Post-operative Radiotherapy Omission in Selected Patients With Early Breast Cancer Trial International VErsion

Trial Title: Post-operative Radiotherapy Omission in Selected Patients With Early Breast Cancer Trial International VErsion

NCT ID: NCT06445738

Condition: Breast Cancer
Breast Cancer Female

Conditions: Official terms:
Breast Neoplasms

Conditions: Keywords:
Omission of radiotherapy
Magnetic Resonance Imaging (MRI)

Study type: Interventional

Study phase: N/A

Overall status: Not yet recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Parallel Assignment

Intervention model description: A two-arm, non-randomised study using MRI and pathological findings to select patients for omission of post-operative radiotherapy.

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Radiation
Intervention name: Arm A: Radiotherapy Omission
Description: Omission of radiotherapy based on pre-surgical MRI and pathology findings at surgery.
Arm group label: Radiotherapy Omission

Other name: A1: Grade 1 or 2/HER2 negative; A2: Grade 3 and/or HER2 positive

Intervention type: Other
Intervention name: Arm B: Standard Treatment
Description: Ineligible for RT omission on study; includes management of MRI-detected lesions.
Arm group label: Standard Treatment

Summary: The PROSPECTIVE trial aims to find out if using the results of Magnetic Resonance Imaging (MRI) for early breast cancer can select people to not have radiotherapy and still have a low chance of the cancer coming back after surgery. The main question it aims to answer is: * Will cancer come back in the same breast as the original cancer in patients who have surgery for their breast cancer, but who don't have radiotherapy afterwards because the results of an MRI before surgery showed favourable characteristics for not having radiotherapy.

Detailed description: Breast cancer is the most common serious malignancy in women and most patients are suitable for therapy involving surgery and adjuvant radiotherapy (RT). For most patients, there is a lack of evidence that breast conserving surgery without adjuvant RT is safe and therefore patients bear the costs, inconvenience and morbidity of RT. Prior attempts to identify large subsets of patients for whom RT can be safely omitted based on clinicopathological features of the index cancer have had limited success, and so RT is currently omitted only in some women over 65 or 70 with small low risk cancers. Identification of a much larger subset of patients in whom adjuvant RT could be safely omitted would be hugely significant, not only to the patients, but to the entire health system. The ANZ 1002 PROSPECT study was a two-arm phase II study that used breast MRI findings and pathological features to identify a group of patients with low risk early breast cancer in whom RT may be safely omitted. The findings at the primary strongly support the hypothesis and suggest that the combination of preoperative MRI and pathological features can identify a substantial group of early breast cancer patients in whom adjuvant RT can be safely omitted. A Health Economic analysis of PROSPECT found that the avoided costs of RT and its potential side effects is likely to substantially outweigh the extra cost of MRI scans and associated investigations. Parallel cross-sectional studies assessing Fear of Cancer Recurrence (FCR) and Health Related Quality of Life (HRQoL) in patients taking part in PROSPECT who either did or did not receive RT and a control group found a substantially lower FCR in PROSPECT patients who omitted RT as well as improved HRQoL. The majority of screened and eligible patients (427/443 and 193/201, respectively) for PROSPECT were recruited from two Australian sites. Before the PROSPECT approach can be widely adopted, the findings need to be replicated in a multicentre, international study. In addition, patient reported outcomes and health economic assessments need to be performed prospectively and longitudinally. PROSPECTIVE is the follow-up to PROSPECT which will address these issues, and also include translational research aspects to further study the natural history and outcomes of this group of lower risk early breast cancers.

Criteria for eligibility:
Criteria:
Inclusion Criteria: For inclusion in the study at Registration, participants must fulfil all of the following criteria: 1. Has provided written, informed consent to participate in the study. 2. Female participants ≥ 50 years old with histologically* confirmed ER-positive and/or HER2-positive invasive breast cancer. 3. In good health and suitable for prolonged follow up with a life expectancy of at least 10 years; willing to be followed up for 10 years. 4. Breast imaging indicating unifocal**, unilateral breast cancer must have been performed before pre-registration. 5. Willing/able to have surgery within 8 weeks of registration or pre-operative MRI, whichever occurs later. 6. Pathology material from index cancer must be available. 7. Have ECOG performance status 0-2. 8. Participants with Grade 3 cancer and/or HER2-positive cancer must agree to comply with systemic treatment recommendations. - Oestrogen receptor and progesterone receptor status of invasive cancer will be assessed by immunohistochemistry on the diagnostic core biopsy specimen. The IHC results will be reported as percentage of nuclei stained and a score of intensity from negative, weak, intermediate or high staining - HER2 neu status will be assessed by immunohistochemistry and will be scored as follows46: - 0 or 1+ (HER2 negative): No staining or membrane staining that is incomplete and is faint/barely perceptible and in ≤ 10% of tumour cells (0); or incomplete membrane staining that is faint/barely perceptible and in > 10% of tumour cells (1+). - 2+ (equivocal): weak to moderate complete membrane staining observed in > 10% of tumour cells. Must order reflex test (same specimen using ISH) or order a new test (new specimen if available using HIS or ISH). - 3+ (HER2 positive): Circumferential membrane staining that is complete, intense and in > 10% of tumour cells. Exclusion Criteria: Any one of the following at Registration is regarded as a criterion for exclusion from the study: 1) Triple negative breast cancer (ER-negative and PR-negative and HER2-negative) where ER and PR positivity is defined as Any one of the following at Registration is regarded as a criterion for exclusion from the study: 1. Triple negative breast cancer (ER-negative and PR-negative and HER2-negative) where ER and PR positivity is defined as ≥ 10% staining on IHC47. 2. Previous ipsilateral in-situ or invasive breast cancer. 3. Participants who have a mastectomy for the index cancer. 4. Lymphovascular invasion. 5. Multifocal/multicentric breast cancer. 6. Distant metastasis at diagnosis. 7. Bilateral breast cancer. 8. Known breast cancer predisposition gene mutation carriers (BRCA 1 or 2, PALB2, CHEK2, ATM, CDK1, p53). 9. Contraindication to MRI scanning. 10. Concurrent illness/conditions which limits life expectancy to 10 years. 11. Inability to give informed consent. 10% staining on IHC47. 2) Previous ipsilateral in-situ or invasive breast cancer. 3) Participants who have a mastectomy for the index cancer. 4) Lymphovascular invasion. 5) Multifocal/multicentric breast cancer. 6) Distant metastasis at diagnosis. 7) Bilateral breast cancer. 8) Known breast cancer predisposition gene mutation carriers (BRCA 1 or 2, PALB2, CHEK2, ATM, CDK1, p53). 9) Contraindication to MRI scanning. 10) Concurrent illness/conditions which limits life expectancy to 10 years. 11) Inability to give informed consent. Allocation: Arm A - Radiotherapy Omission In addition to the above criteria, for inclusion in the omission of radiation therapy arm of the study after surgery, participants must fulfil all the following criteria (see Section 9.5.2). Participants not fulfilling any one of the following criterial will be allocated to Arm B: 1. Female participants ≥ 50 years old with histologically* confirmed ER-positive and/or HER2-positive, unifocal**, unilateral invasive breast cancer. 2. Has nil/minimal or mild parenchymal enhancement on pre-operative MRI. 3. Breast conserving surgery with invasive primary tumour (including any surrounding DCIS) ≤ 20 mm. 4. Radial resection margins must be ≥ 2 mm clear of any invasive cancer and ≥ 2 mm clear of any DCIS. Superficial or deep margins of < 2 mm for invasive cancer and DCIS are allowed if all breast tissue from the subcutaneous tissue or pectoralis fascia respectively was removed and radial margins are ≥ 2 mm for invasive cancer and DCIS. 5. pN0 (pN0 i+ is eligible for inclusion) by sentinel node biopsy and/or axillary dissection. 6. Absence of lymphovascular invasion and extensive intraductal component. 7. Have no additional BIRADS 3+ lesions not shown to be benign on pre-operative or surgical biopsy. 8. Participants must be allocated within 8 weeks after final breast surgery. - Oestrogen receptor and progesterone receptor status of invasive cancer will be assessed by immunohistochemistry on the diagnostic core biopsy specimen. The IHC results will be reported as percentage of nuclei stained and a score of intensity from negative, weak, intermediate or high staining - Where histopathology is unable to identify a 'bridge' of tumour tissue joining two or more apparent invasive cancer foci the following will be used to confirm unifocal disease: - All foci must be of the same histology - All foci must have the same hormone (ER and PR) and HER2 status. In relation to Allocation Criteria #3: the overall tumour size (including additional foci of DCIS) must remain ≤ 20 mm. The tumour size is defined as the longest distance between the outer most edges of all foci, the space between the two or more foci is included in the overall size: Size = ('Focus A + Focus B + 'the distance between A and B'). Allocation: Arm B - Standard Treatment In addition to the above Inclusion Criteria, participants who fulfil one any of the following criteria will receive standard treatment: 1. Has moderate or marked parenchymal enhancement on pre-operative MRI. 2. Has a biopsy-proven malignant occult lesion (mOL) identified on MRI. 3. Suspicious lesion identified on CEM but not on MRI and confirmed on investigation to be a malignant lesion. 4. Surgical pathology does not meet the inclusion criteria. 5. Clinical team meeting determination that RT be recommended. 6. Participant chooses to have RT despite being eligible for RT omission.

Gender: Female

Minimum age: 50 Years

Maximum age: N/A

Healthy volunteers: No

Start date: January 1, 2025

Completion date: January 1, 2039

Lead sponsor:
Agency: Breast Cancer Trials, Australia and New Zealand
Agency class: Other

Source: Breast Cancer Trials, Australia and New Zealand

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06445738