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Intraoperative Boost Radiotherapy With Electrons (IOERT) Followed By Hypofractionated Whole-Breast Irradiation (WBRT)

Intraoperative Boost Radiotherapy With Electrons (IOERT) Followed By Hypofractionated Whole-Breast Irradiation (WBRT)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01295723
Enrollment
200
Registered
2011-02-14
Start date
2011-01-31
Completion date
2022-12-31
Last updated
2022-05-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Invasive Lobular and Ductal Carcinoma

Keywords

Breast cancer, Radiation therapy, Mobetron, IOERT, IORT, Hypofractionated radiation therapy, Partial breast radiation

Brief summary

Hypofractionated intraoperative boost (HIOB) is defined as hypofractionated WBRT (40.5 Gy in 2.7 Gy per fraction) preceded by an intraoperative boost to the tumor bed (10 Gy IOERT). The HIOB study concept will test whether such a combined schedule is superior or iso-effective standard RT in terms of local control and cosmetic outcome.

Detailed description

The purpose of this research study is to find out the effects (good and bad) of adding a dose of radiation to the area of the cancer during surgery to whole breast radiation therapy (WBRT) after surgery. IOERT is the application of electron radiation directly to the residual tumor or tumor bed during cancer surgery. WBRT is a type of radiation therapy used to treat patients who have cancer in the breast covering the entire breast tissue. Both immediate and long-term effects will be measured. For patients with certain types of breast cancer, one standard treatment is removal of the area of cancer and a small amount of normal tissue around it followed by breast radiation. The radiation treatment in this situation usually lasts 3 to 5 1/2 weeks of WBRT followed by 5-8 daily radiation treatments at the site where the lump was removed called a boost. During this study, the single dose of electron irradiation (IOERT) given at the surgical site during the operation will replace the usual 5-8 days of localized radiation and the whole breast radiation will last 3 weeks.

Interventions

RADIATIONHypofractionated Whole Breast Radiation Therapy

Hypofractionated Whole Breast Radiation Therapy must start within 14-56 days postoperatively (week 2-8 post-op) * Single reference dose per fraction: 2.7 Gy (ICRU) * Number of fractions: 15 * Number of fractions per week: 5 * Regular Radiation Therapy breaks: Weekend/ Holidays (not exceeding 7 days break) * Total dose: 50.5 Gy (40.5 WBRT + 10 Gy boost) Radiation: Intraoperative Electron Radiation Therapy

RADIATIONIntraoperative Electron Radiation Therapy

Intraoperative Electron Radiation Therapy (IOERT) is delivered after completion of the lumpectomy and sentinel node procedure. IOERT is performed on mobile or fixed linac with variable electron energies in the range of 4-12 MeV

Sponsors

St. Joseph Hospital of Orange
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histological proven invasive breast carcinoma (ductal and lobular) * Age \> 40 years * Karnofsky performance status \>70% * Single discrete tumor or focal microcalcifications that can be imaged on a specimen radiograph or multifocal disease within the same quadrant with a maximum dimension of 4 cm (invasive foci) * Nodal Status: NO-1 * Clear surgical margins: R0; min 2mm. Re-excision after IOERT is permitted but not required to achieve (-) margin. * All grades G1 - G3 * Any hormonal receptor and Her-2 status * Informed consent

Exclusion criteria

* In-situ Carcinoma without invasive component or multifocal disease \> 4 cm * Tumor stage: T3 or 4 * Nodal Status \> N1 pathologically * Surgical margins \< 2mm * Multicentricity * Previous radiotherapy to the involved breast * Karnofsky Index \< 70% * Mixed connective tissue diseases e.g. rheumatoid polyarthritis, thromboangitis obliterans, systemic lupus. * Distant metastases * Unable to provide written consent

Design outcomes

Primary

MeasureTime frameDescription
Assessment of acute and late toxicity5 yearsAssessment of acute toxicity of breast irradiation according to CTC-toxicity Scoring - systems: * At the end of Radiation Therapy * At time of first follow-up investigation (week 8 - 10) Assessment of late toxicity according to NSABP scoring - systems at 6, 12, 24, 36, 48, and 60 months

Secondary

MeasureTime frameDescription
Cosmetic Evaluation5 yearsAssessment of cosmetic outcome according to 5-point scoring system * Before Whole Breast Radiation Therapy * Not earlier than 7 months after Whole Breast Radiation Therapy * At yearly follow-up (photodocumentation in standardized positions) for 5 years.
Disease Free Survival5 yearsRecurrence assessments as documented at post-op follow-ups per protcol.
Overall Survival5 YearsThe length of time from the start of treatment to death within the 5 year period.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026