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Sintilimab Combined With Anlotinib Therapy for Initially Unresectable Non-small Cell Lung Cancer

23 de março de 2022 atualizado por: YueJuan Cheng, Peking Union Medical College Hospital

Sintilimab Combined With Anlotinib Therapy for Patients With Initially Unresectable Stage II-III Non-small Cell Lung Cancer: A Prospective, Single-arm Study

Concurrent or sequential chemoradiotherapy has been recommended as the standard treatment for locally advanced and unresectable non-small cell lung cancer (NSCLC). However, its efficacy remains to be improved. PD-1/PD-L1 inhibitors have been proven to be effective for late-stage NSCLC, and anti-angiogenesis agents have also been used for the first-line treatment of advanced or metastatic NSCLC. Therefore, we designed this single-arm clinical trial, which aims to investigate the safety and feasibility of sintilimab combined with anlotinib therapy for patients with initially unresectable stage II-III NSCLC.

Visão geral do estudo

Status

Ainda não está recrutando

Descrição detalhada

Concurrent or sequential chemoradiotherapy is the standard treatment for patients with locally advanced NSCLC, but patients receiving chemoradiotherapy have limited improvement in prognosis and are almost impossible to achieve a radical cure. Considering the excellent effect of immunotherapy and anti-angiogenesis therapy in NSCLC, we designed this single-arm clinical study, which aims to investigate the safety and feasibility of sintilimab combined with anlotinib therapy for patients with initially unresectable stage II-III NSCLC, in order to enable patients to achieve further surgical treatment and prolonged survival.

Tipo de estudo

Intervencional

Inscrição (Antecipado)

93

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

  • Nome: Yingyi Wang, Professor
  • Número de telefone: +86 010-69158764
  • E-mail: wangyingyi@pumch.cn

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. According to the 8th edition of the AJCC/UICC TNM staging system for NSCLC, patients with locally advanced (stage II-III C) NSCLC confirmed by histology who are initially unable to undergo surgery and concomitant radiochemotherapy and are confirmed to have at least one measurable lesion according to RECIST 1.1.
  2. Age ≥18 years and ≤75 years.
  3. ECOG PS score: 0 to 1.
  4. The main organs function is normal, that is, the following criteria met:

    1. Good hematopoietic function, defined as absolute neutrophil count ≥1.5×109 /L, platelet count≥100 ×109 /L, hemoglobin ≥90g/L [no blood transfusion or no erythropoietin (EPO) dependence within 7 days before enrollment];
    2. Biochemical test results should meet the following criteria: BIL < 1.25 times the upper limit of normal value (ULN); ALT and AST < 2.5 × ULN; in case of liver metastases, ALT and AST < 5 × ULN; Cr ≤1.5×ULN or creatinine clearance (CCr) ≥60ml/min; Coagulation function is good, INR and PT ≤1.5 × ULN;
    3. The oxygen saturation of the finger tip ≥ 92% both at rest and during walking (without oxygen inhalation).
  5. The life expectancy ≥12 weeks.
  6. Signed and dated informed consent.

Exclusion Criteria:

  1. Subjects at risk of massive hemoptysis or with blood in sputum, including but not limited to tumor lesions no more than 5 mm away from large vessels, tumors invading large vessels, and obvious lung cavity/necrotizing tumors.
  2. Small cell lung cancer (including mixed small cell and non-small cell lung cancer) or central squamous cell carcinoma.
  3. With driver mutation (EGFR/ALK/ROS1).
  4. With uncontrollable hypertension (systolic pressure > 160 mmHg, diastolic pressure > 100 mmHg) even receiving antihypertensive drug therapy.
  5. Has an active autoimmune disease, history of allogeneic stem cell transplantation or organ transplantation that has required systemic treatment. Replacement therapy is not considered a form of systemic treatment and is allowed.
  6. Has an active infection requiring systemic therapy.
  7. Has other malignant tumors (except radical cervical carcinoma in situ, non-melanoma skin cancer, etc.) or concomitant diseases that seriously endanger the patients or affect the patients completing the study at the same time.
  8. With immunodeficiency status, including but not limited to HIV infection and primary immunodeficiency diseases.
  9. Previously treated with ICIs.
  10. Is pregnant, breastfeeding, or expecting to conceive or father a child within the projected duration of the study including 120 days following the last dose of study treatment.

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: Experimental arm

Sintilimab will be given intravenously at a dose of 200mg every 21 days. Anlotinib will be given at a dose of 12mg once daily on days 1-14 of a 21-day cycle.

Tumor evaluation will be conducted after treatment of the tested regimen every 2 cycles. Subsequent treatment will be determined based on the evaluation results: If the patients are not suitable for radical surgery, but the result of efficacy evaluation is CR, PR, or SD, they can continue to receive the tested regimen. If the patients are still not suitable for radical surgery after 6 cycles of the tested regimen, the standard first-line or immunotherapy after chemoradiotherapy or radiotherapy will be given. If patients are eligible for radical surgery, surgery will be performed within 4 weeks after completion of the last tested regimen.

Sintilimab will be given intravenously at a dose of 200mg every 21 days.
Outros nomes:
  • IBI308
  • Tyvyt
Anlotinib will be given at a dose of 12mg once daily on days 1-14 of a 21-day cycle.
Outros nomes:
  • AL3818
  • Cloridrato de anlotinibe

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Surgical conversion rate
Prazo: 18 weeks from the initiation of the tested regime therapy
The surgical conversion rate was defined as the proportion of subjects with the successful conversion over all subjects who received the tested regime.
18 weeks from the initiation of the tested regime therapy

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Objective response rate (ORR)
Prazo: 18 weeks from the initiation of the tested regime therapy
ORR is defined as the percentage of participants who have the best overall response (BOR) of complete response (CR) or partial response (PR) assessed based on RECIST 1.1.
18 weeks from the initiation of the tested regime therapy
R0 resection rate
Prazo: within 28 working days after operation
R0 resection rate is defined as the complete resection rate of all tumor under microscope.
within 28 working days after operation
Major pathological response rate
Prazo: within 28 working days after operation
Major pathological response rate is defined as the percentage of patients who achieved a major pathological response (residual tumor ≤10%).
within 28 working days after operation
Pathological complete response rate
Prazo: within 28 working days after operation
Pathological complete response rate is defined as the percentage of patients who achieved a pathological complete response (residual tumor = 0%).
within 28 working days after operation
Overall survival (OS)
Prazo: 2 years from the initiation of the tested regime therapy
OS is measured from the time from the treatment onset (date of first study dose) until the date of death from any cause.
2 years from the initiation of the tested regime therapy
Progression-free survival (PFS)
Prazo: 2 years from the initiation of the tested regime therapy
PFS is measured from the time from the treatment onset (date of first study dose) until the date of tumor progression or death from any cause.
2 years from the initiation of the tested regime therapy
Disease-free survival (DFS)
Prazo: 2 years from the initiation of the tested regime therapy
DFS is measured from the time from radical surgery until the date of tumor progression or death from any cause.
2 years from the initiation of the tested regime therapy
Treatment-related adverse events
Prazo: 3 months from the end of the tested regime therapy
Incidence and grade of treatment-related adverse events assessed based on CTCAE 5.0
3 months from the end of the tested regime therapy

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Chunmei Bai, Professor, Peking union medical colloge hospital

Publicações e links úteis

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Publicações Gerais

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)

1 de abril de 2022

Conclusão Primária (Antecipado)

1 de abril de 2024

Conclusão do estudo (Antecipado)

1 de abril de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

21 de março de 2022

Enviado pela primeira vez que atendeu aos critérios de CQ

23 de março de 2022

Primeira postagem (Real)

1 de abril de 2022

Atualizações de registro de estudo

Última Atualização Postada (Real)

1 de abril de 2022

Última atualização enviada que atendeu aos critérios de controle de qualidade

23 de março de 2022

Última verificação

1 de março de 2022

Mais Informações

Termos relacionados a este estudo

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

De-identified individual participant data for all primary and secondary outcome measures will be made available.

Prazo de Compartilhamento de IPD

Data will be available within 1 year of study completion

Critérios de acesso de compartilhamento IPD

Data access requests will be reviewed by an external independent Review Panel. Requestors will be required to sign a Data Access Agreement

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA
  • CIF
  • ANALYTIC_CODE
  • CSR

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 .

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