Clinical trial of proton craniospinal irradiation for leptomeningeal metastases

Author:

Yang T Jonathan123,Wijetunga Neil A1,Yamada Josh12,Wolden Suzanne1,Mehallow Michelle1,Goldman Debra A4,Zhang Zhigang4,Young Robert J5,Kris Mark G6,Yu Helena A6,Seidman Andrew D7,Gavrilovic Igor T83,Lin Andrew83,Santomasso Bianca8,Grommes Christian83,Piotrowski Anna F83,Schaff Lauren83,Stone Jacqueline B83,DeAngelis Lisa M83,Boire Adrienne839ORCID,Pentsova Elena83

Affiliation:

1. Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York

2. PROMISE (Precision Radiation for OligoMetastatIc and MetaStatic DiseasE) Program, Memorial Sloan Kettering Cancer Center, New York, New York

3. Brain Tumor Center, Memorial Sloan Kettering Cancer Center, New York, New York

4. Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York

5. Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, New York

6. Division of Solid Tumor Oncology, Thoracic Oncology Service, Memorial Sloan Kettering Cancer Center, New York, New York

7. Division of Solid Tumor Oncology, Breast Medicine Service, Memorial Sloan Kettering Cancer Center, New York, New York

8. Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, New York

9. Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York

Abstract

Abstract Background Leptomeningeal metastases (LM) are associated with limited survival and treatment options. While involved-field radiotherapy is effective for local palliation, it lacks durability. We evaluated the toxicities of proton craniospinal irradiation (CSI), a treatment encompassing the entire central nervous system (CNS) compartment, for patients with LM from solid tumors. Methods We enrolled patients with LM to receive hypofractionated proton CSI in this phase I prospective trial. The primary endpoint was to describe treatment-related toxicity, with dose-limiting toxicity (DLT) defined as any radiation-related grade 3 non-hematologic toxicity or grade 4 hematologic toxicity according to the Common Terminology Criteria for Adverse Events that occurred during or within 4 weeks of completion of proton CSI. Secondary endpoints included CNS progression-free survival (PFS) and overall survival (OS). Results We enrolled 24 patients between June 2018 and April 2019. Their median follow-up was 11 months. Twenty patients were evaluable for protocol treatment–related toxicities and 21 for CNS PFS and OS. Two patients in the dose expansion cohort experienced DLTs consisted of grade 4 lymphopenia, grade 4 thrombocytopenia, and/or grade 3 fatigue. All DLTs resolved without medical intervention. The median CNS PFS was 7 months (95% CI: 5–13) and the median OS was 8 months (95% CI: 6 to not reached). Four patients (19%) were progression-free in the CNS for more than 12 months. Conclusion Hypofractionated proton CSI using proton therapy is a safe treatment for patients with LM from solid tumors. We saw durable disease control in some patients.

Funder

National Institutes of Health

National Cancer Institute

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Clinical Neurology,Oncology

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