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OncoMatch/Clinical Trials/NCT07037680

Radiotherapy Plus Anlotinib in LA-NSCLC Intolerable to cCRT

Is NCT07037680 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Anlotinib for locally advanced non-small cell lung cancer.

Phase 2RecruitingJIANYANG WANGNCT07037680Data as of Jun 2026Location: China

Treatment: AnlotinibConcurrent chemoradiotherapy (cCRT) is the standard treatment for patients with negative epidermal growth factor receptor (EGFR)-mutated unresectable locally advanced non-small cell lung cancer (LA-NSCLC). However, parts of patients only receive sequential chemoradiotherapy (sCRT) due to various reasons. This phase II study aimed to improve the outcomes of patients receiving sCRT by combining anti-angiogenesis therapy (Anlotinib) during radiotherapy course.We hypothesize that the combination of radiotherapy with anlotinib could improve the 2-year PFS rate from 35% with sCRT to 50. The accrual target was 44 patients.

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Anlotinib

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: ALK wild-type

Required: EGFR wild-type

Required: ROS1 wild-type

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

Must have received: systemic chemotherapy

Received systemic chemotherapy or combined chemotherapy and immumitherapy for ≥ 4 weeks without progression

Cannot have received: thoracic radiotherapy

thoracic radiotherapy history ... within three months

Lab requirements

Kidney function

adequate renal function with a negative urine protein

Liver function

adequate hepatic function

Adequate hepatic and renal functions with a negative urine protein

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07037680 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior thoracic radiotherapy disqualifies patients from enrollment.

Does this trial require ALK?

Yes, ALK wild-type is a required biomarker for enrollment.

Does this trial require EGFR?

Yes, EGFR wild-type is a required biomarker for enrollment.

Does this trial require ROS1?

Yes, ROS1 wild-type is a required biomarker for enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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