POSNOC - A Trial Looking at Axillary Treatment in Early Breast Cancer

Sponsor
University Hospitals of Derby and Burton NHS Foundation Trust (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT02401685
Collaborator
University of Nottingham (Other), Sussex Health Outcomes Research & Education in Cancer (SHORE-C) (Other), NCRI Radiotherapy Trials QA Group (RTTQA) (Other), Breast Cancer Trials, Australia and New Zealand (Other)
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2
149
38
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Study Details

Study Description

Brief Summary

POSNOC is a pragmatic, randomised, multicentre, non-inferiority trial.

Aim For women with early stage breast cancer and one or two sentinel node macrometastases, to assess whether adjuvant therapy alone is no worse than adjuvant therapy plus axillary treatment, in terms of axillary recurrence within 5 years.

Stratification: Institution, Age (<50, ≥50), Breast-conserving surgery (BCS) or mastectomy, Estrogen receptor (ER) status (positive, negative), Number of positive nodes (1, 2), Intra-operative sentinel assessment using OSNA (yes, no).

Interventions The study will compare adjuvant therapy alone with adjuvant therapy plus axillary treatment (axillary node clearance (ANC) or axillary radiotherapy (ART)).

Sample Size: 1900 participants

Follow-up: Participants will be followed up for 5 years.

Adjuvant Therapy: All participants will receive adjuvant systemic therapy (chemotherapy and/or endocrine therapy). All participants may receive breast/chest wall radiotherapy. Axillary and supraclavicular fossa radiotherapy is not allowed when randomised to adjuvant therapy alone.

Condition or Disease Intervention/Treatment Phase
  • Other: Adjuvant therapy
  • Procedure: Axillary treatment
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
1900 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
POSNOC - POsitive Sentinel NOde: Adjuvant Therapy Alone Versus Adjuvant Therapy Plus Clearance or Axillary Radiotherapy. A Randomised Controlled Trial of Axillary Treatment in Women With Early Stage Breast Cancer Who Have Metastases in One or Two Sentinel Nodes
Actual Study Start Date :
Aug 1, 2014
Anticipated Primary Completion Date :
Jul 1, 2026
Anticipated Study Completion Date :
Dec 31, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Adjuvant therapy alone

Women in this arm will have adjuvant therapy but no treatment to their armpit after surgery. Axillary and supraclavicular fossa radiotherapy is not allowed when randomised to this arm.

Other: Adjuvant therapy
Adjuvant therapy will include chemotherapy and/or endocrine therapy for all women, and radiotherapy to breast or chest wall if indicated. Human epidermal growth factor receptor 2 (HER2) targeted treatment may also be administered when indicated.

Active Comparator: Adjuvant therapy plus axillary treatment

Women in this arm will have adjuvant therapy plus treatment to their armpit after surgery. Axillary treatment can be axillary node clearance or axillary radiotherapy as per local guidelines.

Other: Adjuvant therapy
Adjuvant therapy will include chemotherapy and/or endocrine therapy for all women, and radiotherapy to breast or chest wall if indicated. Human epidermal growth factor receptor 2 (HER2) targeted treatment may also be administered when indicated.

Procedure: Axillary treatment
Axillary treatment can be axillary node clearance or axillary radiotherapy as per local guidelines.

Outcome Measures

Primary Outcome Measures

  1. Axillary recurrence [5 years]

    Axillary recurrence is defined as pathologically (cytology or biopsy) confirmed recurrence in lymph nodes draining the primary tumour site.

Secondary Outcome Measures

  1. Arm morbidity [3 years]

    Arm morbidity will be assessed by the Lymphoedema and Breast Cancer and QuickDASH (disabilities of the arm, shoulder and hand) questionnaires.

  2. Quality of life [3 years]

    Quality of life will be assessed using the Functional Assessment of Cancer Therapy-Breast+4 questionnaire.

  3. Anxiety (Spielberger State/Trait Anxiety Inventory) [3 years]

    Anxiety will be assessed with the Spielberger State/Trait Anxiety Inventory.

  4. Economic evaluation (EQ-5D-5L (EuroQoL) [3 years]

    Health-related quality of life will be evaluated using the EQ-5D-5L (EuroQoL) instrument.

  5. Local (breast or chest wall) recurrence [5 years]

    Number of participants with local (breast or chest wall) recurrence.

  6. Regional (nodal) recurrence [5 years]

    Number of participants with regional (nodal) recurrence.

  7. Distant metastasis [5 years]

    Number of participants with distant metastasis.

  8. Time to axillary recurrence [5 years]

  9. Axillary recurrence free survival [5 years]

  10. Disease free survival [5 years]

  11. Overall survival [5 years]

  12. Contralateral breast cancer [5 years]

    Number of participants with contralateral breast cancer.

  13. Non-breast malignancy [5 years]

    Number of participants with non-breast malignancy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Unifocal or multi-focal invasive tumour with lesion ≤5 cm in its largest dimension, measured pathologically or largest invasive tumour diameter on radiology should be used for women who are randomised intra-operatively or undergo sentinel node biopsy before neoadjuvant therapy (tumour size should be based only on the single largest tumour; do not add the sizes together from the multiple foci)

  • At sentinel node biopsy have 1 or 2 nodes with macrometastases (tumour deposit >2.0mm in largest dimension or defined as macrometastasis on molecular assay)

  • Fit for axillary treatment and adjuvant therapy

  • Have given written informed consent

Exclusion Criteria:
  • bilateral invasive breast cancer

  • more than 2 nodes with macrometastases

  • neoadjuvant therapy for breast cancer except:

  • if sentinel node biopsy performed prior to neoadjuvant chemotherapy in women with early breast cancer

  • short duration of neoadjuvant endocrine therapy is acceptable (up to 3 months)

  • previous axillary surgery on the same body side as the scheduled sentinel node biopsy

  • not receiving adjuvant systemic therapy

  • previous cancer less than 5 years previously or concomitant malignancy except:

  • basal or squamous cell carcinoma of the skin

  • in situ carcinoma of the cervix

  • in situ melanoma

  • contra- or ipsilateral in situ breast cancer

Contacts and Locations

Locations

Site City State Country Postal Code
1 Royal Adelaide Hospital Adelaide Australia
2 Bankstown-Lidcocombe Hospital Bankstown Australia
3 Maeter Hospital Brisbane Australia
4 Coffs Harbour Health Campus Coffs Harbour Australia
5 Monash Cancer Centre Melbourne Australia
6 Royal Melbourne and Royal Women's Hospital Melbourne Australia
7 Sir Charles Gairdner Hospital Perth Australia
8 Riverina Cancer Care Centre Wagga Wagga Australia
9 Waikato Hospital Hamilton New Zealand
10 Rotorua Hospital Rotorua New Zealand
11 Ashford and St Peter's Hospitals NHS Foundation Trust Ashford United Kingdom
12 Barnsley Hospital Barnsley United Kingdom
13 Belfast City Hospital Belfast United Kingdom
14 City Hospital Birmingham United Kingdom
15 Queen Elizabeth Hospital Birmingham United Kingdom
16 Royal Bolton Hospital Bolton United Kingdom
17 Bradford Royal Infirmary Bradford United Kingdom
18 Princess of Wales Hospital Bridgend United Kingdom
19 Addenbrooke's Hospital Cambridge United Kingdom
20 University Hospital Llandough Cardiff United Kingdom
21 Darrent Valley Hospital Dartford United Kingdom
22 Royal Derby Hospital Derby United Kingdom
23 Eastbourne District General Hospital Eastbourne United Kingdom
24 Western General Hospital Edinburgh United Kingdom
25 Medway Maritime Hospital Gillingham United Kingdom
26 Western Infirmary Glasgow United Kingdom
27 Inverclyde Royal Hospital Greenock United Kingdom
28 Harrogate District Hospital Harrogate United Kingdom
29 University Hospital Crosshouse Kilmarnock United Kingdom
30 Forth Valley Hospital Larbert United Kingdom
31 St James's University Hospital Leeds United Kingdom
32 University Hospitals of Leicester NHS Trust Leicester United Kingdom
33 Guy's and St Thomas' NHS Foundation Trust London United Kingdom
34 Royal Marsden Hospital London United Kingdom
35 Luton and Dunstable University Hospital Luton United Kingdom
36 Macclesfield District General Hospital Macclesfield United Kingdom
37 Maidstone Hospital Maidstone United Kingdom
38 North Manchester General Hospital Manchester United Kingdom
39 Wythenshawe Hospital Manchester United Kingdom
40 Royal Victoria Infirmary Newcastle upon Tyne United Kingdom
41 Royal Gwent Hospital Newport United Kingdom
42 The Norfolk and Norwich University Hospital Norwich United Kingdom
43 Oxford University Hospitals Oxford United Kingdom
44 Peterborough City Hospital Peterborough United Kingdom
45 Derriford Hospital Plymouth United Kingdom
46 Rotherham General Hospital Rotherham United Kingdom
47 Royal Stoke University Hospital Stoke-on-trent United Kingdom
48 Royal Cornwall Hospital Truro United Kingdom
49 Wishaw General Hospital Wishaw United Kingdom
50 New Cross Hospital Wolverhampton United Kingdom

Sponsors and Collaborators

  • University Hospitals of Derby and Burton NHS Foundation Trust
  • University of Nottingham
  • Sussex Health Outcomes Research & Education in Cancer (SHORE-C)
  • NCRI Radiotherapy Trials QA Group (RTTQA)
  • Breast Cancer Trials, Australia and New Zealand

Investigators

  • Principal Investigator: Amit Goyal, University Hospitals of Derby and Burton NHS Foundation Trust

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Dr Amit Goyal, Consultant Oncoplastic Breast Surgeon & Associate Professor, University Hospitals of Derby and Burton NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT02401685
Other Study ID Numbers:
  • RD-5103-001-13
  • ISRCTN Number
First Posted:
Mar 30, 2015
Last Update Posted:
Sep 16, 2021
Last Verified:
Sep 1, 2021
Keywords provided by Dr Amit Goyal, Consultant Oncoplastic Breast Surgeon & Associate Professor, University Hospitals of Derby and Burton NHS Foundation Trust
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2021