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ATOM2: A Randomized Phase II Trial on Ablative Therapy to Oligoresidual Metastasis in EGFR Mutated Non-small Cell Lung Cancer After Osimertinib Treatment

Status: Recruiting
Location: See location...
Intervention Type: Radiation, Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is an open-label, multicentre, randomized phase II clinical trial. Patients with stage IV (AJCC 9th edition) non-small cell lung cancer (NSCLC) harboring EGFR exon 19 deletion or exon 21 L858R mutation, who had less than or equal to 3 active oligoresidual cancer sites amenable to local ablative therapy (LAT) (as determined by physician) after 3-6 months of firstline osimertinib treatment, are eligible. Subjects will be randomized 1:1 to osimertinib with or without LAT.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 18 years of age or older and able to understand and give written informed consent

• Pathologically proven non-small cell lung cancer

• Positive for EGFR exon 19 deletion or EGFR exon 21 L858R mutation (either by tissue or plasma testing)

• Stage IV disease

• Receive first line osimertinib monotherapy for stage IV disease

• Undergo a PET-CT scan after 12-24 weeks of initiation of osimertinib treatment, with no evidence of disease progression, and less than or equal to 3 active disease sites (including primary tumour) amenable to local ablative therapy, as determined by investigator

• At least one brain imaging (CT Brain or MRI Brain with contrast, preferably MRI Brain), either at time of diagnosis or while on osimertinib treatment but before randomization, to document CNS status for stratification. Patients with asymptomatic CNS metastases are eligible. For patients with brain metastases diagnosed at baseline, follow up brain imaging is recommended before randomization.

• Patients with history of palliative radiotherapy are eligible

• Eastern Cooperative Oncology Group (ECOG) performance status 0-1

• Adequate haematological values: haemoglobin ≥9.0g/dL, absolute neutreophil count ≥1.0 x 109/L, platelet count ≥100 x 109/L

• Adequate hepatic function: bilirubin ≤1.5 x ULN, AST/ALT ≤2.5 x ULN

• Adequate renal function: creatinine clearance ≥30ml/min, according to the formula of Cockcroft-Gault equation

• Willing and able to comply with the requirements and restrictions in this protocol

Locations
Other Locations
Hong Kong Special Administrative Region
Department of Clinical Oncology, Prince of Wales Hospital
RECRUITING
Hong Kong
Contact Information
Primary
Molly SC LI, MBBS, MRCP
molly@clo.cuhk.edu.hk
3505 1042
Time Frame
Start Date: 2026-02-11
Estimated Completion Date: 2030-03-03
Participants
Target number of participants: 64
Treatments
Experimental: Radiotherapy arm
* Continue osimertinib as per standard of care (40mg or 80mg daily).~* Undergo radiotherapy to 1-3 disease sites as determined by the investigator.
Active_comparator: Control arm
Continue osimertinib as per standard of care (40mg or 80mg daily)
Sponsors
Leads: Chinese University of Hong Kong

This content was sourced from clinicaltrials.gov