Dynamic Observational Study With PET of 68Ga-HER2-affibody in Anti-HER2 Treatment
NCT ID: NCT04769050
Last Updated: 2022-04-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
50 participants
OBSERVATIONAL
2021-02-18
2023-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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First-line patients
First-line treatment of HER2-positive metastatic breast cancer patients
Docetaxel combined with Trastuzumab±Pertuzumab
Docetaxel, 75 mg/m2 ivgtt d1 q3w Trastuzumab, 6 mg/kg(8 mg/kg for initial dose) ivgtt d1 q3w Pertuzumab, 420mg(840mg for initial dose) ivgtt d1 q3w
Second-line patients
Second-line treatment of HER2-positive metastatic breast cancer patients
T-DM1 or Capecitabine combined with Pyrotinib regimen.
T-DM1, 3.6mg/kg(8 mg/kg for initial dose) ivgtt d1 q3w Capecitabine, 1250 mg/m2 bid po d1-14 q3w Pyrotinib, 400mg po daily (continuously)
Interventions
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Docetaxel combined with Trastuzumab±Pertuzumab
Docetaxel, 75 mg/m2 ivgtt d1 q3w Trastuzumab, 6 mg/kg(8 mg/kg for initial dose) ivgtt d1 q3w Pertuzumab, 420mg(840mg for initial dose) ivgtt d1 q3w
T-DM1 or Capecitabine combined with Pyrotinib regimen.
T-DM1, 3.6mg/kg(8 mg/kg for initial dose) ivgtt d1 q3w Capecitabine, 1250 mg/m2 bid po d1-14 q3w Pyrotinib, 400mg po daily (continuously)
Eligibility Criteria
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Inclusion Criteria
2. Female patients aged over 18 years (including cutoff value).
3. an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.
4. Patients with HER2 positive recurrent or metastatic breast cancer confirmed by histopathology.
5. At least one extracranial measurable lesion according to Response Evaluation Criteria in Solid Tumors (RECIST) criteria version 1.1.
6. Previously received no more than 1 prior lines of systemic chemotherapy for metastatic breast cancer
7. Life expectancy ≥ 12 weeks.
8. Adequate function of major organs meets the following requirements (no blood components and cell growth factors have been used within 14 days before randomization):
* Neutrophils ≥ 1.5×10\^9/L
* Platelets ≥ 75×10\^9/L
* Hemoglobin ≥ 80g/L
* Total bilirubin≤ 1.5 × the upper limit of normal (ULN)
* ALT and AST ≤ 3 × ULN
* BUN and Cr ≤ 1.5 × ULN
* Left ventricular ejection fraction (LVEF) ≥ 50%
* QTcF(Fridericia correction) ≤ 470 ms
Exclusion Criteria
2. Patients who have undergone systemic, radical brain or meningeal metastasis (radiotherapy or surgery), but have been confirmed to have been stable for at least 4 weeks, and who have stopped systemic hormonal therapy for more than 2 weeks without clinical symptoms can be included.
3. Received systemic therapy such as chemotherapy, molecular targeted therapyment;received endocrine therapy within 2 weeks before enrollment.
4. Patients with other malignant tumors within 3 years or at the sametime(except for cured skin basal cell carcinoma and cervical carcinomain situ).
5. Have undergone major surgical procedures or significant trauma within 4 weeks prior to randomization, or are expected to undergo major surgery.
6. Pregnant women, lactating female, or women of childbearing age who are unwilling to take effective contraceptive measures.
7. Have a history of allergies to the drug components of this regimen.
8. Patients with active HBV and HCV infection; stable hepatitis B after drug treatment (HBV virus copy number is higher than the upper limit of reference value) and cured hepatitis C patients (HCV virus copy number exceeds the lower limit of detection method).
9. History of immunodeficiency, including HIV positive, or other acquired or congenital immunodeficiency disease, history of organ transplantation.
10. History of cardiac dysfunction, include(1)angina (2)clinical significant arrythmia or require drug intervention (3)myocardial infarction (4)heart failure (5) other cardiac dysfunction (judged by the physician); any cardiac or nephric abnormal ≥ grade 2 found in screening.
11. Female patients who are pregnancy, lactation or women who are ofchildbearing potential tested positive in baseline pregnancy test.
12. Childbearing female who refuse to accept any contraception practice.
13. Determined by the physician, any serious coexisting disease might be harmful to the patient's safety or avoid the patients from accomplishing the treatment(e.g serious hypertension, diabetes, thyroid dysfunction,active infection etc.).
14. History of neurological or psychiatric disorders, including epilepsy or dementia.
15. Severe infections within 4 weeks prior to first dose (eg, intravenous infusion of antibiotics, antifungal or antiviral drugs according to clinical protocols), or unexplained fever (T \> 38.3 °C ) during screening or prior to first administration
18 Years
75 Years
FEMALE
No
Sponsors
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Fudan University
OTHER
Responsible Party
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Xichun Hu
Director of department of medical oncology
Principal Investigators
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Xichun Hu, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Fudan University
Locations
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Fudan University Shanghai Cancer Center
Shanghai, Shanghai Municipality, China
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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DOLPHIN
Identifier Type: -
Identifier Source: org_study_id
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