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Hypofractionated Brain Radiation In EGFR Mutated Adenocarcinoma Cranial Disease (Hybrid)

S

Sichuan Provincial People's Hospital

Status and phase

Unknown
Phase 3

Conditions

Stage IV EGFR Mutated NSCL With Brain Metastases

Treatments

Radiation: HFSRS
Radiation: WBRT
Drug: Gefitinib 250mg po qd or Tarceva 150mg po qd or Icotinib 125mg po tid Other Name: Gefitinib/Tarceva/Icotinib

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

A multi-center phase III randomized controlled study to evaluate the efficacy of Hypofractionated SRS (HFSRS) along with EGFR-TKI in patients with brain metastasis from non-small cell lung cancer (NSCLC). Assuming that HFSRS is not inferior to EGFR-TKI concurrent with whole brain radiotherapy (WBRT), the primary end point is intracranial PFS (iPFS), while secondary outcomes included overall survival (OS), evaluation of cognitive function, quality of life (QoL) and adverse events.

Full description

WBRT remains to be standard of care for NSCL patients. Long term survival from WBRT may have noticeable cognitive dysfunction. The EGFR TKI has reasonable control for intracranial disease, but the duration of EGFR TKI control disease is variable due to tendency of drug resistance. To maintain intracranial disease control and improve cognitive function, the investigators propose using hypofractionated SRS in multiple brain metastases or large brain lesions alone with TKI.

Enrollment

325 estimated patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Histological or cytological confirmation of non-small cell lung cancer (NSCLC);
  • Diagnosis of brain metastases on a Gadolinium-enhanced MRI.
  • More than 3 sites of intracranial metastases, or the longest diameter of the intracranial lesion is more than 4 cm.
  • Positive EGFR mutation.
  • Life expectancy ≥3months.
  • Have one or more measurable encephalic lesions according to RECIST.
  • Adequate hematological function: Absolute neutrophil count (ANC) ≥1.5 x 109/L, and Platelet count ≥100 x 109/L.
  • Adequate renal function: Serum creatinine ≤1.5 x ULN, or ≥ 50 ml/min.
  • Adequate liver function: Total bilirubin ≤ 1.5 x upper limit of normal (ULN) and Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) < 2.5 x ULN in the absence of liver metastases, or < 5 x ULN in case of liver metastases.
  • Female subjects should not be pregnant.
  • All human subjects should able to comply with the required protocol and follow-up procedures, and able to receive oral medications.
  • Written informed consent provided.

Exclusion criteria

  • Previous usage of EGFR-TKI or antibody to EGFR: gefitinib, erlotinib, herceptin, erbitux.
  • CSF or MRI findings consistent with metastases of spinal cord, meninges or meningeal.
  • Allergic to Icotinib.
  • Lack of physical integrity of the upper gastrointestinal tract, or malabsorption syndrome, or inability to take oral medication, or have active peptic ulcer disease.
  • Pregnancy or breast-feeding women.
  • Participate in the other anti-tumor clinical trials in 4 weeks.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

325 participants in 2 patient groups

WBRT along with TKI
Active Comparator group
Description:
Drug: EGFR-TKI Gefitinib 250mg po qd or Tarceva 150mg po qd or Icotinib 125mg po tid Other Name: Gefitinib/Tarceva/Icotinib Radiation: whole brain radiotherapy 3750Gy/15F Other Name: WBRT
Treatment:
Drug: Gefitinib 250mg po qd or Tarceva 150mg po qd or Icotinib 125mg po tid Other Name: Gefitinib/Tarceva/Icotinib
Radiation: WBRT
HFSRS with EGFR TKI
Experimental group
Description:
Drug: EGFR-TKI Gefitinib 250mg po qd or Tarceva 150mg po qd or Icotinib 125mg po tid Other Name: Gefitinib/Tarceva/Icotinib Radiation: whole brain radiotherapy 25 to 40 Gy/5F Other Name: HFSRS
Treatment:
Drug: Gefitinib 250mg po qd or Tarceva 150mg po qd or Icotinib 125mg po tid Other Name: Gefitinib/Tarceva/Icotinib
Radiation: HFSRS

Trial contacts and locations

1

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Central trial contact

ming zeng, MD PhD; YiFeng Bai, MD PhD

Data sourced from clinicaltrials.gov

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