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NCT Number: NCT07828652

Real-world Treatment Outcomes and Safety of Neoadjuvant Pembrolizumab-containing Therapy in Patients With Triple-negative Breast Cancer: Korean Nationwide Multicenter Study (Pembro-Real World)

The purpose of this study is to evaluate the treatment outcomes and safety of neoadjuvant therapy including pembrolizumab in real-world practice for patients with triple-negative breast cancer (TNBC) in a multi-center study in Korea. In particular, we aim to evaluate the treatment efficacy focusing on the pathologic complete response (pCR) and analyze the association with recurrence rates and survival indicators.

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Key information

About this study

There is a need for research analyzing treatment response, long-term clinical outcomes, and the patterns of short- and long-term immune-related adverse events in TNBC patients who have received neoadjuvant chemotherapy including pembrolizumab in a real-world clinical setting. This study aims to provide real-world evidence by comprehensively analyzing pathological response, recurrence patterns, survival outcomes, and treatment-related adverse events in TNBC patients who received pembrolizumab-based neoadjuvant chemotherapy in actual clinical practice. These findings are expected to provide important evidence for validating clinical trial results in real-world clinical settings and optimizing future treatment strategies for TNBC patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age of 19 years or older at the start of treatment
  • Patients diagnosed with triple-negative breast cancer (TNBC) pathologically
  • Patients diagnosed with clinical stage II or III ④ Patients who started neoadjuvant chemotherapy including pembrolizumab, paclitaxel, carboplatin, doxorubicin, and cyclophosphamide as preoperative neoadjuvant chemotherapy after July 2022

Exclusion criteria

  • History of other invasive malignancies, either concurrently or in the past (except for cancers where at least 5 years have passed since completion of treatment and there has been no recurrence) ② Patients diagnosed with clinical stage II or III who have a history of previous diagnosis and treatment for invasive breast cancer and have experienced local recurrence
  • Patients who have not started pembrolizumab treatment concurrently with chemotherapy ④ Cases where assessment of pathological response is impossible due to the absence of surgery

Treatment and study plan

Medical record use research

Other

Medical record use research

Primary outcomes

  1. primary purpose

    Time frame: until 2027.12.31

    Evaluate pathologic complete response, pCR,ypT0N0

Secondary outcomes

  1. Outcome Measure

    Time frame: until 2027.12.31

    Analysis of overall survival (OS), in real-world practice of neoadjuvant therapy including pembrolizumab in patients with triple-negative breast cancer (TNBC)

Other outcomes

  1. Other Outcome Measure

    Time frame: Until 2027.12.31

    Analysis of event-free survival in real-world practice of neoadjuvant therapy including pembrolizumab in patients with triple-negative breast cancer (TNBC)

  2. Other Outcome Measure

    Time frame: until 2027.12.31

    Analysis of adverse events, etc., in real-world practice of neoadjuvant therapy including pembrolizumab in patients with triple-negative breast cancer (TNBC)

Study contacts

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

Yeon hee Park, MD,phD

CONTACT

[email protected]

82-10-9933-1780

Sponsors and collaborators

Lead sponsor

Yeon Hee Park

Other

Registry information

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 18, 2026
Registry last updated
Sep 18, 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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