-47. doi: 10.1016/j.critrevonc.2017.07.003. |
12. | Nie K, Jiang H, Zhang C , et al. Mutational profiling of non-small-cell lung cancer resistant to osimertinib using next-generation sequencing in Chinese patients. Biomed Res Int 2018; 2018:9010353. doi: 10.1155/2018/9010353. |
13. | Tan CS, Cho BC, Soo RA . Next-generation epidermal growth factor receptor tyrosine kinase inhibitors in epidermal growth factor receptor-mutant non-small cell lung cancer. Lung Cancer 2016; 93:59-68. doi: 10.1016/j.lungcan.2016.01.003. |
14. | Ortiz-Cuaran S, Scheffler M, Plenker D , et al. Heterogeneous mechanisms of primary and acquired resistance to third-generation EGFR inhibitors. Clin Ca Res 2016; 22(19):4837-47. doi: 10.1158/1078-0432.CCR-15-1915. |
15. | Ding T, Zhou F, Chen X , et al. Continuation of gefitinib plus chemotherapy prolongs progression-free survival in advanced non-small cell lung cancer patients who get acquired resistance to gefitinib without T790M mutations. J Thorac Dis 2017; 9(9):2923-34. doi: 10.21037/jtd.2017.07.107. |
16. | Jia Y, Yun CH, Park E , et al. Overcoming EGFR(T790M) and EGFR(C797S) resistance with mutant-selective allosteric inhibitors. Nature 2016; 534(7605):129-32. doi: 10.1038/nature17960. |
17. | Kanda S, Horinouchi H, Fujiwara Y , et al. Cytotoxic chemotherapy may overcome the development of acquired resistance to epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) therapy. Lung cancer 2015; 89(3):287-93. doi: 10.1016/j.lungcan.2015.06.016. |
18. | Bell DW, Brannigan BW, Matsuo K , et al. Increased prevalence of EGFR-mutant lung cancer in women and in East Asian populations: analysis of estrogen-related polymorphisms. Clin Ca Res 2008; 14(13):4079-84. doi: 10.1158/1078-0432.CCR-07-5030. |
19. | Bae NC, Chae MH, Lee MH , et al. EGFR, ERBB2, and KRAS mutations in Korean non-small cell lung cancer patients. Cancer Genet Cytogenet 2007; 173(2):107-13. doi: 10.1016/j.cancergencyto.2006.10.007 |
20. | Soejima K, Yasuda H, Hirano T . Osimertinib for EGFR T790M mutation-positive non-small cell lung cancer. Expert Rev Clin Pharmacol 2017; 10(1):31-8. doi: 10.1080/17512433.2017.1265446. |
21. | Hidaka N, Iwama E, Kubo N , et al. Most T790M mutations are present on the same EGFR allele as activating mutations in patients with non-small cell lung cancer. Lung cancer 2017; 108:75-82. doi: 10.1016/j.lungcan.2017.02.019. |
22. | Niederst MJ, Hu H, Mulvey HE , et al. The allelic context of the C797S mutation acquired upon treatment with third-generation EGFR inhibitors impacts sensitivity to subsequent treatment strategies. Clin Cancer Res 2015; 21(17):3924-33. doi: 10.1158/1078-0432.CCR-15-0560. |
23. | Jakobsen KR, Demuth C, Madsen AT , et al. MET amplification and epithelial-to-mesenchymal transition exist as parallel resistance mechanisms in erlotinib-resistant, EGFR-mutated, NSCLC HCC827 cells. Oncogenesis 2017; 6(4):e307. doi: 10.1038/oncsis.2017.17. |
24. | Ham JS, Kim S, Kim HK , et al. Two cases of small cell lung cancer transformation from EGFR mutant adenocarcinoma during AZD9291 treatment. J Thorac Oncol 2016; 11(1):e1-4. doi: 10.1016/j.jtho.2015.09.013. |
25. | Lim SM, Syn NL, Cho BC , et al. Acquired resistance to EGFR targeted therapy in non-small cell lung cancer: Mechanisms and therapeutic strategies. Cancer Treat Rev 2018; 65:1-10. doi: 10.1016/j.ctrv.2018.02.006. |
[1] | Bao Yi, Mo Juanfen, Wu Jiayuan, Cao Chenxi. Expression of PD1 and BTLA on the CD8+ T Cell and γδT Cell Subsets in Peripheral Blood of Non-Small Cell Lung Cancer Patients [J]. Chinese Medical Sciences Journal, 2019, 34(4): 248-255. |
[2] | Zhao Zhimei, Liu Shichao, Xu Xiajuan, Zhang Zhongfa, Nie Keke, Ji Youxin. Treatment of Skin Reaction Induced by Nivolumab Combined with Radiotherapy in Non-small Cell Lung Cancer: A Case Report [J]. Chinese Medical Sciences Journal, 2018, 33(3): 183-187. |
[3] | Ke-ke Nie, Chuan-xin Geng, Ling Zhang, Shi-chao Liu, Zhong-fa Zhang, Rong Wang, Xiao Zou, You-xin Ji. Clinical Observation of Bevacizumab Combined with S-1 in the Treatment of Pretreated Advanced Esophageal Carcinoma [J]. Chinese Medical Sciences Journal, 2016, 31(4): 221-227. |
[4] | Yan-yan Chen, Liu-bo Wang, Hui-li Zhu, Xiang-yang Li, Yan-ping Zhu, Yu-lei Yin, Fan-zhen Lü, Zi-li Wang, Jie-ming Qu. Relationship Between Programmed Death-ligand 1 and Clinicopathological Characteristics in Non-small Cell Lung Cancer Patients [J]. Chinese Medical Sciences Journal, 2013, 28(3): 147-151. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||
|
Supervised by National Health & Family Plan Commission of PRC
9 Dongdan Santiao, Dongcheng district, Beijing, 100730 China
Tel: 86-10-65105897 Fax:86-10-65133074
E-mail: cmsj@cams.cn www.cmsj.cams.cn
Copyright © 2018 Chinese Academy of Medical Sciences
All right reserved.
京公安备110402430088 京ICP备06002729号-1