- ICH GCP
- Registr klinických studií v USA
- Klinická studie 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
Přehled studie
Postavení
Podmínky
- Hodgkinův lymfom
- Metastatický nemalobuněčný karcinom plic
- Metastatický karcinom ledvin z jasných buněk
- Metastatický kožní melanom
- Neresekovatelný kožní melanom
- Kaposiho sarkom
- Fáze III rakoviny plic AJCC v8
- Fáze IV rakoviny plic AJCC v8
- Neresekabilní maligní solidní novotvar
- Stádium III rakoviny ledvinových buněk AJCC v8
- Stádium IV rakoviny ledvinových buněk AJCC v8
- Metastatický maligní solidní novotvar
- Kožní melanom klinického stadia III AJCC v8
- Metastatický uroteliální karcinom
- Metastatický karcinom z Merkelových buněk
- Metastatický kožní spinocelulární karcinom
- Metastatický kolorektální karcinom
- Stádium IV Kolorektální karcinom AJCC v8
- Kožní melanom klinického stadia IV AJCC v8
- Stádium III Kolorektální karcinom AJCC v8
- Metastatický spinocelulární karcinom hlavy a krku
- Neresekabilní spinocelulární karcinom hlavy a krku
- Neresekabilní nemalobuněčný karcinom plic
- Stádium III rakoviny děložního čípku AJCC v8
- Rakovina děložního čípku stadia IV AJCC v8
- Neresekabilní akrální lentiginózní melanom
- Neresekovatelný slizniční melanom
- Neresekabilní uroteliální karcinom
- Neresekabilní kolorektální karcinom
- Metastatický Kaposiho sarkom
- Metastatický cervikální karcinom
- Metastatický slizniční melanom
- Metastatický bazaliom
- Neresekabilní karcinom děložního hrdla
- Neresekabilní karcinom z Merkelových buněk
- Neresekovatelný kožní spinocelulární karcinom
- Neresekabilní bazaliom
- Metastatický akrální lentiginózní melanom
- Neresekabilní karcinom ledvin z průhledných buněk
- Klinické stadium III kožního karcinomu Merkelových buněk AJCC v8
- Klinické stadium IV kožního karcinomu Merkelových buněk AJCC v8
- Stage IV hlava a krk kožní spinocelulární karcinom AJCC V8
- Stage III hlava a krk kožní spinocelulární karcinom AJCC V8
Detailní popis
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.
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 2
Kontakty a umístění
Studijní kontakt
- Jméno: Shailender Bhatia, MD
- Telefonní číslo: 206-606-6765
- E-mail: sbhatia@uw.edu
Studijní místa
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Kampala, Uganda, 3935
- Uganda Cancer Institute
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Kontakt:
- Jackson Orem
- Telefonní číslo: 0782 320543
- E-mail: jackson.orem@uci.or.ug
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Vrchní vyšetřovatel:
- Jackson Orem
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Popis
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
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
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Experimentální: 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. |
Vzhledem k tomu, IV
Ostatní jména:
Podstoupit MRI
Ostatní jména:
Podstoupit ČT
Ostatní jména:
Undergo collection of urine and/or blood samples
Ostatní jména:
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Objective response
Časové okno: 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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Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
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Duration of response (DOR)
Časové okno: 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
Časové okno: 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)
Časové okno: 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)
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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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Spolupracovníci a vyšetřovatelé
Sponzor
Spolupracovníci
Vyšetřovatelé
- Vrchní vyšetřovatel: Shailender Bhatia, MD, Fred Hutch/University of Washington Cancer Consortium
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Další relevantní podmínky MeSH
- Urogenitální onemocnění
- Onemocnění genitálií
- Patologické procesy
- Urogenitální novotvary
- Novotvary podle místa
- Novotvary
- Mužská urogenitální onemocnění
- Onemocnění ledvin
- Urologická onemocnění
- Ženské urogenitální onemocnění
- Ženské urogenitální onemocnění a těhotenské komplikace
- Střevní nemoci
- Onemocnění imunitního systému
- Infekce
- Virová onemocnění
- Nemoci dýchacích cest
- Novotvary podle histologického typu
- Gastrointestinální novotvary
- Novotvary trávicího systému
- Nemoci trávicího systému
- Gastrointestinální onemocnění
- Střevní novotvary
- Rektální onemocnění
- Onemocnění dělohy
- Onemocnění pohlavních orgánů, ženy
- Plicní onemocnění
- Novotvary hlavy a krku
- Novotvary, žlázové a epiteliální
- Adenokarcinom
- Novotvary dýchacího traktu
- Novotvary hrudníku
- Onemocnění tlustého střeva
- Neoplastické procesy
- DNA virové infekce
- Genitální novotvary, ženy
- Kožní choroby
- Lymfatická onemocnění
- Lymfoproliferativní poruchy
- Imunoproliferativní poruchy
- Urologické novotvary
- Karcinom
- Onemocnění děložního čípku
- Neuroektodermální nádory
- Novotvary, zárodečné buňky a embryonální
- Novotvary, nervová tkáň
- Lymfom
- Novotvary ledvin
- Karcinom, Bronchogenní
- Bronchiální novotvary
- Novotvary dělohy
- Neuroendokrinní nádory
- Sarkom
- Novotvary, pojivové a měkké tkáně
- Herpesviridae infekce
- Nádorové virové infekce
- Nevi a melanomy
- Novotvary kůže
- Novotvary, cévní tkáň
- Karcinom, skvamózní buňky
- Polyomavirové infekce
- Novotvary, bazální buňka
- Karcinom, Neuroendokrinní
- Patologické stavy, příznaky a symptomy
- Onemocnění kůže a pojivové tkáně
- Hemická a lymfatická onemocnění
- Spinocelulární karcinom hlavy a krku
- Novotvary plic
- Kolorektální novotvary
- Metastáza novotvaru
- Karcinom, renální buňka
- Karcinom, nemalobuněčné plíce
- Novotvary děložního čípku
- Melanom
- Hodgkinova nemoc
- Sarkom, Kaposi
- Karcinom, přechodná buňka
- Karcinom, bazální buňka
- Karcinom, Merkelová buňka
- Karcinom s čistými buňkami metastatickými renálními buňkami
- Aminokyseliny, peptidy a proteiny
- Proteiny
- Vyšetřovací techniky
- Klinické laboratorní techniky
- Diagnostické techniky a postupy
- Diagnóza
- Protilátky, monoklonální, humanizované
- Protilátky, monoklonální
- Protilátky
- Imunoglobuliny
- Imunoproteiny
- Krevní proteiny
- Sérové globuliny
- Globuliny
- Techniky chemie, analytické
- Analýza spektra
- Nivolumab
- Manipulace se vzorkem
- Magnetická rezonanční spektroskopie
Další identifikační čísla studie
- RG1125119
- NCI-2026-01874 (Identifikátor registru: CTRP (Clinical Trial Reporting Program))
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
produkt vyrobený a vyvážený z USA
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