OncoMatch

OncoMatch/Clinical Trials/NCT06810609

Immunochemotherapy, Surgery or Chemoradiation, and Durvalumab for Stage IIIA/B NSCLC

Is NCT06810609 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Immunotherapy for lung cancer non-small cell cancer (nsclc).

Phase 2RecruitingUniversity Hospital, BonnNCT06810609Data as of Jun 2026Location: Germany

Treatment: ImmunotherapyThe hypothesis of the study is that induction immunochemotherapy, followed by surgery or chemoradiation and consolidation Durvalumab immunotherapy, can significantly improve event-free survival in patients with resectable or borderline resectable NSCLC at stage IIIA/B compared to existing treatment methods.

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Extracted eligibility criteria

Treatments studied

Other

Immunotherapy

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: ALK wild-type

Required: EGFR wild-type

Disease stage

Required: Stage IIIA, IIIB (IASLC/UICC 8)

Excluded: Stage N3 TUMORS (IASLC/UICC 8)

Selected patients with NSCLC stage IIIA/B: IIIA: one or more lymph node levels involved at EBUS/mediastinoscopy T1/T2 N2. IIIB: one or more lymph node levels involved at EBUS/mediastinoscopy T3/T4 N2.

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 74

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines
Min 0 prior lines

Cannot have received: mediastinal irradiation

Prior treatments including prior mediastinal irradiation

Cannot have received: anti-PD-1 therapy

Exception: Permitted if no permanent discontinuation for toxicity, all AEs resolved to baseline, no ≥ Grade 3 immune-related AE or immune-related neurologic/ocular AE of any grade, no additional immunosuppression other than corticosteroids, no recurrence of AE if re-challenged, not currently requiring >10 mg prednisone or equivalent per day. Endocrine AE ≤ Grade 2 allowed if stably maintained and asymptomatic.

Patients who have received prior anti-PD-1, anti-PD-L1, or anti-CTLA-4

Cannot have received: anti-PD-L1 therapy

Exception: Permitted if no permanent discontinuation for toxicity, all AEs resolved to baseline, no ≥ Grade 3 immune-related AE or immune-related neurologic/ocular AE of any grade, no additional immunosuppression other than corticosteroids, no recurrence of AE if re-challenged, not currently requiring >10 mg prednisone or equivalent per day. Endocrine AE ≤ Grade 2 allowed if stably maintained and asymptomatic.

Patients who have received prior anti-PD-1, anti-PD-L1, or anti-CTLA-4

Cannot have received: anti-CTLA-4 therapy

Exception: Permitted if no permanent discontinuation for toxicity, all AEs resolved to baseline, no ≥ Grade 3 immune-related AE or immune-related neurologic/ocular AE of any grade, no additional immunosuppression other than corticosteroids, no recurrence of AE if re-challenged, not currently requiring >10 mg prednisone or equivalent per day. Endocrine AE ≤ Grade 2 allowed if stably maintained and asymptomatic.

Patients who have received prior anti-PD-1, anti-PD-L1, or anti-CTLA-4

Lab requirements

Blood counts

Hemoglobin ≥ 9.0 g/dL; ANC ≥ 1.5 × 10^9/L; Platelet count ≥ 100 × 10^9/L

Kidney function

Measured or calculated creatinine clearance ≥ 60 mL/min

Liver function

Serum bilirubin ≤ 1.5 × institutional ULN (except Gilbert's syndrome); ALT/AST ≤ 2.5 × institutional ULN

Cardiac function

Stable cardiac function (no MI within 6 months, no heart failure NYHA III-IV)

Adequate normal organ and bone marrow function as defined below: Hemoglobin ≥ 9.0 g/dL. ANC ≥ 1.5 × 10^9/L. Platelet count ≥ 100 × 10^9/L. Serum bilirubin ≤ 1.5 × institutional ULN. ALT/AST ≤ 2.5 × institutional ULN. Creatinine clearance ≥ 60 mL/min. Stable cardiac function (no MI within 6 months, no heart failure NYHA III-IV).

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

Frequently asked questions

Is NCT06810609 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

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.

What disease stage is eligible?

Stage IIIA or IIIB is required.

Is there an age limit?

Yes. Patients must be 74 years or younger.

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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