Efficacy and Safety Profile of Becotatug Vedotin(EGFR-Targeting ADC) in Combination With Pucotenlimab and Cisplatin as Neoadjuvant Therapy for Patients With Locally Advanced Head and Neck Squamous Cell Carcinoma (LA-HNSCC)
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Pathological Complete Response(pCR) Rate
研究概览
简要总结
This clinical trial aims to evaluate the efficacy and safety of Becotatug Vedotin (EGFR-Targeting ADC) in combination with Pucotenlimab and Cisplatin as neoadjuvant therapy for patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC).
The primary objective is to assess whether this combination therapy improves the pathological complete response (pCR) rate and to evaluate its safety and tolerability. The secondary objective includes evaluating 1-year disease-free survival (DFS) rates and major pathological response (MPR) rates in patients treated with this combination therapy.
Main Questions This Trial Aims to Answer:
- Does the combination of Becotatug Vedotin, Pucotenlimab, and Cisplatin lead to higher rates of pathological complete response (pCR) and major pathological response (MPR) in patients with locally advanced head and neck squamous cell carcinoma (LA-HNSCC)?
- What are the safety and tolerability profiles of the combination therapy?
- Does the treatment improve disease-free survival at 1 year after treatment?
What Participants Will Do:
Treatment: Participants will receive Becotatug Vedotin (EGFR-Targeting ADC), Pucotenlimab, and Cisplatin as a combination therapy in the neoadjuvant setting.
Treatment Duration: Treatment will last approximately 6-12 weeks, depending on the patient's individual regimen.
Follow-up Visits: Participants will attend routine check-ups for safety evaluations and pathological assessments approximately 7 weeks after completing neoadjuvant therapy.
Outcomes: Researchers will assess pathological complete response (pCR), major pathological response (MPR), and 1-year disease-free survival (DFS) following treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 70 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Aged 18-70 years (inclusive).
- •Histopathologically confirmed Stage III/IVA head and neck squamous cell carcinoma (HNSCC) of the oropharynx, oral cavity, hypopharynx, or larynx (per 8th edition AJCC Cancer Staging Manual).
- •Measurable primary lesions per RECIST v1.
- •Treatment-naive (no prior anti-tumor therapy for current disease).
- •ECOG performance status 0-
- •Eligible for elective standard surgery plus adjuvant chemoradiotherapy/radiotherapy (investigator-assessed).
- •No active autoimmune diseases.
- •No concurrent malignant tumors.
- •Estimated life expectancy >= 6 months.
- •Available tumor tissue for PD-L1 IHC testing (22C3 DAKO assay).
- •Adequate hematological function (screening): ANC >= 1.5×10⁹/L, platelets >= 100×10⁹/L, Hb >= 100 g/L, WBC >= 3.5×10⁹/L; no blood transfusion or bleeding tendency within 7 days.
- •Normal liver function: ALT, AST, ALP, serum bilirubin <= 1.5×ULN.
- •Normal renal function: Serum Cr <= 1.5×ULN or creatinine clearance > 60 mL/min.
- •HPV status confirmed by p16 IHC and in situ hybridization (ISH).
- •Voluntary participation with signed informed consent; legal guardian-signed consent for incompetent subjects, and witness-supervised consent for illiterate subjects.
排除标准
- •Cachexia or multiple organ failure.
- •Active autoimmune disease of any type.
- •Concomitant second primary malignancy (e.g., esophageal cancer).
- •Severe active infection requiring systemic therapy.
- •Uncontrolled serious medical conditions interfering with study treatment (e.g., severe heart/cerebrovascular disease, uncontrolled diabetes/hypertension, active peptic ulcer).
- •Dementia, altered mental status, or other conditions impairing informed consent or questionnaire completion.
- •Peripheral neuropathy >= Grade 2 per CTCAE v5.
- •Hearing impairment >= Grade 2 per CTCAE v5.
- •History of malignancy within 5 years prior to screening.
- •Known HIV-positive status or diagnosed AIDS.
- •Nasopharyngeal carcinoma or HNSCC at sites other than oral cavity, oropharynx, larynx, hypopharynx (e.g., paranasal sinuses, unknown primary).
- •Receipt of investigational drugs or participation in other interventional trials within 30 days prior to screening.
- •Systemic glucocorticoids (>10 mg prednisone equivalent/day) or other immunosuppressants within 14 days prior to randomization (inhaled/topical steroids and adrenal hormone replacement are permitted without active autoimmune disease).
- •Pregnant/lactating women; subjects of childbearing potential refusing contraception.
- •Active infection requiring treatment or systemic anti-infective use within 1 week prior to first dose.
- •Live vaccine administration within 30 days prior to first dose.
- •Vulnerable populations (e.g., mental illness, cognitive impairment, critically ill status).
- •Other conditions deemed unsuitable for enrollment by the investigator.
研究组 & 干预措施
Combination Therapy with Becotatug Vedotin, Pucotenlimab, and Cisplatin
Participants in this arm will receive a combination of Becotatug Vedotin (EGFR-Targeting ADC), Pucotenlimab (PD-1 Inhibitor), and Cisplatin as neoadjuvant therapy for locally advanced head and neck squamous cell carcinoma (LA-HNSCC). The treatment will be administered for approximately 6-12 weeks, followed by surgery. Participants will be monitored for safety and efficacy through routine check-ups and pathological assessments.
干预措施: Combination Therapy with Becotatug Vedotin, Pucotenlimab, and Cisplatin (Combination Product)
结局指标
主要结局
Pathological Complete Response(pCR) Rate
时间窗: Within 7 weeks after the completion of neoadjuvant therapy
次要结局
- Major Pathological Response(MPR) Rate(Within 7 weeks after the completion of neoadjuvant therapy)
- 1-Year Disease-Free Survival(1 year after enrollment)