HNC-SYSU-005: Response to Neoadjuvant Chemoimmunotherapy in Resectable Locally Advanced Oral Cancer

Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University (Other)
Overall Status
Completed
CT.gov ID
NCT06143761
Collaborator
(none)
206
1
18.9
10.9

Study Details

Study Description

Brief Summary

The goal of this observational study is to investigate the effectiveness of neoadjuvant chemoimmunotherapy (NACI) regimens in treating advanced oral squamous cell carcinoma (OSCC) patients. We analyzed clinicopathologic features of advanced OSCC patients who received PD-1 inhibitors in combination with carboplatin and paclitaxel before surgical tumor resection between 2020 and 2022. The Response Evaluation Criteria in Solid Tumors (RECIST, version 1.1) and pathologic response were used to evaluate the efficacy of the NACI treatment. Adverse events apparently related to NACI treatment were graded according to the Common Terminology Criteria for Adverse Events, version 4.0. Disease-free survival (DFS) and overall survival (OS) were calculated using the Kaplan-Meier survival curves and compared using the log rank test. Additionally, we calculated the area under curve (AUC) to compare the predictive value of PD-L1 expression with baseline serum lipid biomarkers for patient response.

Condition or Disease Intervention/Treatment Phase
  • Drug: PD-1 inhibitor+carboplatin+albumin-bound paclitaxel

Study Design

Study Type:
Observational
Actual Enrollment :
206 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
A Pilot Study of Neoadjuvant Chemoimmunotherapy in Resectable Locally Advanced Head and Neck Squamous Cell Carcinoma
Actual Study Start Date :
Dec 1, 2020
Actual Primary Completion Date :
Jun 30, 2022
Actual Study Completion Date :
Jun 30, 2022

Arms and Interventions

Arm Intervention/Treatment
neoadjuvant chemoimmunotherapy+surgery

Patients who underwent neoadjuvant chemoimmunotherapy before surgery

Drug: PD-1 inhibitor+carboplatin+albumin-bound paclitaxel
A comparative evaluation of patient prognosis between those who received neoadjuvant chemoimmunotherapy-surgery treatment and those who underwent surgery alone.

surgery

Patients who accepted the surgery alone

Outcome Measures

Primary Outcome Measures

  1. Overall survival (OS) [2 years]

    The time(years) from day 1 of study treatment until death from any cause.

  2. Disease-free survival (DFS) [2 years]

    DFS(by months) is defined as the time from treatment until the date of the first relapse (local/regional recurrence or distant metastasis) or death (from any cause) whichever comes firsts and regardless of whether the patient withdraws from treatment or receives another anti-cancer therapy prior to disease DFS is defined as the time from treatment until the date of the first relapse (local/regional recurrence or distant metastasis) or death (from any cause) whichever comes firsts and regardless of whether the patient withdraws from treatment or receives another anti-cancer therapy prior to disease relapse.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Patients with advanced OSCC who received NACI before surgery

  • Confirmation of primary OSCC by two experienced pathologists;

  • Clinical stage III/ IVA (cT1-2/cN1-2/M0 or cT3-4a/cN0-2/M0) according to the 8th Edition of American Joint Committee on Cancer (AJCC) guideline;

  • An Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1;

  • No prior anti-cancer therapy;

  • Locally resectable advanced tumor evaluated by a head and neck surgeon.

Advanced OSCC patients who only received surgery

  • A histopathologic diagnosis of primary OSCC;

  • A clinical stage of III/IVA (AJCC, 8th edition);

  • An ECOG performance status of 0 to 1.

Exclusion Criteria:

Patients with advanced OSCC who received NACI before surgery

  • Patients with other pathological types, without NACI or Surgery;

  • Incomplete pre-treatment data;

  • Lost to follow up were excluded from the study.

Advanced OSCC patients who only received surgery

  • Patients who had received other therapies targeting the head and neck region before the surgery or those with evidence of recurrence or metastasis, as assessed by physical examination reports or imaging studies before surgery

  • Lost to follow up.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sun Yat-Sen Memorial Hospital Guangzhou Guangdong China 510120

Sponsors and Collaborators

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

Investigators

  • Principal Investigator: Jinsong Li, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
ClinicalTrials.gov Identifier:
NCT06143761
Other Study ID Numbers:
  • SYSKY-2023-184-01
First Posted:
Nov 22, 2023
Last Update Posted:
Nov 22, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 22, 2023