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Becotatug Vedotin Plus Tislelizumab and Low-Dose Lenvatinib for Advanced Esophageal Squamous Cell Carcinoma, Phase II

Becotatug Vedotin Combined With Tislelizumab and Low-Dose Lenvatinib in Patients With Advanced Esophageal Squamous Cell Carcinoma Who Failed First-Line Therapy: A Phase II Exploratory Study

Immunotherapy combined with chemotherapy has become the first-line standard of care for advanced esophageal squamous cell carcinoma (ESCC), significantly improving patient survival. However, with the widespread adoption of first-line immunotherapy, most patients eventually develop immune resistance. After first-line treatment failure, there is currently no established standard effective therapy for second-line ESCC. Therefore, more effective and safer treatment options are urgently needed for second-line advanced ESCC.

This is a prospective, single-arm, single-center, open-label, Phase II clinical study aiming to evaluate the efficacy and safety of Becotatug Vedotin combined with Tislelizumab and low-dose Lenvatinib in patients with advanced ESCC who have failed first-line therapy. Eligible patients will receive Becotatug Vedotin combined with Tislelizumab and low-dose Lenvatinib. The primary endpoint is objective response rate (ORR) assessed per RECIST v1.1. Secondary endpoints include progression-free survival (PFS), disease control rate (DCR), duration of response (DOR), overall survival (OS), and safety.

Panoramica dello studio

Descrizione dettagliata

The study consists of two phases: a dose-run-in phase and a dose-expansion phase.

Phase 1 (Dose-Run-In Phase): After signing informed consent, 6 eligible patients will receive Becotatug Vedotin combined with Tislelizumab and low-dose Lenvatinib during the safety run-in period to evaluate the safety and tolerability of the regimen: Becotatug Vedotin (2.0mg/kg, iv, d1, q3w, for 4-6 cycles) combined with Tislelizumab (200mg, iv, d1, q3w) and low-dose Lenvatinib (4 mg, po,once daily at a fixed time). If no more than 1 patient among the 6 treated patients experiences a dose-limiting toxicity (DLT) and no unexpected unacceptable serious adverse events occur, the study will proceed to Phase 2.

Phase 2 (Dose-Expansion Phase): Eligible patients will receive the same combination regimen of Becotatug Vedotin, Tislelizumab, and low-dose Lenvatinib as in Phase 1. Treatment will continue until disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator's decision to discontinue treatment, or study termination, whichever occurs first.

Tipo di studio

Interventistico

Iscrizione (Stimato)

36

Fase

  • Fase 2

Contatti e Sedi

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

Contatto 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.Age ≥ 18 years, male or female. 2.Histopathologically or cytologically confirmed recurrent or metastatic esophageal squamous cell carcinoma.

3.Failed first-line or above standard systemic therapy for advanced disease. 4.Patients must be able to provide tumor specimens (paraffin blocks, paraffin-embedded sections, or fresh tissue sections) from primary or metastatic lesions for pathological testing. The most recent archived tumor tissue specimen may be used. If archived tissue is unavailable, a new biopsy is required.

5.ECOG PS 0-2. 6.Expected survival ≥ 3 months. 7.At least one measurable target lesion assessable by CT or MRI according to RECIST version 1.1 criteria.

8.Adequate organ and bone marrow function, as demonstrated by the following laboratory values:

  1. Bone marrow: Absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L;Platelet count (PLT) ≥ 100×10⁹/L;Hemoglobin (HGB)≥90 g/L.
  2. Liver: Total bilirubin (TBIL) ≤ 1.5 × upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST)≤2.5×ULN; for patients with liver metastases, ALT and AST≤5×ULN.
  3. Kidney: Creatinine clearance (Ccr) ≥ 50 mL/min (calculated using the Cockcroft-Gault formula).
  4. Coagulation: International normalized ratio (INR) ≤ 1.5 × ULN and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN (except for patients receiving therapeutic anticoagulation).
  5. Cardiac function: No severe cardiac dysfunction, with left ventricular ejection fraction (LVEF) ≥ 50%.

9.Female patients of childbearing potential must agree to use contraception during the study and for 6 months after the end of study participation, have a negative serum or urine pregnancy test within 7 days prior to study enrollment, and must not be breastfeeding. Male patients must agree to use contraception during the study and for 6 months after the end of study participation.

10.Patients must be able and willing to comply with the scheduled visits, treatment plans, laboratory tests, and other study-related procedures as outlined in the protocol.

11.Patients must be able to understand the study and voluntarily sign the informed consent form.

Exclusion Criteria:

  1. Prior malignancy within 5 years, except for carcinoma in situ, basal cell carcinoma, or other malignancies considered cured with negligible risk of recurrence.
  2. Known hypersensitivity to any component of the study regimen.
  3. High risk of gastrointestinal bleeding, esophageal fistula, or esophageal perforation.
  4. Untreated or unstable parenchymal brain metastases, spinal cord metastasis or compression, leptomeningeal disease, or meningeal metastases.
  5. Evidence of active infection, including:1)Hepatitis B (HBsAg positive with HBV DNA ≥ 2000 IU/mL, excluding drug-induced or other causes of hepatitis);2)Hepatitis C (anti-HCV antibody positive with HCV RNA above the lower limit of detection);3)Human immunodeficiency virus (HIV) infection;4)Uncontrolled active bacterial, viral, fungal, rickettsial, or parasitic infections that have not resolved prior to study drug administration.
  6. Third-space fluid that cannot be controlled by drainage (e.g., massive ascites, pleural effusion, pericardial effusion), or subjects requiring drainage to control third-space fluid within 14 days prior to first dose.
  7. Any severe or uncontrolled systemic disease in the investigator's judgment.
  8. Poorly controlled cardiac disease, including:

1)Heart failure > New York Heart Association (NYHA) class II; 2)Unstable angina pectoris; 3)Myocardial infarction within 1 year; 4)Clinically significant supraventricular or ventricular arrhythmias requiring treatment; 5)Long QT syndrome, with QTcF > 450 ms (male) or QTcF > 470 ms (female). 9.History of primary immunodeficiency or active autoimmune disease, or current use of immunosuppressants or systemic corticosteroids (≥ 10 mg/day prednisone or equivalent) continuing within 2 weeks prior to enrollment.

10.History of or concomitant interstitial lung disease (ILD), radiation pneumonitis, severe chronic obstructive pulmonary disease (COPD), severe pulmonary insufficiency, or symptomatic bronchospasm.

11.Positive serum pregnancy test or breastfeeding females who do not agree to use adequate contraception during the study and for 6 months after the last dose of study drug.

12.History of organ transplantation, including allogeneic peripheral stem cell or bone marrow transplantation.

13.Peripheral neuropathy ≥ Grade 2 (per CTCAE version 5.0). 14.Prior receipt of any of the following treatments:

  1. Intravenous antibiotic therapy within 7 days prior to first dose.
  2. Investigational drug from another clinical trial within 4 weeks prior to first dose.
  3. Live attenuated vaccine within 4 weeks prior to first dose. Inactivated seasonal influenza vaccines or approved non-replicating COVID-19 vaccines are permitted.
  4. Systemic immunostimulatory agents (including but not limited to interferon, interleukin-2, etc.) within 4 weeks prior to first dose.
  5. Major surgical procedure (e.g., abdominal or thoracic surgery, excluding diagnostic puncture, infusion device placement, or gastrointestinal stent placement) within 4 weeks prior to first dose, or anticipation of major surgery not directed at the tumor during the study treatment period.

    15.History of substance abuse (psychoactive drugs) that cannot be abstained from, or psychiatric disorders.

    16.Concurrent participation in another interventional clinical study. 17.Any other condition that, in the investigator's judgment, makes the subject unsuitable for participation in this clinical trial.

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: Becotatug Vedotin Combined with Tislelizumab and Low-Dose Lenvatinib
Participants in this single arm receive Becotatug Vedotin (2.0mg/kg, iv, D1, Q3W, 4 to 6 cycles) in combination with Tislelizumab (200 mg, iv, D1 Q3W, continued for up to 35 cycles [approximately 2 years]) and Low-Dose Lenvatinib (4 mg, orally, once daily at a fixed time. Treatment continues until disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator decision to discontinue, or study termination, whichever occurs first. ).The study consists of a safety run-in phase (approximately 6 participants) followed by an expansion phase (to a total of approximately 36 participants) .
Becotatug Vedotin 2.0 mg/kg administered as an intravenous infusion on Day 1 of each 21-day cycle for 4 to 6 cycles.
Tislelizumab 200 mg administered as an intravenous infusion on Day 1 of each 21-day cycle, continued for up to 35 cycles (approximately 2 years), or until disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator decision to discontinue, or study termination, whichever occurs first.
Low-Dose Lenvatinib 4 mg administered orally at a fixed time once daily, continued until disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator decision to discontinue, or study termination, whichever occurs first.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective Response Rate (ORR)
Lasso di tempo: From start of treatment until disease progression, assessed up to 24 months
Objective response rate is defined as the proportion of patients who achieve complete response (CR) or partial response (PR) as assessed by the investigator per RECIST version 1.1.
From start of treatment until disease progression, assessed up to 24 months

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Progression-Free Survival (PFS)
Lasso di tempo: From start of treatment to disease progression or death, assessed up to 36 months.
Progression-free survival is defined as the time from the first dose of study treatment to the first documented disease progression per RECIST version 1.1 or death from any cause, whichever occurs first.
From start of treatment to disease progression or death, assessed up to 36 months.
Overall Survival (OS)
Lasso di tempo: From start of treatment to death, assessed up to 36 months.
Overall survival is defined as the time from the first dose of study treatment to death from any cause.
From start of treatment to death, assessed up to 36 months.
Disease Control Rate (DCR)
Lasso di tempo: From start of treatment until disease progression, assessed up to 24 months.
Disease control rate is defined as the proportion of patients who achieve complete response (CR), partial response (PR), or stable disease (SD) as assessed by the investigator per RECIST version 1.1.
From start of treatment until disease progression, assessed up to 24 months.
Duration of Response (DOR)
Lasso di tempo: From first documented response to disease progression or death, assessed up to 24 months.
Duration of response is defined as the time from the first documented objective response (CR or PR) to the first documented disease progression per RECIST version 1.1 or death from any cause, whichever occurs first.
From first documented response to disease progression or death, assessed up to 24 months.
Safety and Tolerability
Lasso di tempo: From first dose of study drug until 30 days after the last dose, assessed up to 24 months.
Safety and tolerability will be assessed by the incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs) according to NCI CTCAE version 5.0.
From first dose of study drug until 30 days after the last dose, assessed up to 24 months.

Collaboratori e investigatori

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

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 luglio 2028

Completamento dello studio (Stimato)

31 dicembre 2029

Date di iscrizione allo studio

Primo inviato

30 giugno 2026

Primo inviato che soddisfa i criteri di controllo qualità

30 giugno 2026

Primo Inserito (Effettivo)

7 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

16 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

14 luglio 2026

Ultimo verificato

1 giugno 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

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

NO

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 .

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