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Nimotuzumab Combined With Immunotherapy and Chemotherapy in the Treatment of Locally Advanced Head and Neck Squamous Cell Carcinoma

A Prospective, Randomized, Phase II Study of Nimotuzumab Combined With Immunotherapy and Chemotherapy in the Treatment of Locally Advanced Head and Neck Squamous Cell Carcinoma

This is a randomized controlled, phase II clinical study designed to explore the efficacy and safety of nimotuzumab combined with immunotherapy and chemotherapy as neoadjuvant treatment for locally advanced head and neck squamous cell carcinoma (LA-HNSCC). The primary endpoint of the study is the 2-year event-free survival (EFS) rate. Enrollment is expected to be completed within 2 years; all patients will be followed up for at least 2 years after the last patient is enrolled.

調査の概要

研究の種類

介入

入学 (推定)

182

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

      • Shanghai、中国
        • 募集
        • Shanghai First People's Hospital
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  1. Age 18 to 75 years inclusive.
  2. Histologically or cytologically confirmed squamous cell carcinoma of the head and neck (HNSCC) (oral cavity, oropharynx, larynx, hypopharynx), stage III-IVB per AJCC 8th edition.
  3. Resectable disease assessed by a multidisciplinary team (MDT) including surgical, radiological, and pathological specialists.
  4. Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1.
  5. For oropharyngeal carcinoma: mandatory p16 immunohistochemistry (testing within standard of care is acceptable; repeat testing not required). p16 testing is not required for other tumor locations.
  6. Availability of tumor tissue (archived or newly obtained) for PD-L1 testing (prior testing is acceptable; repeat testing not required).
  7. At least one measurable lesion per RECIST 1.1.
  8. Life expectancy ≥ 6 months.
  9. Adequate hematologic function:

    White blood cell count ≥ 4.0 × 10⁹/L Absolute neutrophil count ≥ 1.5 × 10⁹/L Platelet count ≥ 100 × 10⁹/L Hemoglobin ≥ 90 g/L

  10. Adequate renal function:

    Serum creatinine ≤ 1.5 × upper limit of normal (ULN) OR

    Creatinine clearance (CrCl) ≥ 60 mL/min calculated by Cockcroft-Gault formula:

    Female: CrCl (mL/min) = (140 - age) × body weight (kg) × 0.85 / (72 × serum creatinine (mg/dL)) Male: CrCl (mL/min) = (140 - age) × body weight (kg) × 1.00 / (72 × serum creatinine (mg/dL))

  11. Adequate hepatic function:

    Total bilirubin ≤ 1.5 × ULN Aspartate aminotransferase (AST) ≤ 2.5 × ULN Alanine aminotransferase (ALT) ≤ 2.5 × ULN

  12. Female subjects: negative pregnancy test within 2 weeks before first study drug, non-lactating.

    Females: highly effective contraception required during study and for 6 months after last study drug.

    Males: highly effective contraception required during study and for 6 months after last study drug.

  13. Written informed consent obtained prior to any study-specific procedures, and willingness to comply with all study visits and protocol requirements.

Exclusion Criteria:

  1. Received PD-1 inhibitors, EGFR monoclonal antibodies, EGFR-TKIs, or anti-angiogenic agents within 4 weeks prior to enrollment.
  2. Participation in another interventional clinical trial within 30 days prior to screening.
  3. In the investigator's judgment, the patient cannot tolerate or has contraindications to platinum-based chemotherapy (cisplatin or carboplatin) as specified in the protocol.
  4. Unresectable disease, poor medical condition for surgery, refusal of surgery for any reason, or excessive tumor burden precluding resection.
  5. History of other malignancy within the past 5 years (except cured basal cell carcinoma of the skin).
  6. History of primary immunodeficiency disease.
  7. Presence of uncontrolled comorbidities, including heart failure, severe pulmonary disease, severe hepatic disease, psychiatric disorders, etc.
  8. Known HIV infection, active viral hepatitis, or active tuberculosis.
  9. Underwent major surgery within 90 days prior to the first study drug, or planning major surgery unrelated to this cancer treatment.
  10. Hypersensitivity to any study drug or their components.
  11. Pregnant (confirmed by serum or urine HCG test) or lactating woman; or subject of childbearing potential unwilling or unable to use effective contraception during study treatment and for at least 6 months after the last dose of study treatment (applicable to both males and females).
  12. Investigator considers the subject not suitable for study participation.
  13. Unwilling to participate or unable to provide written informed consent.
  14. Receipt of a live vaccine within 30 days before the first study drug administration.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:なし(オープンラベル)

武器と介入

参加者グループ / アーム
介入・治療
実験的:Study Group
  1. Nimotuzumab ,Albumin-bound paclitaxel and cisplatin administration on days 3 and 24, tislelizumab (or pembrolizumab) administration on days 1 and 22;
  2. Standard of care surgery
Nimotuzumab 400mg,d3,Q3W,for two cycles。
他の名前:
  • ニモツズマブ
tislelizumab (or pembrolizumab) 200mg,d1,Q3W,for two cycles。
他の名前:
  • ペムブロリズマブ
Albumin-bound paclitaxel 180 mg/m² (or docetaxel 75 mg/m²), administered on day 3, every 3 weeks (Q3W);for two cycles。
他の名前:
  • ドセタキセル
Cisplatin 75 mg/m² (carboplatin AUC=5 may be substituted if cisplatin is not tolerated), administered on day 3, every 3 weeks (Q3W).for two cycles。
他の名前:
  • シスプラチン
  • カルボプラチン
Standard radical surgery of tumor

Concurrent chemoradiotherapy: Radiotherapy: intensity modulated conformal radiotherapy (IMRT) was used with a total dose of 60-66gy (2gy/f, 30-33f).

Chemotherapy: Cisplatin 40 mg/m2, QW, 6-7 times in total; Targeting: nimotuzumab 200mg, QW, 6-7 times in total.

アクティブコンパレータ:Control Group
1.Standard of care surgery
Standard radical surgery of tumor

Concurrent chemoradiotherapy: Radiotherapy: intensity modulated conformal radiotherapy (IMRT) was used with a total dose of 60-66gy (2gy/f, 30-33f).

Chemotherapy: Cisplatin 40 mg/m2, QW, 6-7 times in total; Targeting: nimotuzumab 200mg, QW, 6-7 times in total.

この研究は何を測定していますか?

主要な結果の測定

結果測定
時間枠
2-Year Event-Free Survival (EFS) Rate
時間枠:From first study treatment up to 2 years after the last patient randomized.
From first study treatment up to 2 years after the last patient randomized.

二次結果の測定

結果測定
メジャーの説明
時間枠
Major Pathologic Response (MPR)
時間枠:Within 4 weeks after surgery.
Within 4 weeks after surgery.
Pathological Complete Response (pCR)
時間枠:Within 4 weeks after surgery.
Within 4 weeks after surgery.
Objective Response Rate (ORR)
時間枠:After 2 cycles (each cycle is 21 days) of neoadjuvant treatment.
After 2 cycles (each cycle is 21 days) of neoadjuvant treatment.
2-Year Overall Survival (OS) Rate
時間枠:From first study treatment up to 2 years after the last patient randomized.
From first study treatment up to 2 years after the last patient randomized.
Quality of Life (QoL)
時間枠:Baseline(Screening) After neoadjuvant chemotherapy:Study Group(S)Week6 /Control Group(C)NA Post-surgery:S Week 9/C Week 3 After adjuvant radiotherapy(S Week 21/C Week 15) End of treatment(Week 24) Follow-up: Month 6, Month 12, Month 24

Assessed using the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life Questionnaires QLQ-C30 (V3.0).

EORTC QLQ-C30 V3.0:The scale consists of general domain items and global health and quality of life items. General domain items are further divided into functional domains and symptom domains. The raw scores of general items range from 1 (minimum) to 4 (maximum), while those of global health and quality of life items range from 1 (minimum) to 7 (maximum). All raw scores are finally standardized to scores ranging from 0 to 100.

In functional domains including PF, RF, EF, CF, SF and QL, higher scores indicate better functional status. In symptom domains including FA, NV, PA, DY, SL, AP, CO, DI and FI, higher scores stand for more severe symptoms. For the global health and quality of life domain, higher scores reflect better general health condition and quality of life.

Baseline(Screening) After neoadjuvant chemotherapy:Study Group(S)Week6 /Control Group(C)NA Post-surgery:S Week 9/C Week 3 After adjuvant radiotherapy(S Week 21/C Week 15) End of treatment(Week 24) Follow-up: Month 6, Month 12, Month 24

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年4月20日

一次修了 (推定)

2028年4月30日

研究の完了 (推定)

2030年4月30日

試験登録日

最初に提出

2026年4月29日

QC基準を満たした最初の提出物

2026年5月15日

最初の投稿 (実際)

2026年5月22日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月9日

QC基準を満たした最後の更新が送信されました

2026年7月8日

最終確認日

2026年7月1日

詳しくは

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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