- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07721259
A Vaccine (STEMVAC) for Improving Survival in Patients With Triple-Negative Breast Cancer and Moderate or Extensive Residual Cancer Burden
A Multiantigen Vaccine (STEMVAC) for Adjuvant Treatment of Patients With Moderate or Extensive Residual Triple-Negative Breast Cancer
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
OUTLINE: Patients are randomized to 1 of 2 arms.
ARM A: Patients receive CD105/Yb-1/SOX2/CDH3/MDM2-polyepitope plasmid deoxyribonucleic acid (DNA) vaccine (STEMVAC) with recombinant granulocyte-macrophage colony-stimulating factor (GM-CSF) intradermally (ID) every 3 weeks for 3 doses. Patients then receive booster vaccines ID 9 weeks after vaccine 3 and 18 weeks after booster 1. Patients also undergo collection of blood samples throughout the trial.
ARM B: Patients receive GM-CSF ID every 3 weeks for 3 doses. Patients then receive booster vaccines ID 9 weeks after vaccine 3 and 18 weeks after booster 1. Patients also undergo collection of blood samples throughout the trial.
After completion of study treatment, patients are followed up at 3 weeks after their last vaccination and then every 6 months for 3 years.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
- Navn: Research Coordinator(s)
- Telefonnummer: 866-932-8588
- E-mail: cvitrial@uw.edu
Studiesteder
-
-
Washington
-
Seattle, Washington, Forenede Stater, 98109
- Fred Hutch/University of Washington Cancer Consortium
-
Ledende efterforsker:
- Natasha Hunter, MD
-
Kontakt:
- Research Coordinator(s)
- Telefonnummer: 866-932-8588
- E-mail: cvitrial@uw.edu
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- At least 18 years of age
- Eastern Cooperative Oncology Group (ECOG) performance status score of ≤ 2
- Triple-negative breast cancer as determined by the treating oncologist
- Completed standard of care neoadjuvant chemotherapy in the opinion of their treating oncologist
- Patients whose tumors progress on neoadjuvant therapy may be enrolled
- No clinical evidence of local or distant recurrence
- Plan to receive standard of care adjuvant directed therapy
- Completed standard of care locoregional treatment, including definitive breast and lymph node surgery followed by standard radiation therapy, if recommended
- Residual cancer burden (RCB) index 2 or 3 as calculated per routine anatomic pathology clinical standards
- Absolute neutrophil count (ANC) ≥ 800/μL (within 30 days of first study vaccine administration)
- Hemoglobin (Hgb) ≥ 8 g/dL (within 30 days of first study vaccine administration)
- Platelets ≥ 75,000/ μL (within 30 days of first study vaccine administration)
- Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN), except patients with Gilbert's syndrome, in whom total bilirubin must be < 3.0 mg/dL (within 30 days of first study vaccine administration)
- Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ≤ 1.5 x institutional ULN (within 30 days of first study vaccine administration)
- Creatinine ≤ 1.5 x ULN mg/dL or creatinine clearance > 60 mL/min (within 30 days of first study vaccine administration)
At least 28 days post systemic steroids prior to enrollment, unless used as part of prophylaxis to prevent intravenous (IV) contrast reactions.
- Topical, ocular, intra-articular, intranasal, inhalational corticosteroids (with minimal systemic absorption) are allowed
- Must have recovered from major infections and/or surgical procedures; and in the opinion of the investigator, not have any significant active concurrent medical illnesses or condition precluding protocol treatment
- Patients of child-bearing potential must agree to use dual methods of contraception and have a negative urine pregnancy test at screening, and male patients must use an effective barrier method of contraception if sexually active with a person of child-bearing potential. Acceptable methods of contraception are abstinence, condoms with contraceptive foam, oral, implantable or injectable contraceptives, contraceptive patch, intrauterine device, diaphragm with spermicidal gel, or a sexual partner who is surgically sterilized or post-menopausal
Exclusion Criteria:
- Toxicities related to prior exposure to immune checkpoint inhibitors for which immune checkpoint inhibitors cannot be safely continued as determined by study investigator
Germline BRCA1 or BRCA2 mutations with adjuvant olaparib planned within the study period
- NOTE: If olaparib is not planned, then these patients are eligible
Any known cardiac conditions:
- Symptomatic restrictive cardiomyopathy
- Dilated cardiomyopathy
- Unstable angina within 4 months prior to enrollment
- New York Heart Association functional class III-IV heart failure on active treatment
- Symptomatic pericardial effusion
- Autoimmune disease requiring active systemic treatment
- Known hypersensitivity reaction to the GM-CSF adjuvant; any known contra-indication to GM-CSF
- Pregnant or breast feeding
- Known history of human immunodeficiency virus (HIV) infection, hepatitis B (e.g., hepatitis B virus surface antigen [HBsAg] reactive), or hepatitis C (e.g., hepatitis C virus [HCV] ribonucleic acid [RNA] is detected)
- Major surgery within the 4 weeks prior to initiation of first study vaccine
- Enrollment in any other clinical protocol or investigational trial that involves concurrent administration of experimental therapy and/or therapeutic devices, or investigational drug. Patients who completed prior clinical trials (such as neoadjuvant treatment, surgery or radiation trials) and are on long term follow up are permitted
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Arm A (STEMVAC, GM-CSF)
Patients receive STEMVAC with GM-CSF ID every 3 weeks for 3 doses.
Patients then receive booster vaccines ID 9 weeks after vaccine 3 and 18 weeks after booster 1. Patients also undergo collection of blood samples throughout the trial.
|
Gennemgå indsamling af blodprøver
Andre navne:
Opgivet ID
Andre navne:
Given ID
Andre navne:
|
|
Aktiv komparator: Arm B (GM-CSF)
Patients receive GM-CSF ID every 3 weeks for 3 doses.
Patients then receive booster vaccines ID 9 weeks after vaccine 3 and 18 weeks after booster 1. Patients also undergo collection of blood samples throughout the trial.
|
Gennemgå indsamling af blodprøver
Andre navne:
Given ID
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Invasive breast cancer free survival (IBCFS)
Tidsramme: Time from randomization to local or distant recurrence or death, assessed up to 3 years
|
Kaplan-Meier curves will be generated with median estimation and 95% confidence interval, and log-rank tests will be conducted to compare the survival difference between groups.
Will calculate the 3-year IBCFS rate with a 95% confidence interval from Kaplan-Meier methods using Greenwood standard errors.
|
Time from randomization to local or distant recurrence or death, assessed up to 3 years
|
|
Dynamics and characteristics of circulating tumor deoxyribonucleic acid (ctDNA)
Tidsramme: Up to 3 weeks after last vaccination
|
Through serial ctDNA evaluation, each sample will be assessed for ctDNA detectability and, if detectable, total ctDNA mass (continuous variable, as reported by the assay platform) will be calculated.
ctDNA detectability and quantitative ctDNA measures will be summarized descriptively by timepoint and study arm, and changes over time will be evaluated using methods appropriate to the final endpoint definition, data distribution, and repeated-measures structure of the data.
Associations with IBCFS will also be explored.
Copy number variants (including aneuploidy, chromosome-level gains, losses, and amplifications, as defined by the final assay methodology) will also be tracked and tabulated, and changes over time will be evaluated descriptively in both study arms.
|
Up to 3 weeks after last vaccination
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Incidence of adverse events
Tidsramme: Up to 3 weeks after last vaccination
|
Safety and systemic toxicity will be determined by clinical and laboratory parameters evaluated at protocol-specified time points.
Toxicity will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 6.0.
The type and grade of toxicities observed during the immunization regimen will be summarized, and the duration of toxicities will be summarized using descriptive statistics.
All adverse events reported by the investigator will be tabulated according to the affected body system.
The frequency and severity of adverse events will be summarized using proportions and corresponding 95% confidence intervals.
Demographic and baseline characteristics obtained at enrollment will be summarized in tabular and/or graphical formats using descriptive statistics.
|
Up to 3 weeks after last vaccination
|
|
Immune response
Tidsramme: Up to 3 weeks after last vaccination
|
Immune response to CD105/Yb-1/SOX2/CDH3/MDM2-polyepitope plasmid DNA vaccine (STEMVAC) will be measured in peripheral blood functionally by IFN-g enzyme-linked immunosorbent spot, phenotypically using cytometry by time-of-flight to identify T-cell clonal populations, and genomically, using T-cell receptor beta sequencing of CD4+ CD8+ T-cells.
|
Up to 3 weeks after last vaccination
|
|
Expression of epithelial to mesenchymal transformation (EMT)-associated genes
Tidsramme: Archival tissue is collected after enrollment, within 30 days of baseline visit
|
EMT-associated gene expression profiles in residual triple negative breast cancer in surgical pathology samples will be defined for each patient with particular attention on STEMVAC antigen expression.
Expression of these EMT-related genes will be assessed using RNA extracted from formalin-fixed paraffin-embedded tissue.
|
Archival tissue is collected after enrollment, within 30 days of baseline visit
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Natasha Hunter, MD, Fred Hutch/University of Washington Cancer Consortium
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 efter sted
- Neoplasmer
- Hudsygdomme
- Brystsygdomme
- Brystneoplasmer
- Hud- og bindevævssygdomme
- Tredobbelt negative brystneoplasmer
- Peptider
- Aminosyrer, peptider og proteiner
- Proteiner
- Undersøgelsesteknikker
- Kliniske laboratorieteknikker
- Diagnostiske teknikker og procedurer
- Diagnose
- Biologiske faktorer
- Kulhydrater
- Intercellulære signalpeptider og proteiner
- Glycoproteiner
- Glycoconjugates
- Hæmatopoietiske cellevækstfaktorer
- Cytokiner
- Håndtering af eksemplar
- Granulocyt-makrofag-koloni-stimulerende faktor
- Kolonistimulerende faktorer
Andre undersøgelses-id-numre
- RG1126489
- NCI-2026-04722 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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