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NCT Number: NCT03735966

Neoadjuvant Study of Pyrotinib and Trastuzumab Plus Docetaxel and Carboplatin in HER2 Positive Breast Cancer Patients.

Pyrotinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors.This study is a single-arm, prospective, open label clinical study for evaluating the efficacy and safety of neoadjuvant pyrotinib and trastuzumab plus docetaxel given as neoadjuvant treatment in HER2 positive early stage or locally advanced breast cancer.

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Key information

Age range

18 year–75 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Henan cancer hospital

Zhengzhou, Henan, China

About this study

Neoadjuvant therapy is the standard treatment for locally advanced breast cancer and is used to reduce tumors to make them operable, and to increase breast-conserving rates. In recent years, the anti-HER2 treatment mode, which is double-blocked by a combination of dual-targeted drugs, has obtained clinical approval in adjuvant therapy and neoadjuvant therapy. Pyrotinib is an oral tyrosine kinase inhibitor targeting both HER-1 and HER-2 receptors. Based on previous clinical studies, we designed the study to explore the possibility of Pyrotinib in combination with Trastuzumab plus Docetaxel given as neoadjuvant treatment in HER2 positive early stage or locally advanced breast cancer.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • female patients, 18 years ≤ age ≤ 75 years.
  • Performance Status- Eastern Cooperative Oncology Group (ECOG) 0-1.
  • Histologically confirmed invasive breast cancer(early stage or locally advanced):Primary tumour greater than 2 cm diameter
  • HER2 positive (HER2+++ by IHC or FISH+)
  • Life expectancy of more than 3 months
  • Known hormone receptor status.
  • Required laboratory values including following parameters: ANC: ≥ 1.5 x 10^9/L;Platelet count: ≥ 100 x 10^9/L;Hemoglobin: ≥ 9.0 g/dL;Total bilirubin: ≤ 1.5 x upper limit of normal (ULN);ALT and AST: ≤ 1.5 x ULN (or ≤ 5×ULN in patients with liver metastases);BUN and creatine clearance rate: ≥ 50 mL/min;LVEF: ≥ 50%;QTcF: < 470 ms for female and < 450 ms for male.
  • Signed the informed consent form prior to patient entry.

Exclusion criteria

  • metastatic disease (Stage IV) or inflammatory breast cancer.
  • Previous or current history of malignant neoplasms, except for curatively treated:Basal and squamous cell carcinoma of the skin,Carcinoma in situ of the cervix.
  • clinically relevant cardiovascular disease:Known history of uncontrolled or symptomatic angina, clinically significant arrhythmias, congestive heart failure, transmural myocardial infarction, uncontrolled hypertension ≥180/110);
  • Unable or unwilling to swallow tablets.

Treatment and study plan

Pyrotinib plus trastuzumab and docetaxel and carboplatin

Drug

pyrotinib: 320mg orally daily,6cycles; trastuzumab:8mg/kg iv load followed by 6mg/kg iv 3-weekly for a total of 6cycles; docetaxel:after the biological window, 100mg/m2 for a total of 6 cycles carboplatin:d1 ,AUC 6 iv 3-weekly for a total of 6 cycles

Primary outcomes

  1. Pathological Complete Response (pCR)

    Time frame: through study completion, an average of 1 year

    Percentage of Participants With Pathological Complete Response (pCR) at the Time of Surgery evaluated

Secondary outcomes

  1. EFS

    Time frame: Following surgery until Year 5

    Event-free survival

  2. DFS

    Time frame: Following surgery until Year 5

    Disease-free Survival

  3. DDFS

    Time frame: Following surgery until Year 5

    Distance Disease-free Survival

  4. ORR

    Time frame: Baseline up to cycle 4 (assessed at Baseline, at the time of pre-surgery)up to approximately 12 months

    Objective Response Rate

Sponsors and collaborators

Lead sponsor

Henan Cancer Hospital

Other Gov

Registry information

Official study title

Neoadjuvant Study of Pyrotinib in Combination With Trastuzumab Plus Docetaxel and Carboplatin in Patients With HER2 Positive Early Stage or Locally Advanced Breast Cancer : a Single-arm,Ahead , Open-label Study

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Nov 8, 2018
Registry last updated
Dec 1, 2022

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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