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Nivolumab med eller utan varlilumab vid behandling av patienter med återfallande eller refraktärt aggressiva B-cellslymfom

24 oktober 2026 uppdaterad av: National Cancer Institute (NCI)

En randomiserad fas 2-studie av CDX-1127 (Varlilumab) i kombination med nivolumab hos patienter med återfall eller refraktärt aggressivt B-cellslymfom

This phase II trial studies how well nivolumab with or without varlilumab works in treating patients with aggressive B-cell lymphomas that have come back (recurrent) or do not respond to treatment (refractory). Immunotherapy with monoclonal antibodies, such as varlilumab and nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

Studieöversikt

Status

Aktiv, inte rekryterande

Betingelser

Intervention / Behandling

Detaljerad beskrivning

PRIMARY OBJECTIVE:

I. To determine the anti-tumor activity of combination therapy with CDX-1127 (varlilumab) and nivolumab as compared to nivolumab alone in patients with advanced aggressive B-cell non-Hodgkin lymphomas (NHL) based on the lymphoma response to immunomodulatory therapy criteria or LYRIC.

SECONDARY OBJECTIVES:

I. To assess the safety and tolerability profile of treatment with a combination of CDX-1127 (varlilumab) and nivolumab in patients with advanced aggressive B-cell NHL.

II. To evaluate the duration of response, progression-free survival and overall survival.

EXPLORATORY OBJECTIVES:

I. To determine the effect of combination therapy with CDX-1127 (varlilumab) and nivolumab on the immune system as assessed by immunohistochemistry (IHC), mass cytometry (CyTOF), changes in serum cytokine profile and immunogenicity assays.

II. To describe the pharmacokinetic profile of CDX-1127 (varlilumab) and nivolumab when used in combination.

OUTLINE: Patients are randomized to 1 of 2 groups.

GROUP I: Patients receive nivolumab intravenously (IV) over 30 minutes every 2 weeks for 4 months and every 4 weeks for a total of up to 2 years in the absence of disease progression or unacceptable toxicity. Patients may cross over to Group II at the time of disease progression.

GROUP II: Patients receive varlilumab IV over 90 minutes every 4 weeks for up to 2 years in the absence of disease progression or unacceptable toxicity. Patients also receive nivolumab IV over 30 minutes every 2 weeks for 4 months and every 4 weeks for a total of up to 2 years in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 100 days.

Studietyp

Interventionell

Inskrivning (Faktisk)

54

Fas

  • Fas 2

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

  • Förenta staterna
    • Arizona
      • Phoenix, Arizona, Förenta staterna, 85054
        • Mayo Clinic Hospital in Arizona
      • Scottsdale, Arizona, Förenta staterna, 85259
        • Mayo Clinic in Arizona
    • Florida
      • Jacksonville, Florida, Förenta staterna, 32224-9980
        • Mayo Clinic in Florida
      • Tampa, Florida, Förenta staterna, 33612
        • Moffitt Cancer Center
      • Tampa, Florida, Förenta staterna, 33607
        • Moffitt Cancer Center-International Plaza
      • Tampa, Florida, Förenta staterna, 33612
        • Moffitt Cancer Center - McKinley Campus
    • Georgia
      • Atlanta, Georgia, Förenta staterna, 30342
        • Northside Hospital
    • Illinois
      • Chicago, Illinois, Förenta staterna, 60611
        • Northwestern University
      • Chicago, Illinois, Förenta staterna, 60637
        • University of Chicago Comprehensive Cancer Center
    • Kansas
      • Fairway, Kansas, Förenta staterna, 66205
        • University of Kansas Clinical Research Center
      • Hays, Kansas, Förenta staterna, 67601
        • HaysMed
      • Kansas City, Kansas, Förenta staterna, 66160
        • University of Kansas Cancer Center
      • Lawrence, Kansas, Förenta staterna, 66044
        • Lawrence Memorial Hospital
      • Olathe, Kansas, Förenta staterna, 66061
        • The University of Kansas Cancer Center - Olathe
      • Overland Park, Kansas, Förenta staterna, 66210
        • University of Kansas Cancer Center-Overland Park
      • Overland Park, Kansas, Förenta staterna, 66211
        • University of Kansas Hospital-Indian Creek Campus
      • Pittsburg, Kansas, Förenta staterna, 66762
        • Mercy Hospital Pittsburg
      • Salina, Kansas, Förenta staterna, 67401
        • Salina Regional Health Center
      • Topeka, Kansas, Förenta staterna, 66606
        • University of Kansas Health System Saint Francis Campus
      • Westwood, Kansas, Förenta staterna, 66205
        • University of Kansas Hospital-Westwood Cancer Center
    • Minnesota
      • Rochester, Minnesota, Förenta staterna, 55905
        • Mayo Clinic in Rochester
    • Missouri
      • City of Saint Peters, Missouri, Förenta staterna, 63376
        • Siteman Cancer Center at Saint Peters Hospital
      • Creve Coeur, Missouri, Förenta staterna, 63141
        • Siteman Cancer Center at West County Hospital
      • Kansas City, Missouri, Förenta staterna, 64154
        • University of Kansas Cancer Center - North
      • Kansas City, Missouri, Förenta staterna, 64108
        • University Health Truman Medical Center
      • Lee's Summit, Missouri, Förenta staterna, 64064
        • University of Kansas Cancer Center - Lee's Summit
      • North Kansas City, Missouri, Förenta staterna, 64116
        • University of Kansas Cancer Center at North Kansas City Hospital
      • St Louis, Missouri, Förenta staterna, 63110
        • Washington University School of Medicine
      • St Louis, Missouri, Förenta staterna, 63129
        • Siteman Cancer Center-South County
    • New Hampshire
      • Lebanon, New Hampshire, Förenta staterna, 03756
        • Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
    • New York
      • Buffalo, New York, Förenta staterna, 14263
        • Roswell Park Cancer Institute
      • New York, New York, Förenta staterna, 10016
        • Laura and Isaac Perlmutter Cancer Center at NYU Langone
    • Texas
      • Dallas, Texas, Förenta staterna, 75390
        • UT Southwestern/Simmons Cancer Center-Dallas

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Patients must have a histopathologically confirmed diagnosis of an aggressive B-cell non-Hodgkin lymphoma that is recurrent or refractory to standard therapy

  • For the purpose of this study, aggressive B-cell NHL will be deemed any lymphoma belonging to one of the following groups according to the 2016 revision of the World Health Organization (WHO) classification of lymphoid neoplasms

    • For the purposes of stratification, diagnoses are grouped into 2 categories:

      • Category A

        • Burkitt lymphoma
        • Burkitt-like lymphoma with 11q aberration
        • High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements
        • High-grade B-cell lymphoma, not otherwise specified (NOS)

      • Category B

        • Diffuse large B-cell lymphoma (DLBCL), NOS
        • Diffuse large B-cell lymphoma (DLBCL), NOS; germinal center B-cell type
        • Diffuse large B-cell lymphoma (DLBCL), NOS; activated B-cell type
        • Large B-cell lymphoma with IRF4 rearrangement
        • T-cell/histiocyte-rich large B-cell lymphoma
        • Primary DLBCL of the central nervous system (CNS)
        • Primary cutaneous DLBCL, leg type
        • Epstein-Barr virus (EBV)+ DLBCL, NOS
        • EBV+ mucocutaneous ulcer
        • DLBCL associated with chronic inflammation
        • Lymphomatoid granulomatosis
        • Primary mediastinal (thymic) large B-cell lymphoma
        • Intravascular large B-cell lymphoma
        • ALK+ large B-cell lymphoma
        • Plasmablastic lymphoma
        • Primary effusion lymphoma
        • Human herpesvirus (HHV)-8+ DLBCL, NOS
        • B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin lymphoma

  • Patients must have measurable disease, defined as at least one lesion that is > 15 mm (1.5 cm) in the longest axis on cross-sectional imaging and measurable in two perpendicular dimensions per computed tomography (spiral computed tomography [CT]), positron emission tomography (PET)-CT or magnetic resonance imaging (MRI)

  • Patients must have disease that has relapsed after or is refractory to at least 2 lines of standard therapy; the remaining standard treatment options are unlikely to be effective in the opinion of the treating physician, or patient is felt to be ineligible for such therapies or the patient refuses such therapies; patients who have undergone autologous stem cell transplant are eligible as long as they meet all other criteria

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

  • Life expectancy of greater than 12 weeks

  • White blood cell (WBC) >= 2000/mm^3 (within 14 days of registration)

  • Absolute neutrophil count (ANC) >= 1500/mm^3 (within 14 days of registration)

  • Platelet count >= 100,000/mm^3 (within 14 days of registration)

  • Hemoglobin > 9.0 g/dL (within 14 days of registration)

  • Total bilirubin =< 1.5 x upper limit of normal (ULN) (except patients with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL) (within 14 days of registration)

  • Aspartate transaminase (aspartate aminotransferase [AST]) =< 2.5 x ULN (within 14 days of registration)

  • Calculated creatinine clearance (CrCl) >= 50 mL/min (if using the Cockcroft-Gault formula) (within 14 days of registration)

  • Females of child bearing potential must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin [HCG])

  • Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

  • Patient has received chemotherapy, targeted agent, or radiotherapy within 4 weeks or at least 5 half-lives, whichever is longer, 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

  • Patient has received immunotherapy (including monoclonal antibodies) within 4 weeks prior to registration

  • Patients who have not recovered to grade 1 or less from any adverse events due to agents administered more than 4 weeks earlier (excluding alopecia)

  • Patients who are receiving any other investigational agents

  • Patients should be excluded if they have had prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4 antibody, or any other antibody or drug specifically targeting T-cell co-stimulation or immune checkpoint pathways

  • Patients who have received autologous stem cell transplant (ASCT) =< 12 weeks prior to the first dose of study drug

  • Patients with a prior history of allogeneic stem cell or solid organ transplantation

  • Patients with evidence of active disease in the central nervous system (CNS) defined as either the presence of active lesions on MRI obtained within 4 weeks of registration or progressive neurological decline

    • Patients with primary CNS lymphoma who develop systemic recurrence following standard therapy may be included as long as no active CNS disease is present at the time or enrollment; similarly, patients with secondary involvement of the CNS from a systemic lymphoma may be included as long as the CNS disease has been optimally treated and they demonstrate no evidence of active CNS disease

  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to CDX-1127 (varlilumab) and/or nivolumab

  • History of severe hypersensitivity reaction to any monoclonal antibody

  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements

  • Pregnant women are excluded from this study because CDX-1127 (varlilumab) and nivolumab are 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 CDX-1127 (varlilumab) or nivolumab, breastfeeding should be discontinued if the mother is treated with CDX-1127 (varlilumab) or nivolumab

  • Patients with human immunodeficiency virus (HIV) are eligible for the study provided they meet the other protocol criteria in addition to the following:

    • Undetectable HIV load by standard polymerase chain reaction (PCR) clinical assay within 60 days prior to registration

    • Absolute CD4 count of >= 200 mm^3 within 60 days prior to registration

    • Willing to maintain adherence to combination antiretroviral therapy

    • No history of acquired immunodeficiency syndrome (AIDS) defining condition (other than lymphoma or CD4 cell count < 200 mm^3)

    • Likely to have near normal lifespan if not for the presence of relapsed/refractory lymphoma

      • Patients with evidence of hepatitis B virus (HBV) are eligible provided there is minimal hepatic injury and the patient has undetectable HBV on suppressive HBV therapy; patient must be willing to maintain adherence to HBV therapy
      • Patients with previously treated and eradicated hepatitis C virus (HCV) who have minimal hepatic injury are eligible

  • Patients with active autoimmune disease or history of autoimmune disease that might recur, which may affect vital organ function or require immune suppressive treatment including systemic corticosteroids, should be excluded; these include but are not limited to patients with a history of immune related neurologic disease, multiple sclerosis, autoimmune (demyelinating) neuropathy, Guillain-Barre syndrome, myasthenia gravis; systemic autoimmune disease such as systemic lupus erythematosus (SLE), connective tissue diseases, scleroderma, inflammatory bowel disease (IBD), Crohn's, ulcerative colitis, hepatitis; and 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 positive serology, such as antinuclear antibodies (ANA), anti-thyroid antibodies should be evaluated for the presence of target organ involvement and potential need for systemic treatment but should otherwise be eligible

  • Patients are permitted to enroll if they have vitiligo, type I diabetes mellitus, residual hypothyroidism due to autoimmune condition only requiring hormone replacement, psoriasis not requiring systemic treatment, or conditions not expected to recur in the absence of an external trigger (precipitating event)

  • Patients should be excluded if they have a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of study drug administration; inhaled or topical steroids and adrenal replacement doses =< 10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease; patients are permitted to use topical, ocular, intra-articular, intranasal, and inhalational corticosteroids (with minimal systemic absorption); physiologic replacement doses of systemic corticosteroids are permitted, even if =< 10 mg/day prednisone equivalents; a brief 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 contact allergen) is permitted

  • Patients who have had evidence of active or acute diverticulitis, intra-abdominal abscess, gastrointestinal (GI) obstruction and abdominal carcinomatosis which are known risk factors for bowel perforation should be evaluated for the potential need for additional treatment before coming on study

  • Patients with other active malignancy =< 3 years prior to registration for which active treatment is required must be excluded; patients with composite lymphomas that have a non-B-cell component must be excluded EXCEPTIONS: Non-melanotic skin cancer or carcinoma-in-situ of the cervix

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Crossover tilldelning
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Aktiv komparator: Group I (nivolumab)

Patients receive nivolumab IV over 30 minutes every 2 weeks for 4 months and every 4 weeks for a total of up to 2 years in the absence of disease progression or unacceptable toxicity. Patients may cross over to Group II at the time of disease progression.
Biologisk: Nivolumab

Given IV

Andra namn:
  • BMS-936558
  • MDX-1106
  • NIVO
  • ONO-4538
  • Opdivo
  • CMAB819
  • Nivolumab Biosimilar CMAB819
  • MDX 1106
  • MDX1106
  • BMS 936558
  • ABP 206
  • Nivolumab Biosimilar ABP 206
  • BCD-263
  • Nivolumab Biosimilar BCD-263
  • BMS936558
  • ONO 4538
  • ONO4538
Experimentell: Group II (varlilumab, nivolumab)

Patients receive varlilumab IV over 90 minutes every 4 weeks for up to 2 years in the absence of disease progression or unacceptable toxicity. Patients also receive nivolumab IV over 30 minutes every 2 weeks for 4 months and every 4 weeks for a total of up to 2 years in the absence of disease progression or unacceptable toxicity.
Biologisk: Nivolumab

Given IV

Andra namn:
  • BMS-936558
  • MDX-1106
  • NIVO
  • ONO-4538
  • Opdivo
  • CMAB819
  • Nivolumab Biosimilar CMAB819
  • MDX 1106
  • MDX1106
  • BMS 936558
  • ABP 206
  • Nivolumab Biosimilar ABP 206
  • BCD-263
  • Nivolumab Biosimilar BCD-263
  • BMS936558
  • ONO 4538
  • ONO4538
Läkemedel: Varlilumab

Given IV

Andra namn:
  • CDX 1127
  • CDX-1127
  • Immunoglobulin G1, Anti-(Human CD Antigen CD27) (Human Monoclonal CDX-1127 Clone 1f5 Heavy Chain), Disulfid med Human Monoclonal CDX-1127 Clone 1f5 Kappa-chain, Dimer
  • CDX1127

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Overall Response Rate
Tidsram: 2 years

Will be assessed by computed tomography (CT)-based criteria or positron emission tomography (PET)-CT based criteria. A response will be defined as an objective status of partial remission (PR) or complete remission (CR) for patients evaluated by CT-based criteria and complete metabolic response (CMR) or partial metabolic response (PMR) for patients evaluated by PET-CT based criteria. Exact binomial ninety-five percent confidence intervals for the true success proportion will be calculated in each arm. Comparison of overall response rates between the two treatment groups will be performed using a one-sided Fisher's exact test at significance level 0.15.
2 years

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Duration of Response
Tidsram: 2 years

Defined as the date at which the patient's objective status is first noted to be a PR or CR for patients evaluated by CT-based criteria or CMR or PMR for patients evaluated by PET-CT based criteria to the earliest date progression (documentation of disease progression [PMD] or progressive disease [PD]) is documented. The distribution of duration of response will be estimated using the method of Kaplan-Meier. The comparison of duration of response between two treatment arms will be based on the log-rank test.
2 years
Overall Survival
Tidsram: 37 months

The distribution of survival time will be estimated using the method of Kaplan-Meier. The comparison of overall survival between two treatment arms will be based on the log-rank test.
37 months
Progression Free Survival (PFS)
Tidsram: 37 months

The distribution of PFS will be estimated using the method of Kaplan-Meier. The comparison of progression-free survival between two treatment arms will be based on the log-rank test.
37 months
Proportion of Patients With Grade 3 or Higher Adverse Events
Tidsram: 25 months

Will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events version 5.0. The overall adverse event rates for grade 3 or higher hematologic and non-hematologic adverse events at least possibly related to treatment will be compared between the two treatment groups using the Chi-square test (or Fisher's exact test if the data in the contingency table is sparse).
25 months

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in CD27 Expression in Tissue
Tidsram: Baseline up to 100 days after last dose of study drug

Will be assessed by immunohistochemistry. Will be both graphically and quantitatively summarized and explored. Standard paired comparisons methodologies (Wilcoxon signed rank and McNemar's tests) will be used to assess changes in these variables before and after therapy. In addition, baseline values and changes over time in each measure will be explored in relation to clinical outcome. Differences between responders and non-responders will be assessed using Wilcoxon's rank sum (continuous data) or Fisher's exact (categorical data) test. The relationship between each measure and time to event measures (PFS, overall survival [OS]) will be evaluated using Cox's proportional hazards models and log-rank tests. Logistic regression will be used to model the response rate as a function of treatment and CD27 (as a continuous variable). The distribution of CD27 will be estimated empirically in the entire trial population and used to calculate CD27 values corresponding to each fixed percentile.
Baseline up to 100 days after last dose of study drug
Change in Peripheral Blood Immune Cells
Tidsram: Baseline up to 12 weeks

Will be assessed by cytometry by time of flight (CyTOF). The relationship between presence/absence of a particular subtype of cell and association with outcomes will be evaluated. Evaluation of particular combinations of immune cells (immune signature) and whether they are predictive of outcome will also be evaluated. Will be both graphically and quantitatively summarized and explored. Standard paired comparisons methodologies (Wilcoxon signed rank and McNemar's tests) will be used to assess changes in these variables before and after therapy. In addition, baseline values and changes over time in each measure will be explored in relation to clinical outcome. Differences between responders and non-responders will be assessed using Wilcoxon's rank sum (continuous data) or Fisher's exact (categorical data) test. The relationship between each measure and time to event measures (PFS, OS) will be evaluated using Cox's proportional hazards models and log-rank tests.
Baseline up to 12 weeks
Change in the Identification/Characterization of Intratumoral Immune Cells in Tissue
Tidsram: Baseline up to time of disease progression

Will be assessed by immunohistochemistry and CyTOF. Will be both graphically and quantitatively summarized and explored. Standard paired comparisons methodologies (Wilcoxon signed rank and McNemar's tests) will be used to assess changes in these variables before and after therapy. In addition, baseline values and changes over time in each measure will be explored in relation to clinical outcome. Differences between responders and non-responders will be assessed using Wilcoxon's rank sum (continuous data) or Fisher's exact (categorical data) test. The relationship between each measure and time to event measures (PFS, OS) will be evaluated using Cox's proportional hazards models and log-rank tests.
Baseline up to time of disease progression
Change in Genetic Alterations of Chromosome 9p24.1 in Tissue
Tidsram: Baseline up to time of disease progression

Will be assessed by fluorescence in situ hybridization. The proportion of patients in each of these groups who achieve a response will be evaluated. Will be both graphically and quantitatively summarized and explored. Standard paired comparisons methodologies (Wilcoxon signed rank and McNemar's tests) will be used to assess changes in these variables before and after therapy. In addition, baseline values and changes over time in each measure will be explored in relation to clinical outcome. Differences between responders and non-responders will be assessed using Wilcoxon's rank sum (continuous data) or Fisher's exact (categorical data) test. The relationship between each measure and time to event measures (PFS, OS) will be evaluated using Cox's proportional hazards models and log-rank tests.
Baseline up to time of disease progression
Change in Serum Cytokine Profile
Tidsram: Baseline up to 12 weeks

Will be assessed by enzyme-linked immunosorbent assay. Will be both graphically and quantitatively summarized and explored. Standard paired comparisons methodologies (Wilcoxon signed rank and McNemar's tests) will be used to assess changes in these variables before and after therapy. In addition, baseline values and changes over time in each measure will be explored in relation to clinical outcome. Differences between responders and non-responders will be assessed using Wilcoxon's rank sum (continuous data) or Fisher's exact (categorical data) test. The relationship between each measure and time to event measures (PFS, OS) will be evaluated using Cox's proportional hazards models and log-rank tests.
Baseline up to 12 weeks
Change in Mutation Burden in Tissue
Tidsram: Baseline up to time of disease progression

Will be assessed by whole exome sequencing. Will be both graphically and quantitatively summarized and explored. Standard paired comparisons methodologies (Wilcoxon signed rank and McNemar's tests) will be used to assess changes in these variables before and after therapy. In addition, baseline values and changes over time in each measure will be explored in relation to clinical outcome. Differences between responders and non-responders will be assessed using Wilcoxon's rank sum (continuous data) or Fisher's exact (categorical data) test. The relationship between each measure and time to event measures (PFS, OS) will be evaluated using Cox's proportional hazards models and log-rank tests.
Baseline up to time of disease progression

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

National Cancer Institute (NCI)

Utredare

  • Huvudutredare: Stephen M Ansell, Dana-Farber - Harvard Cancer Center LAO

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

21 december 2018

Primärt slutförande (Faktisk)

26 maj 2023

Avslutad studie (Beräknad)

23 oktober 2027

Studieregistreringsdatum

Först inskickad

31 januari 2017

Först inskickad som uppfyllde QC-kriterierna

31 januari 2017

Första postat (Beräknad)

1 februari 2017

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

13 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

24 oktober 2026

Senast verifierad

1 oktober 2026

Mer information

Termer relaterade till denna studie

Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • NCI-2017-00120
  • UM1CA186709 (U.S.S. NIH-anslag/kontrakt)
  • UM1CA186686 (U.S.S. NIH-anslag/kontrakt)
  • NCI-2017-00120 (Registeridentifierare: CTRP (Clinical Trial Reporting Program))
  • MC168D
  • 10089 (Annan identifierare: CTEP)
  • 10089 (Annan identifierare: Dana-Farber - Harvard Cancer Center LAO)

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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