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- Ensaio Clínico NCT07616453
Efficacy and Safety of Culmerciclib Plus Aromatase Inhibitors in a Response-Adapted Neoadjuvant Strategy for Highly Proliferative ER-Positive/HER2-Negative Breast Cancer (TAYLOR-002)
Neoadjuvant Trastuzumab-rezetecan Plus Pertuzumab or Nab-Paclitaxel, Carboplatin, Trastuzumab, and Pyrotinib After Suboptimal Response to Neoadjuvant Dual HER2-Targeted Therapy Combined With Chemotherapy in HER2-Positive Early Breast Cancer: A Response-Guided Phase II Study (TAYLOR-002)
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
This is a prospective, response-adapted, phase II study designed to evaluate an individualized neoadjuvant treatment strategy based on culmerciclib in combination with aromatase inhibitors in patients with highly proliferative ER-positive/HER2-negative early breast cancer. The study incorporates an adaptive treatment algorithm guided by on-treatment assessment of tumor response, with the aim of optimizing therapeutic efficacy while minimizing unnecessary treatment exposure.
All eligible patients initially receive neoadjuvant treatment with culmerciclib plus endocrine therapy according to the study protocol. Following completion of a predefined initial treatment phase, tumor response is assessed using biological and clinical evaluation methods.
Patients who achieve an adequate response continue the same neoadjuvant regimen to complete the planned course of therapy. In contrast, patients demonstrating a suboptimal response are transitioned to alternative treatment strategies prior to surgery. Subsequent treatment selection and management are conducted according to protocol-defined principles and investigator assessment.
This response-adapted strategy is intended to address the clinical heterogeneity of endocrine sensitivity in ER-positive/HER2-negative breast cancer. By tailoring treatment intensity according to early response, the study seeks to maximize therapeutic benefit in responsive patients while facilitating timely treatment modification for those less likely to benefit from the initial regimen.
Primary and secondary objectives include evaluation of clinical efficacy, safety and tolerability of the response-adapted neoadjuvant strategy, and the feasibility of treatment modification based on early response assessment. Exploratory analyses will investigate potential biomarkers associated with treatment response and resistance, with the goal of informing future individualized treatment approaches.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
Contactos e Locais
Contato de estudo
- Nome: Yunxiang Zhou
- Número de telefone: 15868131018
- E-mail: yxzhou@zju.edu.cn
Locais de estudo
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Zhejiang
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Hangzhou, Zhejiang, China, 310009
- Recrutamento
- 2nd Affiliated Hospital, School of Medicine, Zhejiang University
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Contato:
- Yunxiang Zhou
- Número de telefone: 15868131018
- E-mail: yxzhou@zju.edu.cn
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Contato:
- E-mail: yxzhou@zju.edu.cn
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Subinvestigador:
- Yunxiang Zhou
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-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria Female patients aged ≥18 and ≤75 years. Histologically confirmed estrogen receptor (ER)-positive (≥10%) and HER2-negative breast cancer, according to the 2018 ASCO/CAP guidelines. HER2-negative status is defined as immunohistochemistry (IHC) 0 or 1+, or IHC 2+ with negative in situ hybridization (ISH) (ISH ratio <2.0), as confirmed by a certified pathology laboratory.
Ki-67 ≥20% assessed on core needle biopsy samples. Newly diagnosed, treatment-naïve patients with stage I-IIIA disease according to the AJCC 8th edition.
Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.
Adequate bone marrow function:
- Absolute neutrophil count ≥1.5 × 10⁹/L (without growth factor support within 14 days);
- Platelet count ≥100 × 10⁹/L (without transfusion or supportive therapy within 7 days);
- Hemoglobin ≥100 g/L (without transfusion within 7 days).
Adequate hepatic and renal function:
- Total bilirubin ≤1 × upper limit of normal (ULN);
- Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤3 × ULN (≤5 × ULN in patients with liver metastases);
- Blood urea nitrogen and serum creatinine ≤1.5 × ULN, and creatinine clearance ≥50 mL/min (calculated using the Cockcroft-Gault formula).
Left ventricular ejection fraction (LVEF) ≥50% as assessed by echocardiography. QT interval ≤480 ms on 12-lead electrocardiogram (ECG). Ability and willingness to undergo tumor biopsy. Provision of written informed consent. Exclusion Criteria Prior receipt of any anticancer therapy, including chemotherapy, radiotherapy, targeted therapy, or endocrine therapy.
Concurrent treatment with other anticancer agents. Bilateral breast cancer, inflammatory breast cancer, or occult breast cancer. Stage IV breast cancer. Breast cancer not confirmed by histopathology. History of other malignancies within the past 5 years, except for adequately treated carcinoma in situ of the cervix.
Severe dysfunction of major organs, including heart, liver, or kidneys. Conditions affecting oral drug administration or absorption, including inability to swallow, chronic diarrhea, or intestinal obstruction.
Participation in another interventional clinical trial within 4 weeks prior to enrollment.
Known hypersensitivity to any component of the study drugs; history of immunodeficiency, including HIV infection, active hepatitis B or C infection, other acquired or congenital immunodeficiency disorders, or history of organ transplantation.
History of significant cardiovascular disease, including but not limited to clinically significant arrhythmias requiring treatment, myocardial infarction, heart failure, or any other cardiac condition deemed unsuitable by the investigator.
Pregnant or breastfeeding women; women of childbearing potential with a positive pregnancy test at baseline, or unwilling to use effective contraception during the study period.
Any serious concomitant disease that, in the investigator's judgment, may compromise patient safety or compliance with the study, including but not limited to uncontrolled hypertension, severe diabetes, or active infection.
History of neurological or psychiatric disorders, including epilepsy or dementia.
Any other condition that, in the investigator's opinion, makes the patient unsuitable for participation in the study.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: Culmerciclib plus AI
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CDK2/4/6 inhibitor
Letrozole or anastrozole
|
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Complete cell cycle arrest (CCCA)
Prazo: 4 weeks
|
Ki67≤2.7%
|
4 weeks
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Taxa de Resposta Objetiva (ORR)
Prazo: 24 semanas
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24 semanas
|
|
|
Sobrevivência livre de eventos (EFS)
Prazo: Aproximadamente cinco anos
|
O EFS é definido como o tempo da randomização para qualquer um dos seguintes eventos: impede a cirurgia, recorrência local ou distante, segunda malignidade primária ou morte devido a qualquer causa.
|
Aproximadamente cinco anos
|
|
Evento adverso (AE)
Prazo: Aproximadamente três anos
|
Um EA é definido como qualquer ocorrência médica desagradável em um participante do estudo administrou um medicamento, associado temporalmente à intervenção do estudo, sem presunção de causalidade.
|
Aproximadamente três anos
|
|
the proportion of patients with Residual Cancer Burden (RCB) class 0-1
Prazo: 24 weeks
|
24 weeks
|
|
|
Total Pathological Complete Response (tpCR) Rate
Prazo: 24 weeks
|
24 weeks
|
Colaboradores e Investigadores
Investigadores
- Investigador principal: Yiding Chen, Second Affiliated Hospital, School of Medicine, Zhejiang University
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Efeitos fisiológicos das drogas
- Mecanismos Moleculares de Ação Farmacológica
- Hormônios, substitutos hormonais e antagonistas hormonais
- Inibidores Enzimáticos
- Inibidores da síntese de esteróides
- Antagonistas hormonais
- Antagonistas de estrogênio
- Ações farmacológicas
- Ações e usos químicos
- Inibidores de Aromatase
Outros números de identificação do estudo
- 2026-0417
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