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Adaptive Stereotactic Body Radiation

Adaptive Radiation for Abdominopelvic Metastases

  • RegistryNCT05880667
  • PhasePhase 1
  • StatusRecruiting
  • ConditionAbdominopelvic Metastases
  • SponsorFox Chase Cancer Center
How Adaptive Stereotactic Body Radiation works1 min

The drug

What is being tested.

Radiation therapy is given following generation of planning imaging at the time of simulation. A recent development has been diagnostic quality onboard imaging incorporated within radiation treatment machines. The incorporation of onboard imaging into standard practice has allowed the use Stereotactic Body Radiation (SBRT), which is a precise radiation technique that allows safe delivery of ablative radiation doses.

This is a dose-escalation study where the objective is to find the Maximum Tolerated Dose (MTD) and Recommended Phase 2 Dose (RP2D) of adaptive SBRT for abdominopelvic SBRT. There are 3 doses of interest 8Gy/fraction (level 1), 9Gy/fraction (level 2), and 10Gy/fraction (level 3). The starting dose will be level 2.

We will use a Bayesian Optimal Interval Design (BOIN) to define dose escalation and de-escalation rules based on the proportion of patients experiencing a dose-limiting toxicity (DLT). DLT events are Grade 3 events possibly, probably, or definitely related to the study intervention.

The study

How the trial runs.

Single arm Phase I trial of adaptive stereotactic body radiation (SBRT) for abdominopelvic metastases. Adaptive SBRT will allow for escalation of the prescription dose and target coverage while maintaining grade 3+ toxicity no greater than 10%. Subjects with metastatic cancer to the abdomen or pelvis requiring local control or palliation will be enrolled.

Live record on ClinicalTrials.gov →

Eligibility

Who the study is looking for.

  • Subjects must have histologically or cytologically confirmed cancer that is metastatic (all solid tumor types accepted), with at least one target lesion untreated by radiation, IR techniques, or growing in the abdomen or pelvis. Adjacent lymph nodes in the same region (5 cm or closer) constitute one active lesion. Target lesion must be measurable according to RECIST v 1.1. Previous systemic therapies are allowed.
  • ECOG performance status 0 or 1
  • Estimated survival of >/= 12 months
  • Absolute neutrophil count > 1,500/mcL
  • Platelets > 100,000/mcL

Inclusion criteria as written on the registry, trimmed. The full list, with exclusions, is on the live record.

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