Camrelizumab, Pirfenidone, and Chemotherapy in the Treatment of Advanced Triple-Negative Breast Cancer

Официальное название

Exploratory Clinical Study of Camrelizumab Combined With Pirfenidone and Chemotherapy in the Treatment of Advanced Triple-Negative Breast Cancer

Обзор

This is a prospective, single-arm, exploratory clinical study, planned to enroll 12 patients with advanced triple-negative breast cancer who have received first-line systemic treatment with immune checkpoint inhibitors. The treatment regimen will continue until disease progression, intolerable toxicity, withdrawal of informed consent, or investigator's judgment that treatment must be terminated. Imaging assessment will be performed according to RECIST 1.1 criteria, with the research center's assessment results as the final outcome. Subjects who discontinue treatment will enter the follow-up period: 1) Safety follow-up until 30 days after the last dose; 2) Subjects who discontinue treatment for reasons other than progression disease (PD) or death will undergo efficacy follow-up until disease progression, initiation of other anti-tumor drugs, or death, whichever comes first; 3) All subjects will enter the trial period upon enrollment and receive camrelizumab combined with pirfenidone and chemotherapy.

Вмешательства

• Препарат Camrelizumab Combined With Pirfenidone and Chemotherapy
  Treatment Regimen: Camrelizumab: 200 mg intravenous (IV) every 3 weeks (q3w). Pirfenidone: 200 mg three times daily (tid), escalated to 600 mg tid based on tolerability. Chemotherapy: Investigator's choice of standard regimens (e.g., paclitaxel 175 mg/m² IV q3w or capecitabine 1000 mg/m² orally bid on days 1-14 of a 21-day cycle).

Первичные конечные точки

• ORR（Objective Response Rate） [Срок оценки: At the end of every 2 Cycles (each cycle is 21 days) , From first treatment Cycle until achieving complete response (CR) or partialresponse (PR) per RECIST v1.1.], assessed up to 1 year.]

Вторичные конечные точки (4)

• DCR（Disease Control Rate） [Срок оценки: Patients undergo imaging evaluation in every 2 cycles（each cycyle is 21 days）until achieving SD per RECIST v1.1 or through study completion, assessed up to 1 year.]
• CBR（Clinical Benefit Rate） [Срок оценки: through study completion, an average of 1 year".]
• PFS（Progression-Free Survival） [Срок оценки: up to 1 year]
• OS（Overall Survival） [Срок оценки: up to 1 year]

Критерии участия

Критерии включения

• Female, aged 18-70 years.
• Histologically confirmed recurrent/metastatic TNBC (ER-negative: IHC ER <1%; PR-negative: IHC PR <1%; HER2-negative: IHC -/+, or IHC ++ but FISH/CISH negative), with at least one measurable lesion per RECIST v1.1.
• ECOG performance status 0-2.
• Estimated life expectancy ≥3 months.
• Received first-line chemotherapy + PD-1/PD-L1 inhibitor for metastatic or locally advanced unresectable TNBC, with response of CR/PR or stable disease lasting ≥3 months. For neoadjuvant/adjuvant therapy, disease progression during treatment or within 6 months after completion will be considered as first-line failure.
• Adequate organ function (no transfusion, growth factor, or thrombopoietic agents within 2 weeks before screening):
• Hematology: ANC ≥1.5×10⁹/L; PLT ≥90×10⁹/L; Hb ≥90 g/L.
• Serum chemistry: TBIL ≤1.5×ULN; ALT and AST ≤1.5×ULN; ALP ≤2.5×ULN; BUN and Cr ≤1.5×ULN with creatinine clearance ≥50 mL/min (Cockcroft-Gault).
• TSH ≤ULN (if abnormal, T3 and T4 must be assessed; enrollment allowed if T3/T4 normal).
• Cardiac: LVEF ≥50% by echocardiography; 18-lead ECG with QTcF <480 ms (female).
• Women of childbearing potential must have negative pregnancy test (serum or urine) within 7 days prior to enrollment and agree to use adequate contraception during treatment and for 4 months after last dose.
• Voluntarily signed informed consent and good compliance.

Критерии исключения

• Concurrent participation in another interventional cancer trial.
• Received other antitumor therapy within 14 days before first dose.
• Prior treatment with pirfenidone.
• Untreated active brain metastases or leptomeningeal disease.
• Major non-breast cancer surgery within 4 weeks prior to enrollment or incomplete recovery from such surgery.
• Active or history of autoimmune disease (except vitiligo, resolved childhood asthma without treatment in adulthood).
• Severe cardiac disease (e.g., heart failure with LVEF <50%, uncontrolled arrhythmias, angina requiring medication, significant valvular disease, recent myocardial infarction, poorly controlled hypertension >180/100 mmHg).
• Congenital or acquired immunodeficiency (e.g., HIV infection).
• Live vaccination within 4 weeks before or during study.
• Known allergy to study drugs or excipients.
• Severe concomitant disease or condition that may interfere with study participation per investigator judgment

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Не применимо

Модель

Одна группа

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Список центров уточняется — проверьте первичный протокол.

Идентификаторы

NCT: NCT07161791 · OBU-BC-II-271

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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