Efficacy and Safety of a Third-Course of Neoadjuvant Immunochemotherapy Combined With SBRT in Locally Advanced Head and Neck Squamous Cell Carcinoma Patients With Stable Disease After Two Treatment Courses: A Single-Arm Exploratory Study

NCT06722495 | Not Yet Recruiting

• 1 other identifier: SYSKY-2024-804-02
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

Brief Summary

Neoadjuvant immunotherapy before surgery has shown good efficacy and safety in locally advanced HNSCC, particularly with the use of PD-1 inhibitors combined with chemotherapy, where some patients have achieved a high rate of pathological complete response. However, approximately 40% of patients respond poorly to neoadjuvant immunochemotherapy, with prolonged treatment courses failing to significantly improve outcomes, and some patients may even experience disease progression. For these patients, timely surgery or definitive radiotherapy combined with other well-tolerated therapeutic approaches is needed to improve pathological response rates, enhance long-term survival, and preserve organ function.

Conditions

SBRT; Neoadjuvant Immunochemotherapy; LA HNSCC

Outcome Measures

Primary Outcomes (1)

• Objective response rate

  Proportion of subjects containing complete response and partial response, i.e., the sum of the diameters of the target lesions is at least 30% smaller compared to baseline, derived from the RECIST v1.1 criteria at 3 weeks after the 3rd course of Neoadjuvant immunochemotherapy + SBRT, including by imaging assessment.

  3 weeks after the 3rd course of Neoadjuvant immunochemotherapy + SBRT, including by imaging assessment.

Secondary Outcomes (4)

• Overall response rate

  3 weeks after the 3rd course of Neoadjuvant immunochemotherapy + SBRT, including by imaging assessment.

• Pathological complete response

  10days after surgery

• Major pathologic response

  10days after surgery

• Pathological partial response

  10days after surgery

Study Arms (1)

3-Course of Neoadjuvant Immunochemotherapy combined with SBRT in LA-HNSCC with SD after 2-courses

EXPERIMENTAL

Stereotactic body radiation therapy added between 2-course and 3-course treatment.

Radiation: SBRT

Interventions

SBRT RADIATION

Patient will receive SBRT (8Gy\*3F) in combination with the original regimen of neoadjuvant immunochemotherapy in course 3. Gross tumor target volume (GTV) based on the primary foci clearly identified by clinical and imaging examinations. The GTV was discharged 3 mm to generate a Planning target volume (PTV). the target area (PTV) was dosed accordingly to the PTV.

3-Course of Neoadjuvant Immunochemotherapy combined with SBRT in LA-HNSCC with SD after 2-courses

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Age ≥18 and ≤75 years on the date of signing the informed consent form, male or female.
• Histologically and imaging-confirmed T3-4a or N+M0 stage III-IVb (AJCC 8th) HNSCC, patients have received 2-courses of platinum-based chemotherapy and tirilizumab immunotherapy, and whose efficacy is assessed as Stable Disease (SD).
• Life expectancy is at least 3 months.
• ECOG PS 0-1。
• Haematological analysis： 5.1 Absolute neutrophil count (ANC) ≥1.5×10\^9/L without granulocyte colony-stimulating factor in the last 14 days； 5.2 Absolute T-lymphocyte value ≥ 0.5 times the lower limit of normal value； 5.3 Platelets ≥100×10\^9/L without transfusion or platelet-boosting drugs in the last 14 days； 5.4 Haemoglobin ≥90g/L without transfusion or erythropoietin use in the last 14 days.
• Renal function:
• Creatinine clearance\* (Ccr) ≥60 mL/min; \*Ccr will be calculated using the Cockcroft-Gault formula: Ccr = (140-age) × body weight (kg) / \[0.818 (0.85 for males, 0.85 for females) × blood creatinine (SCr, umol/L) \] or Ccr = (140-age) × body weight (kg)/ \[72 × blood creatinine (SCr, mg/dL) \]; 6.2 Creatinine ≤ 1.5 × upper limit of normal (ULN)； 6.3 Routine urinalysis suggests urinary protein ≤ +; 6.4 Quantitative 24-hour urine protein \<1.0g.
• Liver function:
• Serum total bilirubin (TBil) ≤ 1.5 × ULN; 7.2 AST and ALT ≤ 2.5 × ULN, ≤ 5 × ULN for liver metastases, and TBil ≤ 3 × ULN.
• Coagulation: international normalised ratio (INR) and activated partial thromboplastin time (APTT) ≤ 1.5 × ULN.
• Normal thyroid function, defined as thyroid stimulating hormone (TSH) within the normal range. If baseline TSH is outside the normal range, subjects may be enrolled if total T3 (or FT3) and FT4 are within the normal range.
• Cardiac enzyme profiles within the normal range (enrolment is also permitted if the investigator's combined judgement is that it is a purely laboratory abnormality of no clinical significance).
• Patients must be able to understand and voluntarily sign an informed consent form.

You may not qualify if:

• Hypersensitivity to any of the antineoplastic therapeutic drug components of this research.
• Those who have previously suffered from other malignant tumours and have received radiotherapy.
• have uncontrolled clinical symptoms or cardiac disease including, but not limited to, symptomatic congestive heart failure (Grade 2 and above as determined by the New York Heart Association's Functional Class), unstable angina pectoris, acute myocardial ischaemia, and poorly controlled cardiac arrhythmias. Past history of myocarditis and cardiomyopathy.
• Active autoimmune disease requiring systemic therapy (e.g., use of disease-mitigating drugs, glucocorticoids, or immunosuppressants). Alternative therapies (e.g., thyroxine, insulin, or physiological glucocorticoids for adrenal or pituitary insufficiency) are not considered systemic therapy.
• History of (non-infectious) pneumonia requiring steroids or current pneumonia.
• Have active tuberculosis.
• History of non-infectious pneumonia requiring glucocorticoid therapy within 1 year prior to first dose or current clinically active interstitial lung disease.
• Active or uncontrolled infection requiring systemic therapy.
• History of human immunodeficiency virus (HIV) infection (e.g., HIV-positive).
• Liver disease such as cirrhosis, decompensated liver disease; known active hepatitis B (e.g., hepatitis B surface antigen (HBsAg) positive and HBV-DNA \> upper limit of normal in the laboratory of the research centre) or active hepatitis C virus infection (e.g., HCV antibody positive and HCV RNA level above the lower limit of detection).
• \*Note: Hepatitis B subjects meeting the following criteria may also be enrolled: 10.1 HBV viral load \<1000 copies/ml (200 IU/ml) prior to the first dose, and subjects should receive anti-HBV therapy throughout the study treatment period to avoid viral reactivation; 10.2 In subjects with anti-HBc (+), HBsAg (-), anti-HBs (-) and HBV viral load (-), prophylactic anti-HBV therapy is not required, but close monitoring of viral reactivation is needed.
• Have an active bleeding disorder or other history of severe bleeding.
• Allogeneic organ transplantation (except corneal transplantation) or allogeneic haematopoietic stem cell transplantation.
• Pregnant or breastfeeding, or preparing to become pregnant during the trial period.
• Medical, psychological, or social condition that may interfere with the subject's participation in the research or affect the assessment of the results; or other conditions that, in the opinion of the investigator, make enrolment inappropriate, or that, in the opinion of the investigator, present other potential risks that make participation in this research inappropriate.

Sponsors & Collaborators

• Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University: lead

Study Sites (1)

Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University

Guangzhou, Guangdong, 510120, China

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Model Details: This is a single-arm exploratory clinical study aimed at evaluating the efficacy and safety of combining stereotactic body radiation therapy (SBRT) with subsequent treatments in patients with locally advanced head and neck squamous cell carcinoma (LA HNSCC) who are unresponsive to neoadjuvant immunochemotherapy. The study plans to enroll 20 patients diagnosed with stage III-IVb (AJCC 8th) LA HNSCC who have received two cycles of platinum-based chemotherapy and PD-1 inhibitor immunotherapy, but achieved stable disease (SD) according to RECIST 1.1 criteria. These patients will receive SBRT (8Gy\*3F) during the third cycle of immunochemotherapy, followed by standard surgery and postoperative radiotherapy/chemoradiotherapy. The primary endpoint is the objective response rate (ORR) of the primary lesion after the third cycle, with secondary endpoints including overall ORR, pathologic complete response (pCR), major pathologic response (mPR), and partial pathologic response (pPR).

Study Record Dates

• First Submitted: November 6, 2024
• First Posted: December 9, 2024
• Study Start: December 24, 2024
• Primary Completion (Estimated): September 26, 2026
• Study Completion (Estimated): December 26, 2026
• Last Updated: December 9, 2024

Record last verified: 2024-12

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)