Different exposure duration of adjuvant icotinib in stage II-IIIA non-small cell lung cancer patients with positive EGFR mutation (ICOMPARE study): A randomized, open-label phase 2 study.

Author:

Lyu Chao1,Wang Rui2,Li Shaolei3,Yan Shi4,Wang Yuzhao3,Chen Jinfeng3,Wang Liang3,Liu Yinan3,Guo Zhanlin5,Wang Jia3,Pei Yuquan3,Yu Lei6,Wu Nan4,Chen Jun7,Liu Yanheng8,Li Shanqing9,Han Bing10,Ding Lieming11,Mao Li12,Yang Yue1

Affiliation:

1. Thoracic Surgery II, Peking University Cancer Hospital, Beijing, China;

2. The Fourth Hospital of Hebei Medical University, Shijiazhuang, China;

3. Beijing Cancer Hospital, Beijing, China;

4. Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Thoracic Surgery II, Peking University Cancer Hospital & Institute, Beijing, China;

5. THE Affilated Hospital of Inner Mongolia Medical University, Hohhot, China;

6. Department of Thoracic Surgery, Beijing Tongren Hospital, Capital Medical University, Beijing City, China;

7. Tianjing Medical University General Hospital, Tianjin, China;

8. Inner Mongolia People's Hospital, Hohhot, China;

9. Peking Union Medical College Hospital, Beijing, China;

10. PLA Pocket Force Characteristic Medical Center, Beijing, China;

11. Betta Pharmaceuticals Co., Ltd., Hangzhou, China;

12. Betta Pharmaceuticals, Hangzhou, China;

Abstract

8521 Background: EGFR-TKI has been widely used in the treatment for advanced non-small cell lung cancer (NSCLC). Previous studies, such as the EVIDENCE study and the ADAURA study, have confirmed that patients with EGFR-mutated NSCLC could benefit from adjuvant EGFR-TKI treatment. However, the optimal duration time of adjuvant EGFR-TKIs has not been clearly defined. Methods: In this multicenter, randomized, phase 2 trial, eligible patients with II-IIIA stage EGFR mutation-positive NSCLC after R0 resection were randomized in 1:1 to receive adjuvant icotinib for 1 year (group A) or 2 years (group B). The primary endpoint was disease-free survival (DFS). Results: Between September 2013, and September 2018, 109 patients from 8 centers were enrolled in this study, among whom 55 were randomized to group A and 54 to B. As of August 24, 2020 (data cutoff), the median follow-up was 44.1 months (95%CI 37.1-49.9), 31 (56%) of 55 patients in the 1-year group and 25 (46%) of 54 patients in the 2-year group had DFS events. The median DFS was 48.92 months (95%CI 33.15, 70.11) in 2-year group and 32.89 month (95%CI 26.61, 44.78) in 1-year group, respectively. 2-year icotinib significantly prolonged DFS (HR 0.521, 95%CI 0.278, 0.976; p = 0.039). OS events were observed in 20 patients, the OS was not mature yet. Icotinib was re-given for 32 patients with disease recurrence or metastasis as first-line treatment, objective response occurred in 66.7% of 30 patients with measurable disease. Treatment-related adverse events were recorded in 41 of 55 (75%) patients in 1-year group and 36 of 54 (67%) patients in 2-year group, and grade 3 or 4 treatment-related adverse events occurred in 4 (7%) of 55 patients in the 1-year group versus 3 (6%) of 54 in the 2-year group, respectively. No treatment-related deaths or interstitial lung disease were reported. Conclusions: 2-year adjuvant treatment with icotinib resulted in a significantly lower risk of recurrence than 1-year adjuvant icotinib in patients with stage II-IIIA NSCLC positive EGFR mutations and was not associated with increased toxic effects. Clinical trial information: NCT01929200.

Funder

Betta pharmaceuticals

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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