- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07823270
Neoadjuvant Sacituzumab Tirumotecan Plus Toripalimab in Locally Advanced Esophageal Squamous Cell Carcinoma
11. září 2026 aktualizováno: Hebei Medical University Fourth Hospital
A Prospective, Single-arm, Phase II Study of Neoadjuvant Sacituzumab Tirumotecan (SKB264/MK-2870) Combined With Toripalimab in Patients With Locally Advanced Esophageal Squamous Cell Carcinoma
This study aims to evaluate the efficacy and safety of neoadjuvant sacituzumab tirumotecan (SKB264/MK-2870) combined with toripalimab in patients with locally advanced, resectable esophageal squamous cell carcinoma (ESCC).
Eligible participants will receive 3 cycles of neoadjuvant treatment, followed by radical surgery.
The primary endpoint is the pathologic complete response (pCR) rate.
Přehled studie
Postavení
Zatím nenabíráme
Podmínky
Intervence / Léčba
Detailní popis
This is a prospective, single-arm, phase II study planned to enroll 33 participants with histologically or cytologically confirmed locally advanced esophageal squamous cell carcinoma (clinical stage cT1-2N+M0 or T3-4N0-3M0, stage II-IVA) who are candidates for surgery and require neoadjuvant therapy.
After screening within 28 days before the first dose, eligible participants will receive sacituzumab tirumotecan 4 mg/kg intravenously once every 2 weeks on day 1 for 3 cycles, in combination with toripalimab 3 mg/kg intravenously once every 2 weeks on day 1 for 3 cycles.
When administered on the same day, toripalimab is infused first, followed by sacituzumab tirumotecan after an interval of at least 30 minutes.
Tumor response will be assessed based on RECIST v1.1, and radical surgery will be performed within 28 days after completion of neoadjuvant therapy.
Tumor assessments will be performed every 3 months for the first 2 years after surgery and every 6 months thereafter until radiologically confirmed disease progression.
Survival follow-up will be conducted every 3 to 6 months by telephone.
Safety will be assessed according to NCI CTCAE v5.0.
Typ studie
Intervenční
Zápis (Odhadovaný)
33
Fáze
- Fáze 2
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní kontakt
- Jméno: Zhenhua Li
- Telefonní číslo: +86 185 3111 5825
Studijní místa
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Hebei
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Shijiazhuang, Hebei, Čína, 050011
- Hebei Medical University Fourth Hospital
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Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Ne
Popis
Inclusion Criteria:
- Age >=18 years at the time of informed consent, either sex.
- Histologically or cytologically confirmed locally advanced esophageal squamous cell carcinoma.
- Judged by imaging and esophagoscopy as resectable and requiring neoadjuvant therapy, with clinical stage cT1-2N+M0 or T3-4N0-3M0 (stage II-IVA).
- No prior antitumor therapy for esophageal squamous cell carcinoma.
- At least one measurable lesion per RECIST v1.1.
- ECOG performance status of 0 or 1 within 7 days before dosing.
- Adequate organ and bone marrow function (no transfusion, recombinant human thrombopoietin, or colony-stimulating factor within 2 weeks before the first dose):
- Hematology: NEUT# >=1.5x10^9/L; PLT >=100x10^9/L; hemoglobin >=90 g/L.
- Hepatic: AST and ALT <=2.5xULN (<=5xULN for participants with baseline liver metastases); albumin >=30 g/L; total bilirubin <=1.5xULN.
- Renal: creatinine clearance >=60 mL/min (Cockcroft-Gault formula).
- Coagulation: INR, APTT, and PT <=1.5xULN.
- Normal thyroid function, defined as TSH within the normal range. If baseline TSH is outside the normal range, participants with total T3 (or FT3) and FT4 within the normal range are also eligible.
- Cardiac enzymes within the normal range (isolated laboratory abnormalities judged by the investigator as not clinically significant are allowed).
- Left ventricular ejection fraction >=55%.
- Women of childbearing potential and men with partners of childbearing potential must agree to use effective medical contraception from informed consent until 6 months after the last dose.
- Participants voluntarily join the study, sign the informed consent form, and are able to comply with the scheduled visits and procedures.
Exclusion Criteria:
- Any prior antitumor therapy for the currently diagnosed esophageal squamous cell carcinoma.
- History of other malignancies within 5 years (except cured basal cell carcinoma of the skin, squamous cell carcinoma of the skin, and carcinoma in situ of the cervix).
- Requirement for strong inhibitors or inducers of cytochrome P450 3A4 (CYP3A4) within 2 weeks before the first dose or during the study.
- Documented severe dry eye syndrome, severe meibomian gland disease and/or blepharitis, or a history of corneal disease that interferes with or delays corneal healing.
- Any of the following cardiovascular or cerebrovascular diseases or risk factors:
- Myocardial infarction, unstable angina, acute or persistent myocardial ischemia, grade 3 or 4 heart failure (NYHA classification), symptomatic or poorly controlled severe arrhythmia, cerebrovascular accident, transient ischemic attack, or other severe cardiovascular or cerebrovascular diseases within 6 months before dosing.
- History of myocarditis, primary cardiomyopathy, or specific cardiomyopathy.
- Any deep vein thrombosis (participants stabilized with low molecular weight heparin or similar therapy for >=2 weeks may be allowed), peripheral arterial thromboembolic event, pulmonary embolism, or other severe thromboembolic events within 3 months before dosing.
- Aortic aneurysm, aortic dissecting aneurysm, or other major vascular disease that may be life-threatening or requires surgery within 6 months before dosing.
- Uncontrolled systemic disease as judged by the investigator:
- Poorly controlled diabetes mellitus (two consecutive fasting glucose levels >=9 mmol/L).
- Poorly controlled hypertension (systolic blood pressure >160 mmHg and/or diastolic blood pressure >100 mmHg).
- Symptomatic pleural effusion, pericardial effusion, or ascites requiring repeated drainage.
- History of steroid-requiring (non-infectious) interstitial lung disease (ILD) or non-infectious pneumonitis; current ILD or non-infectious pneumonitis; or suspected ILD or non-infectious pneumonitis that cannot be excluded by imaging at screening.
- Active autoimmune disease requiring systemic treatment within the past 2 years, including disease-modifying drugs, immunosuppressants, or systemic corticosteroids (>10 mg/day prednisone or equivalent). Hormone replacement therapy such as thyroxine, insulin, or physiologic corticosteroid replacement for adrenal or pituitary insufficiency is not considered systemic treatment. Participants receiving systemic corticosteroids >10 mg/day prednisone or other immunosuppressive drugs within 2 weeks before dosing.
- Known active pulmonary tuberculosis. Participants with suspected active pulmonary tuberculosis must undergo clinical evaluation to exclude it.
- Known history of allogeneic organ transplantation or allogeneic hematopoietic stem cell transplantation.
- Active hepatitis B (HBsAg positive with HBV-DNA >=500 IU/mL or above the lower limit of detection, whichever is higher) or hepatitis C (HCV antibody positive with HCV-RNA above the lower limit of detection). Participants who are HBsAg positive are required to receive anti-hepatitis B viral therapy during the study.
- Positive human immunodeficiency virus (HIV) test or history of acquired immunodeficiency syndrome (AIDS); known active syphilis infection.
- Known hypersensitivity to the study drugs or any of their components, or a history of severe hypersensitivity reactions to other biologics.
- Severe infection within 4 weeks before dosing, including but not limited to complications requiring hospitalization, sepsis, or severe pneumonia; active infection requiring systemic anti-infective therapy within 2 weeks before dosing.
- Receipt of non-specific immunomodulatory therapy (including but not limited to interferon, IL-2) or Chinese patent medicines approved for antitumor indications within 2 weeks before dosing.
- Receipt of a live vaccine within 30 days before dosing, or planned receipt of a live vaccine during the study.
- Rapid deterioration during screening before dosing, such as a marked change in performance status.
- Pregnant or breastfeeding women.
- Local or systemic diseases caused by non-malignant conditions, or diseases or symptoms secondary to the tumor, that may lead to high medical risk and/or uncertainty in survival evaluation, such as leukemoid reaction or cachexia.
- Any condition that, in the investigator's judgment, interferes with the evaluation of the study drug, participant safety, or interpretation of study results, or any other condition that makes the participant unsuitable for this study.
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
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Experimentální: Neoadjuvant Sacituzumab Tirumotecan + Toripalimab
Participants receive sacituzumab tirumotecan 4 mg/kg intravenously once every 2 weeks plus toripalimab 3 mg/kg intravenously once every 2 weeks for 3 cycles, followed by radical surgery.
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4 mg/kg administered intravenously on day 1 of each 14-day cycle for 3 cycles.
Premedication is required before each infusion to prevent infusion-related reactions.
3 mg/kg administered intravenously on day 1 of each 14-day cycle for 3 cycles.
When given on the same day, toripalimab is infused first, followed by sacituzumab tirumotecan after an interval of at least 30 minutes.
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Pathologic complete response (pCR) rate
Časové okno: Approximately 3 months after the first dose (after completion of neoadjuvant therapy and radical surgery)
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The proportion of participants with no residual viable tumor cells in the resected primary tumor and regional lymph nodes (ypT0N0) after neoadjuvant therapy, as assessed by central pathologic review.
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Approximately 3 months after the first dose (after completion of neoadjuvant therapy and radical surgery)
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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Major pathologic response (MPR) rate
Časové okno: Approximately 3 months after the first dose(after completion of neoadjuvant therapy and radical surgery)
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The proportion of participants with 10 percent or fewer viable tumor cells remaining in the resected primary tumor and regional lymph nodes after neoadjuvant therapy.
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Approximately 3 months after the first dose(after completion of neoadjuvant therapy and radical surgery)
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Objective response rate (ORR) per RECIST v1.1
Časové okno: Approximately 3 months after the first dose
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The proportion of participants with a confirmed complete response (CR) or partial response (PR) as assessed by the investigator according to RECIST v1.1.
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Approximately 3 months after the first dose
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Event-free survival (EFS)
Časové okno: From the first dose until the event, assessed up to approximately 3 years
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Time from the first dose to any of the following events: any disease progression that precludes surgery, postoperative disease progression or recurrence, or death from any cause, whichever occurs first, as assessed by the investigator according to RECIST v1.1.
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From the first dose until the event, assessed up to approximately 3 years
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Overall survival (OS)
Časové okno: From the first dose until death from any cause, assessed up to approximately 5 years
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Time from the first dose to death from any cause.
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From the first dose until death from any cause, assessed up to approximately 5 years
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Incidence and severity of adverse events (safety and tolerability)
Časové okno: From the first dose until 30 days after the last dose
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Incidence, severity, and relationship to study treatment of all adverse events (AEs), treatment-emergent adverse events (TEAEs), and serious adverse events (SAEs) graded according to NCI CTCAE v5.0; the proportion of participants requiring dose reduction or discontinuation due to AEs; and changes in vital signs, physical examination findings, and laboratory results.
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From the first dose until 30 days after the last dose
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Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Vyšetřovatelé
- Vrchní vyšetřovatel: Ziqiang Tian, Hebei Medical University Fourth Hospital
Publikace a užitečné odkazy
Osoba odpovědná za zadávání informací o studiu tyto publikace poskytuje dobrovolně. Mohou se týkat čehokoli, co souvisí se studiem.
Obecné publikace
- Shapiro J, van Lanschot JJB, Hulshof MCCM, van Hagen P, van Berge Henegouwen MI, Wijnhoven BPL, van Laarhoven HWM, Nieuwenhuijzen GAP, Hospers GAP, Bonenkamp JJ, Cuesta MA, Blaisse RJB, Busch ORC, Ten Kate FJW, Creemers GM, Punt CJA, Plukker JTM, Verheul HMW, Bilgen EJS, van Dekken H, van der Sangen MJC, Rozema T, Biermann K, Beukema JC, Piet AHM, van Rij CM, Reinders JG, Tilanus HW, Steyerberg EW, van der Gaast A; CROSS study group. Neoadjuvant chemoradiotherapy plus surgery versus surgery alone for oesophageal or junctional cancer (CROSS): long-term results of a randomised controlled trial. Lancet Oncol. 2015 Sep;16(9):1090-1098. doi: 10.1016/S1470-2045(15)00040-6. Epub 2015 Aug 5.
- Wang ZX, Cui C, Yao J, Zhang Y, Li M, Feng J, Yang S, Fan Y, Shi J, Zhang X, Shen L, Shu Y, Wang C, Dai T, Mao T, Chen L, Guo Z, Liu B, Pan H, Cang S, Jiang Y, Wang J, Ye M, Chen Z, Jiang D, Lin Q, Ren W, Wang J, Wu L, Xu Y, Miao Z, Sun M, Xie C, Liu Y, Wang Q, Zhao L, Li Q, Huang C, Jiang K, Yang K, Li D, Liu Y, Zhu Z, Chen R, Jia L, Li W, Liao W, Liu HX, Ma D, Ma J, Qin Y, Shi Z, Wei Q, Xiao K, Zhang Y, Zhang Y, Chen X, Dai G, He J, Li J, Li G, Liu Y, Liu Z, Yuan X, Zhang J, Fu Z, He Y, Ju F, Liu Z, Tang P, Wang T, Wang W, Zhang J, Luo X, Tang X, May R, Feng H, Yao S, Keegan P, Xu RH, Wang F. Toripalimab plus chemotherapy in treatment-naive, advanced esophageal squamous cell carcinoma (JUPITER-06): A multi-center phase 3 trial. Cancer Cell. 2022 Mar 14;40(3):277-288.e3. doi: 10.1016/j.ccell.2022.02.007. Epub 2022 Mar 3.
- Yang H, Liu H, Chen Y, Zhu C, Fang W, Yu Z, Mao W, Xiang J, Han Y, Chen Z, Yang H, Wang J, Pang Q, Zheng X, Yang H, Li T, Zhang X, Li Q, Wang G, Chen B, Mao T, Kong M, Guo X, Lin T, Liu M, Fu J. Long-term Efficacy of Neoadjuvant Chemoradiotherapy Plus Surgery for the Treatment of Locally Advanced Esophageal Squamous Cell Carcinoma: The NEOCRTEC5010 Randomized Clinical Trial. JAMA Surg. 2021 Aug 1;156(8):721-729. doi: 10.1001/jamasurg.2021.2373.
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia (Odhadovaný)
1. října 2026
Primární dokončení (Odhadovaný)
1. prosince 2028
Dokončení studie (Odhadovaný)
1. prosince 2030
Termíny zápisu do studia
První předloženo
11. září 2026
První předloženo, které splnilo kritéria kontroly kvality
11. září 2026
První zveřejněno (Aktuální)
16. září 2026
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
16. září 2026
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
11. září 2026
Naposledy ověřeno
1. září 2026
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
- Novotvary podle místa
- Novotvary
- Novotvary podle histologického typu
- Gastrointestinální novotvary
- Novotvary trávicího systému
- Nemoci trávicího systému
- Gastrointestinální onemocnění
- Novotvary hlavy a krku
- Novotvary, žlázové a epiteliální
- Nemoci jícnu
- Karcinom
- Novotvary, dlaždicové buňky
- Karcinom, skvamózní buňky
- Novotvary jícnu
- Spinocelulární karcinom jícnu
- Toripalimab
Další identifikační čísla studie
- ESCC-IIT-JS001-N08
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
NE
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Ne
Studuje produkt zařízení regulovaný americkým úřadem FDA
Ne
Tyto informace byly beze změn načteny přímo z webu clinicaltrials.gov. Máte-li jakékoli požadavky na změnu, odstranění nebo aktualizaci podrobností studie, kontaktujte prosím register@clinicaltrials.gov. Jakmile bude změna implementována na clinicaltrials.gov, bude automaticky aktualizována i na našem webu .