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OpenTrials
Completed

NCT Number: NCT06363812

Probability of OncotypeDx to Reallocate As Low or High Risk of Recurrence Breast Cancer Patients with Uncertain Biology

In some cases of hormone receptor positive, human epidermal growth factor receptor 2 (HER2) negative early breast cancer the benefit of adding adjuvant chemotherapy to hormonal treatment, estimated on the basis of the classical clinico-pathological parameters, is unclear. In these cases the application of a genomic test could be useful in guiding the therapeutic choice.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hospital of Prato

Prato, 59100, Italy

About this study

Oncotype Dx (ODx) is a 21-gene assay that classifies primary ER+ breast tumors into three categories of recurrence risk: High (HR), Intermediate (IR) and Low (LR).

Available data show that

  • patients with ODx low score breast cancer perform well without chemotherapy,
  • chemotherapy has an additive value to endocrine therapy in patients with ODx high score tumors, and
  • the role of chemotherapy is unknown in patients with ODx intermediate score cancer.

In this study, the investigators aim to evaluate the capability of ODx to help in guiding the choice of systemic adjuvant treatment in a group of patients with ER+ and HER2- , node negative (pN0) or micrometastatic (pNmi) breast cancer with uncertain biological behavior for whom there is uncertainty about the indication of adjuvant chemotherapy.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histological diagnosis of infiltrating ductal or lobular ER+ HER2- early breast cancer adequately treated with surgery
  • Nodal status: no regional lymph node metastasis (pN0) or micrometastatic regional lymph node (pN1mic)
  • Uncertain biological behavior defined by all of the following parameters: ER >20% and progesterone receptor (PgR) >20% and Ki67 between 14% and 30% and G2
  • Written informed consent

Exclusion criteria

  • pathologic tumor stage (pT) > 5 cm (not applicable to the internal control group)
  • Prior neoadjuvant therapy
  • Evidence of metastatic disease
  • No axillary exploration (sentinel lymph node biopsy or axillary dissection)
  • Multifocal or multicentral or bilateral tumors

Treatment and study plan

Primary outcomes

  1. the proportion of tumor samples with a useful OncotypeDx

    Time frame: 15 days

    number of low risk and high risk at OncotypeDx divided by the total number of tests

Secondary outcomes

  1. the proportion of patients in which the result of the test has induced a modification in the initial treatment plan

    Time frame: 15 days

    number of cases with a therapeutic change divided by the total number of tested cases

  2. the proportion of tumor samples with an intermediate risk or not evaluable at OncotypeDx

    Time frame: 15 days

    number of intermediate risk and not evaluable at OncotypeDx divided by the total number of tests

Sponsors and collaborators

Lead sponsor

Fondazione Sandro Pitigliani

Other

Collaborators

  • Genomic Health®, Inc.
  • Istituto Toscano Tumori

Registry information

Official study title

Prospective Study Evaluating the Probability of OncotypeDx to Allocate At Low or High Risk of Recurrence Early ER Positive HER2 Negative Breast Cancer Patients with Uncertain Biological Behavior Evaluated by Pathological Parameters

Important dates

Study start
2018
Primary completion
2021
Study completion
2024
First posted
Apr 12, 2024
Registry last updated
Feb 28, 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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