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OncoMatch/Clinical Trials/NCT06331455

Treatment of Pulmonary SUlcus, Pancoast and Chest Wall Non-small Cell Lung Cancer Employing Radiation, Immuno-oncology and Resection

Is NCT06331455 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Durvalumab for lung cancer patients.

Phase 2RecruitingMarc de PerrotNCT06331455Data as of May 2026

Treatment: DurvalumabThe SUPER trial is a prospective Phase II trial. It is designed for patients with stage 2 or 3 non-small cell lung cancer (NSCLC) prior to surgery. Patients who are enrolled in this trial will receive combination of Non-ablative oligofractionated radiation (NORT) and two cycles of Durvalumab, an immunotherapy drug before their surgery.

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Extracted eligibility criteria

Cancer type

Non-Small Cell Lung Carcinoma

Biomarker criteria

Required: PD-L1 (CD274) positive (tumor proportion score >1%) (TPS >1%)

PD-L1 positive tumors defined by tumor proportion score (TPS) >1%

Excluded: EGFR mutation

Known oncogenic driver mutations such as EGFR mutant or ALK mutant [excluded]

Excluded: ALK mutation

Known oncogenic driver mutations such as EGFR mutant or ALK mutant [excluded]

Disease stage

Required: Stage IIB, IIIA, IIIB

Excluded: Stage N3 DISEASE IN THE CONTRALATERAL MEDIASTINUM, CONTRALATERAL HILUM, OR CONTRALATERAL SUPRACLAVICULAR LYMPH NODE

Patients with NSCLC stage IIB to IIIB. The presence of N3 disease in the contralateral mediastinum, contralateral hilum, or contralateral supraclavicular lymph node confirmed histologically [excluded]. History of leptomeningeal carcinomatosis, malignant pleural effusion or distant metastasis (M1) [excluded].

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: anti-PD-1 therapy

Exception: see detailed AE and steroid requirements in source_text

Patients who have received prior anti-PD-1, anti PD-L1 or anti CTLA-4: Must not have experienced a toxicity that led to permanent discontinuation of prior immunotherapy. All AEs while receiving prior immunotherapy must have completely resolved or resolved to baseline prior to screening for this study. Must not have experienced a ≥Grade 3 immune related AE or an immune related neurologic or ocular AE of any grade while receiving prior immunotherapy. NOTE: Patients with endocrine AE of ≤Grade 2 are permitted to enroll if they are stably maintained on appropriate replacement therapy and are asymptomatic. Must not have required the use of additional immunosuppression other than corticosteroids for the management of an AE, not have experienced recurrence of an AE if re-challenged, and not currently require maintenance doses of > 10 mg prednisone or equivalent per day.

Cannot have received: anti-PD-L1 therapy

Exception: see detailed AE and steroid requirements in source_text

Patients who have received prior anti-PD-1, anti PD-L1 or anti CTLA-4: Must not have experienced a toxicity that led to permanent discontinuation of prior immunotherapy. All AEs while receiving prior immunotherapy must have completely resolved or resolved to baseline prior to screening for this study. Must not have experienced a ≥Grade 3 immune related AE or an immune related neurologic or ocular AE of any grade while receiving prior immunotherapy. NOTE: Patients with endocrine AE of ≤Grade 2 are permitted to enroll if they are stably maintained on appropriate replacement therapy and are asymptomatic. Must not have required the use of additional immunosuppression other than corticosteroids for the management of an AE, not have experienced recurrence of an AE if re-challenged, and not currently require maintenance doses of > 10 mg prednisone or equivalent per day.

Cannot have received: anti-CTLA-4 therapy

Exception: see detailed AE and steroid requirements in source_text

Patients who have received prior anti-PD-1, anti PD-L1 or anti CTLA-4: Must not have experienced a toxicity that led to permanent discontinuation of prior immunotherapy. All AEs while receiving prior immunotherapy must have completely resolved or resolved to baseline prior to screening for this study. Must not have experienced a ≥Grade 3 immune related AE or an immune related neurologic or ocular AE of any grade while receiving prior immunotherapy. NOTE: Patients with endocrine AE of ≤Grade 2 are permitted to enroll if they are stably maintained on appropriate replacement therapy and are asymptomatic. Must not have required the use of additional immunosuppression other than corticosteroids for the management of an AE, not have experienced recurrence of an AE if re-challenged, and not currently require maintenance doses of > 10 mg prednisone or equivalent per day.

Lab requirements

Blood counts

Hemoglobin ≥9.0 g/dL; Absolute neutrophil count (ANC) ≥1.0 × 10^9/L; Platelet count ≥75 × 10^9/L

Kidney function

Measured or calculated creatinine clearance >40 mL/min

Liver function

Serum bilirubin in normal range (except Gilbert's syndrome); AST (SGOT)/ALT (SGPT) ≤2.5 x institutional upper limit of normal

Adequate normal organ and marrow function as defined below Hemoglobin ≥9.0 g/dL Absolute neutrophil count (ANC) ≥1.0 × 10^9/L Platelet count ≥75 × 10^9/L Serum bilirubin in normal range with the exception of Gilbert's syndrome (persistent or recurrent hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis or hepatic pathology), who will be allowed only in consultation with their physician AST (SGOT)/ALT (SGPT) ≤2.5 x institutional upper limit of normal Measured creatinine clearance (CL) >40 mL/min or Calculated creatinine CL>40 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976) or by 24-hour urine collection for determination of creatinine clearance

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

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