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- Ensaio Clínico NCT07645846
Neoadjuvant Docetaxel, Cisplatin, and Dual Immunotherapy for Sinonasal Carcinoma (PANDA)
A Multicenter, Single-Arm, Phase II Trial of Neoadjuvant Docetaxel and Cisplatin Combined With Dual Immunotherapy for Locally Advanced Sinonasal Carcinoma (PANDA Study)
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Descrição detalhada
Currently, there is a lack of prospective phase II/III clinical evidence to guide the optimal treatment of locally advanced sinonasal carcinoma (SNC). Based on current clinical guidelines for head and neck squamous cell carcinoma (HNSCC), the investigators hypothesize that the combination of TP chemotherapy with dual immune checkpoint inhibitors (targeting PD-1 and CTLA-4) could significantly improve the major pathological response (MPR) and achieve superior organ function preservation in patients with locally advanced SNC.
By evaluating the TP regimen combined with sintilimab and ipilimumab N01, this trial seeks to validate the feasibility of organ function preservation under this therapeutic modality. If successful, this treatment strategy will establish a novel precision treatment paradigm that effectively balances tumor control with organ function preservation, laying a solid foundation for subsequent phase III randomized controlled trials.
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
Contactos e Locais
Contato de estudo
- Nome: Kaiyue Mao
- Número de telefone: 86-020-87342926
- E-mail: maokaiyue@sysucc.org.cn
Estude backup de contato
- Nome: Xiaoyun Feng
- E-mail: fengxy@sysucc.org.cn
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Inclusion Criteria:
- Disease Status: Newly diagnosed, pathologically confirmed locally advanced (AJCC 8th edition Stage III-IVA) sinonasal carcinoma (SNC).
- Suitable for radical comprehensive treatment, with an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 1.
- 18 to 75 years old.
- Defined by the following laboratory test results obtained within 7 days prior to enrollment: Hematology (without blood transfusion or hematopoietic growth factor therapy within 14 days prior to testing): White blood cell (WBC) count ≥ 4.0 × 10^9/L; Absolute neutrophil count (ANC) ≥ 2.0 × 10^9/L; Platelet (PLT) count ≥ 100 × 10^9/L.
- Hepatic function: Total bilirubin < 1.5 × upper limit of normal (ULN) (patients with known Gilbert's disease and serum bilirubin level ≤ 3 × ULN are eligible); Alanine aminotransferase (ALT), aspartate aminotransferase (AST), and alkaline phosphatase < 1.5 × ULN. For patients positive for hepatitis B surface antigen (HBsAg), HBV-DNA must be ≤ 1000 IU/mL, and prophylactic antiviral therapy is required during the study.
- Renal function: Serum creatinine < 1.5 × ULN, or creatinine clearance ≥ 60 mL/min as calculated by the Cockcroft-Gault formula.
- Coagulation: Activated partial thromboplastin time (APTT) and international normalized ratio (INR) ≤ 1.5 × ULN. Patients receiving stable doses of anticoagulant therapy (e.g., low molecular weight heparin or warfarin) with an INR within the expected therapeutic range are eligible.
- Thyroid function: Thyroid-stimulating hormone (TSH) ≤ ULN; if abnormal, T3 and T4 levels will be evaluated, and patients with normal T3 and T4 levels are eligible.
- Contraception: Women of childbearing potential must agree to use highly effective contraceptive measures (e.g., intrauterine device, contraceptive pills, or condoms) during the treatment period and for at least 3 months after the last dose. They must have a negative serum or urine pregnancy test within 7 days prior to enrollment and must not be lactating. Male patients must agree to use highly effective contraceptive measures during the study period and for at least 3 months after the last dose.
- Informed Consent: Voluntary participation with written informed consent signed.
Exclusion Criteria:
- History of other malignancies within the past 5 years, except for curatively treated basal cell carcinoma of the skin, carcinoma in situ of the cervix, and papillary thyroid carcinoma.
- Presence of residual measurable lesions or new tumor/metastasis according to RECIST 1.1 criteria, or deemed inoperable by a head and neck surgeon.
- History of severe hypersensitivity reactions to other monoclonal antibodies or any components of the PD-1 inhibitors.
- Prior and Concomitant Therapies: Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibody (or any other antibody targeting T-cell costimulation or checkpoint pathways).
- Use of high-dose glucocorticoids or traditional Chinese medicine with anti-tumor properties within 4 weeks prior to the first dose of the study drug.
- Prior vaccination with an anti-tumor vaccine, or receipt of a live vaccine within 4 weeks prior to the first dose of the study drug.
- Receipt of any investigational drug within 4 weeks prior to the first dose of the study drug.
- Presence of comorbidities requiring long-term immunosuppressive therapy, or requiring systemic or local administration of corticosteroids at immunosuppressive doses prior to enrollment.
- Concurrent Trials: Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) clinical study or the follow-up phase of an interventional study.
- Recent Medical Events: Major surgery or severe trauma within 4 weeks prior to the first dose of the study drug.
- Organ Transplantation: History of organ transplantation.
- Autoimmune Diseases: Known or suspected active autoimmune disease.
- Human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS).
- Concurrent positive HBsAg and positive HBV DNA copy number (quantitative detection ≥ 1000 cps/mL). Positive blood screening for chronic hepatitis C (HCV antibody positive). Concurrent HBV and HCV co-infection. (Note: Patients with normal liver function who have been on oral antiviral therapy for more than one week may be eligible).
- Failure to meet relevant laboratory criteria within 7 days prior to enrollment; abnormal coagulation function (PT > 16s, APTT > 53s, TT > 21s, Fib < 1.5 g/L), bleeding tendency, or undergoing active thrombolytic or anticoagulant therapy.
Significantly impaired cardiac, hepatic, pulmonary, renal, or bone marrow function. History of dementia or seizures.
- Severe Infections: Severe infection (CTCAE > Grade 2) within 4 weeks prior to the first dose of the study drug, such as severe pneumonia requiring hospitalization, bacteremia, or infectious complications; baseline chest imaging indicating active pulmonary inflammation; presence of signs and symptoms of infection within 2 weeks prior to the first dose of the study drug, or requiring oral or intravenous antibiotic therapy (excluding prophylactic use of antibiotics).
- Pregnancy and Lactation: Pregnant or lactating women; women of childbearing potential who refuse to use effective contraceptive measures.
- Compliance and Legal Capacity: Refusal or inability to sign the informed consent form; presence of personality or psychiatric disorders; lack of or limited civil capacity.
- Other: Presence of any other treatment contraindications deemed inappropriate by the investigator.
Plano de estudo
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: Neoadjuvant Chemo-Immunotherapy
Patients will receive neoadjuvant therapy consisting of Ipilimumab N01 (1 mg/kg, IV, Day 1 of Cycle 1), Sintilimab (200 mg, IV, Q3W for 3 cycles), Docetaxel (75 mg/m^2, IV, Q3W for 3 cycles), and Cisplatin (60 mg/m^2, IV, Q3W for 3 cycles).
Radical surgery will be performed within 4 weeks after the completion of neoadjuvant therapy.
Postoperative adjuvant radiotherapy with or without chemotherapy will be determined by the investigators and a multidisciplinary team (MDT) based on NCCN and CSCO guidelines.
|
Drug: Ipilimumab N01, 1mg/kg, D1C1. Drug: Sintilimab, 200mg, Q3W, C1C2C3. Drug: Docetaxel, 75mg/m2, Q3W, C1C2C3. Drug: Cisplatin, 60mg/m2, Q3W, C1C2C3. Procedure: Radical Surgery. Radiation: Adjuvant Radiotherapy. |
O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Major Pathological Response Rate(MPR)
Prazo: From enrollment to the end of treatment at 9 weeks
|
Defined as the percentage of participants whose resected tumor specimens show ≤10% viable tumor cells upon microscopic examination following neoadjuvant therapy.
|
From enrollment to the end of treatment at 9 weeks
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Objective Response Rate (ORR)
Prazo: Up to 2 years
|
Defined as the proportion of patients who achieve a Complete Response (CR) or Partial Response (PR) per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
|
Up to 2 years
|
|
2-Year Overall Survival (OS) Rate
Prazo: 2 years from the start of treatment
|
Defined as the percentage of participants who are alive 2 years after the initiation of treatment.
|
2 years from the start of treatment
|
|
Median Overall Survival (mOS)
Prazo: Up to 2 years
|
Defined as the time from the start of treatment to death from any cause in 50% of the evaluated patients.
|
Up to 2 years
|
|
2-Year Progression-Free Survival (PFS) Rate
Prazo: 2 years from the end of the last treatment
|
Defined as the percentage of participants who remain alive and free of disease recurrence, new metastasis, or disease progression 2 years after the completion of the last treatment.
|
2 years from the end of the last treatment
|
|
Median Progression-Free Survival (mPFS)
Prazo: Up to 2 years
|
Defined as the time from the start of treatment until disease progression or death in 50% of the evaluable patients.
|
Up to 2 years
|
|
Duration of Response (DoR)
Prazo: From the first documented CR or PR until the first documented tumor progression or death from any cause, assessed up to 2 years
|
Evaluated per RECIST v1.1.
|
From the first documented CR or PR until the first documented tumor progression or death from any cause, assessed up to 2 years
|
|
Disease Control Rate (DCR)
Prazo: Up to 2 years
|
Defined as the percentage of patients who achieve a Complete Response (CR), Partial Response (PR), or Stable Disease (SD) following treatment.
|
Up to 2 years
|
|
R0 Resection Rate
Prazo: At the time of surgery (assessed up to 4 weeks after completion of neoadjuvant therapy)
|
Defined as the percentage of patients achieving a complete tumor resection with microscopically negative margins.
|
At the time of surgery (assessed up to 4 weeks after completion of neoadjuvant therapy)
|
|
Organ Functional Preservation Rate (OFPR)
Prazo: At 2 years post-treatment
|
Defined as the percentage of living patients at 2 years post-treatment who do not require salvage radical surgery and successfully preserve major physiological functions. Patients must meet all 4 conditions: Maxilla & Oral: No total maxillectomy (limited/scaffold-preserving excision allowed); no permanent tube feeding; intelligible speech; no severe trismus (mouth opening >2.5cm). Orbit & Vision: No enucleation/orbital exenteration; ipsilateral vision better than light perception (≥0.05); no intractable diplopia, severely restricted eye movement, or eyelid dysfunction causing exposure keratitis. Skull Base & Neurological: No massive cranial/dural defect from extensive resection; no persistent CSF leak; no severe treatment-induced CNS complications. Appearance: No obvious facial collapse or disfigurement; adequate subjective satisfaction (FACE-Q scale); no external facial prosthesis required. |
At 2 years post-treatment
|
|
Change in Quality of Life Scores (QOL)
Prazo: Baseline and up to 2 years
|
The psychological state and overall quality of life of the patients will be evaluated using the QOL-V30 questionnaire.
Higher scores generally represent a higher quality of life or level of functioning.
|
Baseline and up to 2 years
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Chunyan Chen, Sun Yat-sen University Cancer Center
- Investigador principal: Xuekui Liu, Sun Yat-sen University Cancer Center
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Outros números de identificação do estudo
- 2026-FXY-123
Plano para dados de participantes individuais (IPD)
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Descrição do plano IPD
Prazo de Compartilhamento de IPD
Critérios de acesso de compartilhamento IPD
Tipo de informação de suporte de compartilhamento de IPD
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