Comparison of Neurocognitive Outcome in Two Standard Regimen for Treatment of Low-risk Medulloblastoma
概览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 96
- 试验地点
- 2
- 主要终点
- Neurocognitive Outcomes using WPPSIIV
概览
简要总结
This is a trial to compare neurocognitive outcomes in the intent-to-treat population 2.5 years after diagnosis between patients with newly diagnosed, non-metastatic, SHH-activated, TP53-wt, non-MYC amplified MF randomized to the interventional arms A ("Head Start 4") or B (HIT-SKK).
详细描述
In this study, two highly effective irradiation-sparing treatment regimens are being compared in patients with low-risk early childhood MB:
- Arm A: The "Head Start" 4 regimen developed by the North American Head Start Consortium. This approach uses intensive Induction chemotherapy and Consolidation with HDCT and has led to equally favorable results in this subgroup -- 3y PFS was 96% for infants and young children with M0, SHH MB; 5y EFS was 93% for M0, DMB on the predecessor "Head Start" 3 study.
- Arm B: The HIT-SKK regimen developed within the GPOH. This regimen combines systemic chemotherapy with intraventricular MTX, leading to 93% 5-year PFS in low-risk patients.
Both treatment regimens use high-dose i.v. MTX, but only the HIT-SKK regimen also uses intraventricular administration of MTX directly into the CSF in addition to i.v. MTX. Given the long-term neurocognitive deficits of MTX have been described in childhood leukemia, and the pathogenesis of MTX-induced CNS-damage has been described, this has raised some concerns. Similarly, highly intensive, HDCT containing "Head Start" chemotherapy carries specific risks for the neurocognitive outcomes. Encouragingly, five years after HIT-SKK treatment including intraventricular MTX, young children with MB have a mean fluid intelligence score of 93.8 points. The full-scale IQ after "Head Start" chemotherapy is 95.4 and likewise within normal range. On the other hand, highly intensive, HDCT/AuHCR containing "Head Start" chemotherapy carries specific risks for the neurocognitive outcomes. However, neurocognitive outcomes after the HIT-SKK and "Head Start" chemotherapy regimens are difficult to compare from existing data, because of small sample sizes and inhomogeneous assessment tools used in prior studies. Therefore, a confirmatory study utilizing the same measures administered at the same time points is required to identify clinically relevant differences. In addition, survival, occurrence of second malignancies, neurological and endocrine deficits, hearing loss, and psychosocial comorbidities are also of high relevance in survivors of MB and may differ after both regimens. Since these also severely limit the survivors' potential for activity and participation in everyday life and affect their parents and siblings as well, this information will also be recorded.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- — 至 5 Years(Child)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- 未提供
排除标准
- 未提供
研究组 & 干预措施
Arm A: "Head Start" 4
Arm A consists of 3 to 5 Induction chemotherapy cycles and one high-dose chemotherapy cycle evaluated in the "Head Start" 4 study.
干预措施: Bridging Chemotherapy (Drug)
Arm A: "Head Start" 4
Arm A consists of 3 to 5 Induction chemotherapy cycles and one high-dose chemotherapy cycle evaluated in the "Head Start" 4 study.
干预措施: Induction Cycles A1-A3 (Drug)
Arm A: "Head Start" 4
Arm A consists of 3 to 5 Induction chemotherapy cycles and one high-dose chemotherapy cycle evaluated in the "Head Start" 4 study.
干预措施: Induction Cycles A4-5 (Drug)
Arm A: "Head Start" 4
Arm A consists of 3 to 5 Induction chemotherapy cycles and one high-dose chemotherapy cycle evaluated in the "Head Start" 4 study.
干预措施: Consolidation Cycle A6 (Drug)
Arm B: HIT-SKK
Arm B consists of 3 to 5 cycles of chemotherapy evaluated in the HIT-SKK'92 (Rutkowski et al. 2005) and HIT-2000 (NCT00303810) clinical studies.
干预措施: Bridging Chemotherapy (Drug)
Arm B: HIT-SKK
Arm B consists of 3 to 5 cycles of chemotherapy evaluated in the HIT-SKK'92 (Rutkowski et al. 2005) and HIT-2000 (NCT00303810) clinical studies.
干预措施: HIT-SKK Chemotherapy Cycles B1-3 (Drug)
Arm B: HIT-SKK
Arm B consists of 3 to 5 cycles of chemotherapy evaluated in the HIT-SKK'92 (Rutkowski et al. 2005) and HIT-2000 (NCT00303810) clinical studies.
干预措施: Modified HIT-SKK Cycle B4-5 (Drug)
结局指标
主要结局
Neurocognitive Outcomes using WPPSIIV
时间窗: 105 months
To compare neurocognitive outcomes 2.5 years after diagnosis between patients randomized to the interventional arms A ("Head Start" 4) and B (HIT-SKK). Full-Scale Intelligence Quotient (IQ) as measured by the Wechsler Preschool and Primary Scale of Intelligence (WPPSIIV) administered to those between the ages of 2 years and 6 months to 7 years and 7 months old at 2.5 years after diagnosis (+/- 6 months).
次要结局
- Incidence of therapy-related deaths(152 months)
- OS(152 months)
- Second malignancies(152 months)
- Number of patients with treatment-related adverse events as assessed by CTCAE v5.0(152 months)
- PFS(152 months)
- rtPFS(152 months)
- Assessment of IQ in patients randomized to Head Start or HIT-SKK(152 months)
- Assessment of Development and Adaptive Functioning using ABAS v2 or v3(152 months)
- Quality of Life Assessment using PedsQL Infant or PedsQL 4.0 parent-reported Quality of Life Measure(152 months)
- Correlation between neurocognitive outcomes and QoL(152 months)
- Assessment of impact on hearing using SIOP Boston scale(152 months)
- Number of patients with Leukoencephalopathy(152 months)
- Compare PFS(152 months)
- Assess rate of patients with cancer predisposition syndromes(152 months)
- Compare rtPFS(152 months)
- Compare OS(152 months)
- Assessment of impact on hearing using Chang scales(152 months)
- Association between neurocognitive and behavioral outcomes(152 months)