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Phase 2 N=68 Randomized Treatment

Neoadjuvant PD-1 Blockade in Resectable Oral Squamous Cell Carcinoma

Oral Squamous Cell Carcinoma

Enrolled (actual)
68
Serious AEs
19.1%
Results posted
Apr 2024
Primary outcome: Primary: Pathologic Response. — 25; 2; 4; 4 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Camrelizumab (Drug); Camrelizumanb plus TPF (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Hospital of Stomatology, Wuhan University
Primary completion
Aug 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Pathologic Response.
25; 2; 4; 4; 5; 26
SECONDARY
Radiographic Response.
0; 0; 3; 16; 20; 14
SECONDARY
Event-free Survival (EFS) Rate on Each Treatment Arm.
SECONDARY
Overall Survival (OS) on Each Treatment Arm.
SECONDARY
Adverse Events (AEs).

Summary

The purpose of this study is to investigate the safety and feasibility of neoadjuvant PD-1 blockade alone or neoadjuvant PD-1 blockade plus TPF induction chemotherapy in subjects with resectable local advanced oral squamous cell carcinoma.

Eligibility Criteria

Inclusion Criteria

  • Histologically documented oral squamous cell carcinoma (biopsy required).
  • Local advanced oral squamous cell carcinoma (clinical stage T1-2N1-3M0, T3-4aN0-3M0) with resection option for potential cure, as assessed by a faculty surgeon at Hospital of Stomatology, Wuhan University.
  • Distant metastasis is excluded by chest CT and emission computed tomograph.
  • Adequate organ function as follows: 1) Leukocyte count ≥ 2,000/mm3; 2) Absolute neutrophil count ≥ 1,000/mm3; 3) Platelet count ≥ 100,000/mm3; 4) Hemoglobin ≥ 90 g/L; 5) Serum albumin ≥30 g/L; 6) Total bilirubin ≤ 1.5 × upper limit of normal (ULN); 7) AST (SGOT) and ALT (SGPT) < 2.5 × ULN; 8) ALP ≤ 2.5 × ULN; 9) Prothrombin time-international normalized ratio ≤ 1.5; 10) Serum creatinine ≤ 1.5 × ULN; 11) INR/PT≤ 1.5; 12) TSH ≤ ULN.
  • ECOG performance status 0-1.
  • Female patient tested HCG negative in serum or urine within 7 days prior to the start of investigational product. Both patient and partner must agree to use contraception prior to study entry and for the duration of study participation and for up to 120 days after the last dose of PD-1 blockade.
  • Patient understands the study regimen, its requirements, risks and discomforts and is able and willing to sign the informed consent form.

Exclusion Criteria

  • History of ≥ 3 grade immune related adverse events (irAEs) or have not recovered to ≤ 1 grade irAEs from previous treatment.
  • History of other treatments for cancer, including surgery, chemotherapy, radiotherapy or molecular targeted therapy within past 5 years.
  • Previous therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4 or any other antibody targeting T cell co-regulatory pathways.
  • Active autoimmune disease or history of refractory autoimmune disease.
  • Active systemic infection requiring therapy.
  • Patients who are receiving psychotropic drug or alcohol/drug abuse.
  • Subjects with concurrent other active malignancies.
  • HIV or untreated active HBV or HCV infections, or vaccinated (HBV, flu, varicella, etc) within 4 weeks before recruitment.
  • Uncontrollable systemic diseases, including diabetes, hypertension, etc.
  • History of stroke or transient ischemic attack within past 6 months.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04649476). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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