跳至主要内容
临床试验/NCT04832620
NCT04832620招募中不适用

Defining Optimal Imaging Strategies for Diagnosis, Treatment, and Treatment Evaluation of Chordomas and Chondrosarcomas of the Axial Skeleton

Leiden University Medical Center2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2021年2月2日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
40
试验地点
2
主要终点
Vp(max), Vp(min)

研究概览

简要总结

Rationale: Chordomas and chondrosarcomas located in the axial skeleton are malignant neoplasms of bone. These tumors share the same clinical challenges, as the effect of the disease is more a function of their local aggressiveness than their tendency to metastasize (20% metastasize). The local aggressive behavior can cause debilitating morbidity and mortality by destruction of nearby located critical neurovascular structures. Imaging has, in addition to histopathology, a role in diagnosis and in guiding (neo)adjuvant and definitive treatment. Despite the low sensitivity to radiotherapy, proton radiotherapy has been successfully used as an adjunct to resection or as definitive treatment for aggressive chordomas and chondrosarcomas, making it a standard indication for proton therapy in the Netherlands.

Chordomas and chondrosarcomas consist, especially after previous therapy, of non-viable and viable tumor components. Identification of these viable components by functional imaging is important to determine the effect of previous therapy, as change in total tumor volume occurs more than 200 days after change of functional imaging parameters.

Objective: The main objective of this study is to determine if functional MRI parameters change within 6 months, and earlier than volumetric changes after start of proton beam therapy. This would allow timely differentiation between affected and unaffected (viable) tumor components, which can be used for therapy adjustment.

Secondary objectives: Determine which set of parameters (PET-CT and secondary MRI) can predict clinical outcome (tumor specific mortality, development of metastases, morbidity secondary to tumor activity and morbidity secondary to treatment); determine what type of imaging can accurately identify viable tumor nodules relative to critical anatomical structures; improving understanding of relevance of changing imaging parameters by correlating these with resected tumor.

Study design: Prospective cohort study Study population: LUMC patients diagnosed with primary or recurrent chordoma or chondrosarcoma in the axial skeleton. A number of 20 new patients per year is expected.

Main study parameters: Volumetric and functional MR imaging parameters including permeability parameters.

Secondary parameters are generated by PET-CT (SUV, MTV and TLG), MR (perfusion, permeability and diffusion), therapy (proton beam dose mapping, surgery) and clinical outcome. End points are disease specific survival, progression free survival (including development of metastases), side effects of treatment, and functional outcome (see CRF). In patients who are treated with surgical resection following neo-adjuvant therapy, the surgical specimen will be correlated with imaging findings.

Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Treatment and clinical management will not be affected in this study, thus the additional burden, risks, and benefits associated with participation in this study are minimal.

Two extra MRI and one PET-CT examination will be planned during proton therapy.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically diagnosed with primary or recurrent chordoma or chondrosarcoma in the axial skeleton (clivus, spine and sacrum)
  • Accepted for standard proton beam therapy

排除标准

  • Diagnosis other than chordoma or chondrosarcoma is made.
  • Patient refuses (parts) of the standard treatment protocol.
  • Patient refuses MRI due to claustrophobia.
  • Patient not suitable for MRI due to the presence of MRI incompatible implants.
  • Incapacitated patients.
  • Patient doesn't allow coded data to be used for analysis.
  • Patient is under 50 years of age.
  • Lesion size less than 1cm.
  • Patients with WHO 3 and higher.

结局指标

主要结局

Vp(max), Vp(min)

时间窗: At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment

MRI permeability parameter - tumor plasma volume

次要结局

  • Max Enhancement (%)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Wash In Rate (sˉ¹)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Brevity of Enhancement (s)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Ktrans(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Ve(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • mean ADC, Min ADC, Max ADC(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Rel Enhancement (%)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Time of arrival T0 (s)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Area under the curve (AUC)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • SUV(At inclusion and and 11 months following the start date fo proton therapy)
  • TLG(At inclusion and and 11 months following the start date fo proton therapy)
  • Max Rel Enhancement (%)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Time To Peak (s)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • Wash Out Rate (sˉ¹)(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • kep(At inclusion, 4 and 8 weeks, 5,11,17 and 23 months after the start date of proton therapy treatment)
  • MTV(At inclusion and and 11 months following the start date fo proton therapy)

研究者

发起方
Leiden University Medical Center
申办方类型
Other
责任方
Principal Investigator
主要研究者

Augustinis D.G. Krol, MD PhD

Radiation oncologist

Leiden University Medical Center

研究点 (2)

Loading locations...

相似试验