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Clinical Trial
. 2023 Aug;8(4):101565.
doi: 10.1016/j.esmoop.2023.101565. Epub 2023 Jun 20.

Randomized phase II adjuvant trial to compare two treatment durations of icotinib (2 years versus 1 year) for stage II-IIIA EGFR-positive lung adenocarcinoma patients (ICOMPARE study)

Affiliations
Clinical Trial

Randomized phase II adjuvant trial to compare two treatment durations of icotinib (2 years versus 1 year) for stage II-IIIA EGFR-positive lung adenocarcinoma patients (ICOMPARE study)

C Lv et al. ESMO Open. 2023 Aug.

Abstract

Background: Despite the prolonged median disease-free survival (DFS) by adjuvant targeted therapy in non-small-cell lung cancer patients with epidermal growth factor receptor (EGFR) mutations, the relationship between the treatment duration and the survival benefits in patients remains unknown.

Patients and methods: In this multicenter, randomized, open-label, phase II trial, eligible patients aged 18-75 years with EGFR-mutant, stage II-IIIA lung adenocarcinoma and who had not received adjuvant chemotherapy after complete tumor resection were enrolled from eight centers in China. Patients were randomly assigned (1 : 1) to receive either 1-year or 2-year icotinib (125 mg thrice daily). The primary endpoint was DFS assessed by investigator. The secondary endpoints were overall survival (OS) and safety. This study was registered at ClinicalTrials.gov (NCT01929200).

Results: Between September 2013 and October 2018, 109 patients were enrolled (1-year group, n = 55; 2-year group, n = 54). Median DFS was 48.9 months [95% confidence interval (CI) 33.1-70.1 months] in the 2-year group and 32.9 months (95% CI 26.6-44.8 months) in the 1-year group [hazard ratio (HR) 0.51; 95% CI 0.28-0.94; P = 0.0290]. Median OS for patients was 75.8 months [95% CI 64.4 months-not evaluable (NE)] in the 2-year group and NE (95% CI 66.3 months-NE) in the 1-year group (HR 0.34; 95% CI 0.13-0.95; P = 0.0317). Treatment-related adverse events (TRAEs) were observed in 41 of 55 (75%) patients in the 1-year group and in 36 of 54 (67%) patients in the 2-year group. Grade 3-4 TRAEs occurred in 4 of 55 (7%) patients in the 1-year group and in 3 of 54 (6%) patients in the 2-year group. No treatment-related deaths or interstitial lung disease was reported.

Conclusions: Two-year adjuvant icotinib was shown to significantly improve DFS and provide an OS benefit in EGFR-mutant, stage II-IIIA lung adenocarcinoma patients compared with 1-year treatment in this exploratory phase II study.

Keywords: EGFR mutations; adjuvant targeted therapy; disease-free survival; icotinib; non-small-cell lung cancer.

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Figures

Figure 1
Figure 1
Trial diagram. EGFR, epidermal growth factor receptor.
Figure 2
Figure 2
Analysis of survival for the intention-to-treat population. (A) Kaplan–Meier plots of DFS. (B) Kaplan–Meier plots of DFS after the EOT. (C) Kaplan–Meier plots of OS. CI, confidence interval; DFS, disease-free survival; EOT, end of treatment; HR, hazard ratio; NE, not evaluable; OS, overall survival.
Figure 3
Figure 3
Forest plots for the HRs (triangles) and 95% CIs (horizontal line) of disease-free survival and overall survival in subgroups of patients for the intention-to-treat population. (A) Forest plots of disease-free survival. (B) Forest plots of overall survival. CI, confidence interval; ECOG, Eastern Cooperative Oncology Group; EGFR, epidermal growth factor receptor; HR, hazard ratio.

References

    1. Xu S.T., Xi J.J., Zhong W.Z., et al. The unique spatial-temporal treatment failure patterns of adjuvant gefitinib therapy: a post hoc analysis of the ADJUVANT trial (CTONG 1104) J Thorac Oncol. 2019;14:503–512. - PubMed
    1. Arriagada R., Auperin A., Burdett S., et al. Adjuvant chemotherapy, with or without postoperative radiotherapy, in operable non-small-cell lung cancer: two meta-analyses of individual patient data. Lancet. 2010;375:1267–1277. - PMC - PubMed
    1. Goldstraw P., Chansky K., Crowley J., et al. The IASLC Lung Cancer Staging Project: proposals for revision of the TNM stage groupings in the forthcoming (eighth) edition of the TNM classification for lung cancer. J Thorac Oncol. 2016;11:39–51. - PubMed
    1. Burdett S., Pignon J.P., Tierney J., et al. Adjuvant chemotherapy for resected early-stage non-small cell lung cancer. Cochrane Database Syst Rev. 2015;3:CD011430. - PMC - PubMed
    1. Pignon J.P., Tribodet H., Scagliotti G.V., et al. Lung adjuvant cisplatin evaluation: a pooled analysis by the LACE Collaborative Group. J Clin Oncol. 2008;26:3552–3559. - PubMed

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