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Intermittent Hypoxic Training as Neoadjuvant Therapy for Lung Squamous Cell Carcinoma

25 de mayo de 2026 actualizado por: zhang yi

Study on the Novel Application of Intermittent Hypoxic Training in Neoadjuvant Therapy for Lung Squamous Cell Carcinoma

The goal of this clinical trial is to learn if adding intermittent hypoxic training (IHT) to standard neoadjuvant chemo-immunotherapy can increase the pathologic complete response (pCR) rate in patients aged 18 to 75 of both sexes with resectable stage II-IIIA lung squamous cell carcinoma. The main questions it aims to answer are:Can the addition of IHT to standard neoadjuvant chemo-immunotherapy significantly improve the pathologic complete response (pCR) rate compared to standard therapy alone? Is IHT safe and well-tolerated in this perioperative setting, and can it improve 2-year recurrence-free survival (RFS) without increasing complications? Researchers will compare the experimental group (standard neoadjuvant chemo-immunotherapy combined with IHT) to the control group (standard neoadjuvant chemo-immunotherapy alone) to see if the combination safely enhances anti-tumor immune responses, improves tumor regression, and extends long-term survival. Participants will:Receive standard neoadjuvant chemo-immunotherapy for 4 cycles (21 days per cycle), consisting of nab-paclitaxel, carboplatin, and pembrolizumab. Undergo Intermittent Hypoxic Training (IHT) if randomized to the experimental group, using the FLY-2265 low oxygen system (13% $FiO_2$ for 5 minutes followed by 21% $FiO_2$ for 5 minutes per cycle; 10 cycles per session, twice daily) for 7 consecutive days starting on Day 1 of each chemo-immunotherapy cycle. Undergo surgery (VATS lobectomy and systematic lymph node dissection) 3 to 4 weeks after the completion of the 4th cycle, provided that the disease has not progressed. Complete regular post-operative follow-up visits (including chest CT scans, brain MRIs, bone scans, tumor markers, and peripheral blood immune monitoring) for up to 5 years to evaluate long-term outcomes.

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Estimado)

60

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100053
        • Xuanwu Hospital, Capital Medical University
        • Contacto:

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  1. Age between 18 and 75 years old (inclusive), regardless of sex.
  2. Diagnosed with histologically confirmed stage II-IIIA (according to the AJCC 8th edition staging system) squamous cell lung carcinoma.
  3. The primary tumor is evaluated by a multidisciplinary team (MDT) and deemed completely resectable.
  4. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1.
  5. Life expectancy of at least 6 months.
  6. Adequate organ, bone marrow, and coagulation functions, meeting the following laboratory criteria within 7 days prior to enrollment:

    • Absolute neutrophil count (ANC) >= 1.5 x 10^9/L;
    • Platelet count >= 100 x 10^9/L;
    • Hemoglobin >= 90 g/L;
    • Total bilirubin <= 1.5 x upper limit of normal (ULN);
    • Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) <= 2.5 x ULN;
    • Serum creatinine <= 1.5 x ULN, or creatinine clearance >= 50 mL/min;
    • International normalized ratio (INR) and activated partial thromboplastin time (APTT) <= 1.5 x ULN.
  7. Female participants of childbearing potential must have a negative serum pregnancy test within 7 days prior to the first dose and agree to use effective contraception during the study and for at least 6 months after the last dose. Male participants must agree to use effective contraception during the study and for at least 6 months after the last dose.
  8. Participant understands the study protocol, voluntarily participates, and signs the written Informed Consent Form (ICF).

Exclusion Criteria:

  1. Histologically confirmed small cell lung cancer, adeno-squamous carcinoma, large cell neuroendocrine carcinoma, or adenocarcinoma (including components of these types).
  2. Patients with driver gene mutations that have approved targeted therapies available (e.g., EGFR mutations, ALK rearrangements, ROS1 fusions, etc.).
  3. Prior systemic antitumor therapy for lung cancer, including chemotherapy, radiotherapy, immunotherapy, targeted therapy, or definitive surgical resection.
  4. Active, known, or suspected autoimmune diseases (e.g., systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, autoimmune hepatitis), or a history of autoimmune disease within the past 2 years.
  5. History of other malignant tumors within the past 5 years, except for adequately treated cured skin basal cell carcinoma, squamous cell carcinoma, or carcinoma in situ (e.g., cervical carcinoma in situ).
  6. Severe cardiovascular or cerebrovascular diseases, including but not limited to:

    • Myocardial infarction or unstable angina within the past 6 months;
    • New York Heart Association (NYHA) Class III or IV congestive heart failure;
    • Clinically significant ventricular arrhythmia or poorly controlled symptomatic arrhythmia;
    • Stroke or transient ischemic attack (TIA) within the past 6 months.
  7. Poorly controlled hypertension (systolic blood pressure >= 160 mmHg and/or diastolic blood pressure >= 100 mmHg despite standard antihypertensive therapy).
  8. Chronic obstructive pulmonary disease (COPD) or other respiratory diseases with severe lung function impairment (e.g., FEV1 < 50% predicted value, or requiring long-term home oxygen therapy).
  9. Active infections requiring systemic intravenous anti-infective treatment within 2 weeks prior to enrollment (e.g., severe pneumonia, bacteremia), or active tuberculosis infection.
  10. Known history of human immunodeficiency virus (HIV) infection, or active Hepatitis B (HBV DNA >= 500 IU/mL or copy number above detection limit) or active Hepatitis C (HCV RNA positive).
  11. History of interstitial lung disease (ILD), drug-induced pneumonitis, radiation pneumonitis requiring steroid treatment, or evidence of active pneumonitis.
  12. Severe claustrophobia, severe high-altitude sickness history, or other medical/psychological conditions that prevent compliance with intermittent hypoxic training (IHT) using the FLY-2265 low oxygen system.
  13. Pregnant or breastfeeding women.
  14. Any other medical condition, clinical laboratory abnormality, or social circumstance that, in the opinion of the investigator, may compromise participant safety, interfere with the evaluation of study interventions, or affect compliance with study procedures.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Intermittent Hypoxic Training + Chemo-immunotherapy
Participants will receive standard neoadjuvant chemo-immunotherapy (nab-paclitaxel + carboplatin + pembrolizumab) for 4 cycles (21 days per cycle). Concurrently, participants will undergo Intermittent Hypoxic Training (IHT) using the FLY-2265 system (13% FiO2 for 5 min, 21% FiO2 for 5 min per cycle; 10 cycles/session, twice daily) for 7 consecutive days starting on Day 1 of each chemo-immunotherapy cycle. Surgery will be performed 3-4 weeks after completing the 4th cycle.
Participants will undergo Intermittent Hypoxic Training (IHT) using the FLY-2265 low oxygen system. The training protocol consists of cycles of inhaling 13% FiO2 (fraction of inspired oxygen) for 5 minutes, followed by 21% FiO2 (room air) for 5 minutes. Each session comprises 10 cycles, administered twice daily, for 7 consecutive days. This 7-day training course starts on Day 1 of each 21-day neoadjuvant treatment cycle, for a total of 4 courses.
Participants will receive standard clinical doses of neoadjuvant chemo-immunotherapy for 4 cycles (21 days per cycle) prior to surgery. The regimen includes: 1) Nab-paclitaxel; 2) Carboplatin; 3) Pembrolizumab. All agents will be administered via intravenous infusion according to standard clinical oncology guidelines.
Otros nombres:
  • Nab-paclitaxel
  • Carboplatino
  • Pembrokizumab
Comparador activo: Standard Neoadjuvant Chemo-immunotherapy Alone
Participants will receive standard neoadjuvant chemo-immunotherapy alone for 4 cycles (21 days per cycle). The regimen consists of nab-paclitaxel, carboplatin, and pembrolizumab at standard clinical doses, identical to the experimental group. No intermittent hypoxic training will be administered. Surgery will be performed 3-4 weeks after completing the 4th cycle.
Participants will receive standard clinical doses of neoadjuvant chemo-immunotherapy for 4 cycles (21 days per cycle) prior to surgery. The regimen includes: 1) Nab-paclitaxel; 2) Carboplatin; 3) Pembrolizumab. All agents will be administered via intravenous infusion according to standard clinical oncology guidelines.
Otros nombres:
  • Nab-paclitaxel
  • Carboplatino
  • Pembrokizumab

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Pathologic Complete Response (pCR) Rate
Periodo de tiempo: At the time of surgery (approximately 3 to 4 weeks after the completion of the 4th cycle of neoadjuvant therapy).
The percentage of participants who achieve pathologic complete response, defined as the complete disappearance of all invasive tumor cells in the completely resectable lung cancer specimen and all sampled regional lymph nodes (ypT0N0) following neoadjuvant therapy.
At the time of surgery (approximately 3 to 4 weeks after the completion of the 4th cycle of neoadjuvant therapy).

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Major Pathological Response (MPR) Rate
Periodo de tiempo: At the time of surgery (approximately 3 to 4 weeks after the completion of the 4th cycle of neoadjuvant therapy).
The percentage of participants with 10% or less viable tumor cells remaining in the resected primary tumor specimen following neoadjuvant therapy.
At the time of surgery (approximately 3 to 4 weeks after the completion of the 4th cycle of neoadjuvant therapy).
Incidence of Treatment-Emergent Adverse Events (TEAEs)
Periodo de tiempo: From the start of neoadjuvant therapy up to 30 days after surgery (approximately 5 months).
Safety and tolerability evaluated by grading and recording adverse events, compliance with intermittent hypoxic training, and delay or discontinuation of neoadjuvant therapy, graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
From the start of neoadjuvant therapy up to 30 days after surgery (approximately 5 months).
2-Year Recurrence-Free Survival (RFS) Rate
Periodo de tiempo: 2 years post-surgery.
The percentage of participants who are alive without tumor recurrence or progression at 2 years after surgery.
2 years post-surgery.
Changes in Peripheral Blood Immune Cell Subsets
Periodo de tiempo: Baseline (before therapy) and prior to surgery (approximately 12 weeks after baseline).
Evaluation of tumor immune microenvironment factors and systemic immunity, including the percentage of CD8+ T cells, CD4+ T cells, and the CD4+/CD8+ T-cell ratio measured by flow cytometry.
Baseline (before therapy) and prior to surgery (approximately 12 weeks after baseline).

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de junio de 2026

Finalización primaria (Estimado)

1 de diciembre de 2027

Finalización del estudio (Estimado)

1 de diciembre de 2028

Fechas de registro del estudio

Enviado por primera vez

25 de mayo de 2026

Primero enviado que cumplió con los criterios de control de calidad

25 de mayo de 2026

Publicado por primera vez (Actual)

1 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

1 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

25 de mayo de 2026

Última verificación

1 de mayo de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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