Clinical trial · Interventional
Stereotactic Body Radiation Therapy in Treating Patients With Stage I Non-Small Cell Lung Cancer
Seamless Phase I/II Study of Stereotactic Lung Radiotherapy (SBRT) for Early Stage, Centrally Located, Non-Small Cell Lung Cancer (NSCLC) in Medically Inoperable Patients
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Stereotactic body radiation therapy may be able to send x-rays directly to the tumor and cause less damage to normal tissue. PURPOSE: This phase I/II trial is studying the side effects and best dose of stereotactic body radiation therapy and to see how well it works in treating patients with stage I non-small cell lung cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Lung Cancer | Malignant Lung Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (9)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| SBRT 40.0 Gy | Radiation | — | UNRESOLVED |
| SBRT 42.5 Gy | Radiation | — | UNRESOLVED |
| SBRT 45.0 Gy | Radiation | — | UNRESOLVED |
| SBRT 47.5 Gy | Radiation | — | UNRESOLVED |
| SBRT 50.0 Gy | Radiation | — | UNRESOLVED |
| SBRT 52.5 Gy | Radiation | — | UNRESOLVED |
| SBRT 55.0 Gy | Radiation | — | UNRESOLVED |
| SBRT 57.5 Gy | Radiation | — | UNRESOLVED |
| SBRT 60.0 Gy | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (9)
- type
- EXPERIMENTAL
- label
- Level 1: 8.0 Gy/FX
- description
- SBRT 40.0 Gy
- interventionNames
- Radiation: SBRT 40.0 Gy
- type
- EXPERIMENTAL
- label
- Level 2: 8.5 Gy/FX
- description
- SBRT 42.5 Gy
- interventionNames
- Radiation: SBRT 42.5 Gy
- type
- EXPERIMENTAL
- label
- Level 3: 9.0 Gy/FX
- description
- SBRT 45.0 Gy
- interventionNames
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 120 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS:
* Histologically or cytologically confirmed non-small cell lung cancer (NSCLC)
* Stage T1-2, N0, M0 disease
* Tumor size ≤ 5 cm
* Tumor must be within or touching the zone of the proximal bronchial tree, defined as a volume of 2 cm in all directions around the proximal bronchial tree (i.e., carina, right and left main bronchi, right and left upper lobe bronchi, intermedius bronchus, right middle lobe bronchus, lingular bronchus right, and left lower lobe bronchi) OR immediately adjacent to the mediastinal or pericardial pleura (PTV touching the pleura)
* Hilar or mediastinal lymph nodes ≤ 1 cm AND no abnormal hilar or mediastinal uptake on positron emission tomography (PET) scan are considered N0
* Mediastinal lymph node sampling by any technique is allowed but not required
* Patients with \> 1 cm hilar or mediastinal lymph nodes on CT scan or abnormal PET scan (including suspicious but nondiagnostic uptake) are eligible provided directed tissue biopsies of all abnormally identified areas are negative for cancer
* Tumor deemed technically resectable, in the opinion of an experienced thoracic cancer surgeon, with a reasonable possibility of obtaining a gross total resection with negative margins, defined as a potentially curative resection (PCR)
* Patient deemed "medically inoperable" due to severe underlying physiological medical problems that would prohibit a PCR, including any of the following:
* Baseline forced expiratory volume at one second (FEV1) \< 40% predicted
* Postoperative FEV1 \< 30% predicted
* Severely reduced diffusion capacity
* Baseline hypoxemia and/or hypercapnia
* Exercise oxygen consumption \< 50% predicted
* Severe pulmonary hypertension
* Diabetes mellitus with severe end-stage organ damage
* Severe cerebral, cardiac, or peripheral vascular disease
* Severe chronic heart disease
* Measurable disease as documented by CT scan or whole-body PET scan within the past 8 weeks
* Patients with lesions that cannot be visualized by CT scan are not eligible
* Pleural effusion allowed provided it is deemed too small to tap under CT guidance and is not evident on chest x-ray
* Pleural effusion that appears on chest x-ray is allowed only after thoracotomy or other invasive procedure
PATIENT CHARACTERISTICS:
* Zubrod performance status 0-2
* Not pregnant
* Negative pregnancy test
* Fertile patients must use effective contraception during and for ≥ 60 days after completion of study therapy
* No other invasive malignancy within the past 2 years except nonmelanomatous skin cancer or carcinoma in situ of the breast, oral cavity, or cervix
* Prior lung cancer allowed provided the patient has been disease-free for ≥ 2 years
PRIOR CONCURRENT THERAPY:
* No prior radiotherapy to the region of the study cancer that would result in overlap of radiotherapy fields
* No prior chemotherapy for the study cancer
* No other concurrent local therapy (including standard-fractionated radiotherapy and/or surgery) or systemic therapy (including standard chemotherapy or biologic targeted agents) specifically intended as treatment for study cancer
* Local or systemic therapy at the time of disease progression allowedReferences
Publications (2)
- DERIVEDBezjak A, Paulus R, Gaspar LE, Timmerman RD, Straube WL, Ryan WF, Garces YI, Pu AT, Singh AK, Videtic GM, McGarry RC, Iyengar P, Pantarotto JR, Urbanic JJ, Sun AY, Daly ME, Grills IS, Sperduto P, Normolle DP, Bradley JD, Choy H. Safety and Efficacy of a Five-Fraction Stereotactic Body Radiotherapy Schedule for Centrally Located Non-Small-Cell Lung Cancer: NRG Oncology/RTOG 0813 Trial. J Clin Oncol. 2019 May 20;37(15):1316-1325. doi: 10.1200/JCO.18.00622. Epub 2019 Apr 3. PMID 30943123
- DERIVEDLevy A, Guckenberger M, Hurkmans C, Nestle U, Belderbos J, De Ruysscher D, Faivre-Finn C, Le Pechoux C. SBRT Dose and Survival in Non-Small Cell Lung Cancer: In Regard to Koshy et al. Int J Radiat Oncol Biol Phys. 2015 Jul 15;92(4):945-6. doi: 10.1016/j.ijrobp.2015.03.032. No abstract available. PMID 26104945