- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg 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
Studieoversigt
Status
Betingelser
- Hodgkin lymfom
- Metastatisk lunge ikke-småcellet karcinom
- Metastatisk klarcellet nyrecellekarcinom
- Metastatisk kutan melanom
- Uoperabelt kutan melanom
- Kaposi Sarkom
- Stadie III lungekræft AJCC v8
- Stadie IV lungekræft AJCC v8
- Ikke-operable malignt fast neoplasma
- Stadie III nyrecellekræft AJCC v8
- Stadie IV nyrecellekræft AJCC v8
- Metastatisk malignt fast neoplasma
- Klinisk fase III kutan melanom AJCC v8
- Metastatisk Urothelial Carcinom
- Metastatisk Merkelcellekarcinom
- Metastatisk hudpladecellekarcinom
- Metastatisk kolorektalt karcinom
- Fase IV kolorektal cancer AJCC v8
- Klinisk fase IV kutan melanom AJCC v8
- Fase III kolorektal cancer AJCC v8
- Metastatisk hoved- og halspladecellekræft
- Uoperabelt hoved- og nakkepladecellekarcinom
- Ikke-småcellet lungekarcinom, der ikke kan opopereres
- Stadie III livmoderhalskræft AJCC v8
- Stadie IV Livmoderhalskræft AJCC v8
- Uoperabelt Akralt lentiginøst melanom
- Uoperabelt slimhindemelanom
- Uoperabelt Urothelial Carcinom
- Ikke-operabelt kolorektalt karcinom
- Metastatisk Kaposi Sarkom
- Metastatisk cervikal karcinom
- Metastatisk slimhindemelanom
- Metastatisk basalcellekarcinom
- Uoperabelt cervikal karcinom
- Uoperabelt Merkelcellekarcinom
- Uoperabelt hudpladecellekarcinom
- Ikke-operabelt basalcellekarcinom
- Metastatisk Akral Lentiginøst Melanom
- Ikke-operabelt klarcellet nyrecellekarcinom
- Klinisk trin III kutan Merkelcellekarcinom AJCC v8
- Klinisk trin IV kutan Merkelcellekarcinom AJCC v8
- Trin IV Hoved- og hals -kutan pladecellecarcinom AJCC V8
- Trin III Hoved og hals kutan pladecellecarcinom AJCC V8
Intervention / Behandling
Detaljeret beskrivelse
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.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 2
Kontakter og lokationer
Studiekontakt
- Navn: Shailender Bhatia, MD
- Telefonnummer: 206-606-6765
- E-mail: sbhatia@uw.edu
Studiesteder
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-
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Kampala, Uganda, 3935
- Uganda Cancer Institute
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Kontakt:
- Jackson Orem
- Telefonnummer: 0782 320543
- E-mail: jackson.orem@uci.or.ug
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Ledende efterforsker:
- Jackson Orem
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
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
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 |
|---|---|
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Eksperimentel: 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. |
Givet IV
Andre navne:
Gennemgå MR
Andre navne:
Gennemgå CT
Andre navne:
Undergo collection of urine and/or blood samples
Andre navne:
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Objective response
Tidsramme: Up to 4 years after completion of study treatment
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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.
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Up to 4 years after completion of study treatment
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Duration of response (DOR)
Tidsramme: 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
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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).
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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
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Disease control
Tidsramme: Up to 4 years after completion of study treatment
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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).
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Up to 4 years after completion of study treatment
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Progression free survival (PFS)
Tidsramme: 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
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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).
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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
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Overall survival (OS)
Tidsramme: 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
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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).
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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
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Disease specific survival
Tidsramme: From date of first dose of study treatment until the date of death, assessed up to 4 years after completion of study treatment
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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).
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From date of first dose of study treatment until the date of death, assessed up to 4 years after completion of study treatment
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Incidence of adverse events
Tidsramme: Up to 90 days years after completion of study treatment
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Will include immune-related adverse events, treatment interruption and treatment discontinuation, and the use of immunosuppressive medications for toxicities.
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Up to 90 days years after completion of study treatment
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Accrual and by compliance with treatment timepoints
Tidsramme: Up to 4 years after completion of study treatment
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Feasibility defined by accrual and by compliance with treatment timepoints in this unique setting.
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Up to 4 years after completion of study treatment
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Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Shailender Bhatia, 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
- Urogenitale sygdomme
- Genitale sygdomme
- Patologiske processer
- Urogenitale neoplasmer
- Neoplasmer efter sted
- Neoplasmer
- Mandlige urogenitale sygdomme
- Nyresygdomme
- Urologiske sygdomme
- Urogenitale sygdomme hos kvinder
- Kvinders urogenitale sygdomme og graviditetskomplikationer
- Tarmsygdomme
- Sygdomme i immunsystemet
- Infektioner
- Virussygdomme
- Luftvejssygdomme
- Neoplasmer efter histologisk type
- Gastrointestinale neoplasmer
- Neoplasmer i fordøjelsessystemet
- Sygdomme i fordøjelsessystemet
- Gastrointestinale sygdomme
- Intestinale neoplasmer
- Endetarmssygdomme
- Livmodersygdomme
- Kønssygdomme, kvindelige
- Lungesygdomme
- Neoplasmer i hoved og hals
- Neoplasmer, kirtel og epitel
- Adenocarcinom
- Neoplasmer i luftvejene
- Thoracale neoplasmer
- Tyktarmssygdomme
- Neoplastiske processer
- DNA-virusinfektioner
- Genitale neoplasmer, kvindelige
- Hudsygdomme
- Lymfesygdomme
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Urologiske neoplasmer
- Karcinom
- Livmoderhalssygdomme
- Neuroektodermale tumorer
- Neoplasmer, kimceller og embryonale
- Neoplasmer, nervevæv
- Lymfom
- Nyre-neoplasmer
- Karcinom, bronkogent
- Bronkiale neoplasmer
- Uterine neoplasmer
- Neuroendokrine tumorer
- Sarkom
- Neoplasmer, bindevæv og blødt væv
- Herpesviridae infektioner
- Tumorvirusinfektioner
- Nevi og melanomer
- Neoplasmer i huden
- Neoplasmer, vaskulært væv
- Karcinom, pladecelle
- Polyomavirus infektioner
- Neoplasmer, basalcelle
- Karcinom, neuroendokrin
- Patologiske tilstande, tegn og symptomer
- Hud- og bindevævssygdomme
- Hemiske og lymfatiske sygdomme
- Planocellulært karcinom i hoved og hals
- Lungeneoplasmer
- Kolorektale neoplasmer
- Neoplasma Metastase
- Karcinom, nyrecelle
- Karcinom, ikke-småcellet lunge
- Uterine cervikale neoplasmer
- Melanom
- Hodgkins sygdom
- Sarkom, Kaposi
- Carcinom, overgangscelle
- Karcinom, basalcelle
- Karcinom, Merkel Cell
- Clear-Cell metastatisk nyrecellekarcinom
- Aminosyrer, peptider og proteiner
- Proteiner
- Undersøgelsesteknikker
- Kliniske laboratorieteknikker
- Diagnostiske teknikker og procedurer
- Diagnose
- Antistoffer, monoklonal, humaniseret
- Antistoffer, monoklonal
- Antistoffer
- Immunoglobuliner
- Immunoproteiner
- Blodproteiner
- Serum globuliner
- Globuliner
- Kemiteknikker, analytisk
- Spektrumanalyse
- Nivolumab
- Håndtering af eksemplar
- Magnetisk resonansspektroskopi
Andre undersøgelses-id-numre
- RG1125119
- NCI-2026-01874 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Plan for individuelle deltagerdata (IPD)
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