Breast-Sparing Proton Therapy for Hodgkin's Disease

NCT ID: NCT02070393

Last Updated: 2015-02-04

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 3 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-09-30
• Study Completion Date: 2015-02-28

Brief Summary

The purpose of this study is to drastically reduce unnecessary breast dose in young females with Hodgkin's Disease who require radiation therapy.

Detailed Description

According to the National Cancer Institute's Surveillance, Epidemiology, and End Results Program, there will be an estimated 8,490 new cases of Hodgkin's Lymphoma (HL) in the United States in 2010, with an estimated 1,320 deaths (Jemal, Siegel et al.). The unadjusted rates of 5 year overall survival are approximately 95%, and remain among the highest of all childhood and adult malignancies. With many children and young adults surviving into advanced age, the impetus has been to develop less toxic yet equally effective treatments. One of the main approaches taken over the last 25 years to minimize long-term treatment toxicity has been to limit the amount and volume of radiation received by patients. This pilot study continues along those lines, attempting to further refine the delivery of radiation therapy (RT) in order to avoid one of the most notorious long-term side-effects: secondary breast cancer.

Multiple studies investigating late toxicity in long-term survivors of pediatric Hodgkin's Lymphoma have shown the risk of breast cancer in young females receiving mediastinal radiation to be 50 times greater than their age-matched counterparts. The Late Effects Study Group, with a median follow-up of 17 years, reported a breast cancer incidence of 16% with a standardized incidence ratio of 55.5 (Bhatia, Yasui et al. 2003). Through utilization of breast-sparing proton therapy, we hope to provide young female patients with the benefits of radiation therapy while decreasing their risk of secondary breast cancer, thus increasing the therapeutic ratio.

In a prior computer-based, in-silico, dose planning study, utilizing the most basic beam orientation (a single PA beam), we showed that dose to breast tissue was reduced by a minimum of at least 80% with proton treatment compared to standard AP-PA photon treatment (in publication). Furthermore, dose to clinical target volume was maintained, and dose to other normal structures was statistically no worse. We now aim to validate these findings by verifying the beam range, in-vivo, via post-treatment combined Positron Emission Tomography-Computer Tomography (PET-CT) imaging in young females undergoing supra-diaphragmatic radiotherapy for Hodgkin's Disease.

Conditions

Hodgkins Disease

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Radiation Treatment using Protons

14 -24 Radiation Treatments (typically 1.5 - 1.8 cobalt-Gray equivalent per fraction for 14-24 treatments).

Group Type: EXPERIMENTAL

Proton

Intervention Type: RADIATION

14-24 Radiation treatments using Protons

Interventions

Proton

14-24 Radiation treatments using Protons

Intervention Type: RADIATION

Other Intervention Names

Breast sparing using proton beams

Eligibility Criteria

Inclusion Criteria

• Female sex
• Age >/= 10 years old and < 30 years old
• Pathologically confirmed classical Hodgkin's Lymphoma
• At least one site of disease located above the diaphragm
• Signed study-specific consent prior to initiation of therapy
• Women of child-bearing potential must have a negative pregnancy blood test within 7 days of starting protocol therapy.

Exclusion Criteria

• Previous radiation therapy to any part of the body.
• Parenchymal lung involvement at initial presentation or any patient that may need whole lung irradiation as per institutional guidelines.
• Lymphocyte predominant histology not eligible.
• Significant infection or other coexistent medical condition that would preclude protocol therapy such as:

• History of HIV/AIDS
• History of collagen Vascular Disease
• Symptomatic congestive heart failure
• Unstable angina pectoris or myocardial infarction within 6 months
• Uncontrolled hypertension (systolic blood pressure > 160 mm Hg or diastolic blood pressure > 100 mm Hg on 2 consecutive measurements separated by 1 week).
• History of uncontrolled diabetes
• Psychiatric illness/social situations that would compromise patient safety or limit compliance with study requirements

• Minimum Eligible Age: 10 Years
• Maximum Eligible Age: 30 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Indiana University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Jeffery Buchsbuam, MD

Role: PRINCIPAL_INVESTIGATOR

Indiana University

Locations

Indiana University Health Proton Therapy Center

Bloomington, Indiana, United States

Countries

United States

Other Identifiers

IUHPTC-01

Identifier Type: -

Identifier Source: org_study_id