Esta página foi traduzida automaticamente e a precisão da tradução não é garantida. Por favor, consulte o versão em inglês para um texto fonte.

Almonertinib Treats Advanced NSCLC Patients With EGFR Mutations Who Are Safety Intolerant After Osimertinib Treatment (ACTIVE)

6 de maio de 2021 atualizado por: Lu Shun, Shanghai Chest Hospital

Evaluate the Safety and Efficacy of Almonertinib in the Treatment of Advanced NSCLC Patients With EGFR-sensitive Mutations Who Are Safety Intolerant After Osimertinib Treatment: a Prospective, Multi-center, Single-arm Clinical Trial

This is a prospective, multi-center, single-arm clinical trial to evaluate the safety and effectiveness of Almonertinib treatment in patients with EGFR mutation positive and advanced non-small cell lung cancer (NSCLC) who are intolerant to the safety of osimertinib treatment.

Visão geral do estudo

Status

Ainda não está recrutando

Intervenção / Tratamento

Descrição detalhada

This is a prospective, multi-center, single-arm clinical trial to evaluate the safety and effectiveness of Almonertinib treatment in patients with EGFR mutation positive and advanced non-small cell lung cancer (NSCLC) who are intolerant to the safety of osimertinib treatment. Patients meeting the criteria for inclusion and exclusion were included in the Almonertinib treatment group and received 110 mg of Almonertinib orally once a day.

Tipo de estudo

Intervencional

Inscrição (Antecipado)

40

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos a 75 anos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

Inclusion Criteria:

  1. Over 18 years old (including 18 years old) and under 75 years old (including 75 years old)
  2. Histologically or cytologically diagnosed as locally advanced or metastatic NSCLC.
  3. The CTCAE ≥ grade 3 AE related to osimertinib treatment in previous treatment with osimertinib, or platelet count <75×109 / L (≥CTCAE grade 2), white blood cell count <3×109 / L (≥ CTCAE grade 2), total bilirubin> 1.5×ULN (≥CTCAE grade 2), transaminase (ALT/AST)>3.0×ULN (≥CTCAE grade 2), and the toxic reaction has been alleviated or restored to ≤CTCAE grade 1 patient.
  4. Tumor tissue samples diagnosed as locally advanced or metastatic NSCLC are confirmed to be EGFR sensitive mutations (including exon 19 deletion or L858R, both alone or coexist with other EGFR mutations). If the tumor tissue is accessible, it is recommended to send the tumor tissue for examination; if the tumor tissue is not accessible or the patient cannot accept a tissue biopsy, a blood sample is also acceptable.
  5. The Eastern Cooperative Oncology Group (ECOG) physical status score is 0 to 1, and it has not deteriorated in the previous 2 weeks, and the minimum expected survival is 12 weeks.
  6. The patient has at least one tumor lesion that can be accurately measured at baseline, and the longest diameter at baseline is ≥10 mm (if it is a lymph node, the short diameter is required to be ≥15 mm). The selected measurement method is suitable for accurate repeat measurement, which can be computed tomography (CT) or magnetic resonance scan (MRI). If there is only one measurable lesion, it can be accepted as the target lesion, and a baseline assessment of the tumor lesion should be performed at least 14 days after the diagnostic biopsy.
  7. Women of childbearing age should take appropriate contraceptive measures from screening to 3 months after stopping the study treatment and should not breastfeed. Before starting the administration, the pregnancy test is negative, or meeting one of the following criteria proves that there is no risk of pregnancy:

    1. Postmenopausal is defined as amenorrhea for at least 12 months after the age is greater than 50 years and all exogenous hormone replacement therapy is stopped.
    2. For women younger than 50 years old, if the amenorrhea is 12 months or more after stopping all exogenous hormone treatments, and the luteinizing hormone (LH) and follicle stimulating hormone (FSH) levels are within the laboratory postmenopausal reference value range, also It can be considered post-menopausal.
    3. Have received irreversible sterilization, including hysterectomy, bilateral ovariectomy or bilateral fallopian tube resection, except for bilateral fallopian tube ligation.
  8. Male patients should use barrier contraception (i.e. condoms) from screening to 3 months after stopping the study treatment.
  9. The subjects themselves participated voluntarily and signed an informed consent form in writing.

Exclusion Criteria:

  1. Have received any of the following treatments:

    1. Have previously received any EGFR tyrosine kinase inhibitor treatment except osimertinib;
    2. The patient had undergone major surgery within 4 weeks before the first administration;
    3. Accept other test drugs, and within 5 half-lives;
    4. Within 7 days before the first administration of the study drug, CYP3A4 strong inhibitors, inducers, or drugs with a narrow therapeutic window that are CYP3A4 sensitive substrates have been used.
  2. Patients with other malignant tumors who need standard treatment or major surgery within 2 years after the first administration of the study treatment.
  3. As judged by the investigator, there are any serious or poorly controlled systemic diseases, such as poorly controlled hypertension, active bleeding-prone constitution, or active infection. No need to check for chronic diseases.
  4. Refractory nausea, vomiting or chronic gastrointestinal disease, inability to swallow study drugs or having undergone extensive bowel resection may affect the full absorption of Almonertinib.
  5. A history of interstitial lung disease, a history of drug-induced interstitial lung disease, a history of interstitial pneumonia requiring steroid therapy, or any evidence of clinically active interstitial lung disease.
  6. Meet any of the following cardiac examination results:

    1. The average corrected QT interval (QTc)> 470 msec obtained from 3 ECG examinations in the resting state, the Fridericia formula is used for QT interval correction (QTcF);
    2. Resting ECG suggests that there are various clinically significant rhythms, conduction or ECG morphological abnormalities (such as complete left bundle branch block, 3 degree atrioventricular block, 2 degree atrioventricular block, and PR between Period> 250 msec);
    3. There are any factors that increase the risk of QTc prolongation or arrhythmia events, such as heart failure, hypokalemia, congenital long QT syndrome, family history of long QT syndrome, or unexplained sudden death or prolonged QT of immediate family members under 40 Any concomitant drugs in the interval;
    4. Left ventricular ejection fraction (LVEF) ≤50%.
  7. Insufficient bone marrow reserve or organ function, reaching the following laboratory limits:

    1. Absolute neutrophil count <1.5×109 / L;
    2. Platelet count <100×109 / L;
    3. Hemoglobin <90 g/L (<9 g/dL);
    4. Alanine aminotransferase> 2.5 times the upper limit of normal (ULN)
    5. Aspartate aminotransferase> 2.5×ULN
    6. Total bilirubin> 1.5×ULN; or Gilbert syndrome (unconjugated hyperbilirubinemia)
    7. Creatinine>1.5×ULN and creatinine clearance rate<50 mL/min (calculated by Cockcroft-Gault formula); only when creatinine>1.5×ULN, creatinine clearance rate needs to be confirmed.
  8. Women who are breastfeeding or whose blood or urine pregnancy test results are positive within 3 days before the first dose of study treatment.
  9. Active fungal, bacterial and/or viral infections requiring systemic treatment.
  10. Have a history of hypersensitivity to any active or inactive ingredients of Almonertinib or to drugs with similar chemical structure to Almonertinib or the same class of Almonertinib.
  11. Any serious or uncontrolled eye disease may increase the safety risk of the patient as judged by the doctor.
  12. Patients who are judged by the investigator who may not comply well with the procedures and requirements of the study.
  13. The investigator judges that there are any patients with conditions that endanger the safety of the patient or interfere with the evaluation of the study.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: N / D
  • Modelo Intervencional: Atribuição de grupo único
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: Almonertinib group
Patients meeting the criteria for inclusion and exclusion were included in the Almonertinib treatment group and received 110 mg of Almonertinib orally once a day.

Almonertinib is a class 1 new drug,the third-generation small molecule EGFR TKI, which can irreversibly and highly selectively inhibit EGFR sensitive mutations (such as exon 19 deletion and L858R mutation) and T790M resistance mutations.

Patients meeting the criteria for inclusion and exclusion were included in the Almonertinib treatment group and received 110 mg of Almonertinib orally once a day.

Outros nomes:
  • HS-10296

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Assess the safety of Almonertinib: Number of AEs/SAEs
Prazo: Continuously throughout the study until 28 days after Termination of the treatment
Number of adverse events (AEs)/serious adverse events (SAEs)
Continuously throughout the study until 28 days after Termination of the treatment

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Assess the anti-tumor activity: Progression Free Survival (PFS)
Prazo: From date of baseline until the date of disease progression or discontinuation from study, assessed up to 24 months

To assess the efficacy of Almonertinib in the treatment of advanced NSCLC patients with EGFR-sensitive mutations who are intolerant to safety after osimertinib treatment by assessment of progression free survival (PFS) using Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).

From date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months.

From date of baseline until the date of disease progression or discontinuation from study, assessed up to 24 months
Assess the anti-tumor activity: Objective response rate (ORR)
Prazo: From date of baseline until the date of disease progression or discontinuation from study, assessed up to 24 months
ORR is defined as the percentage of patients who have at least 1 response of CR or PR prior to any evidence of progression assessed up to 24 months.
From date of baseline until the date of disease progression or discontinuation from study, assessed up to 24 months
Assess the anti-tumor activity: Disease control rate (DCR)
Prazo: From date of baseline until the date of disease progression or discontinuation from study, assessed up to 24 months
The DCR is defined as the proportion of patients with a best overall response of CR, PR, or SD assessed up to 24 months.
From date of baseline until the date of disease progression or discontinuation from study, assessed up to 24 months
Assess the anti-tumor activity: Duration of response (DoR)
Prazo: the time from date of documented progression or death in the absence of disease progression assessed up to 24 months.
DoR is defined as the time from the date of first documented response until the date of documented progression or death in the absence of disease progression assessed up to 24 months.
the time from date of documented progression or death in the absence of disease progression assessed up to 24 months.
Assess the anti-tumor activity: Overall survival (OS)
Prazo: an average of 4 years
Start of study drug to Survival Endpoint through study completion, an average of 4 years.
an average of 4 years
Assess the anti-tumor activity: Depth of Remission (DepOR)
Prazo: through study completion, an average of 1 year
The depth of remission (change in tumor size) refers to the amount of change in the sum of the length of the longest diameter of the target lesion defined by RECIST 1.1 when no new lesions appear or no non-target lesions have progressed compared with the baseline.
through study completion, an average of 1 year

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Investigadores

  • Investigador principal: Meiqi Shi, Jiangsu Cancer Institute & Hospital
  • Investigador principal: Yongsheng Li, The Affiliated Cancer Hospital of Chongqing University
  • Investigador principal: Jianying Zhou, Zhejiang University
  • Investigador principal: Xiuyu Cai, Sun Yat-sen University
  • Investigador principal: Yueyin Pan, The First Affiliated Hospital of University of Science and Technology of China
  • Investigador principal: Wenxiu Yao, Sichuan Cancer Hospital and Research Institute
  • Investigador principal: Chun Huang, Tianjin Cancer Hospital
  • Investigador principal: Minglei Zhuo, Peking University Cancer Hospital & Institute
  • Investigador principal: Conghua Xie, Wuhan University
  • Investigador principal: Qibin Song, Hubei Provincial People's Hospital

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Antecipado)

15 de julho de 2021

Conclusão Primária (Antecipado)

15 de janeiro de 2024

Conclusão do estudo (Antecipado)

15 de janeiro de 2024

Datas de inscrição no estudo

Enviado pela primeira vez

30 de abril de 2021

Enviado pela primeira vez que atendeu aos critérios de CQ

6 de maio de 2021

Primeira postagem (Real)

11 de maio de 2021

Atualizações de registro de estudo

Última Atualização Postada (Real)

11 de maio de 2021

Última atualização enviada que atendeu aos critérios de controle de qualidade

6 de maio de 2021

Última verificação

1 de maio de 2021

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • YX-L-202109

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

NÃO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

Ensaios clínicos em Câncer de pulmão

Ensaios clínicos em Almonertinib

3
Se inscrever