- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07576725
Low Dose, Reduced Frequency Nivolumab for the Treatment of Unresectable or Metastatic Cancer, AFFORD IO Trial
AFFORD IO: A Phase 2 Trial of Low Dose, Reduced Frequency Nivolumab (Anti-PD-1 Antibody) in Patients With Unresectable or Metastatic Cancer
Aperçu de l'étude
Statut
Les conditions
- Lymphome de Hodgkin
- Carcinome pulmonaire non à petites cellules métastatique
- Carcinome rénal métastatique à cellules claires
- Mélanome cutané métastatique
- Mélanome cutané non résécable
- Sarcome de Kaposi
- Cancer du poumon de stade III AJCC v8
- Cancer du poumon de stade IV AJCC v8
- Tumeur solide maligne non résécable
- Cancer des cellules rénales de stade III AJCC v8
- Cancer des cellules rénales de stade IV AJCC v8
- Tumeur solide maligne métastatique
- Mélanome cutané de stade III clinique AJCC v8
- Carcinome urothélial métastatique
- Carcinome métastatique à cellules de Merkel
- Carcinome épidermoïde cutané métastatique
- Carcinome colorectal métastatique
- Cancer colorectal de stade IV AJCC v8
- Mélanome cutané de stade IV clinique AJCC v8
- Cancer colorectal de stade III AJCC v8
- Carcinome épidermoïde métastatique de la tête et du cou
- Carcinome épidermoïde de la tête et du cou non résécable
- Carcinome pulmonaire non à petites cellules non résécable
- Cancer du col de l'utérus de stade III AJCC v8
- Cancer du col de l'utérus de stade IV AJCC v8
- Mélanome lentigineux acral non résécable
- Mélanome muqueux non résécable
- Carcinome urothélial non résécable
- Carcinome colorectal non résécable
- Sarcome de Kaposi métastatique
- Carcinome cervical métastatique
- Mélanome muqueux métastatique
- Carcinome basocellulaire métastatique
- Carcinome cervical non résécable
- Carcinome à cellules de Merkel non résécable
- Carcinome épidermoïde cutané non résécable
- Carcinome basocellulaire non résécable
- Mélanome lentigineux acral métastatique
- Carcinome rénal à cellules claires non résécable
- Carcinome cutané à cellules de Merkel de stade clinique III AJCC v8
- Carcinome cutané à cellules de Merkel de stade clinique IV AJCC v8
- Stage IV Head and Nou Cartane cutané CARCINOMA SELLES A AJCC V8
- Stade III Tête et cou CARCINOME SPÉLIQUE CUDAME AUJCC V8
Description détaillée
OUTLINE:
INDUCTION PHASE: Patients receive nivolumab intravenously (IV) over approximately 30 minutes on days 1 and 45 in the absence of disease progression or unacceptable toxicity. Patients who are benefitting after 45 days proceed to Maintenance Phase.
MAINTENANCE PHASE: Patients receive nivolumab IV over approximately 30 minutes every 90 days (days 90, 180, 270 and 360) in the absence of disease progression or unacceptable toxicity.
All patients also undergo computed tomography (CT)/magnetic resonance imaging (MRI) and blood sample collection throughout the study. Patients may also undergo urine sample collection throughout the study.
After completion of study treatment, patients are followed up at 90 days and then every 12 months for up to 4 years.
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
Contacts et emplacements
Coordonnées de l'étude
- Nom: Shailender Bhatia, MD
- Numéro de téléphone: 206-606-6765
- E-mail: sbhatia@uw.edu
Lieux d'étude
-
-
-
Kampala, Ouganda, 3935
- Uganda Cancer Institute
-
Contact:
- Jackson Orem
- Numéro de téléphone: 0782 320543
- E-mail: jackson.orem@uci.or.ug
-
Chercheur principal:
- Jackson Orem
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
Participants are eligible if they have one of these histologically confirmed, unresectable or metastatic cancer types listed below, based upon historical responsiveness to anti-PD-(L)1 agents
- Non-small cell lung cancer (NSCLC) with documented PD-L1 expression (combined positive score [CPS] ≥ 1) (NOTE: Participants with known driver oncogenic mutations/rearrangements, including EGFR, ALK and ROS-1, will be excluded.)
- Head and neck squamous cell carcinoma (HNSCC) with documented PD-L1 expression (CPS ≥ 1)
- Clear cell renal cell carcinoma (ccRCC) (NOTE: Other subtypes may be permitted after approval by the Medical Monitor)
- Melanoma (cutaneous, acral-lentiginous and mucosal subtypes), and non-melanoma skin cancers, (cutaneous squamous cell carcinoma [CSCC], basal cell carcinoma [BCC] and Merkel cell carcinoma [MCC])
- Hodgkin's lymphoma
- Urothelial carcinoma
- Cervical cancer with documented PD-L1 expression (CPS ≥ 1)
- Colorectal cancer with high microsatellite instability (MSI) or mismatch repair deficiency
- Kaposi sarcoma (KS) without clinical concern for multicentric Castleman's disease (MCD)
- Any cancer type with historical data suggesting an ORR > 20% with anti-PD(L)-1 agents (NOTE: All participants in this category must be approved by the Medical Monitor prior to enrollment.)
- Must have experienced disease progression after or deemed not to be a good candidate for available curative systemic therapy options
- Presence of at least one measurable tumor, per RECIST v1.1
- Age 18 or older. (NOTE: Both men and women, and members of all races and ethnic groups are eligible for this trial.)
- Eastern Cooperative Oncology Group (ECOG) performance score of 0-2
- Absolute neutrophil count (ANC) ≥ 1.0 × 10^9/L
- Platelet count ≥ 75 × 10^9/L
- Hemoglobin ≥ 9 g/dL (NOTE: Participants may have been transfused)
- Total bilirubin level ≤ 1.5 × the upper limit of normal (ULN) (or total bilirubin ≤ 2.5 × upper limit of normal [ULN] in participants with Gilbert's syndrome)
- Estimated creatinine clearance ≥ 30mL/min according to the Cockcroft-Gault formula or according to local institutional standard
- Must consent to undergo serial research blood draws at study defined timepoints, unless deemed unsafe or not feasible by the treating investigator
- Must have an ability to understand and provide consent to the institutional review board (IRB)-approved informed consent form (ICF) document(s)
- Women of childbearing potential must have a negative serum or urine pregnancy test at screening
- Both male and female participants must be willing to use highly effective contraception, as stipulated in national or local guidelines, throughout the study and for at least 180 days after the last treatment administration, if the risk of conception exists
Exclusion Criteria:
- Prior exposure to any immune-checkpoint inhibitor for any reason
- Residual adverse event(s) from prior therapy grade > 1 (National Cancer Institute [NCI]-Common Terminology Criteria for Adverse Events [CTCAE] v6.0) that could interfere with study endpoints or put participant safety at risk, as determined by the treating investigator
- Known active central nervous system (CNS) metastases and/or prior history of leptomeningeal cancer involvement
- Known history of another active malignancy (besides the eligible cancer diagnosis) within the last 3 years from day 1 of nivolumab that could interfere with study endpoints or put participant safety at risk. (NOTE: Exception will be made for adequately treated basal or squamous cell carcinoma of the skin or carcinoma in situ [skin, bladder, cervical, colorectal, breast] or low grade prostatic intraepithelial neoplasia or grade 1 prostate cancer. Any other neoplasm, which has been treated adequately and is adjudged by the treating investigator to have a low risk of progression during the study, could be enrolled only after approval from the medical monitor.)
Known active hepatitis B virus (HBV) or hepatitis C virus (HCV), defined as follows:
- Active HBV is defined as a known positive hepatitis B virus surface antigen (HBsAg) result or positive total hepatitis B virus core antibody (anti-HBc) results in the absence of hepatitis B virus surface antibody (anti-HBsAb). (NOTE: When HBsAg is negative and HBcAb is positive, HBV-DNA should be measured. When HBV-deoxyribonucleic acid [DNA] is negative, this participant could be enrolled with close monitoring of HBV activities.)
- Active hepatitis C virus (HCV) is defined as a known positive HCV antibody result and quantitative HCV-ribonucleic acid (RNA) results greater than the lower limits of detection of the assay. (NOTE: Participants who have had definitive treatment for HCV are permitted if HCV-RNA is undetectable.)
Known uncontrolled HIV infection. (NOTE: HIV-infected participants may be allowed if all the following criteria are met: CD4 count ≥ 100/μL, viral load less than 200 copies/mL, and clinically stable on antiretroviral therapy [ART] for at least 3 months.)
- These participants will be enrolled only after approval from the medical monitor
- Known active autoimmune disease or an allograft requiring systemic immunosuppression with corticosteroids (> 10 mg/day of prednisone or equivalent) or immunosuppressive drugs within the past 2 years before the first dose of nivolumab. (NOTE: Exceptions will be made for participants with autoimmune conditions such as diabetes type I, vitiligo, psoriasis, hypothyroid or hyperthyroid diseases not requiring immunosuppressive treatment; participants receiving physiologic corticosteroid replacement therapy at doses < 10 mg/day of prednisone or equivalent for adrenal or pituitary insufficiency; participants with a condition such as asthma or chronic obstructive pulmonary disease that requires intermittent use of steroids or those who require brief courses of corticosteroids for prophylaxis [e.g., contrast dye allergy], nivolumab-related standard premedication, and/or treatment of non-serious immune related adverse events. Any other situation must be discussed with the medical monitor for risk/benefit assessment.)
- Immunosuppressed status due to severe uncontrolled diabetes, concurrent uncontrolled hematological malignancy, or other comorbidities
- Known history of serious, active infections (aside from well-controlled HIV, as per exclusion criterion #6) requiring systemic antimicrobial agents within 14 days before the first dose of nivolumab. (NOTE: Chronic infections such as herpes simplex virus requiring suppressive therapy may be allowed after discussion with the medical monitor for risk/benefit assessment.)
- Known history of clinically significant interstitial lung disease, or active noninfectious pneumonitis
- Clinically significant (i.e., active) cardiovascular disease such as cerebral vascular accident or myocardial infarction within 6 months prior to first dose of nivolumab, ongoing unstable angina or congestive heart failure (New York Heart Association Classification class II-IV), or serious cardiac arrhythmia that could jeopardize participant safety on the study
- Receipt of live vaccine(s) within 30 days of planned start of nivolumab. (NOTE: Examples of live vaccines include but are not limited to measles, mumps, rubella, varicella-zoster [chickenpox], yellow fever, rabies, bacillus Calmette Guerin [BCG], and typhoid vaccines. Seasonal influenza vaccines for injection are generally killed-virus vaccines and are allowed; however, intranasal influenza vaccines are live, attenuated vaccines and are not allowed.)
- Known severe acute or chronic medical conditions such as uncontrolled seizure disorder, serious psychiatric illness, or laboratory abnormalities, that may increase the risk associated with study participation or may interfere with the interpretation of study endpoints and, in the judgment of the treating investigator, would make the participant inappropriate for entry into this study
- Known active tuberculosis (TB). (NOTE: Participants with latent TB will be allowed, provided they are receiving tuberculosis preventive therapy, after approval of the medical monitor.)
- Known allergy or hypersensitivity to any component of the study drug formulation (including excipients and additives) that could interfere with study endpoints or put participant safety at risk
- Pregnant or breast-feeding woman
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: N / A
- Modèle interventionnel: Affectation à un seul groupe
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Treatment (low dose, reduced frequency nivolumab)
INDUCTION PHASE: Patients receive nivolumab IV over approximately 30 minutes on days 1 and 45 in the absence of disease progression or unacceptable toxicity. Patients who are benefitting after 45 days proceed to Maintenance Phase. MAINTENANCE PHASE: Patients receive nivolumab IV over approximately 30 minutes every 90 days (days 90, 180, 270 and 360) in the absence of disease progression or unacceptable toxicity. All patients also undergo CT/MRI and blood sample collection throughout the study. Patients may also undergo urine sample collection throughout the study. |
Étant donné IV
Autres noms:
Passer une IRM
Autres noms:
Subir une tomodensitométrie
Autres noms:
Undergo collection of urine and/or blood samples
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Objective response
Délai: Up to 4 years after completion of study treatment
|
Defined as the best objective response of complete response (CR) or partial response (PR), as determined by investigator assessment per Response Evaluation Criteria in Solid Tumors (RECIST) version (v)1.1.
|
Up to 4 years after completion of study treatment
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Duration of response (DOR)
Délai: From the earliest date of disease response (CR or PR) until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
Will be assessed per RECIST 1.1.
The Kaplan-Meier (KM) technique will be used to obtain estimates of DOR.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From the earliest date of disease response (CR or PR) until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
|
Disease control
Délai: Up to 4 years after completion of study treatment
|
Defined as achievement of CR, PR, or stable disease as a patient's best objective response to the study treatment, per RECIST v1.1.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
Up to 4 years after completion of study treatment
|
|
Progression free survival (PFS)
Délai: From date of first dose of study treatment until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
The KM technique will be used to obtain estimates of PFS.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From date of first dose of study treatment until the earliest date of disease progression, or the date of death from any cause, assessed up to 4 years after completion of study treatment
|
|
Overall survival (OS)
Délai: From date of first dose of study treatment until the date of death from any cause, assessed up to 4 years after completion of study treatment
|
The KM technique will be used to obtain estimates of OS.
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From date of first dose of study treatment until the date of death from any cause, assessed up to 4 years after completion of study treatment
|
|
Disease specific survival
Délai: From date of first dose of study treatment until the date of death, assessed up to 4 years after completion of study treatment
|
For event-based survival analyses in participants without documentation of the event, survival will be censored on the last date the participant was known to be event free.
The standard error of the KM estimates will be computed using the Greenwood formula (Kalbfleisch & Prentice, 2002), and standard errors from the matrix form of Greenwood's formula for cumulative incidence estimates.
Median time to event, if reached, will be presented with a 90% confidence interval based on the Brookmeyer and Crowley method (Kalbfleisch & Prentice, 2002).
|
From date of first dose of study treatment until the date of death, assessed up to 4 years after completion of study treatment
|
|
Incidence of adverse events
Délai: Up to 90 days years after completion of study treatment
|
Will include immune-related adverse events, treatment interruption and treatment discontinuation, and the use of immunosuppressive medications for toxicities.
|
Up to 90 days years after completion of study treatment
|
|
Accrual and by compliance with treatment timepoints
Délai: Up to 4 years after completion of study treatment
|
Feasibility defined by accrual and by compliance with treatment timepoints in this unique setting.
|
Up to 4 years after completion of study treatment
|
Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: Shailender Bhatia, MD, Fred Hutch/University of Washington Cancer Consortium
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Maladies urogénitales
- Maladies génitales
- Processus pathologiques
- Tumeurs urogénitales
- Tumeurs par site
- Tumeurs
- Maladies urogénitales masculines
- Maladies rénales
- Maladies urologiques
- Maladies urogénitales féminines
- Maladies urogénitales féminines et complications de la grossesse
- Maladies intestinales
- Maladies du système immunitaire
- Infections
- Maladies virales
- Maladies des voies respiratoires
- Tumeurs par type histologique
- Tumeurs gastro-intestinales
- Tumeurs du système digestif
- Maladies du système digestif
- Maladies gastro-intestinales
- Tumeurs intestinales
- Maladies rectales
- Maladies utérines
- Maladies génitales, femme
- Maladies pulmonaires
- Tumeurs de la tête et du cou
- Tumeurs, glandulaires et épithéliales
- Adénocarcinome
- Tumeurs des voies respiratoires
- Tumeurs thoraciques
- Maladies du côlon
- Processus néoplasiques
- Infections par le virus de l'ADN
- Tumeurs génitales, femme
- Maladies de la peau
- Maladies lymphatiques
- Troubles lymphoprolifératifs
- Troubles immunoprolifératifs
- Tumeurs urologiques
- Carcinome
- Maladies du col de l'utérus
- Tumeurs neuroectodermiques
- Tumeurs, cellules germinales et embryonnaires
- Tumeurs, tissu nerveux
- Lymphome
- Tumeurs rénales
- Carcinome bronchique
- Tumeurs bronchiques
- Tumeurs utérines
- Tumeurs neuroendocrines
- Sarcome
- Tumeurs, tissus conjonctifs et mous
- Infections à Herpesviridae
- Infections virales tumorales
- Nevi et mélanomes
- Tumeurs cutanées
- Tumeurs, tissu vasculaire
- Carcinome épidermoïde
- Infections à polyomavirus
- Tumeurs basocellulaires
- Carcinome neuroendocrinien
- Conditions pathologiques, signes et symptômes
- Maladies de la peau et du tissu conjonctif
- Maladies hémiques et lymphatiques
- Carcinome épidermoïde de la tête et du cou
- Tumeurs pulmonaires
- Tumeurs colorectales
- Métastase néoplasmique
- Carcinome à cellules rénales
- Carcinome pulmonaire non à petites cellules
- Tumeurs du col de l'utérus
- Mélanome
- Maladie de Hodgkin
- Sarcome, Kaposi
- Carcinome à cellules transitionnelles
- Carcinome basocellulaire
- Carcinome, cellule de Merkel
- Carcinome à cellules rénales à cellules claires
- Acides aminés, peptides et protéines
- Protéines
- Techniques d'investigation
- Techniques de laboratoire clinique
- Techniques et procédures de diagnostic
- Diagnostic
- Anticorps, monoclonal, humanisé
- Anticorps, monoclonal
- Anticorps
- Immunoglobulines
- Immunoprotéines
- Protéines sanguines
- Globulines sériques
- Globulines
- Techniques de chimie, analytique
- Analyse du spectre
- Nivolumab
- Manipulation des échantillons
- Spectroscopie de résonance magnétique
Autres numéros d'identification d'étude
- RG1125119
- NCI-2026-01874 (Identificateur de registre: CTRP (Clinical Trial Reporting Program))
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
produit fabriqué et exporté des États-Unis.
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 .