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Spots Global Cancer Trial Database for Proton Radiation for Stage II/III Breast Cancer

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Trial Identification

Brief Title: Proton Radiation for Stage II/III Breast Cancer

Official Title: Phase II Study of Postoperative, Cardiac-Sparing Proton Radiotherapy for Patients With Stage II/III,Loco-Regional, Non-Metastatic Breast Cancer Requiring Whole Breast or Chest Wall Irradiation With Lymph Node Irradiation

Study ID: NCT01758445

Interventions

Proton Radiotherapy

Study Description

Brief Summary: The purpose of this study is to look at the rates of acute and long term adverse events of postoperative proton radiotherapy for complex loco-regional irradiation in women with loco-regionally advanced breast cancer. This study specifically includes longitudinal follow up to assess the incidence of cardiac mortality and second malignant neoplasms at 10 and 15 years following proton therapy(PT).

Detailed Description: The proposed Phase II study is seeking to build clinical data as a continuation of the original dosimetric analysis published by Ares et al. performed at Paul-Scherrer Institute (PSI). That comparison demonstrated a benefit form proton planning for patients with non-metastatic breast cancer requiring complex, loco-regional, postoperative radiotherapy.1 The advantages of PT were improved target coverage compared to standard photon irradiation and reduced dose to heart, lungs and contralateral breast. The study goal is to demonstrate a "meaningful benefit" of proton therapy for women with loco-regionally advanced breast cancer. The main clinical endpoints of this trial are the reduction of cardiac morbidity and mortality (coronary artery disease, myocardial infarction, cardiac insufficiency) and the reduction of contralateral, second breast cancer. Both adverse events are presently associated with external beam photon therapy. Both goals require longitudinal follow-up of minimum 5-10 years. Despite the logistical challenges of long term follow-up, the effort is needed in view of the compelling preclinical evidence of dose avoidance or even absence of radiation dose to heart and contralateral breast uniquely accomplishable by protons only.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Northwestern Medicine Chicago Proton Center, Warrenville, Illinois, United States

Maryland Proton Treatment Center, Baltimore, Maryland, United States

Princeton ProCure Managment LLC, Somerset, New Jersey, United States

Oklahoma Proton Center, Oklahoma City, Oklahoma, United States

Hampton University Proton Therapy Institute, Hampton, Virginia, United States

Contact Details

Name: Eugen Hug, MD

Affiliation: Proton Collaborative Group

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

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