Clinical trial · Interventional
A Randomized Comparison of Radiation Therapy Techniques in the Management of Node Positive Breast Cancer
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Radiotherapy has been shown to reduce breast-cancer specific mortality in patients at high risk for distant dissemination. It has also been shown to increase rates of non-breast cancer deaths and morbidity due to cardiovascular and pulmonary toxicity. Although treatment planning has improved significantly through the years, recent reports still demonstrate treatment-related morbidity even with 3-dimensional planned techniques. Thus, while 3D planning represents the state of the art treatment for loco-regional radiotherapy for breast cancer, further improvement is needed to continue to decrease heart and lung exposure. The ultimate goal of the proposed research is to determine whether treatment planning using intensity-modulated radiotherapy (IMRT), the "next generation" of radiation treatment delivery systems, results in less radiation exposure to the heart and lungs than the best current RT technique in women with node positive breast cancer. This proposal will test the potential clinical value of IMRT compared to the best standard 3D plan (partially wide tangent fields, PWTF) in the treatment of breast cancer. These two treatment techniques will be studied in a Phase II randomized trial using quantitative indicators of potential cardiac and lung toxicity. The preliminary data generated from this trial will be used to ultimately justify a multi-institutional comparison of the two treatment techniques with long-term clinical cardiac and pulmonary toxicity as endpoints.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| 3D | Radiation | — | UNRESOLVED |
| IMRT | Radiation | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- 1
- description
- Best Delivery-optimized radiotherapy technique (IMRT)
- interventionNames
- Radiation: IMRT
- type
- ACTIVE_COMPARATOR
- label
- 2
- description
- Best 3-dimensional standard PWTF technique
- interventionNames
- Radiation: 3D
Primary outcomes (1)
- measure
- The Number of Participants With a Significant Increase in Perfusion Defects (PD)
- timeFrame
- 1 Year
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: Eligibility Criteria * Breast cancer diagnosis: Patients must have histologically confirmed adenocarcinoma of the breast requiring comprehensive loco-regional irradiation that includes treatment to the intact breast/chest wall, supraclavicular (SCV), infraclavicular nodes (ICV), and internal mammary nodes (IMN). * Patients must have pathologic T 1, 2, 3 or 4, N 1, 2, or 3 Stage II or III disease as defined by the AJCC Staging System, 6th edition. Patients who do not undergo axillary staging but are at risk for nodal involvement may also be treated. * All patients must have left-sided breast cancer. * Both men and women are eligible. * Patients must be adults (18 years of age or older) * For women of child-bearing age, effective contraception must be used. A written statement must be obtained that the patient is not pregnant. If there is any question of pregnancy at time of therapeutic RT or at time of each SPECT-CT scan, a pregnancy test will be done to confirm the patient is not pregnant. * Performance status should be 0-2 by ECOG criteria. * Patients that have received prior RT may be enrolled on the present study if the new breast lesion can be treated with no overlap of RT fields. * Patients must be aware of the neoplastic nature of her/his disease. * Patients must be informed of the investigational nature of this study and must sign an informed consent in accordance with the Institutional Review Board (IRB) of the University of Michigan and federal guidelines. * Patients' blood tests should indicate they are able to tolerate radiotherapy. Tests must be done within 28 days of registration: CBC with differential and platelet count (Hemoglobin \> 8.0 g/dl; wbc \> 2000/mm3; absolute neutrophil count \> 1000/mm3; platelet count \> 75,000/mm3. Exclusion Criteria: * Patients who are pregnant or are nursing are excluded. * Pathologically node negative breast cancer unless treated with neo-adjuvant chemotherapy. * Performance status \> 2 by ECOG criteria * Patients who are unable to lie on their back and raise their arm above their head in the treatment planning position for radiotherapy * Patients with a clinically unstable medical condition * Patients with a life-threatening disease state * History or suspicion of serious life-threatening allergic reaction to Tc-99m imaging agents. * Patients that have had breast-conservation surgery with positive margins or any patient with negative margins with a tumor positive for an extensive intraductal component. * Patients that are not able to use the ABC device.
References
Publications (1)
- DERIVEDJagsi R, Griffith KA, Moran JM, Ficaro E, Marsh R, Dess RT, Chung E, Liss AL, Hayman JA, Mayo CS, Flaherty K, Corbett J, Pierce L. A Randomized Comparison of Radiation Therapy Techniques in the Management of Node-Positive Breast Cancer: Primary Outcomes Analysis. Int J Radiat Oncol Biol Phys. 2018 Aug 1;101(5):1149-1158. doi: 10.1016/j.ijrobp.2018.04.075. Epub 2018 May 5. PMID 30012527