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Toripalimab Plus Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable NSCLC

2026年9月13日 更新者:Shaodong Hong

A Phase II Study of Toripalimab Combined With Sacituzumab Tirumotecan as Neoadjuvant Therapy for Resectable Non-Small Cell Lung Cancer

This is a prospective, multicenter, single-arm Phase II investigator-initiated trial evaluating neoadjuvant toripalimab plus sacituzumab tirumotecan (SKB264) in treatment-naive adults with resectable or potentially resectable, driver-negative non-small cell lung cancer (NSCLC). Eligible participants have stage II-IIIA or selected IIIB disease (T3N2 or T4N2) and will receive sacituzumab tirumotecan 5 mg/kg plus toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles. Participants deemed operable after multidisciplinary assessment will undergo definitive surgery. The primary endpoint is pathologic complete response. A Simon two-stage minimax design plans to enroll 30 participants.

調査の概要

状態

まだ募集していません

詳細な説明

This prospective, multicenter, single-arm Phase II investigator-initiated trial evaluates neoadjuvant sacituzumab tirumotecan (SKB264), a TROP2-directed antibody-drug conjugate, plus the PD-1 antibody toripalimab in treatment-naive adults with resectable or potentially resectable, driver-negative NSCLC. Participants have stage II-IIIA or selected IIIB disease (T3N2 or T4N2). Sacituzumab tirumotecan 5 mg/kg and toripalimab 3 mg/kg are administered intravenously on Day 1 every 2 weeks for up to 6 cycles. Surgery is planned 4-6 weeks after the final neoadjuvant dose when the participant remains operable following multidisciplinary assessment. Tumor response is assessed using RECIST 1.1. Safety is assessed using NCI CTCAE version 5.0, including adverse events, serious adverse events, perioperative complications, and surgery delays or cancellations. The primary endpoint is pathologic complete response, defined as no residual viable tumor cells in the resected primary tumor and all resected lymph nodes. Major pathologic response is defined as residual viable tumor of 10% or less.

研究の種類

介入

入学 (推定)

30

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

  • 名前:Shaodong Hong Hong, M.D., Ph.D.
  • 電話番号:+8615920527656
  • メール:hongshd@sysucc.org.cn

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:

  • Signed informed consent obtained before any study procedure.
  • Age 18 to 75 years, male or female.
  • Histologically/cytologically confirmed, treatment-naive, resectable or potentially resectable NSCLC: stage II-IIIA and selected IIIB (T3N2, T4N2) per IASLC/UICC TNM 9th edition.
  • Disease staged as cTNM by PET-CT or by neck/chest/abdominal/pelvic CT plus whole-body bone scan and brain MRI.
  • Multidisciplinary team including thoracic surgeon judges lesion resectable or potentially resectable.
  • At least one measurable target lesion per RECIST 1.1.
  • ECOG performance status 0-1.
  • Adequate organ function (baseline, no transfusion, rh-EPO, or G-CSF within 2 weeks before first dose): neutrophils ≥1.5 ×10^9/L; platelets ≥100 ×10^9/L; hemoglobin ≥9 g/dL.
  • AST, ALT, ALP ≤2.5 × ULN; TBil ≤1.5 × ULN.
  • For liver metastases: AST/ALT ≤5 × ULN; TBil ≤2 × ULN.
  • For liver or bone metastases: ALP ≤5 × ULN.
  • Creatinine clearance (Cockcroft-Gault) ≥60 mL/min.
  • INR, APTT, PT ≤1.5 × ULN.
  • TSH within normal range; if TSH abnormal but T3 and free T4 normal, eligible.
  • Women of childbearing potential must have a negative pregnancy test within 7 days before first dose and use effective contraception during treatment and until 12 months after last dose; men with partners of childbearing potential must use effective contraception during treatment and until 12 months after last dose.

Exclusion Criteria:

  • Neuroendocrine histology component in tumor pathology.
  • Known EGFR sensitizing mutation or ALK fusion (for non-squamous NSCLC, EGFR/ALK status must be determined).
  • Other malignancy within 5 years, except those with clinically negligible metastatic risk and curative treatment intent (e.g., adequately treated carcinoma in situ as per protocol examples).
  • Severe or uncontrolled comorbidities, including symptomatic cerebrovascular events or liver disease at Child-Pugh grade ≥A.
  • History of allogeneic stem cell transplantation or solid organ transplantation.
  • Severe dry eye syndrome, severe meibomian gland dysfunction, severe blepharitis, or corneal disorders that may delay corneal healing.
  • History of interstitial lung disease requiring steroids, or active ILD.
  • HIV positive or diagnosed AIDS.
  • Active tuberculosis.
  • Uncontrolled active HBV infection (HBsAg positive with HBV-DNA above local upper limit of normal). HBV-DNA must be <500 IU/mL within 28 days before randomization/inclusion.
  • Active HCV infection (HCV antibody positive and HCV RNA positive).
  • Known hypersensitivity to toripalimab or sacituzumab tirumotecan (or excipients).
  • Live vaccine within 30 days before first dose (except inactivated vaccines allowed where specified by protocol, including local policy).
  • Any systemic or local anticancer treatment before first study treatment.
  • Use of traditional Chinese medicines with anticancer indication within 7 days before first dose, or need to continue such drugs during study.
  • Other investigational drug not discontinued for at least 5 half-lives or 2 months (whichever is longer) before first dose.
  • Any known or suspected autoimmune disease or immunodeficiency, except primary hypothyroidism (stable, not requiring hormones, or stable on physiologic hormone replacement) and stable type 1 diabetes mellitus with controlled blood glucose.
  • Medical or psychiatric conditions likely to cause premature discontinuation or compromise safety, sampling, or follow-up, including severe social or compliance risks.
  • Pregnancy or breastfeeding; unwillingness to use effective contraception as specified.
  • Any other condition considered unsuitable by investigator.

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:なし
  • 介入モデル:単一グループの割り当て
  • 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:Toripalimab plus sacituzumab tirumotecan
Participants will receive sacituzumab tirumotecan 5 mg/kg intravenously on Day 1 every 2 weeks combined with toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy. Surgery will be performed after multidisciplinary assessment when appropriate. Postoperative or adjuvant treatment will be determined according to guidelines and investigator assessment.
Toripalimab 3 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy, administered in combination with sacituzumab tirumotecan.
Sacituzumab tirumotecan (SKB264) 5 mg/kg intravenously on Day 1 every 2 weeks for up to 6 cycles as neoadjuvant therapy, administered in combination with toripalimab.

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
メジャーの説明
時間枠
Pathological Complete Response (pCR) Rate
時間枠:At definitive surgery, up to 18 weeks after first study treatment
Proportion of participants with no residual viable tumor cells in the resected primary tumor and all resected lymph nodes. Participants without surgery or evaluable surgical pathology will be counted as non-pCR.
At definitive surgery, up to 18 weeks after first study treatment

二次結果の測定

結果測定
メジャーの説明
時間枠
Major Pathological Response (MPR) Rate
時間枠:At definitive surgery, up to 18 weeks after first study treatment
Proportion of participants with residual viable tumor of 10% or less in the resected primary tumor and all resected lymph nodes.
At definitive surgery, up to 18 weeks after first study treatment
R0 Resection Rate
時間枠:At definitive surgery, up to 18 weeks after first study treatment
Proportion of participants who undergo R0 resection, defined as microscopically margin-negative resection, after neoadjuvant therapy.
At definitive surgery, up to 18 weeks after first study treatment
Pathological Downstaging Rate
時間枠:At definitive surgery, up to 18 weeks after first study treatment
Proportion of participants with pathological stage lower than baseline clinical stage at definitive surgery.
At definitive surgery, up to 18 weeks after first study treatment
Objective Response Rate (ORR)
時間枠:Up to 18 weeks after first study treatment
Proportion of participants with complete response or partial response according to investigator-assessed RECIST 1.1 after neoadjuvant therapy.
Up to 18 weeks after first study treatment
Event-Free Survival (EFS)
時間枠:Up to 60 months from enrollment
Time from enrollment to disease progression precluding surgery, disease progression or recurrence after surgery, disease progression in participants who do not undergo surgery, or death from any cause, whichever occurs first.
Up to 60 months from enrollment
Overall Survival (OS)
時間枠:Up to 60 months from enrollment
Time from enrollment to death from any cause.
Up to 60 months from enrollment
Incidence of Adverse Events
時間枠:From first study treatment through 90 days after the last study treatment or surgery, whichever occurs later
Incidence of adverse events graded according to NCI CTCAE version 5.0.
From first study treatment through 90 days after the last study treatment or surgery, whichever occurs later

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 (推定)

2026年10月1日

一次修了 (推定)

2028年12月1日

研究の完了 (推定)

2028年12月1日

試験登録日

最初に提出

2026年7月24日

QC基準を満たした最初の提出物

2026年9月13日

最初の投稿 (実際)

2026年9月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月15日

QC基準を満たした最後の更新が送信されました

2026年9月13日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

De-identified individual participant data and data dictionaries from this investigator-initiated Phase II oncology study will not be shared at this time due to current sponsor/institutional policy, data governance requirements, and pending legal/ethics arrangements.

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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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