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NCT Number: NCT01299987

Prospective Phase II Study of Intraoperative Radiotherapy (IORT) in Elderly Patients with Small Breast Cancer

This prospective, multicentric single arm phase II study is based on the protocol of the international TARGIT-A study. The purpose is to investigate the efficacy of a single intraoperative radiotherapy treatment within elderly low risk patients (≥ 70 years, cT1, cN0, cM0, invasive-ductal) which is followed by WBRT only when risk factors are present. In presence of risk factors postoperative WBRT will be added to complete the radiotherapeutic treatment according to international guidelines.

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Key information

Age range

70 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Universitätsmedizin Mannheim UMM

Mannheim, Baden-Wurttemberg, 68167, Germany

About this study

Patients ≥ 70 years with small, low-risk breast cancer who are operated but not irradiated show local relapse rates around 4% after 4 years. With adjuvant whole breast radiotherapy (WBRT) the local relapse rate drops to 1% after 4 years under Tamoxifen (Hughes et al 2004). It has been demonstrated (Polgar et al. 2007, Vaidya et al. 2010) that the efficacy of radiation of the tumor bed only in a selected group can be non-inferior to WBRT. The TARGIT E study should confirm the efficacy of a single dose of intraoperative radiotherapy (IORT) in a well selected group of elderly patients with small breast cancer and absence of risk factors. In presence of risk factors postoperative WBRT will be added to complete the radiotherapeutic treatment according to international guidelines.

Endpoints are the local relapse rate (within 2 cm of the tumor bed), ipsilateral relapse, cancer-specific and overall survival and contralateral breast cancer as well as documentation of quality of life and cosmetic outcome. The expected local relapse rates are 0.5/1/1.5% after 2.5/5/7.5 years, respectively.

Discontinuation of the trial is scheduled if rates of local relapse rates rise to 3/4/6% after 2.5/5/7.5 years. Power calculations result in 265 patients with a calculated loss to follow-up of 20%, an alpha of 0.05 and a beta 0.1. Only centers with access to the Intrabeam® system (Carl Zeiss) can recruit patients into the trial.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • cT1c cN0 cM0
  • ≥ 70 years old
  • invasive-ductal histology
  • compliance
  • informed consent

Exclusion criteria

  • extensive intraductal component (EIC)
  • multifocality /-centricity
  • lymph vessel invasion (L1)
  • clinical signs of distant metastases or clinically suspicious lymph nodes
  • other histology
  • < 70 years old
  • missing informed consent or non-compliance
  • bilateral breast cancer at time of diagnosis
  • known BRACA 1/2 mutations (genetic testing not required)

Treatment and study plan

intraoperative radiotherapy

Radiation

intraoperative single dose radiotherapy (20 Gy)

Other names: IORT

Primary outcomes

  1. Local Relapse

    Time frame: up to ten years

    Rate of local relapse (within 2cm of the initial tumor bed)

Secondary outcomes

  1. Overall Survival

    Time frame: up to ten years

    Death is an event

  2. Ipsi- or Contralateral Breast Cancer

    Time frame: up to ten years

    Rate of ipsilateral and contralateral breast cancer events

  3. Cosmesis

    Time frame: up to 7.5 years

    BCCT.Core analysis of cosmesis

  4. General and breast-specific Quality of Life after IORT

    Time frame: up to 10 years

    EORTC questionnaires QLQ C30 and BR23

  5. Late toxicity after IORT

    Time frame: up to ten years

    LENT-SOMA based toxicity at all FU time points

Sponsors and collaborators

Lead sponsor

Universitätsmedizin Mannheim

Other

Registry information

Official study title

TARGIT-E(Elderly) Prospective Phase II Study of Intraoperative Radiotherapy (IORT) in Elderly Patients with Small Breast Cancer

Acronym: TARGIT-E

Important dates

Study start
2011
Primary completion
2022
Study completion
2022
First posted
Feb 21, 2011
Registry last updated
Mar 30, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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