- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07728955
A Single-arm, Exploratory Clinical Study Evaluating the Efficacy and Safety of Bevacizumab in Combination With Anlotinib and Etoposide as First-line Therapy for Elderly Patients With Small-cell Lung Cancer or Those Who Are Intolerant to Intensive Chemotherapy (SCLC)
A single-arm exploratory clinical study to observe and evaluate the first-line treatment of elderly and treatment-intolerant patients with small cell lung cancer using benmelstobart in combination with anlotinib and etoposide.
Eligible patients are those with histologically or pathologically confirmed small cell lung cancer (SCLC) (AJCC 9th edition), who are treatment-naïve and considered elderly or intolerant to intensive therapy. Eligible subjects receive 4-6 cycles of benmelstobart injection combined with anlotinib hydrochloride and etoposide, followed by maintenance therapy with benmelstobart injection plus anlotinib hydrochloride, continued until disease progression or intolerable toxicity.
The study aims to evaluate the efficacy and safety of first-line treatment with benmelstobart injection in combination with anlotinib hydrochloride and etoposide in patients with advanced SCLC.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Heping Li
- Número de teléfono: +86 13710873975
- Correo electrónico: liheping@mail.sysu.edu.cn
Copia de seguridad de contactos de estudio
- Nombre: Xiuxing Chen
- Número de teléfono: +86 13265129905
- Correo electrónico: Chenxx266@mail.sysu.edu.cn
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- The subject must voluntarily participate in this study after being fully informed and must sign a written informed consent form (ICF), and be willing and able to comply with the study procedures and requirements.
- At the time of signing the ICF, male or female subjects aged ≥65 years, or male or female subjects aged ≥18 years who are assessed by the investigator as not suitable for intensive treatment, defined as: ECOG performance status of 2-3, or comorbidities (CIRS >6 and ≤12), or otherwise judged by the investigator as not suitable for intensive treatment. Intensive treatment is defined as first-line intensive therapy for metastatic small cell lung cancer, i.e., standard chemotherapy with etoposide plus cisplatin or carboplatin combined with immune checkpoint inhibitors and targeted agents.
- Histologically or cytologically confirmed metastatic small cell lung cancer (SCLC), according to the International Association for the Study of Lung Cancer and the American Joint Committee on Cancer TNM staging system, 9th edition (AJCC 9th).
- Subjects must not have received prior systemic therapy for metastatic SCLC. Patients who previously received adjuvant, neoadjuvant, or radical chemoradiotherapy for non-metastatic disease are eligible if disease progression occurred >6 months after completion of the last treatment.
- At least one measurable target lesion according to RECIST v1.1. Lesions previously treated with radiotherapy or other local regional therapy are not considered target lesions unless clear progression is documented after treatment. Lesions must have a longest diameter ≥10 mm on CT or MRI at baseline (lymph nodes must have a short axis ≥15 mm), and must be suitable for repeated accurate measurement per RECIST v1.1.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-3.
- Adequate organ function as defined below, with no blood transfusion or use of hematopoietic growth factors within 14 days prior to testing: Platelets (PLT) ≥80 × 10⁹/L Hemoglobin (HGB) ≥80 g/L Neutrophils (NEUT) ≥1.5 × 10⁹/L Creatinine ≤1.5 × upper limit of normal (ULN) or creatinine clearance (CrCl) ≥30 mL/min (Cockcroft-Gault) ALT and AST ≤2.5 × ULN (≤5 × ULN if liver metastases present) Total bilirubin (TBIL) ≤1.5 × ULN (≤3 × ULN in Gilbert's syndrome) INR or PT ≤1.5 × ULN and APTT ≤1.5 × ULN, or clinically acceptable bleeding risk as assessed by investigator Urine protein <2+ or 24-hour urine protein <1 g Expected survival ≥3 months Women of childbearing potential must agree to use effective contraception during and for 6 months after the study and have a negative serum pregnancy test within 7 days before enrollment and must not be breastfeeding Male subjects must agree to use effective contraception during and for 6 months after the study Willingness to participate and good compliance with follow-up.
Exclusion Criteria:
- Prior anti-cancer therapy within specified time windows: Anti-PD-1/PD-L1 therapy within 3 years before first dose Anti-angiogenic multi-target TKIs (e.g., anlotinib, apatinib) within 3 years Any anti-cancer therapy (chemotherapy, targeted therapy, immunotherapy, etc.) or investigational drug within 28 days before first dose Traditional Chinese medicines with approved anti-cancer indications within 2 weeks before first dose (e.g., Fufang Banmao capsule, Kang'ai injection, Kanglaite capsule/injection, Aidi injection, Yadanzi oil injection/capsule, Xiaoaiping tablets/injection, Huachansu capsule, etc.)
- Other primary malignancies, except: Tumors treated by single surgery with complete remission ≥3 years before enrollment Non-melanoma skin cancer or in situ cancers not requiring treatment Prostate cancer requiring only clinical observation
- Symptomatic or progressing CNS metastases or carcinomatous meningitis. Patients with stable brain metastases may be eligible if: No neurological symptoms No corticosteroid use required and no indication for radiotherapy Largest brain lesion ≤1.5 cm Stable on two brain MRI/CT scans ≥2 weeks apart Additional timing and stability conditions after CNS treatment as specified Off corticosteroids ≥2 weeks if previously treated with CNS radiotherapy ≥4 weeks interval after CNS surgery before first dose
- Cardiovascular conditions including: NYHA class II or higher heart failure Severe arrhythmia requiring treatment Myocardial infarction, unstable angina, or vascular bypass within 6 months LVEF <40% QTcF prolongation (female >470 ms, male >450 ms) or risk factors for torsades de pointes Uncontrolled hypertension (SBP ≥150 mmHg and/or DBP ≥100 mmHg despite treatment)
- Thrombotic events within 6 months (e.g., stroke, TIA, DVT, pulmonary embolism), hypertensive crisis, or encephalopathy.
- History of epilepsy.
- Superior vena cava syndrome.
- Active or uncontrolled pulmonary conditions including interstitial lung disease, radiation pneumonitis, immune-related pneumonitis, active tuberculosis, pneumoconiosis, or severe pulmonary impairment (FEV1, DLCO, or DLCO/VA <40%).
- Severe bone metastasis-related complications (e.g., pathological fracture, spinal cord compression, uncontrolled bone pain).
- Active uncontrolled infection (≥CTCAE grade 2) or fever >38.5°C of unknown cause.
- Uncontrolled third-space fluid accumulation (pleural, peritoneal, pericardial effusion), unless stable after drainage.
- Tumor invasion or unclear boundary with major blood vessels on imaging.
- Bleeding tendency within 2 months or hemoptysis (>2.5 mL/day) within 2 weeks, or unhealed wounds/ulcers/fractures.
- Significant gastrointestinal disease affecting drug absorption (e.g., severe ulcers, cirrhosis, bowel obstruction, IBD, surgery affecting absorption, etc.).
- Live attenuated vaccine within 4 weeks before first dose.
- Severe hypersensitivity to monoclonal antibody therapies.
- Active autoimmune disease requiring systemic therapy within 2 years (excluding replacement therapies).
- Immunodeficiency or ongoing immunosuppressive therapy (>10 mg/day prednisone equivalent) within 2 weeks before dosing.
- HIV positivity, active hepatitis B or C infection as defined by HBV DNA or HCV RNA thresholds.
- Active syphilis, dialysis-dependent renal failure.
- Poorly controlled diabetes (fasting glucose >10 mmol/L).
- History of organ transplantation or planned transplantation.
- Major surgery or significant trauma within 4 weeks before first dose.
- Palliative radiotherapy within 2 weeks before first dose.
- Unresolved prior treatment toxicities (except alopecia/pigmentation/lab abnormalities not clinically significant); peripheral neuropathy not recovered to ≤Grade 2.
- Pregnancy or breastfeeding.
- Severe psychiatric illness, drug abuse, or alcoholism.
- Known allergy to study drug or any of its components.
- Any other clinically significant condition that may compromise safety or interfere with study assessments as judged by the investigator.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Grupo experimental
|
Platinum-free regimen
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Progression-Free Survival (PFS)
Periodo de tiempo: From first dose of study treatment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months.
|
Progression-Free Survival (PFS) is defined as the time from the first dose of study treatment to the first documented disease progression or death due to any cause, whichever occurs first.
|
From first dose of study treatment until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 24 months.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Tasa de control de enfermedades (DCR)
Periodo de tiempo: Hasta la finalización del estudio, un promedio de 1 año.
|
Hasta la finalización del estudio, un promedio de 1 año.
|
|
|
Objective Response Rate(ORR)
Periodo de tiempo: Through study completion, an average of 1 year.
|
ORR is defined as the percentage of participants with a confirmed Complete Response (CR) or Partial Response (PR) as per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
|
Through study completion, an average of 1 year.
|
|
Duration of Response (DoR)
Periodo de tiempo: From the date of first documented response (CR or PR) until the date of first documented disease progression or death, whichever came first, assessed up to 24 months.
|
From the date of first documented response (CR or PR) until the date of first documented disease progression or death, whichever came first, assessed up to 24 months.
|
|
|
Overall Survival (OS)
Periodo de tiempo: From first dose of study treatment until date of death from any cause, assessed up to 36 months.
|
From first dose of study treatment until date of death from any cause, assessed up to 36 months.
|
|
|
Safety and Tolerability
Periodo de tiempo: From first dose of study treatment until 30 days after last dose, assessed up to 24 months.
|
Safety will be evaluated by summarizing the incidence of AEs, irAEs, and SAEs graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v6.0.
|
From first dose of study treatment until 30 days after last dose, assessed up to 24 months.
|
|
Cancer-Specific Survival (CSS)
Periodo de tiempo: From first dose of study treatment until date of death due to small cell lung cancer , assessed up to 36 months.
|
From first dose of study treatment until date of death due to small cell lung cancer , assessed up to 36 months.
|
Colaboradores e Investigadores
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Neoplasias por sitio
- Neoplasias
- Enfermedades de las vías respiratorias
- Enfermedades pulmonares
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Neoplasias Pulmonares
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Carcinoma de pulmón de células pequeñas
- Químicos orgánicos
- Hidrocarburos
- Hidrocarburos, cíclico
- Carbohidratos
- Podoflotoxina
- Tetrahidronaftalenos
- Naftalenos
- Hidrocarburos aromáticos policíclicos
- Hidrocarburos, aromáticos
- Compuestos policíclicos
- Glucósidos
- Glucósidos
- Etopósido
- anlotinib
Otros números de identificación del estudio
- SYSU-SQ-2026014
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .