OncoMatch

OncoMatch/Clinical Trials/NCT06518057

Hippocampal Avoidance in Craniospinal Irradiation for the Treatment of Leptomeningeal Metastases From Breast Cancer or Non-small Cell Lung Cancer

Is NCT06518057 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies non-drug interventions for anatomic stage iv breast cancer ajcc v8.

Phase 2RecruitingUniversity of WashingtonNCT06518057Data as of May 2026

This phase II clinical trial studies how well craniospinal irradiation (CSI) with hippocampal avoidance, using proton therapy or volumetric modulated arc therapy (VMAT), works in treating patients with breast cancer or non-small cell lung cancer (NSCLC) that has spread from the original (primary) tumor to the cerebrospinal fluid (CSF) and meninges (thin layers of tissue that cover and protect the brain and spinal cord) (leptomeningeal metastases). Radiation therapy is an effective treatment in relieving localized symptoms caused by leptomeningeal metastases. However, the type of radiation therapy typically used does not prevent the spread of leptomeningeal disease. CSI (radiation therapy directed at the brain and spinal cord to kill tumor cells) may be able to target all of the areas of possible leptomeningeal tumor spread. CSI may however result in significant neurological side effects due to radiation damage to a part of the brain called the hippocampus. Hippocampal avoidance (HA) reduces the amount of radiation to the hippocampus. Proton or VMAT CSI with HA may be an effective treatment while reducing neurological side effects for patients with leptomeningeal metastases from breast cancer and NSCLC.

Check if I qualify

Extracted eligibility criteria

Cancer type

Breast Carcinoma

Non-Small Cell Lung Carcinoma

Tumor Agnostic

Disease stage

Required: Stage IV

Metastatic disease required

Prior therapy

Cannot have received: radiation therapy

Exception: only if previous radiotherapy to the intended treatment site precludes developing a treatment plan that respects normal tissue tolerances

Previous radiotherapy to the intended treatment site that precludes developing a treatment plan that respects normal tissue tolerances

Lab requirements

Blood counts

hemoglobin > 8 g/dl; absolute neutrophil count > 1,000/mm; platelet count > 100,000/mm

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • University of California San Francisco · San Francisco, California
  • Fred Hutch/University of Washington Cancer Consortium · Seattle, Washington

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify