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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.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

64

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

Inclusion Criteria:

  1. 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.
  2. 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.
  3. 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).
  4. 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.
  5. 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.
  6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-3.
  7. 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:

  1. 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.)
  2. 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
  3. 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
  4. 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)
  5. Thrombotic events within 6 months (e.g., stroke, TIA, DVT, pulmonary embolism), hypertensive crisis, or encephalopathy.
  6. History of epilepsy.
  7. Superior vena cava syndrome.
  8. 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%).
  9. Severe bone metastasis-related complications (e.g., pathological fracture, spinal cord compression, uncontrolled bone pain).
  10. Active uncontrolled infection (≥CTCAE grade 2) or fever >38.5°C of unknown cause.
  11. Uncontrolled third-space fluid accumulation (pleural, peritoneal, pericardial effusion), unless stable after drainage.
  12. Tumor invasion or unclear boundary with major blood vessels on imaging.
  13. Bleeding tendency within 2 months or hemoptysis (>2.5 mL/day) within 2 weeks, or unhealed wounds/ulcers/fractures.
  14. Significant gastrointestinal disease affecting drug absorption (e.g., severe ulcers, cirrhosis, bowel obstruction, IBD, surgery affecting absorption, etc.).
  15. Live attenuated vaccine within 4 weeks before first dose.
  16. Severe hypersensitivity to monoclonal antibody therapies.
  17. Active autoimmune disease requiring systemic therapy within 2 years (excluding replacement therapies).
  18. Immunodeficiency or ongoing immunosuppressive therapy (>10 mg/day prednisone equivalent) within 2 weeks before dosing.
  19. HIV positivity, active hepatitis B or C infection as defined by HBV DNA or HCV RNA thresholds.
  20. Active syphilis, dialysis-dependent renal failure.
  21. Poorly controlled diabetes (fasting glucose >10 mmol/L).
  22. History of organ transplantation or planned transplantation.
  23. Major surgery or significant trauma within 4 weeks before first dose.
  24. Palliative radiotherapy within 2 weeks before first dose.
  25. Unresolved prior treatment toxicities (except alopecia/pigmentation/lab abnormalities not clinically significant); peripheral neuropathy not recovered to ≤Grade 2.
  26. Pregnancy or breastfeeding.
  27. Severe psychiatric illness, drug abuse, or alcoholism.
  28. Known allergy to study drug or any of its components.
  29. Any other clinically significant condition that may compromise safety or interfere with study assessments as judged by the investigator.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione di gruppo singolo
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Gruppo sperimentale
Platinum-free regimen

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression-Free Survival (PFS)
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Tasso di controllo della malattia (DCR)
Lasso di tempo: Fino al completamento degli studi, in media 1 anno.
Fino al completamento degli studi, in media 1 anno.
Objective Response Rate(ORR)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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
Lasso di tempo: 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)
Lasso di tempo: 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.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 agosto 2026

Completamento primario (Stimato)

31 dicembre 2027

Completamento dello studio (Stimato)

31 agosto 2028

Date di iscrizione allo studio

Primo inviato

30 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

22 luglio 2026

Primo Inserito (Effettivo)

27 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

27 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

22 luglio 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • SYSU-SQ-2026014

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .