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Completed

NCT Number: NCT06464341

Nodal Burden and Nodal Recurrence in Patients With Isolated Tumor Cells After Neoadjuvant Chemotherapy Treated With Axillary Dissection or Nodal Radiation: the OPBC-05/EUBREAST-14R/ICARO Study

The purposes of this multicenter retrospective cohort study are to determine the residual nodal burden in patients with isolated tumor cells detected in the SLN or the clipped node after NAC and to determine oncologic outcomes in this group of patients after ALND or nodal RT or observation.

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Key information

Age range

18 year–100 year

Sex eligibility

Female

Study type

Observational

Primary location

Medical University of Vienna, Vienna, Austria

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About this study

In the context of upfront surgery, the extent of disease in the sentinel lymph nodes (SLNs) significantly predicts the chances of additional non-SLN metastases during axillary lymph node dissection (ALND). For patients with minimal SLN disease (isolated tumor cells [ITCs] and micrometastases), the probability of further non-SLN metastases is between 10-20%. In contrast, for patients with macrometastases, the risk increases to 27-33%.

In patients undergoing neoadjuvant chemotherapy (NAC), those with positive SLNs exhibit a greater residual nodal burden compared to those treated with upfront surgery. For patients with remaining micro- or macrometastases post-NAC, additional positive lymph nodes are found in over 60% of ALND specimens, regardless of receptor subtype. Consequently, ALND remains the standard care for any residual nodal disease after NAC.

Residual ITCs after NAC are present in about 1.5% of all patients undergoing NAC. There is limited data on the likelihood of discovering additional positive lymph nodes in this group, with fewer than 35 documented cases examining residual nodal burden. Therefore, the benefit of ALND for minimal residual disease is uncertain, and axillary management for patients with nodal ITCs is not standardized. Although omitting ALND reduces arm morbidity, identifying residual nodal disease can influence adjuvant therapy recommendations. Despite the lack of consensus on the oncologic safety of omitting ALND in this group, care patterns indicate a growing adoption of this approach. Given the rarity of this clinical scenario and the absence of forthcoming prospective studies, this study utilized real-world data from a large international cohort to determine the incidence of residual non-SLN involvement in patients with ITCs in the SLNs post-NAC, and to compare clinical outcomes in patients with and without ALND as definitive axillary treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Consecutive patients affected with T1-4 N0-3 breast cancer
  • For cN+: Biopsy proven confirmation is required
  • For cN0: any axillary staging technique including palpation is allowed
  • Residual ITCs in the SLN or clipped node
  • At least 1-year follow-up (12/2021 or later depending on the time of data collection)
  • For cN0: SLNB with single or dual tracer mapping
  • For cN+: SLNB with dual mapping or targeted axillary dissection (TAD: imaging-guided localization of sampled node in combination with SLN procedure with or without dual mapping)
  • Underwent TAD/SLNB +/- ALND +/- axillary RT

Exclusion criteria

  • Male patients
  • Patients with nodal pCR
  • Patients with residual nodal micro- or macrometastases
  • Stage IV disease at presentation
  • Inflammatory breast cancer (T4d) at presentation

Treatment and study plan

Observational study no intervention

Other

Observational study no intervention

Primary outcomes

  1. Number of Axillary Lymph Node Dissection (ALND)

    Time frame: Day 0

    Evaluation of the number of ALNDs performed

  2. Number of Tailored Axillary Dissection (TAD)

    Time frame: Day 0

    Evaluation of the number of TAD performed

  3. Number of Sentinel Lymph Node Biopsy (SLNB)

    Time frame: one time assessment before surgery

    Evaluation of the number of SLNB performed

  4. Number Axillary Radiotherapy

    Time frame: Up to 2 years

    Evaluation of the number of axillary radiotherapy performed

  5. Number of additional micrometastases

    Time frame: Day 0

    Evaluation of the number of additional micrometastases removed by ALND

  6. Number of additional macrometastases

    Time frame: Day 0

    Evaluation of the number of additional macrometastases removed by ALND

  7. Axillary recurrence

    Time frame: Up to 14 years

    Evaluation of the number of axillary recurrence

Secondary outcomes

  1. Regional recurrence

    Time frame: Up to 14 years

    Evaluation of the number of regional recurrence

  2. Locoregional recurrence

    Time frame: Up to 14 years

    Evaluation of the number of locoregional recurrence

  3. Invasive recurrence

    Time frame: Up to 14 years

    Evaluation of the number of invasive recurrence

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Collaborators

  • Memorial Sloan Kettering Cancer Center

Registry information

Acronym: ICARO

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Jun 18, 2024
Registry last updated
Jan 20, 2025

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

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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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