Study of SHR-A1811 Combined With Pyrotinib and Bevacizumab in Advanced Breast Cancer With Brain Metastasis

Официальное название

A Prospective, Single-arm, Exploratory, Phase Ib/II Study of SHR-A1811 Combined With Pyrotinib and Bevacizumab in Advanced Breast Cancer With Brain Metastasis.

Обзор

In phase Ib, our study is aimed to evaluate the safety and tolerance of SHR-A1811 combined with pyrotinib in breast cancer with brain metastasis, and confirm the recommended phase 2 dose combined with preliminary results of efficacy. In phase II, our study is aimed to evaluate the efficacy and safety of SHR-A1811 combined with pyrotinib and bevacizumab at RP2D in breast cancer with brain metastasis.

Вмешательства

• Препарат SHR-A1811
  ADC
• Препарат Bevacizumab
  bevacizumab biosimilar
• Препарат Pyrotinib
  anti-HER2 inhibitor

Первичные конечные точки

• RP2D in phase Ib [Срок оценки: From the enrolment of the first subject, to the end of Cycle 6 completion or disease progression or dose discontinuation due to AE in the last enrolled subject]
• CNS-ORR by investigator in phase II [Срок оценки: At baseline, at the time point of every 6 weeks]

Вторичные конечные точки (12)

• Incidence of dose-limiting toxicity (DLT) in phase Ib [Срок оценки: At the time point of 21 days from first medication]
• MTD in phase Ib [Срок оценки: From the enrolment of the first subject, to the end of Cycle 6 completion or disease progression or dose discontinuation due to AE in the last enrolled subject]
• Incidence and grade of adverse event (AE) and serious adverse event (SAE) in phase Ib [Срок оценки: From the time of informed consent provided to 3 months after the last dose of study therapy]
• CNS-ORR per RANO-BM in phase Ib [Срок оценки: At baseline, at the time point of every 6 weeks]
• CNS-ORR per RECIST v1.1 in phase Ib [Срок оценки: At baseline, at the time point of every 6 weeks]
• CNS-DCR in phase Ib [Срок оценки: At baseline, at the time point of every 6 weeks]
• DoR in phase Ib [Срок оценки: up to 2 years]
• CNS-ORR per RECIST v1.1 in phase II [Срок оценки: At baseline, at the time point of every 6 weeks]
• CNS-DCR in phase II [Срок оценки: At baseline, at the time point of every 6 weeks]
• DoR in phase II [Срок оценки: up to 2 years]
• PFS in phase II [Срок оценки: up to 2 years]
• OS in phase II [Срок оценки: up to 2 years]

Критерии участия

Критерии включения

• More than 18 years old;
• ECOG PS Score: 0\~2;
• Patients must have a life expectancy ≥ 3 months;
• Brian metastasis confirmed by MRI, at least one measurable brain lesion based on RANO-BM with no prior radiotherapy;
• Mannitol or hormone therapy is allowed to use for brain metastasis before enrolment, but treatment dosage should be stable for one week and not need to be increased;
• Adequate organ function and marrow function;
• Has recovered from any AEs (≤ grade 1) related to prior anti-tumour treatments before first dose of study therapy, except: a. alopecia; b. hyperpigmentation;
• Willing to join in this study, able to provide written informed consent, good compliance and willing to cooperate with follow-up.

Критерии исключения

• Has leptomeningeal metastasis or cystic metastatic lesions confirmed by MRI or lumbar puncture;
• Existence of third space fluid (e.g. massive ascites, pleural effusion, pericardial effusion) that is not well controlled by effective methods, e.g. drainage;
• Has CNS complications with the need for emergency intervention, or brain metastasis with poorly controlled symptoms by hormone or dehydration therapy, such as uncontrollable intracranial hypertension, mental disorder or epilepsy;
• Prior bevacizumab or EGFR-TKI is allowed, but should meet the following requirements at the same time:

• No disease progression during prior bevacizumab or EGFR-TKI;
• More than 3 months from the interruption of bevacizumab or EGFR-TKI to disease progression;
• Has received whole brain radiotherapy, chemotherapy, surgery within 2 weeks before first dose of study therapy; has received trastuzumab-based therapy or endocrine therapy within one week before first dose of study therapy; has received palliative radiotherapy for bone metastasis within 2 weeks before first dose of study therapy;
• Has known clinically significant lung disease, that is, moderate-to-severe lung disease which severely affects respiratory function, including but not limited to: idiopathic pulmonary fibrosis, pneumonitis. Prior ≥ grade 3 interstitial lung disease is not allowed to enrolment;
• Has received full-dose anticoagulants or thrombolytics within 10 days before enrolment, or non-steroid anti-inflammatory drugs with platelet inhibition (except low-dose aspirin (≤325mg qd) for preventive use);
• Existence of unhealed wound, active gastric ulcer, and other diseases which may cause haemorrhage risk (e.g., prior major operation within 4 weeks before enrolment, prior arterial or venous thrombotic event within one year before enrolment, prior cerebralvascular accident);
• Has known hereditary haemorrhagic tendency or coagulation disorder;
• Has joined in other clinical drug trials within 2 weeks before enrolment;
• Use of other antitumor systemic treatment during the study at the same time, except bisphosphonates for the treatment of bone metastasis or osteoporosis prevention;
• Other malignancy within prior 5 years unless curatively treated with no evidence of disease for at least recent 3 years, except: curatively treated in situ cancer of the cervix, skin basal cell carcinoma or skin squamous cell carcinoma;
• Cardiac insufficiency, including but not limited to: congestive heart failure, transmural myocardial infarction, angina which needs drug treatments, clinically significant valvulopathy and high-risk arrhythmia, or QTc abnormity with clinical significance in ECG examination during the screening period (corrected QTc >450 msec \[male\] or QTc >470 msec \[female\] under the resting state);
• Uncontrolled hypertension (under the resting state: systolic pressure >160mmHg or diastolic pressure >100mmHg);
• Other diseases which may affect study results, including but not limited to: 1) known history of immunodeficiency, including HIV-positive, other acquired or innate immunodeficient disease, or known history of organ transplantation; 2) HBsAg-positive and HBV DNA≥1000 IU/mL, or HCV antibody-positive, or treponema pallidum antibody-positive; 3) hypersensitivity to study therapy or any of its excipients; 4) severe infection requiring antibiotics, antiviral or antifungal treatment;
• Female patients during the gestation or suckling period, of childbearing potential and pregnancy test-positive, or unwilling to use an effective method of contraception during the whole study;
• Inability to swallow, intestinal obstruction or existence of other factors affecting medication and absorption;
• Any other conditions not appropriate for study enrolment in the opinion of the investigator.

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение

Нерандомизированное

Модель

Последовательный дизайн

Маскирование

Открытое

Основная цель

Лечение

Центры проведения

Китай · 1 центр

• Fudan Cancer Hospital — Шанхай

Идентификаторы

NCT: NCT06718933 · BCBM-004

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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