Hu3S193 in Treating Women With Ovarian Epithelial, Primary Peritoneal, or Fallopian Tube Cancer
A PHASE II TRIAL OF Hu3S193 THERAPY FOR PATIENTS WITH PLATINUM REFRACTORY OR PLATINUM RESISTANT EPITHELIAL OVARIAN, PRIMARY PERITONEAL AND FALLOPIAN TUBE CANCER
RATIONALE: Monoclonal antibodies, such as Hu3S193, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them.
PURPOSE: This phase II trial is studying how well Hu3S193 works in treating patients with ovarian epithelial cancer, fallopian tube cancer, or peritoneal cavity cancer.
研究概览
详细说明
OBJECTIVES:
Primary
- To evaluate the efficacy of monoclonal antibody Hu3S193 in women with platinum-resistant/refractory ovarian, fallopian tube, or primary peritoneal cancer, based on RECIST criteria (Response Evaluation Criteria in Solid Tumors).
Secondary
- To determine the safety of the study drug.
- To determine the drug pharmacokinetics when administered in multiple weekly injections.
Exploratory analysis
- Clinical Benefit (objective response rate + tumor stabilization).
- Progression Free Survival (PFS).
- Duration of Response.
- Overall Survival.
- 12-month survival rate.
OUTLINE: This is a multicenter study.
Patients receive monoclonal antibody Hu3S193 IV over 1 hour once weekly in weeks 1-8. Treatment repeats every 8 weeks for up to 3 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed monthly.
研究类型
注册 (实际的)
阶段
- 阶段2
联系人和位置
学习地点
-
-
-
Minas Gerais、巴西、30285-000
- Hospital da Baleia
-
Porto Alegre、巴西、90610-000
- Hospital Sao Lucas da PUCRS
-
Rio de Janeiro、巴西、20220-410
- Instituto Nacional de Cancer
-
Sao Paulo、巴西、05651-901
- Hospital israelita Albert Einstein
-
Sao Paulo、巴西、01308-050
- Hospital Sírio-Libanês
-
Sao Paulo、巴西、01246-000
- Hospital das Clinicas FMUSP
-
Sao Paulo、巴西、01401-904
- Hospital Alemao Oswaldo Cruz
-
-
Rio Grande do Sul
-
Porto Alegre、Rio Grande do Sul、巴西、90035-903
- Hospital de Clinicas de Porto Alegre
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
DISEASE CHARACTERISTICS:
Histologically confirmed ovarian epithelial, fallopian tube, or primary peritoneal carcinoma
- Progressive disease
- Disease must express Lewis-Y antigen documented by immunohistochemistry in archived or fresh primary or metastatic tumor biopsies
Measurable disease, including at least one measurable lesion, according to RECIST criteria or CA-125 (Cancer Antigen-125) > 2 times upper normal limit
- Pleural effusion, ascites, bone metastases, and lesions located in previously irradiated areas are not considered measurable
Disease must be considered platinum-refractory or resistant, meeting any of the following criteria:
- Platinum-refractory defined as progression during the initial platinum-based chemotherapy regimen or failure to achieve a complete response (e.g., stable disease or partial response) with evidence of progressive disease (by physical examination, radiological exams, or CA-125) during the initial platinum-based chemotherapy
- Platinum-resistant defined as recurrence within six months of completion of the initial platinum-based regimen (primary platinum-resistance) or recurrence after six months of completion of the initial platinum-based regimen (still considered platinum-sensitive, but incurable by any approach, that will progress to a secondary platinum-resistance scenario) and failure to ≥ 1 re-induction with a platinum-based regimen (secondary platinum-resistance)
- No high tumor burden, as assessed by the investigator
- No rapidly progressing disease, as assessed by clinical evaluation
- No known CNS (Central Nervous System) involvement by tumor
PATIENT CHARACTERISTICS:
Inclusion criteria:
- Karnofsky performance status > 70%
- Life expectancy ≥ 12 weeks
- ANC (absolute neutrophil count) ≥ 1,500/mm³
- Platelet count ≥ 100,000/mm³
- Serum bilirubin ≤ 2.0 mg/dL
- AST (aspartate aminotransferase) and ALT (alanine aminotransferase) ≤ 2.5 times upper limit of normal (ULN) (≤ 5 times ULN if with liver metastases)
- Creatinine ≤ 2.0 mg/dL
- Prothrombin time < 1.3 times control
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
Exclusion criteria:
- NYHA (New York Heart Association) class III or IV heart disease
- Clinically significant arrhythmias by ECG
- Myocardial infarction within the past 6 months
Any other serious illness, including any of the following:
- Severe ascites
- Severe active infections requiring antibiotics
- Bleeding disorders
- Chronic inflammatory bowel disease
- Diseases that might interfere with the collection of accurate results from this study
- Positive for human anti-human antibodies
- Prior history of tumor (excluding adequately treated nonmelanoma skin cancer or carcinoma in situ of the uterine cervix)
- Uncontrolled hypercalcemia (i.e., > 11.5 mg/dL)
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- Recovered from the toxic effects of any prior therapy
- No concurrent systemic steroids or immunosuppressant agents
No more than 1 prior non-platinum-containing regimen for the treatment of platinum-resistant/refractory disease
- Patients who receive 2 or more different non-platinum-containing chemotherapy regimens for platinum-resistant/refractory disease are not eligible
- More than 4 weeks since prior and no other concurrent chemotherapy, radiotherapy, radiopharmaceuticals (e.g., ^32P), biological therapy, anti-estrogen therapy (including tamoxifen), immunotherapy, or surgery
- More than12 weeks since prior investigational agent
- No prior treatment with a murine or humanized antibody and/or antibody fragment
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:hu3S193
|
20 mg/m2, intravenous, weekly for a maximum of 3 cycles (of 8 weeks each)
|
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 |
|---|---|---|
|
Best Overall Response
大体时间:From start of study treatment until the end of Cycle 1 (8 weeks), Cycle 2 (16 weeks) or Cycle 3 (24 weeks).
|
Best response recorded from the start of treatment until disease progression/recurrence. Includes all patients evaluable for efficacy, regardless of used criteria: RECIST or CA-125 (Cancer Antigen 125). Evaluation of target lesions: Complete Response (CR), resolution of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter (LD sum) of target lesions, taking as reference the baseline LD sum; Progressive Disease (PD), a 20% increase in LD sum of target lesions or the appearance of new lesion(s); Stable Disease (SD), no sufficient shrinkage to qualify as PR nor sufficient increase to qualify as PD. Evaluation of non-target lesions: CR, resolution of all non-target lesions and normalization of CA-125 level; SD, persistence of one or more non-target lesions and/or maintenance of CA-125 level above the normal limits; PD, appearance of one or more new lesions and/or unequivocal progression of existing non-target lesions. |
From start of study treatment until the end of Cycle 1 (8 weeks), Cycle 2 (16 weeks) or Cycle 3 (24 weeks).
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of Participants With Adverse Events and Serious Adverse Events
大体时间:From the first dose of investigational product up to 30 days after the last dose of investigational product
|
A listing of all adverse events is located in the Reported Adverse Event module.
|
From the first dose of investigational product up to 30 days after the last dose of investigational product
|
|
Number of Participants With Adverse Events Reasonably Related to the Investigational Product (Incidence Greater Than 5%).
大体时间:From the first dose of investigational product up to 30 days after the last dose of investigational product
|
Adverse events with possible, probable or definite relationship to the investigational product were considered to be reasonably related.
|
From the first dose of investigational product up to 30 days after the last dose of investigational product
|
|
Mean Cmax and Cmin of Hu3S193 Relating to the First 4 Doses.
大体时间:Pre-dose (within 10 minutes) and Post-dose (5 minutes after completion of infusion) on weeks 1, 2, 3, and 4 of Cycle 1.
|
Cmax = Peak (post-dosing) IP (Investigational Product) plasma concentration.
Cmin = Trough (pre-dosing) IP plasma concentration (Cmin).
Plasma concentration of Hu3S193 expressed in µg/mL.
|
Pre-dose (within 10 minutes) and Post-dose (5 minutes after completion of infusion) on weeks 1, 2, 3, and 4 of Cycle 1.
|
|
Mean Cmax and Cmin of Hu3S193 Relating to the First 8 Doses
大体时间:Pre-dose (within 10 minutes) and Post-dose (5 minutes after completion of infusion) on weeks 1, 2, 3, 4, 5, 6, 7 and 8 of Cycle 1.
|
Cmax = Peak (post-dosing) IP plasma concentration.
Cmin = Trough (pre-dosing) IP plasma concentration (Cmin).
Plasma concentration of Hu3S193 expressed in µg/mL.
|
Pre-dose (within 10 minutes) and Post-dose (5 minutes after completion of infusion) on weeks 1, 2, 3, 4, 5, 6, 7 and 8 of Cycle 1.
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Clinical Benefit
大体时间:From start of study treatment until the end of Cycle 3 (24 weeks).
|
The clinical benefit was calculated considering all patients with objective response rate (CR + PR) or stable disease (SD) for at least 24 weeks according RECIST or CA-125 if patients were non-assessable or when assessment by RECIST was unknown. Clinical benefit = 100% x (Number of patients with objective response + Number of patients with stable disease for at least 24 weeks) / Number of patients included in the efficacy population. The evaluation of target and non-target lesions is described at the Outcome Measure titled "Best Overall Response". CR: Complete Response; PR: Partial Response; SD: Stable Disease. |
From start of study treatment until the end of Cycle 3 (24 weeks).
|
|
Progression Free Survival (PFS)
大体时间:From the first day of the investigational product administration until documentation of disease progression or death due to any cause (whichever occurred first). An average of 16.5549 weeks.
|
Progression free survival (PFS) is defined as the duration of time from start of treatment to time of disease progression.
|
From the first day of the investigational product administration until documentation of disease progression or death due to any cause (whichever occurred first). An average of 16.5549 weeks.
|
|
Overall Survival
大体时间:From start of study treatment until death or the date that patients were last known to be alive. An average of 56.126 weeks.
|
Measured from the beginning of therapy until the date of death or for patients without a known date of death, they will be censored at the date they were last known to be alive.
|
From start of study treatment until death or the date that patients were last known to be alive. An average of 56.126 weeks.
|
|
12-Month Survival Rate
大体时间:12 months from the start of study treatment.
|
Rate of patients alive 12 months after starting therapy with the investigational product.
|
12 months from the start of study treatment.
|
合作者和调查者
调查人员
- 学习椅:Oren Smaletz, MD、Recepta Biopharma
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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.