Combining chemotherapy, radiotherapy, and immunotherapy for advanced head and neck cancer

A Prospective, Single-center, Open-label Phase II Clinical Study of Intra-arterial Chemotherapy Combined with Concurrent Radiotherapy and Tislelizumab-jsgr in the Treatment of T4bNanyM0 HNSCC

This study is testing a new treatment that combines chemotherapy, radiation, and immunotherapy for patients with advanced head and neck cancer who can't have surgery to see if it helps them live longer and feel better.

Quick facts

• Phase: Phase 2
• Study type: Interventional
• Enrollment: 50 (estimated)
• Ages: 18 Years and up
• Sex: All
• Sponsor: Beijing Tongren Hospital (Academic / other)
• Drugs / interventions: immunotherapy, chemotherapy
• Locations: 1 site (Beijing, Beijing Municipality)
• Trial ID: NCT06725498 on ClinicalTrials.gov

What this trial studies

This clinical trial explores a novel treatment approach for patients with T4bNanyM0 head and neck squamous cell carcinoma by integrating intra-arterial chemotherapy with radiotherapy and immunotherapy. The study evaluates the effectiveness and safety of a regimen that includes Tislelizumab-jsgr, Cisplatin, and Albumin-Bound Paclitaxel, followed by immune checkpoint inhibitors. Patients who are not candidates for surgical resection will receive a tailored treatment plan aimed at improving survival outcomes. The trial meticulously assesses the response to this combined therapeutic strategy.

Who should consider this trial

Good fit: Ideal candidates include adults aged 18 and older with a confirmed diagnosis of T4bNanyM0 head and neck squamous cell carcinoma and adequate organ function.

Not a fit: Patients with early-stage head and neck cancer or those with severe comorbidities may not benefit from this study.

Why it matters

Potential benefit: If successful, this approach could significantly enhance survival rates for patients with advanced head and neck cancer.

How similar studies have performed: While this approach is innovative, similar studies combining chemotherapy, radiotherapy, and immunotherapy have shown promise in other cancer types, suggesting potential for success.

Eligibility criteria

Inclusion Criteria:

* Patients with T4bNanyM0 Head and neck squamous cell carcinoma (hypopharyngeal cancer, laryngeal cancer, oropharyngeal cancer or oral cavity) with a confirmed diagnosis by histology and/or cytology;
* Expected survival ≥3 months, with adequate organ function;
* Investigators believe they can safely receive treatment with PD-1 combined with platinum and albumin-bound paclitaxel;
* Age ≥18 years;
* ECOG score of 0-1;
* Measurable disease as defined by RECIST v1.1;
* Adequate bone marrow reserve and organ function: Absolute neutrophil count (ANC) ≥1,000/microliter (mcL), platelets ≥75,000/mcL, hemoglobin ≥8g/dL, without transfusion or dependence on erythropoietin (EPO) (within 7 days after assessment);
* Renal function: Serum creatinine ≤1.5 times the upper limit of normal (ULN) OR measured or calculated creatinine clearance ≥60mL/min with creatinine levels \> 1.5 times the institutional ULN. (GFR can also be used in place of creatinine or CrCl). Creatinine clearance should be calculated according to institutional standards;
* Liver function: For subjects with a total bilirubin level \>1.5 ULN, serum total bilirubin ≤1.5 times ULN or direct bilirubin ≤ULN; For patients with liver metastases, aspartate aminotransferase (AST/SGOT) and alanine aminotransferase (ALT/SGPT) ≤2.5 times ULN OR ≤5 times ULN; Albumin \> 2.5 mg/dL;
* Coagulation function: International normalized ratio (INR) or prothrombin time (PT) ≤1.5 times ULN, if the subject is receiving anticoagulant therapy, PT or PTT should be within the permissible range of the anticoagulant used;
* Females should agree to use contraceptive measures (such as intrauterine device (IUD), oral contraceptives, or condoms) during the study and for 6 months after the study ends; Negative serum or urine pregnancy test within 7 days before study entry, and must be non-lactating patients; Males should agree to use contraceptive measures during the study and for 6 months after the study ends.

Exclusion Criteria:

* Patients with a history of prior immunotherapy, radiotherapy, and treatment with EGFR monoclonal antibodies;
* Patients with a history of other (including unknown primary) malignant tumors within the past 5 years;
* Patients who are intolerant to radiotherapy post-surgery;
* Patients known to be allergic to the study medication or its active ingredients, excipients;
* Patients with any unstable systemic diseases, including but not limited to: severe infections, uncontrolled diabetes, unstable angina, cerebrovascular accidents or transient ischemic attacks, myocardial infarction, congestive heart failure, serious arrhythmias requiring medication, liver, kidney, or metabolic disorders;
* Patients with potential immune deficiencies, chronic infections, including HIV, hepatitis, tuberculosis (TB), or autoimmune diseases;
* Patients with potential hematological issues, including bleeding disorders, known prior gastrointestinal bleeding requiring intervention within the past 6 months, active pulmonary embolism or deep vein thrombosis (DVT) that is unstable on anticoagulation regimens;
* A history or any evidence of active noninfectious pneumonia;
* Known active central nervous system (CNS) metastases and/or leptomeningeal disease or carcinomatous meningitis. Subjects with previously treated brain metastases may participate if they are stable (no evidence of imaging progression for at least four weeks prior to the first trial treatment and any neurological symptoms have returned to baseline), with no new or enlarging evidence of brain metastases, and are not on steroids for at least 7 days prior to trial treatment. This exception does not include carcinomatous meningitis, which is excluded regardless of clinical stability;
* Concurrent use (or receipt) of medications within 7 days prior to Day 1 of Cycle 1 that may affect drug metabolism;
* Pregnant or breastfeeding, or expecting to become pregnant or father a child during the anticipated trial period;
* Any uncontrollable concomitant diseases, including but not limited to persistent or active infections, symptomatic congestive heart failure, unstable angina, arrhythmias;
* Prolonged corrected QT (QTc) interval \> 475 ms on screening EKG;
* Ejection fraction \<40% on 2D echocardiogram (ECHO) at screening;
* Any serious medical or psychiatric illness/condition, including substance use disorders, that may interfere with or limit adherence to study requirements/treatment in the investigator's judgment;
* Active autoimmune disease requiring systemic treatment in the past 2 years (i.e., the use of disease-modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapies (e.g., thyroid hormone, insulin, or physiologic corticosteroid replacement for adrenal or pituitary insufficiency, etc.) are not considered a form of systemic treatment.

Where this trial is running

Beijing, Beijing Municipality

• Beijing Tongren Hospital Affiliated to Capital Medical University — Beijing, Beijing Municipality, China (Recruiting)

Study contacts

• Study coordinator: Xiaohong Chen, Dr.

Conditions Head and Neck Squamous Cell Carcinoma