Icotinib Following Chemotherapy Versus Chemotherapy as Adjuvant Therapy in Stage IIA-IIIA NSCLC With EGFR Mutation

Last updated: September 1, 2024
Sponsor: Sun Yat-sen University
Overall Status: Terminated

Phase

3

Condition

Lung Cancer

Lung Disease

Non-small Cell Lung Cancer

Treatment

12-month icotinib

6-month Icotinib

Clinical Study ID

NCT01996098
GASTO1002
wsy003
  • Ages 18-75
  • All Genders

Study Summary

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.

Eligibility Criteria

Inclusion

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 offour 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 toreceive oral medications.

  • Female patients, except those who are postmenopausal or surgically sterilized, musthave a negative pre-study serum or urine pregnancy test.

Exclusion

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 curedbasal cell carcinoma of the skin, cured in situ carcinoma of the uterine cervix andcured 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 tothis.

  • Any unstable systemic disease (including active infection, uncontrolledhypertension, unstable angina, congestive heart failure, myocardial infarctionwithin 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.

Study Design

Total Participants: 251
Treatment Group(s): 2
Primary Treatment: 12-month icotinib
Phase: 3
Study Start date:
January 01, 2014
Estimated Completion Date:
February 15, 2024

Study Description

Adjuvant chemotherapy is recommended for routine use in patients with fully resected stage IIA-IIIA non-small cell lung cancer (NSCLC). Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) show great efficacy in patients with advanced non-small cell lung cancer (NSCLC) with EGFR mutation. Icotinib is a novel EGFR-TKI developed by a group of Chinese scientists. In the phase III ICOGEN trial, icotinib had non-inferiority efficacy to gefitinib with better safety. In phase II trial, chemotherapy followed by 6-month gefitinib as adjuvant therapy can confer longer disease-free survival compared with chemotherapy alone in patients with resected stage IIIA-N2 non-small cell lung cancer harboring EGFR mutations. This study is to studying 6-month or 12-month icotinib following chemotherapy to see how well it works compared to chemotherapy in treating patients with resected stage IIA-IIIA NSCLC harboring EGFR mutation.

Connect with a study center

  • Sun Yat-sen University Cancer Center

    Guangzhou, Guangdong 510060
    China

    Site Not Available

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