A Phase I Clinical Trial of mTOR Inhibition With Sirolimus for Enhancing NY-ESO-1 Protein With MIS416 Vaccine Induced Anti-Tumor Immunity in Ovarian, Fallopian Tube and Primary Peritoneal Cancer
试验速览
- 阶段
- 1 期
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- Incidence of adverse events defined by National Cancer Institute Common Terminology Criteria for Adverse Events version 4.03
研究概览
简要总结
This phase I clinical trial studies the side effects of sirolimus and NY-ESO-1 protein with MIS416 in treating patients stage II-IV ovarian, fallopian tube, or primary peritoneal cancer. Sirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Vaccine therapy, like Y-ESO-1 protein with MIS416, may strengthen the immune system to find and kill tumor cells. Biological therapies, such as sirolimus, use substances made from living organisms that may stimulate or suppress the immune system in different ways and stop tumor cells from growing. Giving sirolimus and vaccine therapy may work betting in treating patients with ovarian, fallopian tube or primary peritoneal cancer.
详细描述
PRIMARY OBJECTIVE:
I. Determine the safety and feasibility of NY-ESO-1 protein with MIS416 in combination with mammalian target of rapamycin (mTOR) inhibitor sirolimus.
SECONDARY OBJECTIVES:
I. To determine the effectiveness of these combinatorial therapies by assessing NY-ESO-1 specific cellular and humoral immunity: peripheral blood NY-ESO-1 specific cluster of differentiation (CD)8+ and CD4+ T-cells; peripheral blood NY-ESO-1 specific antibodies; peripheral blood frequency of CD4+ CD25+ forkhead box P3 (FOXP3)+ regulatory T-cells; explore time to disease progression.
OUTLINE:
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women with stages II-IV epithelial ovarian, fallopian tube, or primary peritoneal carcinoma who have completed standard therapy for primary or recurrent disease (i.e., patients who would normally be observed); eligible patients may have asymptomatic residual measurable disease on physical examination and/or computed tomography (CT) scan, and/or may have an elevated cancer antigen 125 (CA-125); or may be in complete clinical remission after treatment for primary or recurrent disease; these patients would normally enter a period of observation after standard management
- •Any human leukocyte antigen (HLA) type (historic HLA typing is permitted)
- •Tumor expression of NY-ESO-1 by immunohistochemistry (IHC) and/or real-time polymerase chain reaction (RTPCR)
- •No history of previous severe allergic reactions to vaccines or unknown allergens
- •Life expectancy > 6 months
- •Have an Eastern Cooperative Oncology Group (ECOG) performance status of =< 2
- •Hematology and biochemistry laboratory results within the limits normally expected for the patient population, without evidence of major organ failure
- •Absolute neutrophil count (ANC) >= 1,000/uL
- •Platelets (PLT) >= 75,000/uL
- •Hemoglobin (Hgb) >= 8 g/dL
- •Total bilirubin =< 1.5 x upper limits of normal (ULN)
- •Serum glutamic-oxaloacetic transaminase(SGOT)/aspartate aminotransferase (AST) or serum glutamate pyruvate transaminase(SGPT)/alanine aminotransferase (ALT) =< 3 x ULN
- •Serum creatinine =< 2 x ULN
- •Prothrombin time(PT)/international normalized ratio(INR) =< 1.5
- •Electrocardiogram, showing no indications of cardiac problems like congestive heart failure, myocardial infarction, and cardiomyopathy
- •Have been informed of other treatment options
- •Ability to swallow and retain oral medication
- •Participants of child-bearing potential must agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control) prior to study entry; should a woman become pregnant or suspect she is pregnant while she is participating in this study, she should inform her treating physician immediately
- •Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure
- •Patients may have received previous NY-ESO-1 vaccine therapy
排除标准
- •Metastatic disease to the central nervous system
- •Other serious illnesses (e.g., serious infections requiring antibiotics, bleeding disorders)
- •History of severe autoimmune disorders requiring use of steroids or other immunosuppressives
- •Concomitant systemic treatment with corticosteroids, anti-histamine or non-steroidal antiinflammatory drugs for >2 weeks,, and other platelet inhibitory agents, strong inhibitors/inducers of cytochrome P450-3A4 (CYP450-3A4)
- •Chemotherapy, radiation therapy, or immunotherapy within 4 weeks prior to first dosing of study drug (6 weeks for nitrosoureas); concomitant hormonal therapies for breast cancers are allowed
- •Patients with a positive fecal occult blood test excluding hemorrhoids
- •Clinically significant heart disease (New York Heart Association [NYHA] class III or IV) within six months
- •Participation in any other clinical trial involving another investigational agent within 4 weeks prior to first dosing of study drug
- •Known hepatitis B, hepatitis C, or human immunodeficiency virus (HIV)
- •Mental impairment that may compromise the ability to give informed consent and comply with the requirements of the study
- •Lack of availability of a patient for immunological and clinical follow-up assessment
- •Known pulmonary hypertension
- •Known hypersensitivity to sirolimus
- •Evidence of current drug or alcohol abuse or psychiatric impairment, which in the Investigator's opinion will prevent completion of the protocol therapy or follow-up
- •Pregnant or nursing female patients
- •Unwilling or unable to follow protocol requirements
- •Any condition which in the investigator's opinion deems the patient an unsuitable candidate to receive study drug (i.e., any significant medical illness or abnormal laboratory finding that would, in the investigator's judgment, increase the subject's risk by participating in this study)
研究组 & 干预措施
Cohort I (NY-ESO-1 protein with MIS416)
Patients receive NY-ESO-1 protein with MIS416 vaccine SC on days 1, 15, 29, 57, 85, and 113 in the absence of disease progression or toxicity.
干预措施: Laboratory Biomarker Analysis (Other)
Cohort I (NY-ESO-1 protein with MIS416)
Patients receive NY-ESO-1 protein with MIS416 vaccine SC on days 1, 15, 29, 57, 85, and 113 in the absence of disease progression or toxicity.
干预措施: Recombinant NY-ESO-1 Protein (Biological)
Cohort II (NY-ESO-1 protein with MIS416, sirolimus)
Patients receive NY-ESO-1 protein with MIS416 vaccine as in Cohort I. Patients also receive sirolimus PO daily for 2 weeks followed by 2 weeks off starting on days 1, 29, 57, and 85.
干预措施: Laboratory Biomarker Analysis (Other)
Cohort II (NY-ESO-1 protein with MIS416, sirolimus)
Patients receive NY-ESO-1 protein with MIS416 vaccine as in Cohort I. Patients also receive sirolimus PO daily for 2 weeks followed by 2 weeks off starting on days 1, 29, 57, and 85.
干预措施: Recombinant NY-ESO-1 Protein (Biological)
Cohort II (NY-ESO-1 protein with MIS416, sirolimus)
Patients receive NY-ESO-1 protein with MIS416 vaccine as in Cohort I. Patients also receive sirolimus PO daily for 2 weeks followed by 2 weeks off starting on days 1, 29, 57, and 85.
干预措施: Sirolimus (Drug)
结局指标
主要结局
Incidence of adverse events defined by National Cancer Institute Common Terminology Criteria for Adverse Events version 4.03
时间窗: Up to 30 days
The toxicity rate for each adverse event will be estimated using a two-sided, 95%, exact binomial confidence interval (Clopper-Pearson).
次要结局
- NY-ESO-1 specific CD4+ and CD8+ T-cells cellular immunity assessed in peripheral blood by enzyme-linked immunosorbent spot (ELISPOT) and intracellular cytokine staining (ICS)(Up to 12 months)
- NY-ESO-1 specific humoral immunity(Up to 12 months)
- Time to disease progression as documented by Response Evaluation Criteria in Solid Tumors version 1.1(Up to 12 months)