TerminatedEarly Phase 1NCT01525446

Proton Stereotactic Body Radiation Therapy for Early-Stage Non-Small Cell Lung Cancer

Stereotactic body radiation therapy (SBRT) is a special form of treatment which pinpoints high doses of radiation directly to cancer. Standard radiation (or photon radiation) is commonly used for SBRT to treat Non-Small Cell Lung Cancer (NSCLC). Proton beam radiation is a special type of radiation only available at a few institutions in the US and has not been previously used in SBRT to treat NSCLC. The use of protons for SBRT may improve the accuracy of the treatment and may help to minimize the dose delivered unnecessarily to healthy tissue. In this study, the investigators are evaluating the safety and effectiveness of proton-based SBRT for early-stage NSCLC located in the periphery of the lung.

Checked against the public recordLast updated Feb 17, 2016 · Source: ClinicalTrials.gov

StatusTerminated
PhaseEarly Phase 1
U.S. locations1
SponsorMassachusetts General Hospital
01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Early Phase 1
Sponsor
Massachusetts General Hospital
Interventions being studied
Radiation: SBRT with proton beam radiation
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Histologically or cytologically confirmed non-small cell lung cancer (need not be newly diagnosed) * Stage clinical T1 N0 M0 or T2 N0 M0 * NSCLC must be limited to a single lesion * NSCLC must be peripherally located (\> 2 cm from proximal bronchial tree and \> 1 cm from mediastinal pleura) * NSCLC must be considered medically inoperable * Life expectancy greater than 6 months Exclusion Criteria: * Pregnant or breastfeeding * Prior radiation therapy to the lungs or mediastinum * Prior malignancy in the last 2 years unless treated definitively and disease free or carcinoma in situ or early stage skin cancers that have been definitively treated * Receiving other study agents or other types of cancer therapy * Uncontrolled intercurrent illness * Pacemaker or defibrillator-dependent

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Massachusetts General HospitalBoston, Massachusetts

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Feb 17, 2016. Always confirm current availability with the study team.

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