Status:

UNKNOWN

Radiotherapy Combined With Almonertinib for Stage III EGFR-Mutated Lung Cancer

Lead Sponsor:

Laibin People's Hospital

Conditions:

Lung Cancer Stage III

Eligibility:

All Genders

18-80 years

Phase:

PHASE2

PHASE3

Brief Summary

Study Object: Stage III lung cancer with epidermal growth factor receptor (EGFR) sensitive mutation. Study Method: The study subjects will be randomly assigned to the intervention group and the contr...

Detailed Description

The following tasks need to be completed at the time of enrollment: screening, signing the informed consent form, random assignment according to the randomization table, detailed patient medical histo...

Eligibility Criteria

Inclusion

  • Patients initially diagnosed with lung cancer through imaging and pathological examination.
  • Genetic testing confirms EGFR-sensitive mutations.
  • Staging according to the international eighth edition of lung cancer TNM is between stage ⅢA to ⅢC.
  • Age between 18 to 80 years old, without severe organ diseases such as heart, liver, kidney, etc.
  • ⑤ General condition assessed with a performance status (PS) score of ≤2 points.

Exclusion

  • ① Patients with upper gastrointestinal physiological disorders, malabsorption syndrome, intolerance to oral medications, or peptic ulcers.
  • Patients who have received previous radiotherapy or chemotherapy for lung conditions.
  • Patients with concomitant chronic obstructive pulmonary disease, atelectasis, or other conditions that cause difficulties in lesion measurements.
  • Patients with active pulmonary tuberculosis. ⑤ Patients with respiratory failure. ⑥ Patients with allergies to the investigational drugs used in this study. ⑦ Pregnant or lactating women. ⑧ Patients with any other diseases, neurological or metabolic disorders, physical examination or laboratory findings that may raise reasonable suspicions of certain diseases or conditions, which would either disqualify the use of the investigational drugs or place the subjects at high risk of treatment-related complications.

Key Trial Info

Start Date :

September 1 2023

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

December 8 2025

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT05994339

Start Date

September 1 2023

End Date

December 8 2025

Last Update

August 29 2023

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