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항암제 약물, 카보 탄 티닙의 첨가, 면역 요법 약물 Cemiplimab (regn2810), 청소년 및 고급 adrenocortical cancer 성인의 첨가

2026년 11월 5일 업데이트: National Cancer Institute (NCI)

Adolescents 및 adrenocortical cancer를 가진 성인의 Cemiplimab (Cabo-Cemiplimab)과 Cabozantinib와 함께 Cabozantinib의 2 상 연구

This phase II trial compares the effect of giving cabozantinib with or without cemiplimab in patients with adrenocortical cancer that has spread to nearby tissue or lymph nodes (locally advanced), and that cannot be removed by surgery (unresectable) or that has come back after a period of improvement (recurrent) or that has spread from where it first started (primary site) to other places in the body (metastatic). Cabozantinib is in a class of medications called tyrosine kinase inhibitors. It works by blocking the action of an abnormal protein that signals cancer cells to multiply, which may help keep cancer cells from growing. Immunotherapy with monoclonal antibodies, such as cemiplimab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving cabozantinib with cemiplimab may kill more tumor cells in patients with locally advanced unresectable or recurrent/metastatic adrenocortical cancer.

연구 개요

상태

모병

정황

개입 / 치료

상세 설명

PRIMARY OBJECTIVE:

I. To determine whether the combination of cabozantinib plus cemiplimab (REGN2810) (Cabo-Cemiplimab [REGN2810]) improves progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors (RECIST) version (v.) 1.1 relative to cabozantinib alone in patients with locally advanced unresectable or recurrent/metastatic advanced adrenocortical cancer.

SECONDARY OBJECTIVES:

I. To assess tolerability and adverse events of Cabo-Cemiplimab (REGN2810) in advanced adrenocortical cancer (ACC) patients.

II. To assess objective response rate as per RECIST v 1.1. III. To assess duration of objective response, time to progression (TTP), and overall survival (OS) in ACC patients receiving Cabo-Cemiplimab (REGN2810).

EXPLORATORY OBJECTIVE:

I. To assess PFS from re-registration (per RECIST 1.1) and OS for patients who crossover to receive Cabo-Cemiplimab after progressing on cabozantinib alone.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM A: Patients receive cabozantinib orally (PO) once daily (QD) on days 1-21 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients undergo computed tomography (CT) scan or magnetic resonance imaging (MRI) and blood sample collection throughout the study. Upon disease progression, patients may elect to crossover to receive combination therapy on Arm B.

ARM B: Patients receive cemiplimab intravenously (IV) over 30 minutes on day 1 and cabozantinib PO QD on days 1-21 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan or MRI and blood sample collection throughout the study.

After completion of study treatment, patients are followed up every 12 weeks until disease progression and then every 6 months for 4 years post-registration.

연구 유형

중재적

등록 (추정된)

48

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

  • 미국
    • Arizona
      • Phoenix, Arizona, 미국, 85054
        • 모병
        • Mayo Clinic Hospital in Arizona
        • 연락하다:
          • Site Public Contact
          • 전화번호: 855-776-0015
        • 수석 연구원:
          • Julie E. Hallanger Johnson
    • California
      • La Jolla, California, 미국, 92093
        • 모병
        • UC San Diego Moores Cancer Center
        • 연락하다:
        • 수석 연구원:
          • Yu-Wei Chen
      • Madera, California, 미국, 93636
        • 모병
        • Valley Children's Hospital
        • 연락하다:
        • 수석 연구원:
          • Ruetima Titapiwatanakun
    • Colorado
      • Aurora, Colorado, 미국, 80045
        • 모병
        • UCHealth University of Colorado Hospital
        • 수석 연구원:
          • Laura Graham
        • 연락하다:
          • Site Public Contact
          • 전화번호: 720-848-0650
    • Florida
      • Jacksonville, Florida, 미국, 32224-9980
        • 모병
        • Mayo Clinic in Florida
        • 연락하다:
          • Site Public Contact
          • 전화번호: 855-776-0015
        • 수석 연구원:
          • Julie E. Hallanger Johnson
    • Illinois
      • Chicago, Illinois, 미국, 60611
        • 모병
        • Lurie Children's Hospital-Chicago
        • 연락하다:
          • Site Public Contact
          • 전화번호: 773-880-4562
        • 수석 연구원:
          • Elizabeth A. Sokol
      • Chicago, Illinois, 미국, 60611
        • 모병
        • Northwestern University
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
      • Danville, Illinois, 미국, 61832
        • 모병
        • Carle at The Riverfront
        • 수석 연구원:
          • Priyank P. Patel
        • 연락하다:
      • DeKalb, Illinois, 미국, 60115
        • 모병
        • Northwestern Medicine Cancer Center Kishwaukee
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
      • Effingham, Illinois, 미국, 62401
        • 모병
        • Carle Physician Group-Effingham
        • 연락하다:
        • 수석 연구원:
          • Priyank P. Patel
      • Geneva, Illinois, 미국, 60134
        • 모병
        • Northwestern Medicine Cancer Center Delnor
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
      • Glenview, Illinois, 미국, 60026
        • 모병
        • Northwestern Medicine Glenview Outpatient Center
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
          • Site Public Contact
          • 전화번호: 312-695-1102
      • Grayslake, Illinois, 미국, 60030
        • 모병
        • Northwestern Medicine Grayslake Outpatient Center
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
          • Site Public Contact
          • 전화번호: 312-695-1102
      • Lake Forest, Illinois, 미국, 60045
        • 모병
        • Northwestern Medicine Lake Forest Hospital
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
      • Mattoon, Illinois, 미국, 61938
        • 모병
        • Carle Physician Group-Mattoon/Charleston
        • 연락하다:
        • 수석 연구원:
          • Priyank P. Patel
      • Normal, Illinois, 미국, 61761
        • 모병
        • Carle BroMenn Medical Center
        • 수석 연구원:
          • Priyank P. Patel
        • 연락하다:
      • Normal, Illinois, 미국, 61761
        • 모병
        • Carle Cancer Institute Normal
        • 수석 연구원:
          • Priyank P. Patel
        • 연락하다:
      • Oak Brook, Illinois, 미국, 60523
      • Orland Park, Illinois, 미국, 60462
      • Shiloh, Illinois, 미국, 62269
        • 모병
        • Memorial Hospital East
        • 연락하다:
        • 수석 연구원:
          • Nikolaos Trikalinos
      • Urbana, Illinois, 미국, 61801
        • 모병
        • Carle Cancer Center
        • 연락하다:
        • 수석 연구원:
          • Priyank P. Patel
      • Warrenville, Illinois, 미국, 60555
        • 모병
        • Northwestern Medicine Cancer Center Warrenville
        • 수석 연구원:
          • Mary F. Mulcahy
        • 연락하다:
    • Iowa
      • Ankeny, Iowa, 미국, 50023
        • 모병
        • UI Health Care Mission Cancer and Blood - Ankeny Clinic
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-3305
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Carroll, Iowa, 미국, 51401
        • 모병
        • Saint Anthony Regional Hospital
        • 연락하다:
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Clive, Iowa, 미국, 50325
        • 모병
        • UI Health Care Mission Cancer and Blood - West Des Moines Clinic
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-3305
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, 미국, 50314
        • 모병
        • Broadlawns Medical Center
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-282-2200
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, 미국, 50314
        • 모병
        • Mercy Medical Center - Des Moines
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-3305
        • 수석 연구원:
          • Richard L. Deming
      • Des Moines, Iowa, 미국, 50309
        • 모병
        • Iowa Methodist Medical Center
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-6727
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, 미국, 50309
        • 모병
        • UI Health Care Mission Cancer and Blood - Des Moines Clinic
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-3305
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Des Moines, Iowa, 미국, 50314
        • 모병
        • UI Health Care Mission Cancer and Blood - Laurel Clinic
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-3305
        • 수석 연구원:
          • Seema Harichand-Herdt
      • Fort Dodge, Iowa, 미국, 50501
        • 모병
        • UI Healthcare Mission Cancer and Blood - Fort Dodge
        • 수석 연구원:
          • Seema Harichand-Herdt
        • 연락하다:
      • Waukee, Iowa, 미국, 50263
        • 모병
        • UI Health Care Mission Cancer and Blood - Waukee Clinic
        • 연락하다:
          • Site Public Contact
          • 전화번호: 515-241-3305
        • 수석 연구원:
          • Seema Harichand-Herdt
    • Massachusetts
      • Boston, Massachusetts, 미국, 02215
        • 모병
        • Dana-Farber Cancer Institute
        • 수석 연구원:
          • Stephanie A. Berg
        • 연락하다:
          • Site Public Contact
          • 전화번호: 877-442-3324
    • Michigan
      • Ann Arbor, Michigan, 미국, 48109
        • 모병
        • University of Michigan Rogel Cancer Center
        • 수석 연구원:
          • Francis P. Worden
        • 연락하다:
    • Minnesota
      • Rochester, Minnesota, 미국, 55905
        • 모병
        • Mayo Clinic in Rochester
        • 연락하다:
          • Site Public Contact
          • 전화번호: 855-776-0015
        • 수석 연구원:
          • Julie E. Hallanger Johnson
    • Missouri
      • City of Saint Peters, Missouri, 미국, 63376
        • 모병
        • Siteman Cancer Center at Saint Peters Hospital
        • 연락하다:
        • 수석 연구원:
          • Nikolaos Trikalinos
      • Creve Coeur, Missouri, 미국, 63141
        • 모병
        • Siteman Cancer Center at West County Hospital
        • 연락하다:
        • 수석 연구원:
          • Nikolaos Trikalinos
      • Kansas City, Missouri, 미국, 64108
        • 모병
        • Children's Mercy Hospitals and Clinics
        • 수석 연구원:
          • Keith J. August
        • 연락하다:
      • Springfield, Missouri, 미국, 65807
        • 모병
        • CoxHealth South Hospital
        • 수석 연구원:
          • Jay W. Carlson
        • 연락하다:
          • Site Public Contact
          • 전화번호: 417-269-4520
      • St Louis, Missouri, 미국, 63110
        • 모병
        • Washington University School of Medicine
        • 연락하다:
        • 수석 연구원:
          • Nikolaos Trikalinos
      • St Louis, Missouri, 미국, 63129
        • 모병
        • Siteman Cancer Center-South County
        • 연락하다:
        • 수석 연구원:
          • Nikolaos Trikalinos
      • St Louis, Missouri, 미국, 63136
        • 모병
        • Siteman Cancer Center at Christian Hospital
        • 연락하다:
        • 수석 연구원:
          • Nikolaos Trikalinos
    • Nebraska
      • Bellevue, Nebraska, 미국, 68123
        • 모병
        • Nebraska Medicine-Bellevue
        • 연락하다:
        • 수석 연구원:
          • Apar Kishor Ganti
      • Omaha, Nebraska, 미국, 68198
        • 모병
        • University of Nebraska Medical Center
        • 연락하다:
        • 수석 연구원:
          • Apar Kishor Ganti
      • Omaha, Nebraska, 미국, 68118
        • 모병
        • Nebraska Medicine-Village Pointe
        • 연락하다:
          • Site Public Contact
          • 전화번호: 402-559-5600
        • 수석 연구원:
          • Apar Kishor Ganti
    • New Jersey
      • Basking Ridge, New Jersey, 미국, 07920
        • 모병
        • Memorial Sloan Kettering Basking Ridge
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
      • Middletown, New Jersey, 미국, 07748
        • 모병
        • Memorial Sloan Kettering Monmouth
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
      • Montvale, New Jersey, 미국, 07645
        • 모병
        • Memorial Sloan Kettering Bergen
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
    • New York
      • Commack, New York, 미국, 11725
        • 모병
        • Memorial Sloan Kettering Commack
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
      • Harrison, New York, 미국, 10604
        • 모병
        • Memorial Sloan Kettering Westchester
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
      • New York, New York, 미국, 10065
        • 모병
        • Memorial Sloan Kettering Cancer Center
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
      • Uniondale, New York, 미국, 11553
        • 모병
        • Memorial Sloan Kettering Nassau
        • 연락하다:
          • Site Public Contact
          • 전화번호: 212-639-7592
        • 수석 연구원:
          • Nitya P. Raj
    • North Carolina
      • Cary, North Carolina, 미국, 27518
        • 정지된
        • Duke Cancer Center Cary
      • Durham, North Carolina, 미국, 27710
        • 모병
        • Duke University Medical Center
        • 연락하다:
          • Site Public Contact
          • 전화번호: 888-275-3853
        • 수석 연구원:
          • Diane L. Reidy-lagunes
      • Raleigh, North Carolina, 미국, 27609
        • 모병
        • Duke Cancer Center Raleigh
        • 연락하다:
        • 수석 연구원:
          • Diane L. Reidy-lagunes
    • Ohio
      • Columbus, Ohio, 미국, 43210
        • 모병
        • Ohio State University Comprehensive Cancer Center
        • 연락하다:
        • 수석 연구원:
          • Bhavana Konda
    • Oklahoma
      • Oklahoma City, Oklahoma, 미국, 73104
        • 모병
        • University of Oklahoma Health Sciences Center
        • 연락하다:
        • 수석 연구원:
          • Adanma Anji Ayanambakkam Attanathi
    • Pennsylvania
      • Pittsburgh, Pennsylvania, 미국, 15224
        • 모병
        • Children's Hospital of Pittsburgh of UPMC
        • 연락하다:
        • 수석 연구원:
          • Brittani K. Seynnaeve
    • South Carolina
      • Boiling Springs, South Carolina, 미국, 29316
        • 모병
        • Prisma Health Cancer Institute - Spartanburg
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Columbia, South Carolina, 미국, 29203
        • 모병
        • Prisma Health Richland Hospital
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Easley, South Carolina, 미국, 29640
        • 모병
        • Prisma Health Cancer Institute - Easley
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Greenville, South Carolina, 미국, 29605
        • 모병
        • BI-LO Charities Children's Cancer Center
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Greenville, South Carolina, 미국, 29605
        • 모병
        • Prisma Health Cancer Institute - Faris
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Greenville, South Carolina, 미국, 29605
        • 모병
        • Prisma Health Cancer Institute - Butternut
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Greenville, South Carolina, 미국, 29615
        • 모병
        • Prisma Health Cancer Institute - Eastside
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Greer, South Carolina, 미국, 29650
        • 모병
        • Prisma Health Cancer Institute - Greer
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
      • Seneca, South Carolina, 미국, 29672
        • 모병
        • Prisma Health Cancer Institute - Seneca
        • 수석 연구원:
          • Aniket Saha
        • 연락하다:
    • Tennessee
      • Memphis, Tennessee, 미국, 38105
        • 모병
        • Saint Jude Children's Research Hospital
        • 연락하다:
        • 수석 연구원:
          • Catherine G. Lam
    • Texas
      • Austin, Texas, 미국, 78723
      • Dallas, Texas, 미국, 75390
        • 모병
        • UT Southwestern/Simmons Cancer Center-Dallas
        • 연락하다:
        • 수석 연구원:
          • Suzanne M. Cole
      • Dallas, Texas, 미국, 75235
        • 모병
        • Parkland Memorial Hospital
        • 연락하다:
        • 수석 연구원:
          • Suzanne M. Cole
      • Dallas, Texas, 미국, 75237
        • 모병
        • UT Southwestern Simmons Cancer Center - RedBird
        • 수석 연구원:
          • Suzanne M. Cole
        • 연락하다:
      • Fort Worth, Texas, 미국, 76104
      • Fort Worth, Texas, 미국, 76104
        • 모병
        • UT Southwestern/Simmons Cancer Center-Fort Worth
        • 연락하다:
        • 수석 연구원:
          • Suzanne M. Cole
      • Richardson, Texas, 미국, 75080
        • 모병
        • UT Southwestern Clinical Center at Richardson/Plano
        • 연락하다:
        • 수석 연구원:
          • Suzanne M. Cole
      • San Antonio, Texas, 미국, 78207
        • 모병
        • Children's Hospital of San Antonio
        • 연락하다:
        • 수석 연구원:
          • Julie Voeller
      • San Antonio, Texas, 미국, 78229
        • 모병
        • University of Texas Health Science Center at San Antonio
        • 연락하다:
        • 수석 연구원:
          • Aaron J. Sugalski
    • Virginia
      • Richmond, Virginia, 미국, 23235
        • 모병
        • VCU Massey Cancer Center at Stony Point
        • 연락하다:
        • 수석 연구원:
          • Asit K. Paul
      • Richmond, Virginia, 미국, 23298
        • 모병
        • VCU Massey Comprehensive Cancer Center
        • 수석 연구원:
          • Asit K. Paul
        • 연락하다:
    • Washington
      • Seattle, Washington, 미국, 98195
        • 모병
        • University of Washington Medical Center - Montlake
        • 연락하다:
          • Site Public Contact
          • 전화번호: 800-804-8824
        • 수석 연구원:
          • Keith D. Eaton
      • Seattle, Washington, 미국, 98109
        • 모병
        • Fred Hutchinson Cancer Center
        • 연락하다:
          • Site Public Contact
          • 전화번호: 800-804-8824
        • 수석 연구원:
          • Keith D. Eaton

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

12년 이상 (어린이, 성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • STEP 1: Patients must have documented histologically or cytologically confirmed adrenocortical carcinoma

  • STEP 1: Locally advanced unresectable or recurrent/metastatic disease

  • STEP 1: Evaluable disease as defined by RECIST v 1.1

  • STEP 1: Up to 3 prior lines of systemic therapy will be allowed in the unresectable/recurrent/metastatic setting. Treatment naïve patients will be allowed.

    • Note: Combination etoposide, doxorubicin, cisplatin, and mitotane (EDP-M) is considered 1 line of therapy. For patients who received mitotane ≤ 6 months prior to registration, mitotane should be discontinued 28 days prior to study registration AND a mitotane level must be documented to be < 2 mg/L prior to registration. Patients who have received mitotane within 6 months of enrollment and who have mitotane levels ≥ 2 mg/L will not be eligible to enroll

  • STEP 1: No prior treatment with cabozantinib or other cMET inhibitors, or anti-CTLA-4, or anti-PD-1/PD-L1 therapy

  • STEP 1: Prior external beam radiation therapy (any area radiated within a month prior to study registration cannot be used as an index lesion and only growth outside of the radiation field can be considered for disease progression), systemic cytotoxic chemotherapy, targeted therapies will be allowed, as long as not administered within 14 days before study registration, and provided any acute treatment-related associated toxicities have recovered to ≤ grade 1 except for alopecia, peripheral neuropathy or other residual toxicities that are not deemed clinically significant

  • STEP 1: Potential trial participants should have recovered from clinically significant adverse events, and wound healing is clinically adequate of their most recent therapy/intervention prior to enrollment

  • STEP 1: Age 12 years and above; and BSA ≥ 1.2m^2

  • STEP 1:

    • Eastern Cooperative Oncology Group (ECOG) performance 0 - 2 (age 18 and above); or
    • Patients 12 to <16 years of age will be assessed by the Lansky scale and should have a score ≥ 50; or
    • Patients ≥ 16 to <18 years of age will be assessed by the Karnofsky scale, and should have a score ≥ 50

  • STEP 1: Absolute neutrophil count (ANC) ≥ 1,000/mcL without colony stimulating factor support within 2 weeks prior

    • Transfusion support is allowed if ≥ 7 days from obtaining required initial laboratory

  • STEP 1: Platelet count ≥ 100,000/mcL

    • Transfusion support is allowed if ≥ 7 days from obtaining required initial laboratory

  • STEP 1: Hemoglobin ≥ 8 g/dL

    • Transfusion support is allowed if ≥ 7 days from obtaining required initial laboratory

  • STEP 1: Total bilirubin ≤ 1.5 x upper limit of normal (ULN)

    • For patients with known Gilbert's disease, bilirubin ≤ 3 mg/dL

  • STEP 1: Aspartate aminotransferase (AST)(serum glutamic oxaloacetic transaminase [SGOT])/ alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) ≤ 3 x upper limit of normal (ULN)

  • STEP 1: Random Urine Creatinine Ratio (UPCR) ≤ 1 mg/mg

  • STEP 1: Calculated (Calc.) creatinine clearance ≥ 30 mL/min

  • STEP 1: Mitotane level < 2 mg/L*

    • Only applicable for patients who have received mitotane ≤ 6 months prior to registration

  • STEP 1: Must have assessment of adrenal steroid production within 3 months prior to registration as patients will be stratified based on corticosteroid production

    • Patients will be classified as corticosteroid producing if random plasma adrenocorticotropic hormone (ACTH) is < 20 pg/mL plus random serum cortisol is > 20 mcg/dL in the absence of anti-cortisol therapy. Patients already on anti-cortisol therapy will be classified as having corticosteroid producing tumors regardless of their plasma ACTH and serum cortisol levels, as these levels can be affected by anti-cortisol therapy

  • STEP 1: Not pregnant and not nursing, because this study involves an agent that has known genotoxic, mutagenic and teratogenic effects based on animal reproduction studies. Therefore, for women of childbearing potential only, a negative urine or serum pregnancy test, per institution standard, done ≤ 14 days prior to registration is required

  • STEP 1: Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional within 28 days of registration. To be eligible for this trial, patients should be class II or better

  • STEP 1: No known history of congenital long QT syndrome

  • STEP 1: No known history of myocarditis

  • STEP 1: No myocardial infarction (MI) or unstable angina within 6 months of registration

  • STEP 1: No clinically significant gastrointestinal abnormalities that may increase the risk for gastrointestinal bleeding within 6 months of registration including, but not limited to: active peptic ulcer, known endoluminal metastatic lesion(s) with history of bleeding, inflammatory bowel disease, or other gastrointestinal conditions with increased risk of perforation

  • STEP 1: No history of gastrointestinal (GI) perforation within 6 months of registration

  • STEP 1: No known tumor with invasion into the GI tract from the outside causing increased risk of perforation or bleeding within 28 days of registration

  • STEP 1: No current radiologic or clinical evidence of pancreatitis

  • STEP 1: No history of clinically significant non-healing wounds or ulcers within 28 days of registration

  • STEP 1: No uncontrolled hypertension within 14 days of registration (defined as sustained systolic blood pressure (SBP) ≥ 150 mmHg and/or diastolic blood pressure (DBP) ≥ 90 mmHg despite optimal medical management)

  • STEP 1: No known endobronchial lesions involving the main or lobar bronchi and/or lesions infiltrating major pulmonary vessels that increase the risk of pulmonary hemorrhage. (CT with contrast is recommended to evaluate such lesions.). No hemoptysis greater than ½ teaspoon (2.5 mL) or any other signs of pulmonary hemorrhage within the 3 months prior to registration

  • STEP 1: No history of pneumonitis

  • STEP 1: No known tumor invading or encasing any major blood vessels

  • STEP 1: No history of fracture within 28 days of registration

  • STEP 1: No known brain metastases or cranial epidural disease unless adequately treated with radiotherapy and/or surgery (including radiosurgery) and stable for at least 4 weeks after major surgery (e.g., removal or biopsy of brain metastasis) before registration. Eligible patients must be neurologically asymptomatic and without corticosteroid treatment at the time of the start of study treatment

  • STEP 1: Major surgery (e.g., laparoscopic nephrectomy, GI surgery, within 2 weeks before registration. Minor surgeries within 10 days before registration. Patients with clinically relevant ongoing complications from prior surgery are not eligible

  • STEP 1: Verbalizes the ability to swallow oral tablet formulation

  • STEP 1: No history of allergic reaction attributed to compounds of similar chemical or biological composition to cabozantinib

  • STEP 1: Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen will be eligible

  • STEP 1: HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months prior to registration are eligible for this trial

  • STEP 1: For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated

  • STEP 1: Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load

  • STEP 1: 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 systemic lupus erythematosus (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, Sjögren'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

  • STEP 1: No steroid use > 10 mg prednisone equivalents daily. A brief course of corticosteroids for prophylaxis or for treatment of non-autoimmune conditions (e.g., delayed-type hypersensitivity reaction caused by contact allergen) is permitted, as is steroid pre-medication for contrast allergy

  • STEP 1: Chronic concomitant treatment with strong inhibitors of CYP3A4 is not allowed on this study. Patients on strong CYP3A4 inhibitors must discontinue the drug for 14 days prior to registration on the study

  • STEP 1: Chronic concomitant treatment with strong CYP3A4 inducers is not allowed. Patients must discontinue the drug 14 days prior to the start of study treatment

  • STEP 1: Herbal supplements and traditional Chinese medicines are not allowed

  • STEP 1: Active treatment with coumarin agents (e.g., warfarin), direct thrombin inhibitors (e.g., dabigatran), direct Xa inhibitor betrixaban or platelet inhibitors (e.g., clopidogrel) within 5 days of registration. Allowed use of anticoagulants include: 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, apixaban. Also use of anticoagulants is allowed in patients with known brain metastases who are on a stable dose of the anticoagulant for at least 1 week prior to registration without clinically significant hemorrhagic complications from the anticoagulation regimen or the tumor

  • STEP 2 (CROSSOVER): Patients must have demonstrated radiographic progression of disease on cabozantinib monotherapy (Arm A) per RECIST version 1.1 criteria

    • Patients must cross-over to Arm C within 4 weeks (+/- 1 week) after radiographic documented progression and do not need to have a repeat radiographic assessment prior to starting cabozantinib and cemiplimab (REGN2810). The progression CT may serve as eligibility for crossover and as the baseline tumor measurement

  • STEP 2 (CROSSOVER): Patients that were discontinued on cabozantinib, or currently meet criteria for discontinuation of cabozantinib due to toxicity are not eligible to cross-over.

    • Note: Patients who underwent dose reduction of cabozantinib during treatment on Arm A will not re-escalate dose at or after cross-over to Cabo-Cemiplimab (REGN2810) (Arm B)

  • STEP 2 (CROSSOVER): Not pregnant and not nursing, because this study involves an agent that has known genotoxic, mutagenic and teratogenic effects. Therefore, for women of childbearing potential only, a negative serum or urine pregnancy test done ≤ 14 days prior to re-registration is required

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 크로스오버 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Arm A (cabozantinib)

Patients receive cabozantinib PO QD on days 1-21 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan or MRI and blood sample collection throughout the study. Upon disease progression, patients may elect to crossover to receive combination therapy on Arm B.
절차: Biospecimen Collection

Undergo blood sample collection

다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
절차: Computed Tomography

Undergo CT scan

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
의약품: Cabozantinib

Given PO
실험적: Arm B (cabozantinib and cemiplimab)

Patients receive cemiplimab IV over 30 minutes on day 1 and cabozantinib PO QD on days 1-21 of each cycle. Cycles repeat every 21 days for 2 years in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan or MRI and blood sample collection throughout the study.
절차: Biospecimen Collection

Undergo blood sample collection

다른 이름들:
  • 생물학적 샘플 수집
  • 생체 표본 수집
  • 표본 수집
  • 샘플 수집
절차: Magnetic Resonance Imaging

Undergo MRI

다른 이름들:
  • MRI
  • 자기 공명
  • 자기공명영상 스캔
  • 의료영상, 자기공명 / 핵자기공명
  • 씨
  • MR 이미징
  • MRI 검사
  • NMR 이미징
  • NMRI
  • 핵자기공명영상
  • 자기공명영상(MRI)
  • SMRI
  • 자기공명영상(시술)
  • 구조적 MRI
절차: Computed Tomography

Undergo CT scan

다른 이름들:
  • CT
  • 고양이
  • 고양이 스캔
  • 컴퓨터 축 단층 촬영
  • 전산화 단층 촬영
  • CT 스캔
  • 단층 촬영
  • 컴퓨터 축 단층 촬영(시술)
  • 컴퓨터 단층촬영(CT) 스캔
  • 진단 CAT 스캔
  • 진단 CAT 스캔 서비스 유형
의약품: Cabozantinib

Given PO

생물학적: Cemiplimab

Given IV

다른 이름들:
  • REGN2810
  • 세미플리맙 RWLC
  • 세미플리맙-rwlc
  • 리브타요
  • REGN 2810
  • REGN-2810

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Progression free survival (PFS)
기간: From registration to either progression or death, assessed up to 4 years post-registration

Per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v 1.1). Will be analyzed using an intention-to-treat approach. Kaplan-Meier methodology will be used to estimate the distributions for the treatment arms. The hazard ratio, median PFS, and estimated PFS rates at 5, 10 and 15 months will be estimated along with corresponding 95% confidence intervals. A one-sided log rank-test will be used to compare the PFS distributions between the two treatment arms.
From registration to either progression or death, assessed up to 4 years post-registration

2차 결과 측정

결과 측정
측정값 설명
기간
Incidence of adverse events
기간: Up to 4 years post-registration

Adverse events will be recorded using National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0 for each patient. Frequency tables and summary statistics will be used and with the appropriate methods of evaluating categorical and continuous data.
Up to 4 years post-registration
Objective response rate
기간: Up to 4 years post-registration

Will be assessed based on RECIST 1.1 criteria and will be summarized by treatment arm. will be calculated as the number of patients who achieve a response (partial response, complete response) divided by the total number of patients randomized to the corresponding treatment arm. A contingency table comparing treatment arms and responders to non-responders will be generated and a Fisher's exact test with a p-value cutoff of 0.05 will be used for determining whether evidence of a significant association between treatment and response is found.
Up to 4 years post-registration
Duration of response
기간: From first date of the patient achieving either a complete or partial response and progression (via RECIST v 1.1), assessed up to 4 years post-registration

Kaplan-Meier methodology will be used to estimate the distributions of duration of response and a log-rank test between treatment arm will be calculated with corresponding p-value.
From first date of the patient achieving either a complete or partial response and progression (via RECIST v 1.1), assessed up to 4 years post-registration
Time to progression
기간: From registration date and progression date, assessed up to 4 years post-registration

Kaplan-Meier methodology will be used to estimate the distributions of time to progression.
From registration date and progression date, assessed up to 4 years post-registration
Overall survival
기간: From registration to death, assessed up to 4 years post-registration

Kaplan-Meier methodology will be used to estimate the distributions of overall survival.
From registration to death, assessed up to 4 years post-registration

기타 결과 측정

결과 측정
측정값 설명
기간
Median PFS for patients who cross over
기간: From re-registration to progression or death, assessed up to 4 years post-registration

Calculated with corresponding 95% confidence interval.
From re-registration to progression or death, assessed up to 4 years post-registration

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

National Cancer Institute (NCI)

수사관

  • 수석 연구원: Bhavana Konda, Alliance for Clinical Trials in Oncology

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 2월 22일

기본 완료 (추정된)

2029년 6월 2일

연구 완료 (추정된)

2029년 6월 2일

연구 등록 날짜

최초 제출

2025년 3월 26일

QC 기준을 충족하는 최초 제출

2025년 3월 26일

처음 게시됨 (실제)

2025년 3월 28일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 6일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 5일

마지막으로 확인됨

2026년 8월 1일

추가 정보

이 연구와 관련된 용어

추가 관련 MeSH 약관

기타 연구 ID 번호

  • NCI-2025-02021
  • U10CA180821 (미국 NIH 보조금/계약)
  • NCI-2025-02021 (레지스트리 식별자: CTRP (Clinical Trial Reporting Program))
  • A092204 (기타 식별자: CTEP)
  • A092204 (기타 식별자: Alliance for Clinical Trials in Oncology)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

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.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다