- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07646080
Exploratory Study on Toripalimab and Anlotinib Combined With Standard Chemotherapy for Refractory Dermatofibrosarcoma Protuberans
9. juni 2026 opdateret af: Yanjie Zhang, MD
This study aims to evaluate the efficacy and safety of toripalimab and anlotinib hydrochloride combined with standard chemotherapy in patients with refractory dermatofibrosarcoma protuberans (DFSP) resistant to imatinib therapy, and to provide evidence for the exploration of DFSP treatment.
Studieoversigt
Status
Ikke rekrutterer endnu
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Tilmelding (Anslået)
20
Fase
- Fase 2
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Haihua Yuan
- Telefonnummer: +86-021-56691101-7261
- E-mail: ayuan790415@shsmu.edu.cn
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Ingen
Beskrivelse
Inclusion Criteria
- Male or female patients aged ≥18 years.
- Locally advanced, unresectable or metastatic dermatofibrosarcoma protuberans (DFSP) with histologically confirmed specific subtypes; disease progression following standard imatinib therapy, or no satisfactory alternative treatment options. Specific subtypes include: fibrosarcomatous DFSP (FS-DFSP) or DFSP with transformation to high-grade sarcoma, such as undifferentiated pleomorphic sarcoma, leiomyosarcoma, rhabdomyosarcoma, etc.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- At least one measurable lesion at baseline according to RECIST 1.1 criteria.
Adequate organ and bone marrow function within 14 days prior to enrollment:
- Hemoglobin ≥9 g/dL
- Platelet count ≥75,000/mm³
- Absolute neutrophil count ≥1500/mm³
- Serum albumin ≥2.5 g/dL
- PT, aPTT, and INR ≤1.5 × ULN
- AST and ALT ≤3 × ULN, or <5 × ULN in patients with liver metastases
- Total bilirubin ≤1.5 × ULN (without liver metastasis), or <3 × ULN (with Gilbert syndrome or liver metastasis at baseline)
- Creatinine clearance ≥30 mL/min calculated by the Cockcroft-Gault formula
- Left ventricular ejection fraction (LVEF) ≥50% as assessed by ECHO or MUGA scan within 28 days prior to enrollment.
Exclusion Criteria
Patients with any of the following will be excluded:
- Spinal cord compression, leptomeningeal disease, or clinically active central nervous system (CNS) metastases.
- Active primary immunodeficiency, known HIV infection, active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection.
- History of non-infectious interstitial lung disease (ILD)/non-infectious pneumonitis requiring corticosteroid therapy, current ILD/non-infectious pneumonitis, or suspected ILD/non-infectious pneumonitis that cannot be ruled out by imaging at screening.
- Myocardial infarction within 6 months prior to enrollment, symptomatic congestive heart failure (CHF, NYHA class II-IV), unstable angina, or recent cardiovascular event (including stroke) within <6 months.
Pulmonary criteria:
- Clinically significant pulmonary comorbidities including but not limited to underlying pulmonary disease (e.g., pulmonary embolism, severe asthma, severe COPD, restrictive lung disease, pleural effusion within 3 months before enrollment);
- Documented autoimmune, connective tissue, or inflammatory disease (e.g., rheumatoid arthritis, Sjögren's syndrome, sarcoidosis, etc.) or suspected pulmonary involvement at screening; full disease details must be documented in the eCRF;
- Prior pneumonectomy.
- Poor compliance unable to cooperate with study treatment and procedures.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Toripalimab, Anlotinib Hydrochloride Combined with Standard Chemotherapy
All enrolled patients will receive study intervention starting on Day 1 of each 3-week cycle until disease progression, intolerable toxicity, or study withdrawal: Toripalimab 240 mg (fixed dose) administered intravenously once every 3 weeks (Q3W); Anlotinib 10 mg administered orally once daily on Days 1-14 of each 3-week cycle; and standard chemotherapy based on anthracycline or gemcitabine once every 3 weeks (Q3W).
|
All enrolled patients will receive study intervention starting on Day 1 of each 3-week cycle until disease progression, intolerable toxicity, or study withdrawal: Toripalimab 240 mg (fixed dose) administered intravenously once every 3 weeks (Q3W).
All enrolled patients will receive study intervention starting on Day 1 of each 3-week cycle until disease progression, intolerable toxicity, or study withdrawal: Anlotinib 10 mg administered orally once daily on Days 1-14 of each 3-week cycle.
All enrolled patients will receive study intervention starting on Day 1 of each 3-week cycle until disease progression, intolerable toxicity, or study withdrawal: standard chemotherapy based on anthracycline or gemcitabine once every 3 weeks (Q3W).
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective Response Rate (ORR)
Tidsramme: From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
The Objective Response Rate (ORR) is defined as the percentage of patients whose best response on or before the first occurrence of disease progression is a complete response (CR) or partial response (PR).
Tumor responses were assessed by investigators using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1.
|
From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Duration of Response (DoR)
Tidsramme: From the date of first documented response (complete response [CR] or partial response [PR]) to the time of disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
Duration of Response (DoR) is defined as the time from the date of first documented response (CR or PR) to date of first occurrence of disease progression as determined by the investigator, or death from any cause, whichever occurs first.
|
From the date of first documented response (complete response [CR] or partial response [PR]) to the time of disease progression or death from any cause, whichever occurs first, assessed up to 24months.
|
|
Progression-Free Survival (PFS)
Tidsramme: Through study completion, an average of 2 years.
|
Progression-Free Survival (PFS) is defined as the time from the start of study treatment to the first occurrence of disease progression, or death, whichever occurs first.
Tumor responses were assessed by investigators using RECIST version 1.1.
|
Through study completion, an average of 2 years.
|
|
Overall Survival (OS)
Tidsramme: Through study completion, an average of 2 years.
|
Overall Survival (OS) is defined as the time from the date of the first study treatment (Day 1) to the date of death from any cause.
|
Through study completion, an average of 2 years.
|
|
Disease Control Rate (DCR)
Tidsramme: From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24 months.
|
Disease Control Rate (DCR) is defined as the proportion of patients whose best response is CR, PR or SD maintained more than 8 weeks.
Tumor responses were assessed by investigators using RECIST version 1.1.
|
From the date of first study treatment until disease progression or death from any cause, whichever occurs first, assessed up to 24 months.
|
|
Best Overall Response (BOR)
Tidsramme: Through study completion, average follow-up of 2 years.
|
Best overall response (BOR) is defined as the best tumor response achieved at any time during treatment, categorized as Complete Response (CR), Partial Response (PR), Stable Disease (SD), or Progressive Disease (PD) per RECIST 1.1 criteria.
Responses require confirmation at least 4 weeks later.
|
Through study completion, average follow-up of 2 years.
|
|
Time to Response (TTR)
Tidsramme: From first dose until first confirmed response, assessed up to 48 months.
|
Time to response (TTR) is defined as the time from the date of first study drug administration to the date of first documented and confirmed CR or PR per RECIST 1.1.
|
From first dose until first confirmed response, assessed up to 48 months.
|
|
Adverse Events (AEs)
Tidsramme: From first study drug administration through 40 days after the last dose; overall average follow-up duration is 2 years.
|
Incidence, severity (graded per NCI CTCAE version 5.0), and causality of adverse events (AEs).
Special attention will be paid to AEs of special interest associated with toripalimab, anlotinib, and anthracycline- or gemcitabine-based chemotherapy, including myelosuppression, hypertension, diarrhea, rash, liver function abnormalities, endocrine disorders, and cardiac toxicity (monitored via periodic left ventricular ejection fraction and electrocardiography).
|
From first study drug administration through 40 days after the last dose; overall average follow-up duration is 2 years.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Anslået)
15. juni 2026
Primær færdiggørelse (Anslået)
31. december 2028
Studieafslutning (Anslået)
31. december 2029
Datoer for studieregistrering
Først indsendt
14. april 2026
Først indsendt, der opfyldte QC-kriterier
9. juni 2026
Først opslået (Faktiske)
12. juni 2026
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
12. juni 2026
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
9. juni 2026
Sidst verificeret
1. juni 2026
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- JY2026-036
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
INGEN
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
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Kliniske forsøg med Dermatofibrosarcoma Protuberans (DFSP)
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The Plastic Surgery Hospital, Chinese Academy of...1、 Department of Plastic and Reconstructive Surgery, Peking University... og andre samarbejdspartnereIkke rekrutterer endnuPlanocellulært hudkræft | Dermatofibrosarcoma Protuberans (DFSP)
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Assistance Publique - Hôpitaux de ParisGlaxoSmithKlineAfsluttetDermatofibrosarkomer af DARIER FERRAND(DFSP)Frankrig
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Mayo ClinicAfsluttetDermatofibrosarcoma ProtuberansForenede Stater
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Sarcoma Alliance for Research through CollaborationAfsluttetDermatofibrosarcoma ProtuberansForenede Stater
-
European Organisation for Research and Treatment...AfsluttetSarkomFrankrig, Belgien, Holland, Det Forenede Kongerige
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National Taiwan University HospitalUkendt
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National Cancer Institute (NCI)AfsluttetTilbagevendende bløddelssarkom hos voksne | Stage IV Blødt vævssarkom for voksne | Dermatofibrosarcoma Protuberans | Voksen fibrosarkomForenede Stater
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ECOG-ACRIN Cancer Research GroupNational Cancer Institute (NCI)Ikke rekrutterer endnuSarkom | Blødt vævssarkom | Leiomyosarkom | Fibrosarkom | Angiosarkom | Ondartet perifer nerveskedetumor | Pleomorfisk liposarkom | Synovialt sarkom | Udifferentieret Pleomorphic Sarkom | Alveolær blød del sarkom | Myxofibrosarkom | Stage III blødt vævssarkom i stammen og ekstremiteterne AJCC v8 | Dedifferentieret... og andre forhold
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National Cancer Institute (NCI)AfsluttetUterin carcinosarkom | Endometrial Stromal Sarkom | Tilbagevendende bløddelssarkom hos voksne | Tilbagevendende uterin sarkom | Stage III Blødt vævssarkom for voksne | Stadie III uterin sarkom | Stage IV Blødt vævssarkom for voksne | Stadium IV Uterin Sarkom | Dermatofibrosarcoma Protuberans | Rhabdomyosarkom... og andre forholdCanada, Forenede Stater
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Children's Oncology GroupNational Cancer Institute (NCI)AfsluttetStage III Blødt vævssarkom for voksne | Stage IV Blødt vævssarkom for voksne | Stadie I Voksen blødt vævssarkom | Stage II Blødt vævssarkom for voksne | Dermatofibrosarcoma Protuberans | Angiosarkom hos voksne | Voksen epiteloid sarkom | Voksen ekstraskeletalt osteosarkom | Voksen fibrosarkom | Voksen leiomyosarkom og andre forholdForenede Stater, Canada, Australien, New Zealand, Puerto Rico
Kliniske forsøg med Toripalimab
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Zhongnan HospitalIkke rekrutterer endnuLivmoderhalskræft | Metastatisk | TilbagevendendeKina
-
Mabwell (Shanghai) Bioscience Co., Ltd.RekrutteringUrothelialt karcinomKina
-
Tongji HospitalIkke rekrutterer endnuMuskelinvasiv blæreurotelcarcinom
-
Sun Yat-sen UniversityRekrutteringLungekræft, ikke-småcelletKina
-
Nanjing Immunophage Biotech Co., LtdIkke rekrutterer endnuAvanceret solid tumorKina
-
Jiangsu Cancer Institute & HospitalIkke rekrutterer endnuNSCLC | NSCLC (ikke-småcellet lungekræft)Kina
-
Coherus Biosciences, Inc.Ikke rekrutterer endnuAvancerede eller metastatiske solide tumorer
-
First Affiliated Hospital of Zhejiang UniversityRekrutteringTNBC, Triple Negative Breast CancerKina
-
Mabwell (Shanghai) Bioscience Co., Ltd.Ikke rekrutterer endnuAvanceret Urothelial CarcinomKina
-
Henan Cancer HospitalUkendtEsophageal pladecellekarcinom