Phase II Study Of Iodine-131 Anti-B1 Antibody Plus CHOP For Patients With Previously Untreated Mantle Cell Lymphoma
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 25
- 主要终点
- Number of Participants With the Indicated Unconfirmed Response (Complete Response, Complete Response Unconfirmed, and Partial Response)
研究概览
简要总结
The primary efficacy endpoint of this study is to determine the duration of response of the sequential administration of Iodine-131 Anti-B1 Antibody followed by six cycles of CHOP for patients with previously untreated Mantle Cell Lymphoma (MCL). The secondary efficacy endpoints for this study are to determine the response rate, confirmed response rate, complete response rate, confirmed complete response rate, duration of response for confirmed responders, duration of response for complete responders, duration of response for confirmed complete responders, progression-free survival, time to treatment failure, and the predictive value of detection of minimal residual disease by molecular techniques on response duration. The pharmacokinetic endpoint is to determine the total body residence time of Iodine-131 Anti-B1 Antibody following the dosimetric dose. The safety endpoints are to determine the incidence of adverse experiences, hematologic toxicity, (e.g., nadir, time to nadir, and time to recovery), use of supportive care, percent of patients converting to human anti-murine antibody (HAMA) positivity, the effects of Iodine-131 Anti-B1 Antibody on the growth and function of hematopoietic progenitor cells, and survival of patients with previously untreated MCL treated with Iodine-131 Anti-B1 Antibody followed by six cycles of CHOP.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients must have a confirmed initial diagnosis of mantle cell non-Hodgkin's lymphoma by histology according to the WHO classification .
- •Patients must have Ann Arbor bulky stage II, stage III, or stage IV disease at diagnosis. Bulky stage II disease is defined as a mediastinal mass greater than one-third of the maximum chest diameter, or any other mass greater than or equal to 10 cm in maximum diameter.
- •Patients must have less than an average of 25% of the intratrabecular marrow space involved by NHL in bilateral bone marrow biopsy specimens as assessed microscopically at study entry. A unilateral bone marrow biopsy demonstrating <10% involvement with NHL is also adequate.
- •Patients must have evidence that their tumor tissue expresses the CD20 antigen. Immunoperoxidase stains of paraffin-embedded tissue showing positive reactivity with L26 antibody or immunoperoxidase stains of frozen tissue showing positive reactivity with Anti-B1 Antibody (Coulter Clone) or similar commercially available CD20 antibody or evidence of CD20 positivity by flow cytometry are acceptable evidence of CD20 positivity. This must be performed within 42 days of study entry.
- •Patients must have a performance status of at least 60% on the Karnofsky Performance Scale and an anticipated survival of at least 3 months.
- •Patients must have an ANC greater than or equal to 1500 cells/mm3 and a platelet count greater than or equal to 100,000 cells/mm3 within 14 days of study enrollment. These blood counts must be sustained without support of hematopoietic cytokines or transfusion of blood products.
- •Patients must have adequate renal function (defined as serum creatinine <1.5 times the upper limit of normal) and hepatic function (defined as total bilirubin <1.5 times the upper limit of normal and AST <5 times the upper limit of normal) within 14 days of study enrollment.
- •Patients must have bi-dimensionally measurable disease. At least one lesion must be greater than or equal to 2.0 x 2.0 cm by computerized tomography scan.
- •Females of childbearing potential must have a negative serum pregnancy test within 7 days prior to study enrollment.
- •Patients must have a cardiac left ventricular ejection fraction of greater than or equal to 50% by ventriculography or echocardiogram.
排除标准
- •Patients who have received prior chemotherapy, biologic therapy, steroids, or radiation therapy as treatment for their MCL
- •Patients with active obstructive hydronephrosis
- •Patients with serious illness that would preclude evaluation
- •Patients with prior malignancy other than lymphoma, except for adequately treated skin cancer, in situ cervical cancer, or other cancer for which the patient has been disease free for 5 years
- •Patients with known HIV infection
- •Patients who are HAMA positive
- •Patients with known brain or leptomeningeal metastases.
- •Patients who are pregnant or breastfeeding. Males and females must agree to use a contraceptive method while on study and for 6 months after receiving Iodine-131 Anti-B1 Antibody.
- •Patients with active infection requiring IV anti-infectives at the time of study enrollment.
结局指标
主要结局
Number of Participants With the Indicated Unconfirmed Response (Complete Response, Complete Response Unconfirmed, and Partial Response)
时间窗: Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months)
Participants with response include those with complete response (CR: complete disappearance of all detectable clinical and radiographic evidence of disease and the disappearance of all disease-related symptoms), complete response unconfirmed (CRu: CR, with one of the following: residual lymph node mass \>1.5 centimeters \[cm\] that has regressed by more than 75% in the sum of the product of the diameters or indeterminate bone marrow), or partial response (PR: \>=50% reduction in the sum of the products of the longest perpendicular diameters of all measurable lesions; no new lesions).
次要结局
- Number of Participants With the Indicated Confirmed Response (Confirmed Complete Response, Complete Response Unconfirmed, and Partial Response)(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Mean Nadir Value for Hemoglobin(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Time to Recovery From the Indicated Hematology Parameters(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Number of Participants Negative for Human Anti-Murine (Mouse) Antibody (HAMA) at Screening Who Converted to HAMA Positivity or Remained Negative During the Course of the Study(Screening; at Week 7, Week 13, then every 6 months until disease progression or death (up to 143 months))
- Duration of Response for All Unconfirmed Responders (CR + CRu + PR)(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Time to Treatment Failure(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Mean Nadir Value for Absolute Neutrophil Count (ANC)(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Overall Survival(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Duration of Response for All Confirmed Responders (CR + CRu + PR)(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Progression-free Survival(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Number of Participants With Any Adverse Event (AE) or Serious Adverse Event (SAE)(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Mean Nadir Values for Platelets and White Blood Cell (WBC) Count(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Time to Nadir for the Indicated Hematology Parameters(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Number of Participants With an Adverse Event of Cytopenia(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Duration of Response for Unconfirmed Complete Responders(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))
- Duration of Response for Confirmed Complete Responders(Every 13 weeks up to 2 years, or every 6 months until disease progression or death (average of 77.8 months))