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Online Adaptive stereotactic radiotherapy for abdominopelvic lymphnode oligometastasis.

Online Adaptive stereotactic radiotherapy for abdominopelvic lymphnode oligometastasis. - STEAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON45533
Enrollment
53
Registered
2017-07-12
Start date
2017-05-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

abdominopelvic lymphnode oligometastasis

Interventions

Before every fraction of the radiotherapy, a CT scan will be made.
abdomen
oligometastasis

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: * Indication to SBRT after discussion in Institutional Tumor Board * Patients with abdominal and/or pelvic lymph node metastases of solid tumors * No more than 5 metastatic lesions in no more than 2 organs and a controlled primary tumor site * Diagnostic imaging includes at least a PET-scan and CT *thorax/abdomen, of which one is not older than 4 weeks at the time of referral for SBRT. * Primary tumor must be treated at least 4 months before the diagnosis of the metastasis * Patients must be 18 years or older

Exclusion criteria

Exclusion criteria: * Prior radiotherapy in the same field. * Second primary malignancy except in situ carcinoma of the cervix, adequately treated non-melanoma skin cancer, or other malignancy treated at least 3 years previously without evidence of recurrence. * Pregnancy. * Serious concomitant systemic disorders that would compromise the safety of the patient or his/her ability to complete the study, at the discretion of the investigator.

Design outcomes

Primary

MeasureTime frame
Determine local control of Stereotactic radiotherapy treatment in patients with abdominal and pelvic lymph node oligometastases.

Secondary

MeasureTime frame
Determine overall survival Toxicity of treatment ( NCI CTCAE).

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)