- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07647068
Autologous Tumor Infiltrating Lymphocytes With Interleukin-2 for the Treatment of Locally Advanced, Recurrent or Metastatic Gastrointestinal Stromal Tumors
A Phase 2 Study to Evaluate the Efficacy and Safety of Adoptive Transfer of Autologous Tumor Infiltrating Lymphocytes in Patients With Unresectable, Recurrent, or Metastatic Gastrointestinal Stromal Tumors
Studieoversigt
Status
Betingelser
Intervention / Behandling
- Procedure: MR scanning
- Procedure: Computertomografi
- Medicin: Cyclofosfamid
- Medicin: Fludarabin
- Biologisk: Filgrastim
- Procedure: Positron emissionstomografi
- Biologisk: Aldesleukin
- Procedure: Multigated Acquisition Scan
- Procedure: Røntgen af brystet
- Procedure: Bioprøvesamling
- Procedure: Ekkokardiografitest
- Procedure: Surgical Procedure
- Biologisk: Tumor Infiltrating Lymphocyte Therapy
Detaljeret beskrivelse
PRIMARY OBJECTIVE:
I. To evaluate the efficacy of a non-myeloablative lymphodepleting preparative regimen followed by infusion of autologous TIL and high-dose aldesleukin in patients with locally advanced, recurrent, or metastatic gastrointestinal stromal tumor (GIST) using the objective response rate (ORR).
SECONDARY OBJECTIVES:
I. To further evaluate the efficacy of this therapy using complete response (CR) rate, duration of response (DOR), disease control rate (DCR), progression-free survival (PFS), and overall survival (OS).
II. To characterize the safety profile of this therapy in patients with locally advanced, recurrent, or metastatic gastrointestinal stromal tumors (GIST).
OUTLINE:
Patients receive cyclophosphamide intravenously (IV) over 2 hours on days -8 and -7, fludarabine IV over 30 minutes on days -6 to -2 and TIL IV over 20-30 minutes on day 0 in the absence of disease progression or unacceptable toxicity. Starting within 24 hours of TIL infusion, patients receive aldesleukin IV over 15 minutes every 8 hours for up to 6 doses on days 0-3 in the absence of disease progression or unacceptable toxicity. Starting on day 1 or day 2, patients may receive filgrastim subcutaneously (SC) until neutrophil count > 1 x 10^9/L for 3 consecutive days or > 5 x 10^9/L. Patients with stable disease, partial response or recurrence may receive a second course of treatment. Patients also undergo chest x-ray at screening and urine and blood sample collection, computed tomography (CT), magnetic resonance imaging (MRI) or positron emission tomography (PET) throughout the study. Additionally, patients may also undergo echocardiography or multigated acquisition scan (MUGA) at screening and may also undergo a second surgery to collect cells on study.
After completion of study treatment, patients are followed up at 4-6 weeks, 12 weeks, every 3 months for 3 visits, then every 6 months up to month 24.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
- Navn: The Ohio State University Comprehensive Cancer Center
- Telefonnummer: 1-800-293-5066
- E-mail: OSUCCCClinicaltrials@osumc.edu
Studiesteder
-
-
Ohio
-
Columbus, Ohio, Forenede Stater, 43210
- Ohio State University Comprehensive Cancer Center
-
Ledende efterforsker:
- Joal Beane, MD
-
Kontakt:
- Joal Beane, MD
- Telefonnummer: 812-453-6178
- E-mail: Joal.Beane@osumc.edu
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Measurable locally advanced, recurrent, or metastatic GIST
- Patients with locally advanced disease should be unresectable by conventional surgical approaches
- Patients with distant metastatic spread must be refractory to approved standard systemic therapies (such as imatinib and sunitinib) if they are eligible to receive these treatments
- Patients must be co-enrolled on the companion protocol Cell Harvest and Preparation to Support Adoptive Cell Therapy Clinical Protocols and Pre-Clinical Studies (institutional review board [IRB] #2024C0043), and have available TIL cultures for therapy
- Patients with 3 or fewer brain metastases that are less than 1 cm in diameter and asymptomatic are eligible. Lesions that have been treated with stereotactic radiosurgery must be clinically stable for 1 month after treatment for the patient to be eligible. Patients with surgically resected brain metastases are eligible
- Greater than or equal to 18 years of age and less than or equal to age 75
- Able to understand and sign the informed consent document
- Clinical performance status of Eastern Cooperative Oncology Group (ECOG) 0 or 1
- Life expectancy of greater than three months
- Patients of both genders who are of child-bearing potential must be willing to practice birth control from the time of enrollment on this study and for up to four months after receiving the treatment
Serology:
- Seronegative for HIV antibody. (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who are HIV seropositive can have decreased immune-competence and thus be less responsive to the experimental treatment and more susceptible to its toxicities.)
- Seronegative for hepatitis B antigen, and seronegative for hepatitis C antibody. If hepatitis C antibody test is positive, then patient must be tested for the presence of antigen by reverse transcriptase-polymerase chain reaction (RT-PCR) and be HCV ribonucleic acid (RNA) negative
- Women of child-bearing potential must have a negative pregnancy test because of the potentially dangerous effects of the treatment on the fetus
- Absolute neutrophil count greater than 1000/mm^3 without the support of filgrastim
- White blood cells (WBC) ≥ 3000/mm^3
- Platelet count ≥ 100,000/mm^3
- Hemoglobin > 8.0 g/dl
- Serum alanine aminotransferase (ALT)/aspartate aminotransferase (AST) ≤ to 3.5 times the upper limit of normal
- Serum creatinine ≤ to 1.6 mg/dl and calculated creatinine clearance (Crockcroft-Gault or 24-hour urine creatinine) ≥ 30 mL/min
- Total bilirubin ≤ to 2.0 mg/dl, except in patients with Gilbert's syndrome who must have a total bilirubin less than 3.0 mg/dl
More than four weeks must have elapsed since any prior systemic therapy at the time the patient receives the preparative regimen, and patients' toxicities must have recovered to a grade 1 or less (except for toxicities such as alopecia or vitiligo)
- Note: Patients may have undergone minor surgical procedures within the past 3 weeks, as long as all toxicities have recovered to grade 1 or less
Exclusion Criteria:
- Women of child-bearing potential who are pregnant or breastfeeding because of the potentially dangerous effects of the treatment on the fetus or infant
- Any form of primary immunodeficiency (such as severe combined immunodeficiency disease)
- Concurrent opportunistic infections (The experimental treatment being evaluated in this protocol depends on an intact immune system. Patients who have decreased immune competence may be less responsive to the experimental treatment and more susceptible to its toxicities)
- Active systemic infections (e.g.: requiring anti-infective treatment), coagulation disorders or any other active major medical illnesses
- History of major organ autoimmune disease
- Concurrent systemic steroid therapy including physiologic replacement dosing of systemic steroids (i.e. prednisone ≤ 10 mg/day or equivalent) as well as topical or inhaled corticosteroids are not allowed
- History of severe immediate hypersensitivity reaction to any of the agents used in this study
- History of active coronary or ischemic symptoms
Documented left ventricular ejection fraction (LVEF) of less than or equal to 45%
Note: testing is required in patients with:
- Age ≥ 65 years old
Clinically significant atrial and or ventricular arrhythmias including but not limited to:
- Atrial fibrillation, ventricular tachycardia, second or third degree heart block or have a history of ischemic heart disease, chest pain
Documented forced expiratory volume in 1 second (FEV1) less than or equal to 60% predicted tested in patients with:
- A prolonged history of cigarette smoking (20 pack [pk]/year of smoking within the past 2 years)
- Symptoms of respiratory dysfunction
- Patients who are receiving any other investigational agents
Studieplan
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: Treatment (TIL, aldesleukin)
Patients receive cyclophosphamide IV over 2 hours on days -8 and -7, fludarabine IV over 30 minutes on days -6 to -2 and TIL IV over 20-30 minutes on day 0 in the absence of disease progression or unacceptable toxicity.
Starting within 24 hours of TIL infusion, patients receive aldesleukin IV over 15 minutes every 8 hours for up to 6 doses on days 0-3 in the absence of disease progression or unacceptable toxicity.
Starting on day 1 or day 2, patients may receive filgrastim SC until neutrophil count > 1 x 10^9/L for 3 consecutive days or > 5 x 10^9/L.
Patients with stable disease, partial response or recurrence may receive a second course of treatment.
Patients also undergo chest x-ray at screening and urine and blood sample collection, CT, MRI or PET throughout the study.
Additionally, patients may also undergo echocardiography or MUGA at screening and may also undergo a second surgery to collect cells on study.
|
Gennemgå MR
Andre navne:
Gennemgå CT
Andre navne:
Givet IV
Andre navne:
Givet IV
Andre navne:
Givet SC
Andre navne:
Gennemgå PET
Andre navne:
Givet IV
Andre navne:
Gennemgå MUGA
Andre navne:
Gennemgå røntgen af thorax
Andre navne:
Gennemgå urin- og blodprøvetagning
Andre navne:
Gennemgå ekkokardiografi
Andre navne:
Undergo a second surgery
Andre navne:
Given IV
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Objective response rate
Tidsramme: Up to 24 months
|
Will be estimated by the proportion of patients with a best response of complete response (CR) or partial response (PR) by Response Evaluation Criteria in Solid Tumors criteria, with corresponding exact 95% confidence limit being reported.
|
Up to 24 months
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
CR rate
Tidsramme: Up to 24 months
|
Will be estimated by the proportion of patients with a best response of complete response (CR) by Response Evaluation Criteria in Solid Tumors criteria
|
Up to 24 months
|
|
Duration of response
Tidsramme: Up to 24 months
|
The distribution among patients achieving CR or PR will be characterized by median and quartiles.
|
Up to 24 months
|
|
Disease control rate
Tidsramme: Up to 24 months
|
Up to 24 months
|
|
|
Progression-free survival
Tidsramme: From the initial date of treatment to the date of documented progression, or the date of death (in the absence of progression), assessed up to 24 months
|
Will be estimated by the Kaplan-Meier method.
The corresponding median survival times (with 95% confidence limits) will be determined, as will the cumulative percentage of patients remaining progression-free (and the cumulative percentage-alive) at selected time points after initial treatment (e.g., 3, 6,12, 18 months).
|
From the initial date of treatment to the date of documented progression, or the date of death (in the absence of progression), assessed up to 24 months
|
|
Overall survival
Tidsramme: From the initial date of treatment to the recorded date of death, assessed up to 24 months
|
Will be estimated by the Kaplan-Meier method.
The corresponding median survival times (with 95% confidence limits) will be determined, as will the cumulative percentage of patients remaining progression-free (and the cumulative percentage-alive) at selected time points after initial treatment (e.g., 3, 6,12, 18 months).
|
From the initial date of treatment to the recorded date of death, assessed up to 24 months
|
|
Incidence of adverse events
Tidsramme: Up to 30 days after treatment
|
Will be described and graded using the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0.
The maximum grade of toxicity for each category of interest will be recorded for each patient and the summary results will be tabulated by category and grade.
|
Up to 30 days after treatment
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Joal Beane, MD, Ohio State University Comprehensive Cancer Center
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Neoplasmer
- Neoplasmer efter histologisk type
- Gastrointestinale neoplasmer
- Neoplasmer i fordøjelsessystemet
- Sygdomme i fordøjelsessystemet
- Gastrointestinale sygdomme
- Neoplasmer, bindevæv og blødt væv
- Neoplasmer, bindevæv
- Gastrointestinale stromale tumorer
- Peptider
- Aminosyrer, peptider og proteiner
- Proteiner
- Organiske kemikalier
- Undersøgelsesteknikker
- Kliniske laboratorieteknikker
- Diagnostiske teknikker og procedurer
- Diagnose
- Kulbrinter
- Biologiske faktorer
- Kulhydrater
- Fysiske fænomener
- Kemiteknikker, analytisk
- Spektrumanalyse
- Fosforamid -sennep
- Nitrogen sennepsforbindelser
- Sennepsforbindelser
- Kulbrinter, halogeneret
- Phosphoramider
- Organophosphorforbindelser
- Intercellulære signalpeptider og proteiner
- Glycoproteiner
- Glycoconjugates
- Elektromagnetiske fænomener
- Magnetiske fænomener
- Elektromagnetisk stråling
- Stråling
- Stråling, ioniserende
- Kolonistimulerende faktorer
- Hæmatopoietiske cellevækstfaktorer
- Cytokiner
- Cyclofosfamid
- Håndtering af eksemplar
- Magnetisk resonansspektroskopi
- fludarabin
- Aldesleukin
- Kirurgiske procedurer, operative
- Røntgenstråler
- Granulocytkolonistimulerende faktor
- Filgrastim
Andre undersøgelses-id-numre
- OSU-22356 (Anden identifikator: Ohio State University Comprehensive Cancer Center)
- NCI-2026-03863 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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