- ICH GCP
- USA klinikai vizsgálatok nyilvántartása
- Klinikai vizsgálat 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
A tanulmány áttekintése
Állapot
Körülmények
- Hodgkin limfóma
- Áttétes tüdő nem kissejtes karcinóma
- Áttétes tiszta sejtes vesesejtes karcinóma
- Áttétes bőr melanoma
- Nem reszekálható bőr melanoma
- Kaposi szarkóma
- III. stádiumú tüdőrák AJCC v8
- IV. stádiumú tüdőrák AJCC v8
- Nem reszekálható rosszindulatú szilárd daganat
- III. stádiumú vesesejtes rák AJCC v8
- IV. stádiumú vesesejtes rák AJCC v8
- Áttétes rosszindulatú szilárd daganat
- Clinical Stage III bőr melanoma AJCC v8
- Áttétes uroteliális karcinóma
- Metasztatikus Merkel-sejtes karcinóma
- Áttétes bőr laphámsejtes karcinóma
- Áttétes kolorektális karcinóma
- IV. stádiumú vastag- és végbélrák AJCC v8
- IV. klinikai stádiumú bőr melanoma AJCC v8
- III. stádiumú vastag- és végbélrák AJCC v8
- Áttétes fej és nyak laphámsejtes karcinóma
- Nem reszekálható fej és nyak laphámsejtes karcinóma
- Nem reszekálható tüdő nem kissejtes karcinóma
- III. stádiumú méhnyakrák AJCC v8
- IV. stádiumú méhnyakrák AJCC v8
- Nem reszekálható Acral Lentiginous melanoma
- Nem reszekálható nyálkahártya melanoma
- Nem reszekálható urotheliális karcinóma
- Nem reszekálható kolorektális karcinóma
- Áttétes Kaposi-szarkóma
- Áttétes méhnyak karcinóma
- Áttétes nyálkahártya melanoma
- Áttétes bazális sejtes karcinóma
- Nem reszekálható méhnyak karcinóma
- Nem reszekálható Merkel-sejtes karcinóma
- Nem reszekálható bőrlaphámrák
- Nem reszekálható bazális sejtes karcinóma
- Áttétes acralis lentiginous melanoma
- Nem reszekálható tiszta sejtes vesesejtes karcinóma
- III. klinikai stádiumú bőr Merkel sejtes karcinóma AJCC v8
- IV. klinikai stádiumú bőr Merkel-sejtes karcinóma AJCC v8
- IV. Szakasz fej- és nyakú bőr laphámsejtes karcinóma AJCC V8
- III. Szakasz fej- és nyakú bőr laphámsejtes karcinóma AJCC V8
Részletes leírás
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.
Tanulmány típusa
Beiratkozás (Becsült)
Fázis
- 2. fázis
Kapcsolatok és helyek
Tanulmányi kapcsolat
- Név: Shailender Bhatia, MD
- Telefonszám: 206-606-6765
- E-mail: sbhatia@uw.edu
Tanulmányi helyek
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-
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Kampala, Uganda, 3935
- Uganda Cancer Institute
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Kapcsolatba lépni:
- Jackson Orem
- Telefonszám: 0782 320543
- E-mail: jackson.orem@uci.or.ug
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Kutatásvezető:
- Jackson Orem
-
-
Részvételi kritériumok
Jogosultsági kritériumok
Tanulmányozható életkorok
- Felnőtt
- Idősebb felnőtt
Egészséges önkénteseket fogad
Leírás
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
Tanulási terv
Hogyan készül a tanulmány?
Tervezési részletek
- Elsődleges cél: Kezelés
- Kiosztás: N/A
- Beavatkozó modell: Egyetlen csoportos hozzárendelés
- Maszkolás: Nincs (Open Label)
Fegyverek és beavatkozások
Résztvevő csoport / kar |
Beavatkozás / kezelés |
|---|---|
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Kísérleti: 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. |
Adott IV
Más nevek:
Végezzen MRI-t
Más nevek:
Végezzen CT-t
Más nevek:
Undergo collection of urine and/or blood samples
Más nevek:
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Mit mér a tanulmány?
Elsődleges eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
|
Objective response
Időkeret: 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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Másodlagos eredményintézkedések
Eredménymérő |
Intézkedés leírása |
Időkeret |
|---|---|---|
|
Duration of response (DOR)
Időkeret: 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
Időkeret: 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)
Időkeret: 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).
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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)
Időkeret: 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).
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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
Időkeret: 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
Időkeret: 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
Időkeret: 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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Együttműködők és nyomozók
Szponzor
Együttműködők
Nyomozók
- Kutatásvezető: Shailender Bhatia, MD, Fred Hutch/University of Washington Cancer Consortium
Tanulmányi rekorddátumok
Tanulmány főbb dátumok
Tanulmány kezdete (Becsült)
Elsődleges befejezés (Becsült)
A tanulmány befejezése (Becsült)
Tanulmányi regisztráció dátumai
Először benyújtva
Először nyújtották be, amely megfelel a minőségbiztosítási kritériumoknak
Első közzététel (Tényleges)
Tanulmányi rekordok frissítései
Utolsó frissítés közzétéve (Tényleges)
Az utolsó frissítés elküldve, amely megfelel a minőségbiztosítási kritériumoknak
Utolsó ellenőrzés
Több információ
A tanulmányhoz kapcsolódó kifejezések
További vonatkozó MeSH feltételek
- Urogenitális betegségek
- Nemi szervek betegségei
- Patológiás folyamatok
- Urogenitális neoplazmák
- Neoplazmák webhelyenként
- Neoplazmák
- Férfi urogenitális betegségek
- Vesebetegségek
- Urológiai betegségek
- Női urogenitális betegségek
- Női urogenitális betegségek és terhességi szövődmények
- Bélbetegségek
- Immunrendszeri betegségek
- Fertőzések
- Vírusos betegségek
- Légúti betegségek
- Neoplazmák szövettani típus szerint
- Gasztrointesztinális neoplazmák
- Emésztőrendszeri neoplazmák
- Emésztőrendszeri betegségek
- Emésztőrendszeri betegségek
- Bél neoplazmák
- Rektális betegségek
- Méhbetegségek
- Nemi szervek betegségei, nő
- Tüdőbetegségek
- A fej és a nyak daganatai
- Neoplazmák, mirigyes és epiteliális
- Adenokarcinóma
- Légúti neoplazmák
- Mellkasi neoplazmák
- Vastagbélbetegségek
- Neoplasztikus folyamatok
- DNS vírusfertőzések
- Nemi szervek daganatai, nők
- Bőrbetegségek
- Nyirokrendszeri betegségek
- Limfoproliferatív rendellenességek
- Immunproliferatív rendellenességek
- Urológiai neoplazmák
- Karcinóma
- A méhnyak betegségei
- Neuroektodermális daganatok
- Neoplazmák, csírasejt és embrionális
- Neoplazmák, idegszövet
- Limfóma
- Vese neoplazmák
- Karcinóma, bronchogén
- Bronchiális neoplazmák
- Méh neoplazmák
- Neuroendokrin daganatok
- Szarkóma
- Neoplazmák, kötő- és lágyszövetek
- Herpesviridae fertőzések
- Tumor vírusfertőzések
- Nevi és melanómák
- Bőr neoplazmák
- Neoplazmák, vaszkuláris szövetek
- Karcinóma, laphámsejtes
- Polyomavírus fertőzések
- Neoplazmák, bazális sejt
- Karcinóma, neuroendokrin
- Kóros állapotok, jelek és tünetek
- Bőr- és kötőszöveti betegségek
- Hemikus és nyirokbetegségek
- A fej és a nyak laphámsejtes karcinóma
- Tüdő neoplazmák
- Kolorektális neoplazmák
- Neoplazma metasztázis
- Karcinóma, vesesejt
- Karcinóma, nem kissejtes tüdő
- A méhnyak neoplazmái
- Melanóma
- Hodgkin-kór
- Szarkóma, Kaposi
- Carcinoma, átmeneti sejt
- Karcinóma, bazális sejt
- Karcinóma, Merkel sejt
- Tiszta sejtes metasztatikus vesesejtes karcinóma
- Aminosavak, peptidek és fehérjék
- Fehérjék
- Nyomozási technikák
- Klinikai laboratóriumi technikák
- Diagnosztikai technikák és eljárások
- Diagnózis
- Antitestek, monoklonális, humanizált
- Antitestek, monoklonális
- Antitestek
- Immunoglobulinok
- Immunoproteinek
- Vérfehérjék
- Szérumglobulinok
- Globulinok
- Kémiai technikák, analitikus
- Spektrumelemzés
- Nivolumab
- Minta kezelése
- Mágneses rezonancia spektroszkópia
Egyéb vizsgálati azonosító számok
- RG1125119
- NCI-2026-01874 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Terv az egyéni résztvevői adatokhoz (IPD)
Tervezi megosztani az egyéni résztvevői adatokat (IPD)?
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