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NCT Number: NCT06240195

Biomarkers of Efficacy and Tolerability of Sacituzumab-Govitecan in the Treatment of Patients With Triple-negative Breast Cancer in the Metastatic Phase: Prospective Multicenter Real-world Study

Observational, prospective, multicenter study. Collection of data relating to the effectiveness of sacituzumab govitecan SG, in a real-world context and planned research of predictive biomarkers of efficacy/tolerability carried out on multiple platforms at the center coordinator.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

"Regina Elena" National Cancer Institute

Rome, 00144, Italy

Location status: Recruiting

Location contact

Patrizia Vici, Doctor

CONTACT

[email protected]

06-5266.5584 ext. +39

About this study

Identification and inclusion in the study of patients affected by metastatic triple-negative breast cancer mTNBC, treated with sacituzumab govitecan SG as indicated at the participating centers.

Histological and biomolecular characteristics will be evaluated both on the tumor at diagnosis and on tissue resulting from biopsy of the metastatic site, where available. Otherwise, the analyzes will come anyway carried out on the most recent and available tumor tissue, whether deriving from primary tumor or site metastatic.

The search for biomarkers predictive of efficacy/tolerability will be carried out on tumor tissue (where possible both primary and metastatic) and on circulating plasma collected at two separate time points (T0 and T1).

Biomolecular characterization on the biological material of the enrolled patients (tumor tissue and plasma) will be carried out at the end of the study.

The feasibility of organoid development and single-cell sequencing will be evaluated on a small subgroup of patients, among those enrolled at the coordinating center, considering the need for tumor tissue prepared fresh for both methods.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years;
  • Histological diagnosis of TNBC;
  • Locally advanced unresectable or metastatic disease;
  • Indication for treatment with SG in monotherapy according to clinical practice (patients pre-treated with at least two lines of systemic therapy, of which at least one in an advanced stage);
  • Availability of at least one tumor tissue sample (from primary tumor or metastasis) to be sent to the coordinating center (IRE);
  • Written informed consent;
  • Availability to comply with the procedures established by the protocol, according to the methods and times described.

Exclusion criteria

  • Patients with a history of other malignancies;
  • Contraindications to the use of sacituzumab govitecan SG;
  • Untreated and/or clinically unstable (symptomatic) brain metastases.

Treatment and study plan

Data Collection

Other

Collection of data relating to the effectiveness of sacituzumab govitecan and evaluation in a real-world context and planned research of predictive biomarkers of efficacy/tolerability

Primary outcomes

  1. Biomolecular investigations conducted on multiple platforms

    Time frame: 30 months

    Identify the predictive factors of the efficacy of sacituzumab govitecan in terms of PFS through biomolecular investigations conducted on multiple platforms, using tumor tissue (where possible both primary and metastatic) and peripheral blood, circulating plasma collected at two separate time points (T0 and T1) of mTNBC patients treated in the real-world setting.

Secondary outcomes

  1. PFS in patients.

    Time frame: 30 months

    Assess any differences in terms of PFS in patients treated in second line compared to patient treated in lines subsequent to the second. Evaluate the dynamics of quantitative variation over time of any circulating microRNAs predictive of efficacy and tolerability. Evaluate the differences in any predictive biomarkers of efficacy/tolerability, tissue and/or circulating, in patients treated in second line vs patients treated in subsequent lines. Assess any differences in PFS in relation to: previous treatment(s) in the early setting and metastatic, disease sites, dose reductions/treatment discontinuation.

  2. Tolerability of the treatment

    Time frame: 30 months

    Evaluate the tolerability of the treatment in terms of adverse events, defined according to Common Terminology Criteria for Adverse Events (CTCAE, v. 5) and identify factors predictive of toxicity. Evaluate objective response rate (ORR) and overall survival (OS). Assess the variation in any biomarkers of efficacy in primary tumor tissue vs. tissue from metastatic localization (in cases where both samples are available). Select a small subgroup of patients from whose tumor tissue to develop organoids will be treated with SG, and on which potential will be quantified longitudinally over time biomarkers of response to treatment.

  3. Development of organoids

    Time frame: 30 months

    Select a small subgroup of patients from the tumor tissue for single cell testing RNA sequencing to compare with data from bulk RNA sequencing to study the microenvironment tumoral.

Study contacts

Contact information is provided by the study sponsor or research team.

Eriseld Krasniqi, Doctor

CONTACT

[email protected]

Patrizia Vici, Doctor

CONTACT

[email protected]

06-5266.5584 ext. +39

Sponsors and collaborators

Lead sponsor

Regina Elena Cancer Institute

Other

Collaborators

  • Azienda Policlinico Umberto I
  • Campus Bio-Medico University
  • Catholic University of the Sacred Heart
  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS
  • Hospital San Pietro Fatebenefratelli
  • Ospedale "Gaetano Bernabeo" , Ortona
  • Ospedale "SS Annunziata", Chieti
  • Ospedale Sandro Pertini, Roma
  • Ospedale di Belcolle - Viterbo
  • San Giovanni Addolorata Hospital
  • presidio Ospedaliero santo spirito in Sassia, Roma

Registry information

Acronym: BIO-PROSA

Important dates

Study start
2023
Primary completion
2025
Study completion
2027
First posted
Feb 2, 2024
Registry last updated
Jun 5, 2026

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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