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A Clinical Study of Furmonertinib Combined with Chemotherapy as Neoadjuvant Therapy for Resectable Stage II-IIIA EGFRm NSCLC

A Clinical Study of Furmonertinib Combined with Chemotherapy as Neoadjuvant Therapy for Resectable Stage II-IIIA EGFRm NSCLC

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200062769
Enrollment
Unknown
Registered
2022-08-18
Start date
2022-08-25
Completion date
Unknown
Last updated
2023-04-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non small cell lung cancer

Interventions

Furmonertinib+ chemotherapy:Furmonertinib+ Pemetrexed + Carboplatin

Sponsors

Jiangsu Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients should voluntarily participate in the study, sign the informed consent form, have good compliance and cooperate with the follow-up; 2. Age 18-75 years old, with no restriction on gender; 3. Resectable stage II-IIIA NSCLC confirmed by pathological and imaging examinations; 4. EGFR-sensitive mutations (either exon 19 deletion or L858R in exon21); 5. ECOG score 0-1; 6. Treatment-na?ve patients who have not received any anti-tumor therapy previously; 7. No serious abnormalities of hematopoietic function, heart, lung, liver,kidney function and immune system.

Exclusion criteria

Exclusion criteria: 1. Received surgical treatment for lung tumors; 2. Received neoadjuvant chemotherapy or radiotherapy; 3. Confirmed with hepatocellular carcinoma (HCC) or any active liver disease uncontrolled by treatment; 4. Treated but uncontrolled diabetes mellitus, asthma, autoimmune diseases and other chronic diseases; 5. Received cellular therapy within the last 1 year; 6. Participated in other clinical trials (including research vaccines, drugs,medical devices, etc.) within one month.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;Pathological complete response rate;

Secondary

MeasureTime frame
Major pathological response rate;R0 resection rate;NAT treatment completion rate;Disease free survival;Overall survival;Adverse events/Serious adverse events;

Countries

China

Contacts

Public ContactZhaohui Fan

Jiangsu Cancer Institute & Hospital

503868005@qq.com+86 13705173269

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026