NCT Number: NCT01899989
Stereotactic Body Radiation Therapy for Inoperable Locally-advanced Non-small Cell Lung Cancer
The purpose of this study is to determine if the use of exploratory immunologic biomarkers, functional MRI images can serve as early predictors for response of NSCLC. It also will provide important information on the perceived side effects from a patient perspective. Patients may participate if they have tumors ≥3 cm without lymph node involvement (for which chemotherapy is not part of the standard of care). Patients will only receive stereotactic body radiation therapy (SBRT) per standard dose guidelines.
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Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
Memorial Sloan Kettering Cancer Center at Basking Ridge, Basking Ridge, New Jersey, United States
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
All patients:
- Histologically confirmed non-small cell lung cancer
- Medically or technically inoperable as per thoracic surgeon or patient's preference not to undergo surgical resection
- Age ≥ 18 years
- Women of childbearing potential must have a negative blood pregnancy test
- Ability to provide written informed consent
Cohort A:
- Stage IIA-IIIA (TanyN1M0 or T2b-4N0M0) Selected patients with single station N2 nodal involvement in close proximity to the primary tumor target may be considered eligible at the discretion of the PI if all normal tissue guidelines can be met
- Eligible for chemo-therapy
- Karnofsky Performance Status ≥70%
- Men and women of childbearing potential must be willing to use effective contraception while on treatment and for at least 3 months thereafter
- Patients must show adequate organ function as defined by:
- Calculated creatinine clearance ≥40 mL/min for patients receiving pemetrexed (by Cockcroft-Gault)
- Calculated creatinine clearance ≥30 mL/min for patients receiving gemcitabine or paclitaxel (by Cockcroft-Gault) Total bilirubin less than 1.5 x ULN (unless known Gilbert's disease)
- AST and ALT less than 3 x ULN
- Absolute neutrophil count greater than 1500/mm3
- Platelet count greater than 100,000/mm3
Cohort B:
- T2a-4N0M0 who are not candidates for cohort A or who will not be treated with chemotherapy (due to patient preference or at the recommendation of the treating physician).
Exclusion criteria
All patients:
- Prior radiation therapy to the lungs
- Prior surgery or chemotherapy for this presentation of lung cancer (history of prior lung cancer that has been treated and deemed inactive by the clinician is acceptable. Recurrent tumors may be treated on protocol as long as SBRT will be the definitive treatment.)
- N2-3 lymph node involvement based on PET/EBUS-FNA/mediastinoscopy (Any N2 disease that is more than just minimal single station involvement is excluded)
- Direct tumor extension into including aorta or pulmonary artery
- Chronic corticosteroid use equivalent to ≥ prednisone 10 mg daily
Prior treatment with a CD137 agonist, ipilimumab, or the CTLA-4 inhibitor, or PD-1/PDL-1 inhibitor
- Unstable congestive heart failure
Cohort A:
- Continuous oxygen use
Patients meeting the following exclusion criteria will be excluded from the functional MRI portion only:
- Metallic implant,exclusions will be determined per institutional policies
- Pacemaker and defibrillators are excluded
- Stents etc. will be evaluated according to MSKCC policy
- Unmanageable claustrophobia
- High risk for nephrogenic systemic fibrosis
Treatment and study plan
cisplatin or carboplatin-based
DrugStandard chemotherapy with a histology-selected cisplatin or carboplatin-based doublet will be administered intravenously as adjuvant therapy. Gemcitabine will be used for squamous cell carcinomas and pemetrexed will be used for non-squamous non-small cell lung cancer. Cisplatin or carboplatin will be used in combination with the histology-selected agent. The choice of cisplatin or carboplatin will be at the discretion of the treating medical oncologist.
Primary outcomes
-
maximum tolerated dose (Cohort A)
Time frame: 2 years
standard 3+3 dose-escalation scheme
Secondary outcomes
-
≥ grade 4 or persistent ≥ grade 3 late toxicities (Cohorts A & B)
Time frame: ≥3 months post SBRT
All patients will be assessed for toxicities according to CTCAE v 4.0 at least once during SBRT.
-
overall survival (Cohorts A & B)
Time frame: 2 years
Response and progression will be evaluated per standard of care for radiographic progression on CT scans.
Sponsors and collaborators
Lead sponsor
Memorial Sloan Kettering Cancer Center
Other
Registry information
Important dates
- Study start
- 2013
- Primary completion
- 2024
- Study completion
- 2024
- First posted
- Jul 16, 2013
- Registry last updated
- Oct 4, 2024
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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