Clinical trial · Observational
Osimertinib With Chemotherapy as First-line Therapy for EGFR Mutation-positive NSCLC
Osimertinib With Chemotherapy as First-line Therapy for Patients With Locally Advanced or Metastatic Epidermal Growth Factor Receptor (EGFR) Mutation-positive Non-Small Cell Lung Cancer (NSCLC): A Multicentre, Observational Study (FOREFRONT)
NCT06376084CI-TRIAL-00122476FOREFRONTactive not recruitingClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To estimate parameters related to clinical outcomes in a real-world seeting, including investigator reported PFS and OS .
Conditions
Conditions (10)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bronchial Neoplasms | — | UNRESOLVED | — |
| Carcinoma, Bronchogenic | Bronchogenic Carcinoma | ONTOLOGY_EXACT | 0.98 |
| Carcinoma, Non-Small-Cell Lung | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| Lung Diseases | — | UNRESOLVED | — |
| Lung Neoplasms | Lung Neoplasm | ONTOLOGY_EXACT | 0.98 |
| Neoplasms | Neoplasm | ONTOLOGY_EXACT | 0.90 |
| Neoplasms by Site | Neoplasm by Site | ONTOLOGY_EXACT | 0.98 |
| Respiratory Tract Diseases | — | UNRESOLVED | — |
| Respiratory Tract Neoplasms | Respiratory System Neoplasm | ALIAS | 0.90 |
| Thoracic Neoplasms | Thoracic Neoplasm |
Interventions
Interventions (0)
Data not yet available
No intervention recorded.
Design
Arms and outcomes
Arms (0)
[]Primary outcomes (1)
- measure
- Real-World Progression Free Survival (rwPFS)
- timeFrame
- Follow up approximately 36 months after last patient in
- description
- rwPFS is defined as the time from the date of first-line initiation until disease progression or death by investigator report as recorded in the CRF
Secondary outcomes (5)
- measure
- Chemotherapy regimen
- timeFrame
- Follow up approximately 36 months after last patient in
- description
- Chemotherapy information i.e. dose, number of induction chemotherapy cycles and duration of chemotherapy maintenance, any dose changes and reasons for these changes and date of last administration will also be recorded.
- measure
- Duration of chemotherapy (induction and maintenance cycles)
- timeFrame
- Follow up approximately 36 months after last patient in
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Age ≥18 years * Histologically or cytologically documented nonsquamous NSCLC. NSCLC of mixed histology is allowed. * Stage IIIB or IIIC or Stage IV metastatic NSCLC or recurrent NSCLC (based on the American Joint Committee on Cancer Edition 8) not amenable to curative surgery or definitive chemoradiation. * EGFR sensitive mutation-positive (Ex19del and/or 21 L858R) * WHO performance status of 0 to 2 at screening with no clinically significant deterioration in the previous 2 weeks. * Patients who receive Osimertinib plus chemotherapy as first-line treatment based on physician's medical assessment are eligible (For patients who received prior chemotherapy alone/Osimertinib monotherapy/Osimertinib plus chemotherapy as first-line therapy ahead of enrolment, they are diseases progression-free at the time of enrolment and the duration of prior therapy ≤3 months). * Patients with asymptomatic CNS metastases or patients who have completed definitive therapy, are not on steroids and have a stable neurological status for at least 2 weeks after completion of the definitive therapy and steroids are allowed. * Prior adjuvant and neo-adjuvant therapies (chemotherapy, radiotherapy, immunotherapy, biologic therapy, investigational agents), or definitive radiation/chemoradiation with or without regimens including immunotherapy, biologic therapies, investigational agents are permitted as long as treatment was completed at least 12 months prior to the development of recurrent disease. Exclusion Criteria: * Spinal cord compression and symptomatic brain metastases * Past medical history of ILD, drug-induced ILD, radiation pneumonitis that required steroid treatment, or any evidence of clinically active ILD * Any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension and active bleeding diatheses, etc * Any banned substance in label
References
Publications (1)
- DERIVEDZhang B, Ning F, Liu X, Li N, Wang P, Yao W, Han B, Wang Q, Zhong H. First-line therapy of osimertinib with chemotherapy in Chinese patients with EGFR mutation-positive non-small cell lung cancer: protocol for a multicenter, prospective, observational study. Front Oncol. 2025 Sep 5;15:1625714. doi: 10.3389/fonc.2025.1625714. eCollection 2025. PMID 40978050