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Neoadjuvant Docetaxel, Cisplatin, and Dual Immunotherapy for Sinonasal Carcinoma (PANDA)

22 de junho de 2026 atualizado por: Chen Chunyan, Sun Yat-sen University

A Multicenter, Single-Arm, Phase II Trial of Neoadjuvant Docetaxel and Cisplatin Combined With Dual Immunotherapy for Locally Advanced Sinonasal Carcinoma (PANDA Study)

The main objective of this prospective study is to evaluate the effectiveness and safety of a novel neoadjuvant therapy for patients with locally advanced sinonasal carcinoma (SNC). The treatment consists of the standard TP chemotherapy regimen (docetaxel and cisplatin) combined with dual immunotherapy (sintilimab and ipilimumab N01) administered before surgery. Researchers aim to determine the major pathological response (MPR) rate and long-term survival outcomes, while also exploring if this combination treatment approach can help better preserve critical facial and organ functions for SNC patients.

Visão geral do estudo

Status

Ainda não está recrutando

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

Intervencional

Inscrição (Estimado)

23

Estágio

  • Fase 2

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

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

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

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

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

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

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Estimado)

31 de julho de 2026

Conclusão Primária (Estimado)

1 de agosto de 2028

Conclusão do estudo (Estimado)

1 de agosto de 2030

Datas de inscrição no estudo

Enviado pela primeira vez

9 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

9 de junho de 2026

Primeira postagem (Real)

12 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

25 de junho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

22 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

  • 2026-FXY-123

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Descrição do plano IPD

De-identified individual participant data (IPD) that underlie the results reported in the publication will be shared. Study protocol and statistical analysis plan will also be available.

Prazo de Compartilhamento de IPD

Data will become available beginning 6 months and ending 36 months following the publication of the primary research article.

Critérios de acesso de compartilhamento IPD

Data will be shared with qualified researchers whose proposed use of the data has been approved by an independent review committee identified for this purpose. Proposals should be directed to the corresponding author. To gain access, data requestors will need to sign a formal data access agreement, and the data will only be used for achieving the aims specified in the approved proposal.

Tipo de informação de suporte de compartilhamento de IPD

  • PROTOCOLO DE ESTUDO
  • SEIVA

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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