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A Study of Ta-NPs Plus Radiotherapy for Locally Recurrent Retroperitoneal Sarcoma

5. Mai 2026 aktualisiert von: Xingchen Peng, West China Hospital

Ta-NPs Combined With Radiotherapy for Locally Recurrent Retroperitoneal Soft Tissue Sarcoma: A Prospective, Single-Arm Clinical Study

This prospective, single-arm, open-label phase I study evaluates the safety and tolerability of intratumoral injection of tantalum nanoparticles (Ta-NPs) followed by radiotherapy in patients with locally recurrent retroperitoneal soft tissue sarcoma. Using a standard 3+3 dose-escalation design, three dose levels of Ta-NPs (injection volumes of 2%, 5%, and 10% of tumor volume, all at 30 mg/mL) are tested in sequential cohorts to identify dose-limiting toxicities.

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

9

Phase

  • Phase 1

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

  • Name: Xingchen Peng, MD, PhD
  • Telefonnummer: +8618980606753
  • E-Mail: pxx2014@163.com

Studienorte

    • Sichuan
      • Chengdu, Sichuan, China, 610041
        • Sichuan University West China Hospital, Chengdu, Sichuan

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene
  • Älterer Erwachsener

Akzeptiert gesunde Freiwillige

Nein

Beschreibung

Inclusion Criteria:

  1. Age ≥18 years, male or female.
  2. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  3. Histopathologically confirmed diagnosis of dedifferentiated liposarcoma (DD-LPS) or leiomyosarcoma (LMS) with local or regional recurrence after prior standard treatment with curative intent. Prior treatment must include:

    a) Curative/radical or extended resection of the primary or first recurrent lesion. b) Possible prior treatments (if received) must be completed at least 4 weeks before enrollment, including: radiotherapy (external beam radiotherapy to the abdominopelvic region; detailed radiotherapy plan and DVH must be available to assess normal organ doses), chemotherapy (anthracycline- and/or ifosfamide-based systemic chemotherapy), or targeted therapy (e.g., anlotinib). c) All acute adverse events from prior treatments must have resolved to normal or Grade 1 per CTCAE.

  4. At least one lesion suitable for intratumoral injection (either directly or under imaging guidance) and radiotherapy, with a volume ≤3000 cm³ (tumor volume = length × width × height measured by CT/MRI), and measurable by imaging.
  5. Adequate hematologic and organ function within 7 days before first dose, meeting the following laboratory criteria:

    1. Hematology (without G-CSF within 14 days): Absolute neutrophil count (ANC) ≥1.5×10^9/L; (without platelet transfusion within 14 days): Platelet count (PLT) ≥90×10^9/L; (without red blood cell transfusion or erythropoietin within 14 days): Hemoglobin (Hb) ≥90 g/L.
    2. Renal function: Serum creatinine (Cr) ≤1.5×upper limit of normal (ULN), or calculated creatinine clearance (Cockcroft-Gault) ≥50 mL/min (only required if baseline Cr >1.5×ULN).
    3. Liver function: Total bilirubin (TBIL) ≤1.5×ULN (or ≤3.0×ULN for Gilbert's syndrome or liver metastases); AST, ALT, and alkaline phosphatase (ALP) ≤2.5×ULN; serum albumin ≥2.8 g/dL.
    4. Coagulation: International normalized ratio (INR) or prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤1.5×ULN.
    5. Cardiac: Left ventricular ejection fraction (LVEF) ≥50%.
  6. Expected survival ≥6 months.
  7. Willing and able to provide written informed consent, good compliance, and able to complete follow-up.

Exclusion Criteria:

  1. Presence of distant metastasis (M1 stage) that is not suitable for local radiotherapy intervention.
  2. Active skin ulceration, infection, erosion, necrosis, bleeding at the injection site, or risk of hollow organ perforation.
  3. The target lesion(s) have received radiotherapy within the past 6 months.
  4. Known allergy or intolerance to the active ingredient or excipients of Ta-NPs or similar nanoparticles.
  5. Pregnant or breastfeeding women; subjects (or their partners) who plan to become pregnant or have unprotected sexual intercourse without appropriate contraceptive measures (e.g., condoms, intrauterine devices, or partner sterilization) from screening through 3 months after study completion.
  6. HIV-positive; HCV-positive; HBsAg-positive or HBcAb-positive with detectable HBV DNA (quantitative assay ≥500 IU/mL).
  7. Active pulmonary tuberculosis, or history of pulmonary tuberculosis that has not been controlled after treatment.
  8. Other severe, uncontrolled concomitant diseases that may affect protocol compliance or interfere with interpretation of results, including active opportunistic or progressive (severe) infection, uncontrolled diabetes mellitus, cardiovascular disease (New York Heart Association Class III or IV heart failure, second-degree or higher atrioventricular block, myocardial infarction within the past 6 months, unstable arrhythmia or unstable angina, cerebral infarction within 3 months, etc.), or pulmonary disease (interstitial pneumonia, obstructive lung disease, symptomatic bronchospasm history).
  9. Active central nervous system (CNS) metastases or leptomeningeal disease. Subjects with treated brain metastases may be eligible if there is no evidence of progression on MRI for at least 8 weeks after treatment and within 28 days before first dose, and if systemic corticosteroids (>10 mg prednisone equivalent/day) are not required for at least 2 weeks before study drug administration.
  10. Major surgical procedure (excluding diagnostic surgery) within 4 weeks before start of treatment.
  11. History of psychoactive substance abuse without ability to abstain, or history of psychiatric disorders.
  12. History of other malignancies within the past 5 years, except those that have been clearly cured or are curable, such as basal cell or squamous cell skin cancer, superficial bladder cancer or prostate carcinoma in situ, cervical carcinoma in situ, or breast carcinoma in situ.
  13. Any other severe, acute, or chronic medical or psychiatric condition or laboratory abnormality that, in the investigator's opinion, may increase the risk associated with study participation or may interfere with the interpretation of study results.
  14. Any condition that is not in the best interest of the participant.

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Nicht randomisiert
  • Interventionsmodell: Sequenzielle Zuweisung
  • Maskierung: Keine (Offenes Etikett)

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: Arm 1: Low-Dose Ta-NPs (2% Tumor Volume) Plus Radiotherapy
Participants in this arm receive a single intratumoral injection of Ta-NPs at a concentration of 30 mg/mL, with the injection volume calculated as 2% of the baseline tumor volume . Injection is performed under imaging guidance (ultrasound or CT) prior to radiotherapy. Radiotherapy starts 24 hours after injection. Dose-limiting toxicity (DLT) is monitored during the first 28 days after Ta-NPs injection.
Ta-NPs at a concentration of 30 mg/mL administered via intratumoral injection at a volume equal to 2% of the baseline tumor volume (calculated as length × width × height). Injection is performed under imaging guidance (ultrasound/CT) prior to radiotherapy.
External beam radiotherapy delivered using a medical linear accelerator (energy ≥6 MV X-ray) with image-guided radiotherapy (IGRT). Techniques include intensity-modulated radiotherapy (IMRT) or volumetric modulated arc therapy (VMAT). Total dose follows NCCN/CSCO guidelines for soft tissue sarcoma. Fractionation: conventional fractionation (1.8-2.0 Gy per fraction, once daily, 5 days per week).
Experimental: Arm 2: Medium-Dose Ta-NPs (5% Tumor Volume) Plus Radiotherapy
Participants in this arm receive a single intratumoral injection of Ta-NPs at a concentration of 30 mg/mL, with the injection volume calculated as 5% of the baseline tumor volume . Injection is performed under imaging guidance (ultrasound or CT) prior to radiotherapy. Radiotherapy starts 24 hours after injection. Dose-limiting toxicity (DLT) is monitored during the first 28 days after Ta-NPs injection.
External beam radiotherapy delivered using a medical linear accelerator (energy ≥6 MV X-ray) with image-guided radiotherapy (IGRT). Techniques include intensity-modulated radiotherapy (IMRT) or volumetric modulated arc therapy (VMAT). Total dose follows NCCN/CSCO guidelines for soft tissue sarcoma. Fractionation: conventional fractionation (1.8-2.0 Gy per fraction, once daily, 5 days per week).
Ta-NPs at a concentration of 30 mg/mL administered via intratumoral injection at a volume equal to 5% of the baseline tumor volume (calculated as length × width × height). Injection is performed under imaging guidance (ultrasound/CT) prior to radiotherapy.
Experimental: Arm 3: High-Dose Ta-NPs (10% Tumor Volume) Plus Radiotherapy
Participants in this arm receive a single intratumoral injection of Ta-NPs at a concentration of 30 mg/mL, with the injection volume calculated as 10% of the baseline tumor volume . Injection is performed under imaging guidance (ultrasound or CT) prior to radiotherapy. Radiotherapy starts 24 hours after injection. Dose-limiting toxicity (DLT) is monitored during the first 28 days after Ta-NPs injection.
External beam radiotherapy delivered using a medical linear accelerator (energy ≥6 MV X-ray) with image-guided radiotherapy (IGRT). Techniques include intensity-modulated radiotherapy (IMRT) or volumetric modulated arc therapy (VMAT). Total dose follows NCCN/CSCO guidelines for soft tissue sarcoma. Fractionation: conventional fractionation (1.8-2.0 Gy per fraction, once daily, 5 days per week).
Ta-NPs at a concentration of 30 mg/mL administered via intratumoral injection at a volume equal to 10% of the baseline tumor volume (calculated as length × width × height). Injection is performed under imaging guidance (ultrasound/CT) prior to radiotherapy.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of Dose-Limiting Toxicity (DLT)
Zeitfenster: From day of Ta-NPs injection through day 28 post-injection
DLT is defined as any adverse event occurring during the DLT observation period (from the first intratumoral injection of Ta-NPs through Day 28 post-injection) that is judged by the investigator to be at least possibly related to Ta-NPs and meets prespecified DLT criteria.
From day of Ta-NPs injection through day 28 post-injection

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of Adverse Events
Zeitfenster: From signing of informed consent through 90 days after last dose
Incidence, severity, and causality of adverse events (AEs), treatment-emergent AEs (TEAEs), Grade ≥3 treatment-related AEs (TRAEs), serious AEs (SAEs), and injection site toxicity (including extravasation) assessed by CTCAE v6.0.
From signing of informed consent through 90 days after last dose
Pharmacokinetics (PK) of Ta-NPs
Zeitfenster: Blood: Day 0 (pre-injection, 0 hour), and at 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours, Day 4, Day 8, Day 15, Day 28; Urine: Collected in intervals: 0-6 hours, 6-12 hours, 12-24 hours (Day 1), Day 2, Day 8, Day 15
Concentration-time profiles and derived PK parameters of tantalum element in whole blood, plasma, and urine after intratumoral injection of Ta-NPs, measured by inductively coupled plasma mass spectrometry (ICP-MS).
Blood: Day 0 (pre-injection, 0 hour), and at 1 hour, 2 hours, 4 hours, 8 hours, 12 hours, 24 hours, Day 4, Day 8, Day 15, Day 28; Urine: Collected in intervals: 0-6 hours, 6-12 hours, 12-24 hours (Day 1), Day 2, Day 8, Day 15
Objective Response Rate (ORR)
Zeitfenster: Assessed at Week 3 (±2 days) after start of treatment, at treatment completion, and at Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 15, Month 18, Month 21, and Month 24 post-treatment initiation.
Proportion of participants achieving complete response (CR) or partial response (PR) according to RECIST 1.1 criteria, assessed for injected and non-injected lesions.
Assessed at Week 3 (±2 days) after start of treatment, at treatment completion, and at Month 1, Month 2, Month 3, Month 6, Month 9, Month 12, Month 15, Month 18, Month 21, and Month 24 post-treatment initiation.
Local Control Rate at 6 Months
Zeitfenster: 6 months post injection
Proportion of participants with no disease progression (as defined by RECIST 1.1) at 6 months after intratumoral injection.
6 months post injection
Progression-Free Survival (PFS)
Zeitfenster: From injection until disease progression or death (up to approximately 36 months)
Time from intratumoral injection to first documented disease progression (per RECIST 1.1) or death from any cause, whichever occurs first.
From injection until disease progression or death (up to approximately 36 months)
Overall Survival (OS)
Zeitfenster: From injection until death (up to approximately 36 months)
Time from intratumoral injection to death from any cause.
From injection until death (up to approximately 36 months)
Salvage Surgery Success Rate
Zeitfenster: At the time of salvage surgery
Proportion of participants who undergo salvage surgery after treatment and achieve complete (R0) resection.
At the time of salvage surgery

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Changes in Tumor Immune Microenvironment
Zeitfenster: Baseline (pre-treatment) and post-treatment (at time of salvage surgery or biopsy if clinically indicated)
Dynamic changes in key immune cell subsets (e.g., CD8+ T cells) within the tumor microenvironment before and after combination treatment, assessed by multiplex immunofluorescence.
Baseline (pre-treatment) and post-treatment (at time of salvage surgery or biopsy if clinically indicated)
Changes in Peripheral Blood Immune Profile
Zeitfenster: Baseline (pre-injection), Day 8, Day 15, Day 29, and at treatment completion
Dynamic changes in peripheral blood immune cell subsets (e.g., CD8+ T cells) measured by flow cytometry, and changes in serum cytokine levels (e.g., IFN-γ, TNF-α, IL-6) measured by ELISA.
Baseline (pre-injection), Day 8, Day 15, Day 29, and at treatment completion

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Allgemeine Veröffentlichungen

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. Mai 2026

Primärer Abschluss (Geschätzt)

31. Dezember 2026

Studienabschluss (Geschätzt)

1. Mai 2027

Studienanmeldedaten

Zuerst eingereicht

27. April 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

5. Mai 2026

Zuerst gepostet (Tatsächlich)

11. Mai 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

11. Mai 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

5. Mai 2026

Zuletzt verifiziert

1. Mai 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

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Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

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