Clinical trial · Interventional
Icotinib Following Chemotherapy Versus Chemotherapy as Adjuvant Therapy in Stage IIA-IIIA NSCLC With EGFR Mutation
A Multicenter, Randomized, Phase III Trial of Chemotherapy Followed by 6-month or 12-month Icotinib Versus Chemotherapy as Adjuvant Therapy in Stage IIA-IIIA Non-small Cell Lung Cancer Harboring Epidermal Growth Factor Receptor Mutation
NCT01996098CI-TRIAL-00080452ICTANterminatedPhase 3ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Slow accural.
Summary
Brief summary (as posted)
The purpose of this study is studying icotinib following chemotherapy to see how well it works compared to chemotherapy in treating patients with resected stage IIA-IIIA NSCLC harboring EGFR mutation.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 12-month icotinib | Drug | — | UNRESOLVED |
| 6-month Icotinib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- EXPERIMENTAL
- label
- 6-month icotinib
- description
- Icotinib 125 mg three times daily (375 mg per day) by mouth for 6 months
- interventionNames
- Drug: 6-month Icotinib
- type
- EXPERIMENTAL
- label
- 12-month icotinib
- description
- Icotinib 125 mg three times daily (375 mg per day) by mouth for 12 months
- interventionNames
- Drug: 12-month icotinib
- type
- NO_INTERVENTION
- label
- Chemotherapy alone
- description
- No intervention
Primary outcomes (1)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Written informed consent provided. * Aged 18-75 years. * Had completely resected pathological confirmed stage IIA-IIIA NSCLC. * EGFR activating mutation in exon 19 or 21. * Had completed four cycles of platinum-based adjuvant chemotherapy. * Able to start the investigational therapy within 4 weeks after the completion of four cycles of adjuvant chemotherapy. * ECOG performance status of 0-1. * Had a life expectancy of 12 weeks or more. * Adequate hematological function, adequate liver function and renal function. * Able to comply with the required protocol and follow-up procedures, and able to receive oral medications. * Female patients, except those who are postmenopausal or surgically sterilized, must have a negative pre-study serum or urine pregnancy test. Exclusion Criteria: * Had had previous chemotherapy besides four cycles of adjuvant chemotherapy, radiotherapy, or agents directed at the HER axis (e.g. erlotinib, gefitinib, cetuximab, trastuzumab). * Had a history another malignancy in the last 5 years with the exception of cured basal cell carcinoma of the skin, cured in situ carcinoma of the uterine cervix and cured epithelial carcinoma of the bladder. * Any evidence confirmed tumor recurrence before investigational therapy. * Known severe hypersensitivity to icotinib or any of the excipients of this product. * Evidence of clinically active interstitial lung disease. * Eye inflammation not fully controlled or conditions predisposing the subject to this. * Any unstable systemic disease (including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, myocardial infarction within the previous 6 months, serious cardiac arrhythmia requiring medication, hepatic, renal, or metabolic disease). * Known human immunodeficiency virus (HIV) infection. * Pregnancy or breast-feeding women. * Ingredients mixed with small cell lung cancer patients. * History of neurologic or psychiatric disorders.
References
Publications (1)
- DERIVEDLi N, Ou W, Cheng C, You J, Yang L, Chen FX, Liang Y, Yang Z, Wang BX, Chang ZH, Lin YB, Yang W, Xu F, Ding G, Chen XS, Hu R, Li S, Jiang H, Hu XX, Long H, Wang SY. Adjuvant icotinib for resected EGFR-mutated stage II-IIIA non-small-cell lung cancer (ICTAN, GASTO1002): a randomized comparison study. Signal Transduct Target Ther. 2025 Aug 28;10(1):273. doi: 10.1038/s41392-025-02358-w. PMID 40866342