Clinical trial · Interventional
Real-world Experience With Combination Chemotherapy and Osimertinib in Poor Prognostic Group of Metastatic EGFR-mutated Lung Adenocarcinoma
NCT06918782CI-TRIAL-00088306not yet recruitingPhase 2ClinicalTrials.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)
The aims of this study are to determine the potential clinical benefits (in terms of PFS, objective response and OS) of add-on systemic chemotherapy (pemetrexed+carboplatin/cisplatin) to first-line osimertinib treatment among the poor prognostic group of metastatic EGFR-mutant lung adenocarcinoma, i.e. failure of plasma ctDNA EGFR mutant clearance at week 3 after osimertinib treatment
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 (NSCLC) | Malignant Lung Neoplasm | CURATED_EXACT | 0.85 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Osimertinib plus platinum doublet chemotherapy | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Combination chemotherapy and osimertinib
- description
- Incorporating chemotherapy with ongoing osimertinib treatment involves initiating osimertinib at the standard dose of 80mg orally once daily. This regimen includes a combination of pemetrexed and carboplatin or cisplatin administered intravenously every 3 weeks for a maximum of 6 cycles, followed by maintenance pemetrexed at a dosage of 500mg/m2 every 3 weeks in cases of non-progressive disease.
- interventionNames
- Drug: Osimertinib plus platinum doublet chemotherapy
Primary outcomes (1)
- measure
- real-world 1-year progression-free survival
- timeFrame
- The duration of osimertinib treatment extends from the initiation of therapy until either disease progression or death from any cause, whichever occurs first. Progression-free survival (PFS) will be monitored for up to 1 year.
Secondary outcomes (5)
- measure
- rw response rate
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: 1. Adults above 18 years old, both male and female; 2. Pathologically confirmed lung adenocarcinoma with stage IIIB/C or IV disease (TNM staging version 8); 3. Confirmed EGFR common sensitizing mutations (exon 21 L858R or exon 19 del) by locally approved molecular testing methods (allele-specific PCR or NGS) based on tumour tissues or plasma ctDNA; 4. Clinically decided for first-line systemic treatment with osimertinib; 5. Detectable pre-treatment plasma EGFR mutations (by Cobas EGFR Mutation Test v2) and failed clearance 3 weeks (+/- 5 days) after osimertinib treatment; 6. At least one measurable target lesion by RECIST v1.1 criteria; 7. Performance state (ECOG) ≤ 1 and life expectancy ≥ 12 weeks; 8. Females in reproductive age with negative pregnancy test and highly effective means of contraception during and ≥ 4 months after intervention period; 9. Males should agree to have highly effective means of contraception during and ≥ 4 months after intervention period; and 10. Written informed consent obtained. Exclusion Criteria: 1. Mixed NSCLC and small cell carcinoma; 2. Prior systemic anticancer treatment (targeted therapy, chemotherapy or immunotherapy) for metastatic stage NSCLC; 3. Prior adjuvant chemotherapy or targeted therapy within 6 months; 4. Local radiotherapy within 2 weeks or major surgery within 4 weeks; 5. Inadequate haematological function (haemoglobin \< 9 g/dL, neutrophils \< 1.5 x 109/L, platelets \< 100 x 109/L), renal function (serum creatinine ≥ 1.5 x upper limit of normal (ULN) or creatinine clearance \< 45 ml/min) or liver function (total bilirubin \> 1.5 x ULN, ALT/AST/ALP \> 3 x ULN; ALT/AST/ALP \> 5 x ULN for liver metastases; ALP \> 5 x ULN for bone metastases); 6. Major medical comorbidities with significant organ dysfunction; 7. Known active hepatitis B or C infection. Chronic hepatitis B on antiviral allowed as per institutional guideline for chemotherapy; 8. Malignancies other than NSCLC; and 9. Known hypersensitivity to pemetrexed or carboplatin.
References
Publications (0)
Data not yet available
No reference posted for this study.