Camden, New Jersey 08103


Purpose:

This is a pilot study looking at using stereotactic radiosurgery and full dose chemotherapy to treat stage II and III lung cancer that is not amendable to surgical resection.


Study summary:

Current standard of care for treatment of locally advanced (unresectable stage II and all of stage III) non-small cell lung cancer (NSCLC) is chemo-radiation which consists of 7 weeks of radiation and chemotherapy given at a reduced dose (as opposed to systemic dose when chemotherapy given by itself). While outcomes have improved over time they remain humbling, with current approaches associated with overall poor results both in terms of local (30% of patients have local failure) and distant control (40% of patients have distant failure) with a median overall survival of 17 months. This study is evaluating treatment with full dose chemotherapy and stereotactic body radiotherapy (SBRT). SBRT uses high doses of radiation in a very precise and conformal manner, the number of treatments are much reduced versus conventional radiation (SBRT would be able to be completed in 2 weeks or less). The biologically effective dose of SBRT is much higher than that of conventional radiation; despite being a shorter number of treatments the effective radiation dose is higher. SBRT would be completed in 2 weeks and since radiation would be completed in a shorter time span, would allow patients to have higher (systemic) chemotherapy doses. The purpose of this study is to explore SBRT in addition to systemic doses of chemotherapy in the treatment of locally advanced NSCLC.


Criteria:

Inclusion criteria: - Nonsmall cell lung cancer (NSCLC) (any histology) - unresectable stage II - Stage III - Tumor less than 8 cm - Karnofsky performance scale (KPS) of 50 or better - Three or fewer mediastinal or hilar lymph nodes Exclusion criteria - Small cell lung cancer (SCLC) - Stage I and stage IV patients - Stage II patients eligible for surgical resection - Concurrent severe disease that the treating physician feels will interfere with therapy this can include significant cardiovascular or pulmonary disease. - KPS 40 or less (bed bound) - Tumor size greater than 8 cm - Inability to safely treat target lesions (at discretion of treating physician, this would most likely be secondary to not being able to place fiducial markers for tracking) - Four or more medisatinal or hilar lymph nodes


NCT ID:

NCT02568033


Primary Contact:

Kimberly Krieger
Phone: 856-735-6237


Backup Contact:

N/A


Location Contact:

Camden, New Jersey 08103
United States

Kim Krieger
Phone: 856-735-6237

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2019

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