- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07694986
Trial of Therapies With IT cDC1s Combined w/ IT Trastuzamab for Her+ or IT Nivolumab for Her- BC LMD
6 juillet 2026 mis à jour par: H. Lee Moffitt Cancer Center and Research Institute
Phase 2 Trial With a Safety Run-in of Combinatorial Therapies With Intrathecal (IT) Dendritic Cell Vaccines (cDC1s) inHER+ (Combined With IT Trastuzumab) and HER2- (Combined With IT Nivolumab) Breast Cancer (BC) Leptomeningeal Disease (LMD)
The purpose of this study is to learn about the effects of the study treatment, Dendritic Cell Vaccine (DCV), in combination with trastuzumab or nivolumab to confirm the highest dose of the study treatment that can be given safely to participants with Breast Cancer (BC) with Leptomeningeal Disease (LMD).
Aperçu de l'étude
Statut
Recrutement
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
30
Phase
- Phase 2
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Julianne Hardesty
- Numéro de téléphone: 813-745-4098
- E-mail: Julianne.Hardesty@moffitt.org
Lieux d'étude
-
-
Florida
-
Tampa, Florida, États-Unis, 33612
- Recrutement
- Moffitt Cancer Center
-
Sous-enquêteur:
- Hien Liu, MD
-
Chercheur principal:
- Peter Forsyth, MD
-
Sous-enquêteur:
- Sepideh Mokhtari, MD
-
Sous-enquêteur:
- Yolanda Pina, MD
-
Sous-enquêteur:
- James Liu, MD
-
Sous-enquêteur:
- Aixa Soyano Muller, MD
-
Sous-enquêteur:
- Michael Yu, MD
-
Sous-enquêteur:
- Hyo Han, MD
-
Sous-enquêteur:
- Brian Czerniecki, MD
-
Sous-enquêteur:
- Kamran Ahmed, MD
-
Sous-enquêteur:
- Andre Beer Furlan, MD
-
Sous-enquêteur:
- Arnold Etame, MD
-
Sous-enquêteur:
- Joaquim Farinhas, MD
-
Sous-enquêteur:
- Alisha Fell, ARNP
-
Sous-enquêteur:
- Patrick Grogan, MD
-
Sous-enquêteur:
- Nam Tran, MD
-
Sous-enquêteur:
- Michael Vogelbaum, MD
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Inclusion Criteria:
- Histologically or cytologically confirmed diagnosis of BC by ASCO/CAP guidelines (Wolff et al, 2018), or radiographically definite LMD from BC.
- Trial participants must have a diagnosis of LMD. They must have the presence of malignant cells in the CSF (CSF+; note now cytology is considered diagnostic of LMD if the cytology is read as positive or suspicious; [Chamberlain et al., 2017] OR characteristic radiographic abnormalities of LMD). Signs and symptoms of LMD in and of themselves are not sufficient for inclusion.
- Patients must have an ECOG performance scale of ≤2.
- Proton cranial spinal RT OR cranial spinal RT using IMRT are the preferred modalities of RT to treat LMD if possible, before study. At least WBRT is required for participation.
- Coincident brain or spinal cord metastases are allowed if these are stable and do not require local therapy at the time of enrollment. Individuals with previously treated stable brain metastases are eligible to participate.
- Stereotactic radiosurgery (SRS) and/or prior radiotherapy is permitted ≥2 weeks before the initial dendritic cell (DC) vaccine dose. A follow-up brain MRI should be obtained before the DC vaccine to determine the stability of the lesions. An interval of at least 2 weeks after the end of brain radiation or surgical resection of brain lesions or cytotoxic, targeted, immune, or investigational agent is required.
- Must be ≥18 years of age on the day of signing the consent.
- Life expectancy of ≥8 weeks.
- Demonstrate adequate organ function as defined in Table 5. All screening labs should be performed within 14 days of treatment initiation.
- Ability to understand and the willingness to sign a written informed consent document.
- Corticosteroids at doses equivalent to ≤4 mg of dexamethasone daily or equivalent for symptom control are acceptable. This should be minimized when possible.
- If the disease has progressed on current treatment before consent, patients may continue current systemic cancer therapies by PI discretion see Section 7.7.5 (Systemic Therapies Allowed) and Section 5.2, 1 and 2 (Exclusion Criteria).
- Patients with systemic disease are eligible and will be managed as detailed in Section 7.7.5.
- Pregnancy test: negative serum or urine pregnancy test at screening for women of childbearing potential. Must be repeated once a month during treatment.
- Contraception: Highly effective contraception for both male and female subjects throughout the study, and for the following specified durations after the last treatment administration as follows: highly effective contraception must be used by males for at least 90 days after the last treatment administration, if the risk of conception exists, to cover the spermatogenesis Cycle, and at least 5 months after the last dose of nivolumab or 7 months after the last dose of trastuzumab for females.
- The patient has an Ommaya reservoir or equivalent device that allows routine access to CSF and administration of DC1s.
- Patient must be able to tolerate MRIs of brain with contrast for routine disease assessments.
Exclusion Criteria:
- Receiving other treatments specifically administered to treat LMD within the last 2 weeks or 5 half-lives of the agent, whichever is less. However, all other treatments to control systemic disease or bulk CNS disease will be eligible, provided the therapy is not a Phase I agent, an agent that significantly and unequivocally penetrates the CSF (eg, high-dose methotrexate, thiotepa, high-dose ara-C) by PI discretion. H & P section: Patients may continue on IV trastuzumab, fam-trastuzumab deruxtecan-nxki, pertuzumab, tucatinib, or other HER2-directed, hormonal, or other therapeutic agents if controlling systemic disease and leptomeningeal metastases developed while on these therapies. In addition, at time of systemic progression, patients may start additional agents at the discretion of the treating physician according to criteria in Section 6.7.1. and not start on new systemic therapies until LMD disease assessment.
- Use of any immunotherapy within the last 4 weeks.
- Unable or unwilling to have a contrast-enhanced brain MRI.
- Known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or in situ cervical cancer that has undergone potentially curative therapy.
- Has an active infection requiring systemic therapy which in the investigator's opinion will increase the risk to the patient.
- Had major surgical procedure, or significant traumatic injury within 2 weeks. Ommaya placement is allowed.
- Patients with shunts are excluded from the study (including but not limited to ventriculoperitoneal and ventriculoatrial shunts).
- History of an intracranial thrombosis or thrombi extending up to the skull base. The choice of modality is at the investigator or provider's discretion.
- Has a history of current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
- Is pregnant or breastfeeding or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 90 days after the last dose of trial treatment.
- Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1, 2 antibodies). Testing is not mandatory.
- Has known active or chronic hepatitis B (HBV) or hepatitis C virus (HCV). Testing is not mandatory.
- ORGAN TRANSPLANTATION: Prior organ transplantation including allogenic stem-cell transplantation.
- Other severe acute or chronic medical conditions or psychiatric conditions including recent (within the past year) or active suicidal ideation or behavior; or laboratory abnormalities that may increase the risk associated with study participation or study treatment administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the patient inappropriate for entry into this study.
- Has received a live vaccine within 30 days before the first dose of study drug. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (eg, FluMist) are live attenuated vaccines and are not allowed. Current COVID vaccines are not live vaccines.
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Non randomisé
- Modèle interventionnel: Affectation séquentielle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Safety Run-In HER2- Cohort
Participants with HER2-negative breast cancer leptomeningeal disease (TNBC or HR-positive) receive intrathecal HER3-pulsed cDC1 vaccines in combination with IT nivolumab.
|
Autologous peptide-pulsed cDC1 vaccine administered intrathecally.
Autres noms:
50 mg intrathecal every 2 weeks for HER2-negative participants.
|
|
Expérimental: Safety Run-In HER2+ Cohort
Participants with HER2-positive breast cancer leptomeningeal disease receive intrathecal (IT) HER2/HER3 peptide-pulsed cDC1 vaccines in combination with IT trastuzumab.
|
Autologous peptide-pulsed cDC1 vaccine administered intrathecally.
Autres noms:
150 mg intrathecal weekly for HER2-positive participants.
|
|
Expérimental: Phase 2 Efficacy Cohort
Following completion of the safety run-in and confirmation of the RP2D, participants will receive treatment based on HER2 status: HER2-positive participants will receive IT cDC1 vaccines plus IT trastuzumab. HER2-negative participants will receive IT cDC1 vaccines plus IT nivolumab. |
Autologous peptide-pulsed cDC1 vaccine administered intrathecally.
Autres noms:
50 mg intrathecal every 2 weeks for HER2-negative participants.
150 mg intrathecal weekly for HER2-positive participants.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Safety Run-In: Maximum Tolerated Dose (MTD)
Délai: Up to 28 days
|
MTD of IT cDC1s combined with IT trastuzumab for HER2+ patients or with IT nivolumab for HER2- patients.
|
Up to 28 days
|
|
Phase 2: Median Overall Survival
Délai: Up to 1 year
|
Median survival from initiation of study treatment.
|
Up to 1 year
|
|
Phase 2: One-Year Survival Rate
Délai: Up to 1 year
|
Proportion of participants alive at one year after treatment initiation.
|
Up to 1 year
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Progression Free Survival (PFS)
Délai: Up to 1 year
|
Progression-free survival is defined as the time from first study treatment (Cycle 1 Day 1) until documented disease progression or death from any cause, whichever occurs first.
|
Up to 1 year
|
|
Objective Response Rate (ORR)
Délai: Up to 1 Year
|
The proportion of participants achieving an objective response during study treatment.
Response in leptomeningeal/CNS disease will be assessed using Response Assessment in Neuro-Oncology Leptomeningeal Metastases (RANO-LM) criteria, and response in non-CNS/systemic disease will be assessed using RECIST version 1.1 criteria.
|
Up to 1 Year
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Collaborateurs
Les enquêteurs
- Chercheur principal: Peter Forsyth, MD, Moffitt Cancer Center
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 août 2026
Achèvement primaire (Estimé)
1 août 2029
Achèvement de l'étude (Estimé)
1 août 2030
Dates d'inscription aux études
Première soumission
6 juillet 2026
Première soumission répondant aux critères de contrôle qualité
6 juillet 2026
Première publication (Réel)
10 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
10 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
6 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies du système nerveux
- Tumeurs par site
- Tumeurs
- Maladies de la peau
- Maladies du sein
- Tumeurs du système nerveux
- Tumeurs du système nerveux central
- Maladies de la peau et du tissu conjonctif
- Tumeurs mammaires
- Tumeurs méningées
- Acides aminés, peptides et protéines
- Protéines
- Anticorps, monoclonal, humanisé
- Anticorps, monoclonal
- Anticorps
- Immunoglobulines
- Immunoprotéines
- Protéines sanguines
- Globulines sériques
- Globulines
- Trastuzumab
- Nivolumab
Autres numéros d'identification d'étude
- MCC-23481
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .