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AMC 120, Glofitamab Plus Chemoimmunotherapy in Newly Diagnosed HIV-Associated Large B-Cell Lymphoma (The "Glofit-RCHOP Study")

2026年8月12日 更新者:National Cancer Institute (NCI)

A Feasibility Study of Glofitamab Plus Chemoimmunotherapy in Newly Diagnosed HIV-Associated Large B-Cell Lymphoma

This phase I trial studies the safety and side effects of glofitamab plus a chemoimmunotherapy regimen called R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in treating patients newly-diagnosed with HIV-associated large B-cell lymphoma. Glofitamab is a bispecific monoclonal antibody, which can bind to two different antigens that are expressed by cancer cells (CD3 and CD20) at the same time. This may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. Cyclophosphamide is in a class of medications called alkylating agents. It works by damaging the cell's deoxyribonucleic acid (DNA) and may kill cancer cells. It may also lower the body's immune response. Doxorubicin is in a class of medications called anthracyclines. Doxorubicin damages the cell's DNA and may kill cancer cells. It also blocks a certain enzyme needed for cell division and DNA repair. Vincristine is in a class of medications called vinca alkaloids. It works by stopping cancer cells from growing and dividing and may kill them. Prednisone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Giving glofitamab in combination with the R-CHOP regimen may be a safe treatment for patients with newly-diagnosed with HIV-associated large B-cell lymphoma.

研究概览

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

介入性

注册 (估计的)

15

阶段

  • 阶段1

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

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

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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:
  • 生物样本采集
  • 收集的生物样本
  • 标本采集
  • 样本收集
鉴于IV
其他名称:
  • 胞毒素
  • CTX
  • (-)-环磷酰胺
  • 2H-1,3,2-氧氮杂膦,2-[双(2-氯乙基)氨基]四氢-,2-氧化物,一水合物
  • 卡洛生
  • 环磷酰胺
  • 环草醛
  • 克拉芬
  • CP一水合物
  • 循环电池
  • 环胚素
  • 环爆碱
  • 环磷酰胺一水合物
  • 环磷烷
  • 环磷脂
  • 环素
  • 环孢菌素
  • 胞磷
  • 胞磷烷
  • 磷脂龙
  • Genoxal
  • Genuxal
  • 雷多西那
  • 米托生
  • 新星
  • 重免疫
  • 赛克磷酰胺
  • WR- 138719
  • 阿斯塔B 518
  • B-518
  • WR-138719
  • 乙518
  • B518
  • WR 138719
  • WR138719
  • Frindovyx
给定采购订单
其他名称:
  • 达美松
  • 奥拉松
  • .delta.1-可的松
  • 1, 2-脱氢可的松
  • 阿达松
  • 皮质醇
  • 达考汀
  • 德考坦
  • 去氧硫醇
  • 德克顿
  • Delta 1-可的松
  • 三角穹顶
  • 三角可烯
  • 三角可的松
  • 三角洲脱氢可的松
  • 德尔蒂森
  • 三角洲
  • 经济松
  • 利沙克特
  • 美保生-F
  • 麦考坦
  • 奥菲索罗纳
  • 帕纳福特
  • 松脂-S
  • 伞骨
  • Perrigo 泼尼松
  • 预测
  • 泼尼松-M
  • 泼尼可特
  • 泼尼地布
  • 泼尼龙加
  • 预付款
  • 泼尼松 Intensol
  • 泼尼松
  • 泼尼通
  • 普罗米芬
  • 雷约斯
  • 伺服松
  • SK-泼尼松
鉴于IV
其他名称:
  • 致癌素
  • 基克里斯汀
  • 硫酸亮绿新碱
  • 硫酸白新碱
  • 长春
  • 长春甙
  • 万可乐
  • 硫酸长春新碱
鉴于IV
其他名称:
  • 阿霉素
  • 5,12-并萘二酮,10-[(3-氨基-2,3,6-三脱氧-α-L-来氧代-己吡喃糖基)氧基]-7,8, 9,10-四氢-6,8,11-三羟基-8-(羟基乙酰基)-1-甲氧基-, 盐酸盐, (8S-cis)- (9CI)
  • 广告管理公司
  • 盐酸阿霉素
  • 阿霉素 PFS
  • 阿霉素RDF
  • 阿霉素,盐酸盐
  • Adriblastina
  • 阿得拉碱
  • 阿地美达
  • 氯霉素
  • DOX
  • DOXO细胞
  • 多索伦
  • 阿霉素盐酸盐
  • 农杆菌
  • FI 106
  • FI-106
  • 羟基柔红霉素
  • 橡胶
  • FI106
鉴于IV
其他名称:
  • 利妥昔单抗
  • 美罗华
  • 总部基地 798
  • BI 695500
  • C2B8单克隆抗体
  • 嵌合抗 CD20 抗体
  • CT-P10
  • IDEC-102
  • IDEC-C2B8
  • IDEC-C2B8单克隆抗体
  • 单克隆抗体IDEC-C2B8
  • PF-05280586
  • 里亚布尼
  • 利妥昔单抗ABBS
  • 利妥昔单抗ARRX
  • 利妥昔单抗生物类似药 ABP 798
  • 利妥昔单抗生物仿制药 BI 695500
  • 利妥昔单抗生物类似药 CT-P10
  • 利妥昔单抗生物类似药 GB241
  • 利妥昔单抗生物仿制药 IBI301
  • 利妥昔单抗生物类似药 JHL1101
  • 利妥昔单抗生物仿制药 PF-05280586
  • 利妥昔单抗生物类似药 RTXM83
  • 利妥昔单抗生物仿制药 SAIT101
  • 利妥昔单抗生物仿制药 SIBP-02
  • 利妥昔单抗生物类似药 TQB2303
  • 利妥昔单抗PVVR
  • 利妥昔单抗-arrx
  • 利妥昔单抗-pvvr
  • RTXM83
  • Ruxience
  • 特鲁希玛
  • 里克松
  • 伊克达尔
  • 马布塔斯
  • 利妥昔单抗-abbs
  • BI-695500
  • BI695500
  • 闪电战
  • IDEC 102
  • IDEC102
  • PF 05280586
  • PF05280586
  • 里特维亚
  • 利妥昔单抗-blit
  • 利西名
  • RTXM 83
  • RTXM-83
  • ABP-798
  • ABP798
  • CT P10
  • CTP10
  • 2013年大奖赛
  • GP-2013
  • GP2013
  • 利妥昔单抗生物仿制药 GP2013
接受PET/CT
其他名称:
  • CT
  • 猫
  • 电脑扫描
  • 计算机轴向断层扫描
  • 计算机断层扫描
  • CT扫描
  • 断层扫描
  • 计算机轴向断层扫描(程序)
  • 计算机断层扫描 (CT) 扫描
  • 诊断猫扫描
  • 诊断猫扫描服务类型
接受PET/CT
其他名称:
  • 医学成像、正电子发射断层扫描
  • 宠物
  • 宠物扫描
  • 正电子发射断层扫描
  • PT
  • 正电子发射断层扫描(程序)
鉴于IV
其他名称:
  • RO7082859
  • 抗 CD20 x 抗 CD3 双特异性单克隆抗体 RO7082859
  • RO 7082859
  • 科伦维
  • 格洛非他单抗gxbm
  • RO-7082859
经历回声
其他名称:
  • 超声心动图
  • 欧共体
进行肿瘤组织活检
其他名称:
  • Bx
  • 活组织检查类型
  • 活检
Undergo bone marrow biopsy or aspiration
Undergo bone marrow biopsy or aspiration
其他名称:
  • 骨髓活检
  • 活组织检查,骨髓

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.
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.
Up to 2 years after completion of study treatment
Complete response rates (CRR)
大体时间:Up to 8 cycles (Cycles = 21 days)
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.
Up to 8 cycles (Cycles = 21 days)
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)
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.
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
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.
From treatment initiation and date of death from any cause, assessed up to 2 years after completion of study treatment
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

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

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Stefan K Barta、AIDS Malignancy Consortium

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年10月9日

初级完成 (估计的)

2028年4月30日

研究完成 (估计的)

2028年4月30日

研究注册日期

首次提交

2026年6月13日

首先提交符合 QC 标准的

2026年6月13日

首次发布 (实际的)

2026年6月16日

研究记录更新

最后更新发布 (实际的)

2026年8月13日

上次提交的符合 QC 标准的更新

2026年8月12日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

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

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

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.

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