AMC 120, Glofitamab Plus Chemoimmunotherapy in Newly Diagnosed HIV-Associated Large B-Cell Lymphoma (The "Glofit-RCHOP Study")
A Feasibility Study of Glofitamab Plus Chemoimmunotherapy in Newly Diagnosed HIV-Associated Large B-Cell Lymphoma
研究概览
地位
条件
- 浆母细胞淋巴瘤
- 原发性渗出性淋巴瘤
- 艾滋病相关弥漫性大 B 细胞淋巴瘤
- 弥漫性大 B 细胞淋巴瘤,未另行说明
- 高级 B 细胞淋巴瘤,未另行说明
- High Grade B-Cell Lymphoma With MYC and BCL2 Rearrangements
- Lugano Classification Stage II Adult Non-Hodgkin Lymphoma AJCC v8
- Lugano Classification Stage III Adult Non-Hodgkin Lymphoma AJCC v8
- Lugano Classification Stage IV Adult Non-Hodgkin Lymphoma AJCC v8
详细说明
PRIMARY OBJECTIVE:
I. To establish the feasibility and safety of the regimen glofitamab plus rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (Glofit-RCHOP) in people with newly diagnosed Human Immunodeficiency Virus (HIV)-associated large B-cell lymphoma (LBCL).
SECONDARY OBJECTIVES:
I. To evaluate the toxicity of Glofit-RCHOP when utilized in combination with antiretroviral therapy (ART) as assessed by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
II. To evaluate the overall response rate (ORR) and complete response rate (CRR) for Glofit-RCHOP in newly diagnosed HIV-associated LBCL using Lugano criteria.
III. To evaluate progression-free survival (PFS), duration of response (DoR), and overall survival (OS) for Glofit-RCHOP in newly diagnosed HIV-associated LBCL.
EXPLORATORY OBJECTIVES:
I. To prospectively assess if circulating tumor deoxyribonucleic acid (ctDNA) levels at baseline and ctDNA dynamics (e.g., changes in ctDNA levels after 3 cycles and at end of treatment) can predict outcomes of therapy (PFS and OS).
II. To characterize the genetic subtypes of newly diagnosed HIV-associated LBCL based on commonly occurring genetic alterations.
III. To assess dynamic changes in cluster of differentiation 4 (CD4) and cluster of differentiation 8 (CD8) counts during treatment with Glofit-RCHOP.
IV. To assess the relationship between T-cell subsets, serum levels of cytokines, and inflammation-associated/microbial-translocation molecular profiles with clinical response in HIV-associated aggressive B-cell lymphomas treated with Glofit-RCHOP.
V. To assess the impact of Glofit-RCHOP on quality of life (QoL). VI. To assess the prognostic significance of myelocytomatosis oncogene (MYC) overexpression (defined as MYC immunohistochemistry [IHC] ≥ 40%).
VII. To assess the association of HIV viral load prior to starting glofitamab on frequency and severity of cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS).
OUTLINE:
Patients receive RCHOP consisting of: rituximab intravenously (IV) over 90-360 minutes, cyclophosphamide IV over 1 hour, doxorubicin IV over 3-10 minutes, and vincristine IV over 3-10 minutes on day 1 of each cycle, and prednisone orally (PO) once daily (QD) on days 1-5 of each cycle. Patients also receive glofitamab IV over 4 hours on days 8 and 15 of cycle 2 and on day 8 of cycles thereafter. Cycles of RCHOP repeat every 21 days for 6 cycles, and cycles of glofitamab repeat every 21 days for 8 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo echocardiogram (ECHO), bone marrow biopsy or aspiration, positron emission tomography/computed tomography (PET/CT), and blood sample collection throughout the study. Patients may also undergo tumor tissue biopsy during screening.
After completion of study treatment, patients are followed every 3 months.
研究类型
注册 (估计的)
阶段
- 阶段1
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Participant is able to understand and willing to sign a written informed consent document
- Participants must have histologically (via at least a core or ideally, incisional or excisional biopsy) documented CD20 positive newly diagnosed HIV-associated LBCL as per World Health Organization (WHO) 5th edition, diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS); high grade B-cell lymphoma-NOS or DLBCL/high grade B-cell lymphoma with MYC and BCL2 rearrangement. Plasmablastic lymphoma and primary effusion lymphoma may be included only if CD20-positive
Stage II-IV disease (as per Lugano Staging Criteria) that is measurable as defined below:
- Measurable lymph nodes with longest diameter > 1.5 cm, or
- Measurable extranodal lesions with longest diameter > 1.0 cm
- Participants with bone marrow involvement only will be eligible as long as the morphological bone marrow involvement is documented on a bone marrow biopsy. These participants, however, will need to be willing to undergo subsequent bone marrow biopsies for response assessment and documentation
Evidence of HIV infection. Participants must have documentation of HIV-1 infection by means of any one of the following:
- Documentation of HIV diagnosis in the medical record by a licensed health care provider;
- Documentation of receipt of ART (at least two different medications that do not constitute a prescription for pre-exposure prophylaxis) by a licensed health care provider. Documentation may be a record of an ART prescription in the participant's medical record, a written prescription in the name of the participant for ART, or pill bottles for ART with a label showing the participant's name;
- HIV-1 ribonucleic acid (RNA) detection by a licensed HIV-1 RNA assay at any time;
Any licensed HIV screening antibody and/or HIV antibody/antigen combination assay confirmed by a second licensed HIV assay such as a HIV-1 Western blot confirmation or HIV rapid multispot antibody differentiation assay.
- Note: The term "licensed" refers to a kit that has been certified or licensed by an oversight body within the participating country and validated internally (e.g., United States [US] Food and Drug Administration [FDA]).
World Health Organization and Centers for Disease Control and Prevention guidelines mandate that confirmation of the initial test result must use a test that is different from the one used for the initial assessment. A reactive initial rapid test should be confirmed by either another type of rapid assay or an E/CIA that is based on a different antigen preparation and/or different test principle (e.g., indirect versus competitive), or a Western blot or a plasma HIV-1 RNA viral load.
- Participants with HIV must be on treatment with effective ART that is in accordance with the current International AIDS Society guidelines concurrently with chemotherapy. Use of experimental antiretroviral agents or those containing zidovudine (including Combivir and Trizivir) or ritonavir (includes Norvir® or Kaletra®), cobicistat, didanosine (Videx® or Videx EC®), or similar potent CYP3 inhibitors are prohibited. In order to be eligible, participants taking zidovudine or ritonavir, cobicistat, didanosine, or other CYP3 inhibitors must change to a different regimen 7 days prior to protocol therapy initiation. Changes to ART therapy during the study may be made if medically necessary (toxicity, failure of regimen, etc.). Participants must be on ART for at least 7 days prior to initiation of protocol therapy except for ART-naïve participants who need to get started on ART within the 1st cycle of study treatment (before cycle 2 day 1). ART needs to be approved by protocol chair or co-chair prior to enrollment
- Age ≥ 18 years. Because no dosing or adverse event (AE) data are currently available on the use of glofitamab in combination with RCHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in participants < 18 years of age, children are excluded from this study
- Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2 (Karnofsky ≥50%)
- Absolute neutrophil count (ANC) ≥ 1,000/mcL unless decreased due to bone marrow involvement. Also, in participants with the Duffy antigen null phenotype, neutrophil counts may be lower and a lower threshold required for enrollment can be discussed with the protocol chair on a case-by-case basis
- Platelets ≥ 75,000/mcL unless decreased due to bone marrow involvement
- Hemoglobin of ≥ 8 g/dL unless decreased due to bone marrow involvement
- Aspartate aminotransferase (AST [serum glutamic oxaloacetic transaminase (SGOT)])/alanine aminotransferase (ALT [serum glutamate pyruvate transaminase (SGPT)]) ≤ 3 × institutional upper limit of normal (ULN; ≤ 5 × ULN is acceptable if secondary to liver involvement by lymphoma)
- Total serum bilirubin ≤ 1.5 × institutional ULN (< 3.0 × ULN for participants with Gilbert syndrome). If, however, the elevated bilirubin is felt to be secondary to ART, the total bilirubin must be ≤ 3.5 mg/dL, provided that the direct bilirubin is normal and the AST and ALT ≤ 3 x the ULN
- Glomerular filtration rate (GFR) no lower than 30 mL/min/1.73 m^2. GFR can be measured directly or estimated using the site's institutional standards
- Participants must have adequate cardiac function defined as a left ventricular ejection fraction of at least 45% as determined by echocardiogram or multigated acquisition within 6 weeks before enrollment
- The effects of glofitamab on the developing human fetus are unknown. For this reason and because CD20/CD3 bispecific antibodies, as well as other therapeutic agents used in this trial, are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; total abstinence) from study entry and for at least 1 months from the last glofitamab administration or 12 months from the last rituximab administration, whichever is the longest. Women of childbearing potential, defined as pre- or perimenopausal females with an intact uterus, must have a negative serum β-HCG within 7 days prior to enrollment. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform the treating physician immediately. Men treated with glofitamab must also agree to use adequate contraception with partners who are women of childbearing potential (condom plus an additional contraceptive method, such as bilateral tubal occlusion, male sterilization, hormone-releasing intrauterine devices, and copper intrauterine devices) or use contraceptive measures such as a condom with pregnant female partners to avoid exposing the embryo during intercourse, from study entry, for the duration of study participation, and 1 months after the last glofitamab dose or 12 months after completion of rituximab administration, whichever is the longest
- Any CD4 count is allowed
- Participants with leptomeningeal disease are eligible if the treating physician determines that immediate central nervous system (CNS) specific treatment is not required and is unlikely to be required during the first cycle of therapy, except during the initial safety run-in phase, during which participants with leptomeningeal disease will be excluded. For the first three study participants, enrollment will be halted until the third participant completes two target doses (30 mg) of glofitamab and dose-limiting toxicity (DLT) assessment is completed
- Participants 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 are eligible for this trial
Exclusion Criteria:
- Participants who are receiving any other investigational agents
- Participants with active parenchymal central nervous system (CNS) lymphomatous involvement are excluded; however, asymptomatic leptomeningeal disease is allowed as long as participants have ongoing CNS directed therapy, except during the initial safety-run in phase, during which participants with leptomeningeal disease will also be excluded
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to agents used in study
- Uncontrolled intercurrent illness including, but not limited to: symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, significant pulmonary disease (including, but not limited to clinically significant obstructive pulmonary disease or history of bronchospasm), clinically significant liver disease (including viral or other hepatitis or cirrhosis) or psychiatric illness/social situations that, in the opinion of the investigator, would limit compliance with study requirements or make participation in this protocol unreasonably hazardous
- Because there is an unknown but potential risk for AEs in nursing infants secondary to treatment of the mother with the study agent(s), breastfeeding should be discontinued if the mother is treated with the study agent(s). These potential risks may also apply to other agents used in this study
- Participants with refractory HIV disease will not be eligible. Refractory HIV will be defined as prior ART exposure and HIV viral load > 1000 copies/uL and no options for HIV control evaluated by HIV genotyping. Participants with HIV viral load > 1000 copies/uL can be enrolled if additional ART will be initiated
Participants who have had chemotherapy other than allowable pre-trial therapy outlined below, or radiotherapy other than palliative radiation for medical emergencies (i.e., cord compression or impending fracture), within the last four weeks.
Allowable prior therapy:
- A maximum of one cycle of combination chemotherapy, including CHOP ± rituximab and etoposide-prednisone-Oncovin-cyclophosphamide-hydroxydaunorubicin (EPOCH) ± rituximab. The start of previous chemotherapy cycle must occur at least 21 days but no more than 35 days prior to beginning treatment under this protocol, and this cycle will count towards the maximum of six cycles under this study (i.e., cycle received prior to study enrollment will count as cycle 1) OR
- One prior course of limited therapy including cyclophosphamide and/or glucocorticoids and/or rituximab to improve fitness for combination chemotherapy (i.e., those with impaired hepatic function, renal function and or performance status due to lymphomatous involvement). The start of this therapy may occur up to 35 days prior to beginning treatment under this protocol; cyclophosphamide administration must have been completed at least 14 days prior to initiation of protocol therapy. Such treatment will not count towards the maximum of six cycles under this study (i.e., participants will receive six cycles on study and start with cycle 1 of RCHOP)
- Participants must not have had previous anthracycline treatment within the last two years, except for one cycle off protocol or liposomal doxorubicin. Any prior exposure to liposomal doxorubicin is allowed as long as the left ventricular ejection fraction is ≥ 45%. It is at the discretion of the investigator if prior exposure to doxorubicin more than two years prior is acceptable
- Participants with active tuberculosis and other active opportunistic infections requiring active treatment
- Participants with active fungal infection or history of opportunistic infection requiring continuous prophylaxis or treatment with fluconazole, voriconazole or posaconazole. Oral candidiasis or fungal nail bed infections are permitted
- Participants with chronic hepatitis B (defined by a positive test for hepatitis B surface antigen [HBsAg]). All participants will be required to be screened for Hepatitis B. Participants with resolved infection (i.e., participants who are HBsAg negative but positive for antibodies to hepatitis B core antigen [anti-HBc] and/or antibodies to hepatitis B surface antigen [anti-HBs]) must be screened using real-time polymerase chain reaction (PCR) measurement of Hepatitis B virus (HBV) DNA levels. Participants who are PCR positive will be excluded. EXCEPTION: Participants with serologic findings suggestive of HBV vaccination (anti-HBs positivity as the only serologic marker) AND a known history of prior HBV vaccination, do not need to be tested for HBV DNA by PCR. For participants who have evidence of prior Hepatitis B exposure and are PCR negative, hepatitis B (Hep B) reactivation prophylaxis is mandated using institutional guidelines
- If hepatitis C antibody positive, participants will be excluded from study unless hepatitis C viral load is undetectable. Additionally, participants must have no evidence of cirrhosis and have liver function tests (LFTs)
- Participants with baseline peripheral neuropathy > grade 2 or painful >/= grade 2 neuropathy
- Participants who have not recovered from AEs due to prior anti-cancer therapy (i.e., have residual toxicities > grade 1) with the exception of alopecia
Concomitant medications: Participants should only be excluded from trial participation when clinically relevant known or predicted drug-drug interactions or potential overlapping toxicities will impact safety or efficacy. Please include scientific or clinically based rationale for exclusion.
- Please note that this must account for all agents to be used on this study, including commercial agents. Please refer to the FDA product labels for all commercial agents and include information on prohibited concomitant medications in all applicable sections of the protocol
- A wash out period prior to the start of cycle 1 of at least 4 weeks for prior use of any monoclonal antibody, systemic immunotherapeutic agents, immunosuppressive agents (such as, but not limited to cyclosporin, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor) is required
- Unable to comply with the requirements of the protocol, or unable to provide adequate informed consent in the opinion of the principal investigator (PI)
- Major surgery, other than diagnostic surgery, occurring within 4 weeks prior to study entry. Splenectomy will not be considered an exclusionary major surgery
- Having received a live, attenuated vaccine within 28 days prior to registration
- Myocardial infarction within the preceding 3 months
- Prior solid organ or allogeneic hematopoietic cell transplant
- Prior diagnosis of progressive multifocal leukoencephalopathy (PML)
- Known or suspected history of hemophagocytic lymphohistiocytosis (HLH)
History of autoimmune disease, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener granulomatosis, Sjögren syndrome, Guillain-Barré syndrome, multiple sclerosis, vasculitis, or glomerulonephritis. The following exceptions apply:
- Patients with a history of autoimmune-related hypothyroidism on a stable dose of thyroid-replacement hormone
- Patients with controlled Type 1 diabetes mellitus who are on an insulin regimen are eligible for study
- Patients with a history of disease-related immune thrombocytopenic purpura, autoimmune hemolytic anemia, or other stable autoimmune diseases
Participants with eczema, psoriasis, lichen simplex chronicus, or vitiligo with dermatologic manifestations only (e.g., participants with psoriatic arthritis are excluded) are eligible for the study provided all of following conditions are met:
- Rash must cover < 10% of body surface area
- Disease is well controlled at baseline and requires only low-potency topical corticosteroids
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Treatment (RCHOP, glofitamab)
Patients receive RCHOP consisting of: rituximab IV over 90-360 minutes, cyclophosphamide IV over 1 hour, doxorubicin IV over 3-10 minutes, and vincristine IV over 3-10 minutes on day 1 of each cycle, and prednisone PO QD on days 1-5 of each cycle.
Patients also receive glofitamab IV over 2-8 hours on days 8 and 15 of cycle 2 and on day 8 of cycles thereafter.
Cycles of RCHOP repeat every 21 days for 6 cycles, and cycles of glofitamab repeat every 21 days for 8 cycles in the absence of disease progression or unacceptable toxicity.
Patients also undergo ECHO, bone marrow biopsy or aspiration, PET/CT, and blood sample collection throughout the study.
Patients may also undergo tumor tissue biopsy during screening.
|
辅助研究
进行血液样本采集
其他名称:
鉴于IV
其他名称:
给定采购订单
其他名称:
鉴于IV
其他名称:
鉴于IV
其他名称:
鉴于IV
其他名称:
接受PET/CT
其他名称:
接受PET/CT
其他名称:
鉴于IV
其他名称:
经历回声
其他名称:
进行肿瘤组织活检
其他名称:
Undergo bone marrow biopsy or aspiration
Undergo bone marrow biopsy or aspiration
其他名称:
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Ability to deliver at least 4 full cycles of glofitamab-rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (Glofit-RCHOP) (Feasibility)
大体时间:Up to cycle 4 (Cycles = 21 days)
|
Feasibility status is defined by the ability to deliver at least 4 cycles of Glofit-RCHOP (i.e.
study cycles 1-4).
The proportion of the participants who completed at least 4 cycles of Glofit-RCHOP treatment (i.e.
cycles 1-4) will be estimated.
Will report 95% confidence interval of the above proportion.
For the regimen Glofit-RCHOP to be declared feasible, at least 12 out of 15 evaluable participants must complete at least 4 full cycles of Glofit-RCHOP.
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Up to cycle 4 (Cycles = 21 days)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Incidence and severity of adverse events (AEs) and serious AEs
大体时间:Up to 2 years after completion of study treatment
|
Will be assessed by National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
Cytokine release syndrome (CRS), immune effector cell-associated neurotoxicity syndrome (ICANS), and immune effector cell-associated hemophagocytic lymphohistiocytosis-like syndrome will be graded using the American Society for Transplantation and Cellular Therapy Cytokine Release Syndrome criteria.
All reported toxicities, regardless of attribution, by toxicity type and maximum grade will be summarized, and sorted by number of participants experiencing the toxicity.
Safety data will be based mainly on the frequency and attribution of AEs, the frequency of discontinuation of treatment due to toxicity during study treatment, and the proportion of participants experiencing grade 3 or higher AEs related to the treatment components.
AEs will be summarized by presenting the number and percentage of participants having any AE.
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Up to 2 years after completion of study treatment
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Complete response rates (CRR)
大体时间:Up to 8 cycles (Cycles = 21 days)
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Defined as the proportion of participants who achieve complete response (CR) among evaluable participants until end of treatment.
CRR will be estimated using proportion and corresponding 95% confidence intervals using the Clopper-Pearson method.
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Up to 8 cycles (Cycles = 21 days)
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|
Overall response rate (ORR)
大体时间:Up to 8 cycles (Cycles = 21 days)
|
Defined as the proportion of participants who achieve CR or partial response among evaluable participants.
ORR will be estimated using proportion and corresponding 95% confidence intervals using the Clopper-Pearson method.
|
Up to 8 cycles (Cycles = 21 days)
|
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Progression-free survival (PFS)
大体时间:From treatment initiation and date of documented progression or date of death from any cause, assessed up to 2 years after completion of study treatment
|
Point estimates (e.g.
median and 12 months PFS) with 95% confidence intervals will be calculated using the Kaplan-Meier product limit method to summarize the results.
Differences in PFS by groups will be tested using the log-rank test.
The association between baseline covariates and PFS will be assessed using a Cox proportional hazards regression model.
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From treatment initiation and date of documented progression or date of death from any cause, assessed up to 2 years after completion of study treatment
|
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Overall survival (OS)
大体时间:From treatment initiation and date of death from any cause, assessed up to 2 years after completion of study treatment
|
Point estimates (e.g.
median and 12 months OS) with 95% confidence intervals will be calculated using the Kaplan-Meier product limit method to summarize the results.
Differences in OS by groups will be tested using the log-rank test.
The association between baseline covariates and OS will be assessed using a Cox proportional hazards regression model.
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From treatment initiation and date of death from any cause, assessed up to 2 years after completion of study treatment
|
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Duration of response (DoR)
大体时间:From the date of first documented response and disease progression or death from any cause, assessed up to 2 years after completion of study treatment
|
For DoR, responders who do not exhibit any disease progression or death during the follow-up will be censored at the last day of follow-up.
|
From the date of first documented response and disease progression or death from any cause, assessed up to 2 years after completion of study treatment
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Change in circulating tumor deoxyribonucleic acid
大体时间:From baseline up to cycle 7 (Cycles = 21 days)
|
Will be reported using descriptive statistics such as mean, standard deviation, median, interquartile range (IQR), and range for continuous variables and counts and percentages for categorical variables.
Group comparison will be done using a Student's t-test and/or Mann-Whitney U test for two groups and Analysis of Variance (ANOVA) and/or Kruskal-Wallis test for comparing more than two groups.
Biomarkers measured multiple times will be analyzed using the change from the baseline (CFB).
Linear regression model, logistic regression model, Cox proportional hazard regression model, Pearson's correlation coefficients, and Spearman's correlation coefficients will be used to examine the association between exploratory endpoints and other endpoints.
|
From baseline up to cycle 7 (Cycles = 21 days)
|
|
Genetic subtypes of HIV-associated large B-cell lymphoma
大体时间:Up to 2 years after completion of study treatment
|
Will be reported using descriptive statistics such as mean, standard deviation, median, IQR, and range for continuous variables and counts and percentages for categorical variables.
Group comparison will be done using a Student's t-test and/or Mann-Whitney U test for two groups and ANOVA and/or Kruskal-Wallis test for comparing more than two groups.
Biomarkers measured multiple times will be analyzed using the CFB.
Linear regression model, logistic regression model, Cox proportional hazard regression model, Pearson's correlation coefficients, and Spearman's correlation coefficients will be used to examine the association between exploratory endpoints and other endpoints.
|
Up to 2 years after completion of study treatment
|
|
Change in CD4 and CD8
大体时间:From baseline up to 12 months after completion of R-CHOP
|
Will be reported using descriptive statistics such as mean, standard deviation, median, IQR, and range for continuous variables and counts and percentages for categorical variables.
Group comparison will be done using a Student's t-test and/or Mann-Whitney U test for two groups and ANOVA and/or Kruskal-Wallis test for comparing more than two groups.
Biomarkers measured multiple times will be analyzed using the CFB.
Linear regression model, logistic regression model, Cox proportional hazard regression model, Pearson's correlation coefficients, and Spearman's correlation coefficients will be used to examine the association between exploratory endpoints and other endpoints.
|
From baseline up to 12 months after completion of R-CHOP
|
|
T-cell subsets, serum levels of cytokines, and inflammation-associated/microbial-translocation molecular profiles
大体时间:Up to 2 years after completion of study treatment
|
Will be reported using descriptive statistics such as mean, standard deviation, median, IQR, and range for continuous variables and counts and percentages for categorical variables.
Group comparison will be done using a Student's t-test and/or Mann-Whitney U test for two groups and ANOVA and/or Kruskal-Wallis test for comparing more than two groups.
Biomarkers measured multiple times will be analyzed using the CFB.
Linear regression model, logistic regression model, Cox proportional hazard regression model, Pearson's correlation coefficients, and Spearman's correlation coefficients will be used to examine the association between exploratory endpoints and other endpoints.
|
Up to 2 years after completion of study treatment
|
|
Participant-Reported Outcomes (PRO)-CTCAE and Participant-Reported Outcomes Measurement Information System
大体时间:At baseline and months 3, 6, 12, 18, and 24
|
Summary scores of the two PRO instruments will be obtained, and descriptive statistics and mean changes from baseline will be measured.
|
At baseline and months 3, 6, 12, 18, and 24
|
|
MYC expression
大体时间:Up to 2 years after completion of study treatment
|
Defined as MYC immunohistochemistry ≥ 40%.
Will be reported using descriptive statistics such as mean, standard deviation, median, IQR, and range for continuous variables and counts and percentages for categorical variables.
Group comparison will be done using a Student's t-test and/or Mann-Whitney U test for two groups and ANOVA and/or Kruskal-Wallis test for comparing more than two groups.
Biomarkers measured multiple times will be analyzed using the CFB.
Linear regression model, logistic regression model, Cox proportional hazard regression model, Pearson's correlation coefficients, and Spearman's correlation coefficients will be used to examine the association between exploratory endpoints and other endpoints.
|
Up to 2 years after completion of study treatment
|
|
HIV viral load prior to starting glofitamab step up dosing
大体时间:Cycle 1 (Cycles = 21 days)
|
Will assess the association with CRS and ICANS.
Will be reported using descriptive statistics such as mean, standard deviation, median, IQR, and range for continuous variables and counts and percentages for categorical variables.
Group comparison will be done using a Student's t-test and/or Mann-Whitney U test for two groups and ANOVA and/or Kruskal-Wallis test for comparing more than two groups.
Biomarkers measured multiple times will be analyzed using the CFB.
Linear regression model, logistic regression model, Cox proportional hazard regression model, Pearson's correlation coefficients, and Spearman's correlation coefficients will be used to examine the association between exploratory endpoints and other endpoints.
|
Cycle 1 (Cycles = 21 days)
|
合作者和调查者
调查人员
- 首席研究员:Stefan K Barta、AIDS Malignancy Consortium
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
- 肿瘤
- 免疫系统疾病
- 组织学类型的肿瘤
- 淋巴系统疾病
- 淋巴增生性疾病
- 免疫增生性疾病
- 淋巴瘤,非霍奇金
- 淋巴瘤,B细胞
- 淋巴瘤
- 半身和淋巴疾病
- 浆母细胞淋巴瘤
- 淋巴瘤,大 B 细胞,弥漫性
- 淋巴瘤,原发性积液
- 氨基酸,肽和蛋白质
- 蛋白质
- 有机化学品
- 杂环化合物
- 杂环化合物,2环
- 杂环化合物,融合环
- 调查技术
- 临床实验室技术
- 诊断技术和程序
- 诊断
- 手术程序,手术
- 细胞学技术
- 细胞诊断
- 碳氢化合物
- 碳氢化合物,循环
- 碳水化合物
- 生物碱
- 多环芳烃
- 碳氢化合物,芳香族
- 多环化合物
- 糖苷
- 吲哚
- 抗体,单克隆
- 抗体
- 免疫球蛋白
- 免疫蛋白
- 血蛋白
- 血清球蛋白
- 球蛋白
- 怀孕
- 怀孕
- 类固醇
- 融合环化合物
- 诊断技术,手术
- 化学技术,分析
- 频谱分析
- 磷酰胺芥末
- 氮芥末化合物
- 芥末化合物
- 碳氢化合物,卤素
- 磷酰胺
- 有机磷化合物
- 妊娠二培养子
- VINCA生物碱
- Secologanin色素生物碱
- 吲哚生物碱
- 吲哚衍生物
- 吲哚王
- 蒽环类动物
- 萘烯
- 氨基糖苷
- 抗体,单克隆,鼠的衍生
- Daunorubicin
- 利妥昔单抗
- 强的松
- 环磷酰胺
- 阿霉素
- 长春新碱
- 活检
- 标本处理
- 磁共振光谱
- CT-P10
- Deltacortene
- prepnylidene
- Glofitamab
其他研究编号
- NCI-2026-04195 (注册表标识符:CTRP (Clinical Trial Reporting Program))
- UM1CA121947 (美国 NIH 拨款/合同)
- AMC-120 (其他标识符:CTEP)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.