DRKS00024109招募中1 期
A phase I safety, dose finding and feasibility trial of GD2IL18CART in patients with relapsed or refractory GD2 positive solid cancers - GD2IL18CART
niversität Münster0 个研究点目标入组 178 人开始时间: 2024年4月2日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 178
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- N/a: Single Arm Study
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 1 Years 至 one（—）
- 性别
- All
入选标准
- •Male or female patients must have a diagnosis of relapsed and/or refractory (r/r) neuroblastoma, Ewing sarcoma, osteosarcoma or advanced breast cancer, judged to be incurable with conventional treatment.
- •Among patients with advanced breast cancer,
- •- patients with hormone receptor positive disease must have exhausted all endocrine therapy options including a combination with a CDK4/6 inhibitor and chemotherapy must not be a reasonable therapy option,
- •- patients with HER2 positive disease should have received Trastuzumab-Emtansin (T-DM1) and/or T-DXd in second line after a HER2 directed antibody in the (neo)adjuvant setting or in first line therapy,
- •- patients with triple negative disease must have received at least 2 prior lines of chemotherapy including Sacituzumab-Govitecan in the metastatic setting, and patients with combined positive score (CPS) >10 and/or immune cell score (IC) >= 1% should have received an immune checkpoint inhibitor previously.
- •For neuroblastoma, patients with locoregional recurrence must have received surgery and/or radiotherapy followed by relapse chemotherapy. Patients with metastatic recurrence after initial classification as intermediate risk must have received high risk therapy. Patients with recurrence after initial classification as high risk must have received relapse chemotherapy alone or combined with immunotherapy.
- •Patients with Ewing sarcoma must have received front-line therapy and at least one prior line of relapse chemotherapy according to standard regimens (alkylating agents in combination with topoisomerase inhibitors; irinotecan with temozolomide; gemcitabine and docetaxel; high-dose ifosfamide; carboplatin with etoposide. Patients with an isolated lung relapse must have received pulmonary irradiation either during frontline or relapse therapy.
- •Patients with osteosarcoma must have received front-line therapy and at least one prior line of relapse chemotherapy (alkylating agents and/or etoposide and/or carboplatin or gemcitabine and docetaxel). Patients with an isolated relapse manifestation (lung metastasis or local relapse) must have unresectable disease.
- •All patients must meet the following disease-specific criteria:
- •GD2 expression on tumor cells in archival or newly obtained biopsy (recommended after GD2 antibody therapy) in the central reference lab. GD2-positive tumor is defined as = 50% of tumor cells expressing = 2+ GD2 using an immunofluorescence staining (IF) assay for specific detection of GD2 expression in formalin-fixed, paraffin-embedded neoplastic tissue or frozen tumor tissue along with a semi- quantitative evaluation.
- •Evaluable disease based on RECIST v1.1 (all disease entities) or by MIBG-scan or PET-scan or bone marrow biopsy/aspirate (neuroblastoma)
- •Age =1 and <80 years
- •Absolute CD3+ T cell count =200/µl
- •ECOG performance score of 0-2 if >16 years old or Lansky performance score of >=60 if =16 years old at screening
- •No childbearing potential or negative pregnancy test at screening and before chemotherapy in women with childbearing potential
- •Signed and dated informed consent/assent by patients and/or parents, before conduct of any trial-specific procedure.
排除标准
- •Patients will be entered into this trial only if they meet none of the following criteria:
- •Active solid brain metastases
- •Current autoimmune disease or history of autoimmune disease with potential CNS involvement
- •Active clinically significant CNS dysfunction (including but not limited to uncontrolled seizure disorders, cerebrovascular ischemia or hemorrhage, dementia, paralysis)
- •History of an additional malignancy other than non-melanoma skin cancer or carcinoma in situ unless disease free for =3 years
- •Pulmonary function: Patients with pre-existing severe lung disease or an oxygen requirement of >28% O2 supplementation or active pulmonary infiltrates on X-ray
- •Cardiac function: Pediatric patients: fractional shortening <28% or left ventricular ejection fraction <50% by echocardiography, adult patients: left ventricular ejection fraction <50% by echocardiography
- •Renal function: GFR =29 mL/min/1.73 m2 by CKD-EPI for patients =18 yrs or creatinine clearance =29 mL/min/1.73 m2 by Schwartz formula for patients <18 yrs of age
- •Liver function: Patients with a serum bilirubin >3 times upper limit of normal or an AST or ALT >5 times upper limit of normal, unless due to liver infiltration by the underlying malignant disease in the estimation of the Investigator
- •Hematological function: Patients must have an absolute neutrophil count (ANC) = 500/µl and a platelet count = 50 × 10e3/µl
- •Presence of any active infection
- •Rapidly progressive disease that in the estimation of the Investigator would compromise ability to complete study therapy
- •Pregnant or breast-feeding females
- •Concurrent or recent prior therapies:
- •-High-dose chemotherapy with autologous stem cell transplantation or requiring autologous stem cell rescue or anticancer biologicals (e.g. mifamurtide, interferons) or immune checkpoint inhibitors or radiation therapy or major surgery within 30 days prior to leukapheresis
- •-Neuroblastoma patients who have relapsed after allogeneic or haploidentical stem cell transplantation must be at least 100 days posttransplant, with no evidence of GVHD and not taking immunosuppressive agents for at least 30 days prior to leukapheresis.
- •-I131 MIBG therapy (neuroblastoma) must be completed at least 3 months prior to apheresis.
- •-GD2-specific antibody therapy with dinutuximab beta or naxitamab within 40 days (5 half lives)
- •-Antiproliferative chemotherapies, epigenetic agents, antibody drug conjugates or antibodies targeting alternative antigens than GD2 within 3 weeks prior to leukapheresis
- •-Immunosuppressive agents other than steroids within 2 weeks prior to leukapheresis
- •-Short-acting molecularly targeted agents (kinase inhibitors) within 7 days prior to leukapheresis
- •-Systemic corticosteroids with the exception of physiologic replacement dosing within 7 days prior to leukapheresis
- •-Live vaccines within 30 days prior to leukapheresis
- •Hypersensitivity against any drug or its ingredients/impurities that is scheduled or likely to be given during trial participation, e.g. as part of the mandatory preparative chemotherapy, pre-medication for infusion, rescue medication/salvage therapies for treatment related toxicities
- •Contraindication of trial related procedures as judged by the Investigator, e.g. tumor biopsy
- •Female patients of child-bearing potential not willing to practice a highly effective form of birth control from the time of signing the informed consent form and for 12 months after dosing t
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