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再発性、転移性、または難治性の上咽頭がんにおける標的薬物カボザンチニブの有無にかかわらず、ニボルマブおよびイピリムマブ免疫療法をテストする

2026年10月30日 更新者：National Cancer Institute (NCI)

プラチナ治療および免疫療法後に進行した進行上咽頭癌患者を対象とした、カボザンチニブ併用または非併用でのニボルマブおよびイピリムマブのランダム化第2相試験

This phase II trial tests how well nivolumab and ipilimumab immunotherapy with or without cabozantinib works in treating patients with nasopharyngeal cancer that has come back (after a period of improvement) (recurrent), has spread from where it first started (primary site) to other places in the body (metastatic), or for which no treatment is currently available (incurable). Immunotherapy with monoclonal antibodies, such as nivolumab and ipilimumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Cabozantinib is in a class of medications called kinase inhibitors. It works by blocking the action of an abnormal protein that signals cancer cells to multiply. This helps slow or stop the spread of cancer cells. Giving immunotherapy with nivolumab and ipilimumab and targeted therapy with cabozantinib may help shrink and stabilize nasopharyngeal cancer.

調査の概要

状態

一時停止

条件

介入・治療

詳細な説明

PRIMARY OBJECTIVE:

I. To determine if the progression-free survival (PFS) of the triplet combination (cabozantinib S-malate, nivolumab, and ipilimumab [CaboNivoIpi]) is more favorable than the doublet (nivolumab and ipilimumab [NivoIpi]).

SECONDARY OBJECTIVES:

I. To compare safety and tolerability between the two arms (Common Terminology Criteria for Adverse Events [CTCAE] version [v]5.0.).

II. To compare overall response rate (ORR) between the two arms via both Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 and immune-modified Response Evaluation Criteria in Solid Tumors (iRECIST) criteria.

III. To compare overall survival (OS) between the two arms. IV. To assess response by primary or acquired PD-1/L1 inhibitor resistance in the prior line of therapy.

EXPLORATORY OBJECTIVE:

I. To evaluate molecular and immunologic predictors of response (Epstein-Barr virus [EBV] viral load; PD-L1 score) between arms.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM A: Patients receive nivolumab intravenously (IV) over 30 minutes and ipilimumab IV over 30 minutes on day 1 of each cycle. Cycles repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Patients undergo computed tomography (CT) or magnetic resonance imaging (MRI) and collection of blood samples throughout the trial.

ARM B: Patients receive nivolumab IV over 30 minutes and ipilimumab IV over 30 minutes on day 1 and cabozantinib S-malate orally (PO) daily on days 1-28 of each cycle. Cycles repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Patients may continue with cabozantinib S-malate after 2 years per treating investigator. Patients undergo CT or MRI and collection of blood samples throughout the trial.

After completion of study treatment, patients are followed up every 8-12 weeks until progression of disease occurs or a new non-protocol anti-cancer therapy is initiated and then every 6 months for up to 2 years.

研究の種類

介入

入学 (推定)

50

段階

  • フェーズ2

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

  • アメリカ
    • California
      • Irvine、California、アメリカ、92612
        • UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care
      • Los Angeles、California、アメリカ、90033
        • USC / Norris Comprehensive Cancer Center
      • Los Angeles、California、アメリカ、90020
        • Keck Medicine of USC Koreatown
      • Los Angeles、California、アメリカ、90033
        • Los Angeles General Medical Center
      • Newport Beach、California、アメリカ、92663
        • USC Norris Oncology/Hematology-Newport Beach
      • Orange、California、アメリカ、92868
        • UC Irvine Health/Chao Family Comprehensive Cancer Center
      • Palo Alto、California、アメリカ、94304
        • Stanford Cancer Institute Palo Alto
    • Georgia
      • Atlanta、Georgia、アメリカ、30308
        • Emory University Hospital Midtown
    • Idaho
      • Boise、Idaho、アメリカ、83706
        • Saint Alphonsus Cancer Care Center-Boise
      • Caldwell、Idaho、アメリカ、83605
        • Saint Alphonsus Cancer Care Center-Caldwell
      • Coeur d'Alene、Idaho、アメリカ、83814
        • Kootenai Health - Coeur d'Alene
      • Nampa、Idaho、アメリカ、83687
        • Saint Alphonsus Cancer Care Center-Nampa
      • Post Falls、Idaho、アメリカ、83854
        • Kootenai Clinic Cancer Services - Post Falls
      • Sandpoint、Idaho、アメリカ、83864
        • Kootenai Clinic Cancer Services - Sandpoint
    • Illinois
      • Chicago、Illinois、アメリカ、60611
        • Northwestern University
      • Chicago、Illinois、アメリカ、60637
        • University of Chicago Comprehensive Cancer Center
      • Chicago、Illinois、アメリカ、60612
        • University of Illinois
      • Danville、Illinois、アメリカ、61832
        • Carle at The Riverfront
      • DeKalb、Illinois、アメリカ、60115
        • Northwestern Medicine Cancer Center Kishwaukee
      • Effingham、Illinois、アメリカ、62401
        • Carle Physician Group-Effingham
      • Evanston、Illinois、アメリカ、60201
        • NorthShore University HealthSystem-Evanston Hospital
      • Geneva、Illinois、アメリカ、60134
        • Northwestern Medicine Cancer Center Delnor
      • Glenview、Illinois、アメリカ、60026
        • NorthShore University HealthSystem-Glenbrook Hospital
      • Glenview、Illinois、アメリカ、60026
        • Northwestern Medicine Glenview Outpatient Center
      • Grayslake、Illinois、アメリカ、60030
        • Northwestern Medicine Grayslake Outpatient Center
      • Harvey、Illinois、アメリカ、60426
        • Ingalls Memorial Hospital
      • Highland Park、Illinois、アメリカ、60035
        • NorthShore University HealthSystem-Highland Park Hospital
      • Lake Forest、Illinois、アメリカ、60045
        • Northwestern Medicine Lake Forest Hospital
      • Mattoon、Illinois、アメリカ、61938
        • Carle Physician Group-Mattoon/Charleston
      • New Lenox、Illinois、アメリカ、60451
        • UC Comprehensive Cancer Center at Silver Cross
      • Orland Park、Illinois、アメリカ、60462
        • University of Chicago Medicine-Orland Park
      • Orland Park、Illinois、アメリカ、60462
        • Northwestern Medicine Orland Park
      • Urbana、Illinois、アメリカ、61801
        • Carle Cancer Center
      • Warrenville、Illinois、アメリカ、60555
        • Northwestern Medicine Cancer Center Warrenville
    • Iowa
      • Ankeny、Iowa、アメリカ、50023
        • UI Health Care Mission Cancer and Blood - Ankeny Clinic
      • Clive、Iowa、アメリカ、50325
        • Mercy Cancer Center-West Lakes
      • Clive、Iowa、アメリカ、50325
        • UI Health Care Mission Cancer and Blood - West Des Moines Clinic
      • Council Bluffs、Iowa、アメリカ、51503
        • Heartland Oncology and Hematology LLP
      • Council Bluffs、Iowa、アメリカ、51503
        • Methodist Jennie Edmundson Hospital
      • Council Bluffs、Iowa、アメリカ、51503
        • Nebraska Cancer Specialists/Oncology Hematology West PC - MEJ
      • Des Moines、Iowa、アメリカ、50309
        • Iowa Methodist Medical Center
      • Des Moines、Iowa、アメリカ、50314
        • Mercy Medical Center - Des Moines
      • Des Moines、Iowa、アメリカ、50309
        • UI Health Care Mission Cancer and Blood - Des Moines Clinic
      • Des Moines、Iowa、アメリカ、50314
        • UI Health Care Mission Cancer and Blood - Laurel Clinic
      • Waukee、Iowa、アメリカ、50263
        • UI Health Care Mission Cancer and Blood - Waukee Clinic
    • Massachusetts
      • Boston、Massachusetts、アメリカ、02111
        • Tufts Medical Center
    • Minnesota
      • Bemidji、Minnesota、アメリカ、56601
        • Sanford Joe Lueken Cancer Center
    • Missouri
      • St Louis、Missouri、アメリカ、63128
        • Mercy Hospital South
    • Montana
      • Anaconda、Montana、アメリカ、59711
        • Community Hospital of Anaconda
      • Billings、Montana、アメリカ、59101
        • Billings Clinic Cancer Center
      • Bozeman、Montana、アメリカ、59715
        • Bozeman Health Deaconess Hospital
      • Great Falls、Montana、アメリカ、59405
        • Benefis Sletten Cancer Institute
      • Kalispell、Montana、アメリカ、59901
        • Logan Health Medical Center
      • Missoula、Montana、アメリカ、59804
        • Community Medical Center
    • Nebraska
      • Omaha、Nebraska、アメリカ、68114
        • Nebraska Methodist Hospital
      • Omaha、Nebraska、アメリカ、68114
        • Oncology Associates PC
      • Omaha、Nebraska、アメリカ、68114
        • Nebraska Cancer Specialists/Oncology Hematology West PC - MECC
    • New Jersey
      • Basking Ridge、New Jersey、アメリカ、07920
        • Memorial Sloan Kettering Basking Ridge
      • Middletown、New Jersey、アメリカ、07748
        • Memorial Sloan Kettering Monmouth
      • Montvale、New Jersey、アメリカ、07645
        • Memorial Sloan Kettering Bergen
    • New York
      • Commack、New York、アメリカ、11725
        • Memorial Sloan Kettering Commack
      • Harrison、New York、アメリカ、10604
        • Memorial Sloan Kettering Westchester
      • New York、New York、アメリカ、10065
        • Memorial Sloan Kettering Cancer Center
      • Uniondale、New York、アメリカ、11553
        • Memorial Sloan Kettering Nassau
    • North Carolina
      • Chapel Hill、North Carolina、アメリカ、27599
        • UNC Lineberger Comprehensive Cancer Center
      • Charlotte、North Carolina、アメリカ、28204
        • Novant Health Presbyterian Medical Center
      • Huntersville、North Carolina、アメリカ、28078
        • Novant Health Cancer Institute - Huntersville
      • Matthews、North Carolina、アメリカ、28105
        • Novant Health Cancer Institute - Matthews
      • Mooresville、North Carolina、アメリカ、28117
        • Novant Health Cancer Institute - Mooresville
    • North Dakota
      • Bismarck、North Dakota、アメリカ、58501
        • Sanford Bismarck Medical Center
      • Fargo、North Dakota、アメリカ、58122
        • Sanford Roger Maris Cancer Center
      • Fargo、North Dakota、アメリカ、58122
        • Sanford Broadway Medical Center
    • Ohio
      • Cincinnati、Ohio、アメリカ、45220
        • Good Samaritan Hospital - Cincinnati
    • Oklahoma
      • Lawton、Oklahoma、アメリカ、73505
        • Cancer Centers of Southwest Oklahoma Research
      • Oklahoma City、Oklahoma、アメリカ、73104
        • University of Oklahoma Health Sciences Center
      • Tulsa、Oklahoma、アメリカ、74146
        • Oklahoma Cancer Specialists and Research Institute-Tulsa
    • Oregon
      • Ontario、Oregon、アメリカ、97914
        • Saint Alphonsus Cancer Care Center-Ontario
      • Portland、Oregon、アメリカ、97239
        • Oregon Health and Science University
    • South Carolina
      • Charleston、South Carolina、アメリカ、29425
        • Medical University of South Carolina
    • South Dakota
      • Sioux Falls、South Dakota、アメリカ、57117-5134
        • Sanford USD Medical Center - Sioux Falls
      • Sioux Falls、South Dakota、アメリカ、57104
        • Sanford Cancer Center Oncology Clinic
    • Tennessee
      • Nashville、Tennessee、アメリカ、37232
        • Vanderbilt University/Ingram Cancer Center
    • Virginia
      • Richmond、Virginia、アメリカ、23235
        • VCU Massey Cancer Center at Stony Point
      • Richmond、Virginia、アメリカ、23298
        • VCU Massey Comprehensive Cancer Center
    • West Virginia
      • Morgantown、West Virginia、アメリカ、26506
        • West Virginia University Healthcare
      • Parkersburg、West Virginia、アメリカ、26101
        • Camden Clark Medical Center
    • Wisconsin
      • Eau Claire、Wisconsin、アメリカ、54701
        • Marshfield Medical Center-EC Cancer Center
      • Marshfield、Wisconsin、アメリカ、54449
        • Marshfield Medical Center-Marshfield
      • Minocqua、Wisconsin、アメリカ、54548
        • Marshfield Medical Center - Minocqua
      • Rice Lake、Wisconsin、アメリカ、54868
        • Marshfield Medical Center-Rice Lake
      • Stevens Point、Wisconsin、アメリカ、54482
        • Marshfield Medical Center-River Region at Stevens Point
      • Weston、Wisconsin、アメリカ、54476
        • Marshfield Medical Center - Weston

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

説明

Inclusion Criteria:

  • Patients must have histologically documented nasopharyngeal carcinoma (NPC) regardless of World Health Organization (WHO) classification (keratinizing squamous cell carcinoma, non-keratinizing, or basaloid squamous cell carcinoma) and regardless of association with Epstein-Barr virus (EBV) and/or human papillomavirus (HPV)

  • Recurrent, metastatic and incurable disease treated with platinum-gemcitabine and prior PD-1/L1 blockade (as first or second-line therapy)

  • Patients are eligible regardless of prior smoking history, p16 immunohistochemistry (IHC) status, PD-L1 expression status, EBV tumor status, EBV viral load at baseline, or tumor genomic alteration status

  • Patients must have at least one measurable lesion (by RECIST v1.1) which has not been previously irradiated that can be accurately measured in at least one dimension (longest diameter to be recorded for non-nodal lesions as >= 10 mm (>= 1 cm) (and short axis for nodal lesions, LN >= 15 mm) with CT scan, MRI, or calipers by clinical exam

  • Patients may have had no more than 2 prior lines of prior systemic therapy for recurrent, metastatic NPC

  • No prior VEGFR targeted therapy permitted

  • Age >= 18 years

  • Eastern Cooperative Oncology Group Performance (ECOG) performance status 0-2

  • Absolute neutrophil count (ANC) >= 1,000/mm^3

  • Hemoglobin >= 9 g/dL

  • Platelet count >= 100,000/mm^3

  • Creatinine or creatinine clearance =< 1.5 mg/dL or >= 30 Modification of Diet in Renal Disease (MDRD)

  • Total bilirubin =< 1.5 x institutional upper limit of normal (ULN); except subjects with Gilbert syndrome who can have a total bilirubin < 3 mg/dL

  • Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGT]) =< 3 x upper limit of normal (ULN)

    • Up to =< 5 allowed with liver metastases

  • Not pregnant and not nursing, because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown. Therefore, for women of childbearing potential only, a negative urine or serum pregnancy test, per institution standard, done =< 7 days prior to registration is required.

    • Pregnant women are excluded from this study because nivolumab, ipilimumab, and cabozantinib are all Class C or D agents with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants, secondary to treatment of the mother with any of the study agents, breastfeeding should be discontinued if the mother is treated with as part of this study (in either arm)

  • No active tumor bleeding: or radiographic evidence of major blood vessel infiltration as judged by the treating investigator

  • Prior -anti-cancer therapy is allowed: Patients need to be recovered from adverse events due to prior anti-cancer therapy (i.e., have residual toxicities > grade 1), with the exception of alopecia. Any life-threatening events clearly attributable to prior immunotherapy exposure that have a high possibility of recurring should warrant exclusion: including severe pneumonitis, grade 4 bullous dermatitis/drug reaction with eosinophilia and systemic symptoms (DRESS), neurologic events such as autoimmune encephalitis transverse myelitis, and/or myocarditis. Maintenance hormonal replacement or long-term hormonal therapy exposure is permitted.

    • No chemotherapy or radiotherapy within 3 weeks (6 weeks for nitrosoureas or mitomycin C) prior to registration. Palliative (limited-field) radiation therapy is permitted, if all of the following criteria are met:

      • Repeat imaging demonstrates no new sites of bone metastases.
      • The lesion being considered for palliative radiation is not a target lesion

  • No patients with a prior malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of the investigational regimen

  • Brain metastases allowed: Patients with treated brain metastases are eligible if follow-up brain imaging 3 weeks after central nervous system (CNS)-directed therapy shows no evidence of progression. Patients with new or progressive brain metastases (active brain metastases) or leptomeningeal disease are eligible if the treating physician determines that immediate CNS specific treatment is not required and is unlikely to be required during the first cycle of therapy

  • Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months prior to registration are eligible for this trial

  • For patients with evidence of chronic hepatitis B (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated

    • Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently receiving treatment, they are eligible if they have an undetectable HCV viral load

  • Solid organ or tissue transplant is allowed: - subsequent therapy with nivolumab increases the risk of organ/tissue rejection. Patients must be instructed that it is crucial they stay in touch with their transplant team during treatment

  • No active autoimmune disease: or history of autoimmune disease that might recur, and which may affect vital organ function or require immune suppressive treatment including systemic corticosteroids. These include but are not limited to patients with a history of

    • Immune related neurologic disease,
    • Multiple sclerosis,
    • Autoimmune (demyelinating) neuropathy,
    • Guillain-Barre syndrome (GBS),
    • Myasthenia gravis;
    • Systemic autoimmune disease such as SLE,
    • Connective tissue diseases,
    • Scleroderma, inflammatory bowel disease (IBD),
    • Crohn's, ulcerative colitis,
    • Patients with a history of toxic epidermal necrolysis (TEN),
    • Stevens-Johnson syndrome, or phospholipid syndrome should be excluded because of the risk of recurrence or exacerbation of disease

  • Patients with vitiligo, endocrine deficiencies including thyroiditis managed with replacement hormones including physiologic corticosteroids are eligible

  • Patients with rheumatoid arthritis and other arthropathies, Sjogren's syndrome, and psoriasis controlled with topical medication and patients with only positive serology, such as antinuclear antibodies (ANA) or anti-thyroid antibodies, should be evaluated for the presence of target organ involvement and potential need for systemic treatment but should otherwise be eligible

  • Pneumonitis should be evaluated for the nature of the disease process, need for treatment prior study treatment, and the risk of exacerbation with study treatment

  • Able to swallow oral medication: No known medical condition causing an inability to swallow oral formulations of agents

  • No condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of study registration. Patients are permitted the use of topical, ocular, intra-articular, intranasal, and inhalational corticosteroids (with minimal systemic absorption). Adrenal replacement steroid doses > 10 mg daily prednisone are permitted. A brief (less than 3 weeks) course of corticosteroids for prophylaxis (e.g., contrast dye allergy) or for treatment of non-autoimmune conditions (e.g., delayed-type hypersensitivity reaction caused by a contact allergen) is permitted

  • Concomitant anticoagulation with coumarin agents (e.g., warfarin), direct thrombin inhibitors (e.g., dabigatran), direct factor Xa inhibitor betrixaban, or platelet inhibitors (e.g., clopidogrel) is prohibited. Allowed anticoagulants are the following:

    • Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH).
    • Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors rivaroxaban, edoxaban, or apixaban in subjects without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week before first dose of study treatment without clinically significant hemorrhagic complications from the anticoagulation regimen or the tumor

  • Concomitant use of any medications or substances that are strong inhibitors or inducers of CYP3A4 is discouraged; if unavoidable, the dose of cabozantinib on study should be adjusted accordingly. Any complementary medications (e.g., herbal supplements or traditional Chinese medicines) intended to treat the disease under study are prohibited

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか？

デザインの詳細

  • 主な目的：処理
  • 割り当て：ランダム化
  • 介入モデル：並列代入
  • マスキング：なし（オープンラベル）

武器と介入

参加者グループ / アーム
介入・治療
アクティブコンパレータ：Arm A (nivolumab, ipilimumab)

Patients receive nivolumab IV over 30 minutes and ipilimumab IV over 30 minutes on day 1 of each cycle. Cycles repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Patients undergo CT or MRI and collection of blood samples throughout the trial.
生物学的：Ipilimumab

Given IV

他の名前：
  • 抗細胞傷害性 T リンパ球関連抗原 4 モノクローナル抗体
  • BMS-734016
  • イピリムマブ バイオシミラー CS1002
  • MDX-010
  • MDX-CTLA4
  • ヤーボイ
  • MDX010
  • BMS734016
  • BMS 734016
手順：Magnetic Resonance Imaging

Undergo MRI

他の名前：
  • MRI
  • 磁気共鳴
  • 磁気共鳴画像スキャン
  • 医用画像、磁気共鳴 / 核磁気共鳴
  • 氏
  • MRイメージング
  • MRI スキャン
  • NMRイメージング
  • NMRI
  • 核磁気共鳴イメージング
  • 磁気共鳴画像法 (MRI)
  • sMRI
  • 磁気共鳴画像法（手順）
  • 構造MRI
生物学的：Nivolumab

Given IV

他の名前：
  • BMS-936558
  • MDX-1106
  • NIVO
  • ONO-4538
  • オプジーボ
  • CMAB819
  • ニボルマブ バイオシミラー CMAB819
  • MDX1106
  • BMS 936558
  • ABP206
  • ニボルマブ バイオシミラー ABP 206
  • BCD-263
  • ニボルマブ バイオシミラー BCD-263
  • BMS936558
  • 小野 4538
  • オノ4538
手順：Biospecimen Collection

Undergo collection of blood samples

他の名前：
  • 生物学的サンプルの収集
  • 採取された生体試料
  • 標本収集
  • サンプル収集
手順：Computed Tomography

Undergo CT scan

他の名前：
  • CT
  • 猫
  • CATスキャン
  • コンピューター断層撮影
  • コンピュータ化されたアキシャルトモグラフィー
  • CTスキャン
  • トモグラフィー
  • コンピューター断層撮影 (手順)
  • コンピューター断層撮影 (CT) スキャン
  • 診断CATスキャン
  • 診断CATスキャンサービスタイプ
実験的：Arm B (nivolumab, ipilimumab, cabozantinib)

Patients receive nivolumab IV over 30 minutes and ipilimumab IV over 30 minutes on day 1 and cabozantinib S-malate PO daily on days 1-28 of each cycle. Cycles repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Patients may continue with cabozantinib S-malate after 2 years per treating investigator. Patients undergo CT or MRI and collection of blood samples throughout the trial.
生物学的：Ipilimumab

Given IV

他の名前：
  • 抗細胞傷害性 T リンパ球関連抗原 4 モノクローナル抗体
  • BMS-734016
  • イピリムマブ バイオシミラー CS1002
  • MDX-010
  • MDX-CTLA4
  • ヤーボイ
  • MDX010
  • BMS734016
  • BMS 734016
手順：Magnetic Resonance Imaging

Undergo MRI

他の名前：
  • MRI
  • 磁気共鳴
  • 磁気共鳴画像スキャン
  • 医用画像、磁気共鳴 / 核磁気共鳴
  • 氏
  • MRイメージング
  • MRI スキャン
  • NMRイメージング
  • NMRI
  • 核磁気共鳴イメージング
  • 磁気共鳴画像法 (MRI)
  • sMRI
  • 磁気共鳴画像法（手順）
  • 構造MRI
薬：Cabozantinib S-malate

Given PO

他の名前：
  • BMS-907351
  • カボメティクス
  • コメトリック
  • XL-184
  • XL184
  • 特大 184
生物学的：Nivolumab

Given IV

他の名前：
  • BMS-936558
  • MDX-1106
  • NIVO
  • ONO-4538
  • オプジーボ
  • CMAB819
  • ニボルマブ バイオシミラー CMAB819
  • MDX1106
  • BMS 936558
  • ABP206
  • ニボルマブ バイオシミラー ABP 206
  • BCD-263
  • ニボルマブ バイオシミラー BCD-263
  • BMS936558
  • 小野 4538
  • オノ4538
手順：Biospecimen Collection

Undergo collection of blood samples

他の名前：
  • 生物学的サンプルの収集
  • 採取された生体試料
  • 標本収集
  • サンプル収集
手順：Computed Tomography

Undergo CT scan

他の名前：
  • CT
  • 猫
  • CATスキャン
  • コンピューター断層撮影
  • コンピュータ化されたアキシャルトモグラフィー
  • CTスキャン
  • トモグラフィー
  • コンピューター断層撮影 (手順)
  • コンピューター断層撮影 (CT) スキャン
  • 診断CATスキャン
  • 診断CATスキャンサービスタイプ

この研究は何を測定していますか？

主要な結果の測定

結果測定
メジャーの説明
時間枠
Progression-free survival (PFS)
時間枠：From randomization to the first of either progression or death from any cause, or censored at last known tumor assessment date, assessed up to 2 years

PFS will be estimated using the Kaplan-Meier method, where the log-rank test will be used to compare the 2 treatment arms.
From randomization to the first of either progression or death from any cause, or censored at last known tumor assessment date, assessed up to 2 years

二次結果の測定

結果測定
メジャーの説明
時間枠
Overall survival (OS)
時間枠：From randomization to death from any cause, or censored at last known follow-up, assessed up to 2 years

OS will be estimated using the Kaplan-Meier method, where the log-rank test will be used to compare the 2 treatment arms.
From randomization to death from any cause, or censored at last known follow-up, assessed up to 2 years
Incidence of adverse events
時間枠：Up to 2 years

The maximum grade for each type of adverse event will be summarized using Common Terminology Criteria for Adverse Events version 5.0. The frequency and percentage of grade 3+ adverse events will be compared between the 2 treatment arms. Comparisons between arms will be made by using either the chi-square or Fisher's exact test.
Up to 2 years
Response by subgroups of interest
時間枠：Up to 2 years

Will also report and compare the overall response rate (ORR) between different subgroups of interest (primary or acquired PD-1/L1 inhibitor resistance in the prior line of therapy (further defined below), etc.). These comparisons will be done via chi-square or Fisher's exact tests. We'll also assess primary versus acquired resistance to prior PD-1 inhibition in each arm as well. While not a formal stratification, in the interim and final analysis we'll also descriptively assess these subgroups between arms as well.
Up to 2 years
ORR
時間枠：Up to 2 years

The response rate will be compared via chi-square or Fisher's exact tests between the 2 treatment arms using both the Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 criteria and also separately for the immune-modified RECIST criteria.
Up to 2 years
Predictors of response
時間枠：Up to 2 years

Will correlate the baseline data (Epstein-Barr virus viral load, p16 immunohistochemistry status, smoking history, and PD-L1 score) with ORR data. For this analysis, logistic regression models will be assessed using the baseline data to predict binary response data. Odds ratios and 95% confidence intervals will be reported. Will also summarize the data using descriptive statistics and graphical methods.
Up to 2 years

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

National Cancer Institute (NCI)

捜査官

  • 主任研究者：Ari J Rosenberg、Alliance for Clinical Trials in Oncology

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2024年2月19日

一次修了 (推定)

2028年12月6日

研究の完了 (推定)

2028年12月6日

試験登録日

最初に提出

2023年6月13日

QC基準を満たした最初の提出物

2023年6月13日

最初の投稿 (実際)

2023年6月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年11月2日

QC基準を満たした最後の更新が送信されました

2026年10月30日

最終確認日

2026年10月1日

詳しくは

本研究に関する用語

追加の関連 MeSH 用語

その他の研究ID番号

  • NCI-2023-04469
  • U10CA180821 (米国 NIH グラント/契約)
  • NCI-2023-04469 (レジストリ識別子：CTRP (Clinical Trial Reporting Program))
  • A092105 (その他の識別子：CTEP)
  • A092105 (その他の識別子：Alliance for Clinical Trials in Oncology)

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page.

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

はい

米国FDA規制機器製品の研究

いいえ

米国で製造され、米国から輸出された製品。

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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