Phase II trial of hippocampal-sparing whole brain irradiation with simultaneous integrated boost for metastatic cancer

Author:

Westover Kenneth D12ORCID,Mendel J Travis1,Dan Tu1,Kumar Kiran1,Gao Ang13,Pulipparacharuv Suprabha1,Iyengar Puneeth1,Nedzi Lucien1,Hannan Raquibul1,Anderson John1,Choe Kevin S4,Jiang Wen1,Abdulrahman Ramzi1,Rahimi Asal1,Folkert Michael1,Laine Aaron1,Presley Chase15,Cullum C Munro5,Choy Hak1,Ahn Chul3,Timmerman Robert1

Affiliation:

1. Department of Radiation Oncology, Fairfax, Virginia

2. Department of Biochemistry, Fairfax, Virginia

3. Department of Clinical Science, Fairfax, Virginia

4. The University of Texas Southwestern Medical Center, Dallas, Texas; Inova Schar Cancer Institute, Fairfax, Virginia (K.S.C.)

5. Department of Psychiatry, Fairfax, Virginia

Abstract

Abstract Background Advanced radiotherapeutic treatment techniques limit the cognitive morbidity associated with whole-brain radiotherapy (WBRT) for brain metastasis through avoidance of hippocampal structures. However, achieving durable intracranial control remains challenging. Methods We conducted a single-institution single-arm phase II trial of hippocampal-sparing whole brain irradiation with simultaneous integrated boost (HSIB-WBRT) to metastatic deposits in adult patients with brain metastasis. Radiation therapy consisted of intensity-modulated radiation therapy delivering 20 Gy in 10 fractions over 2–2.5 weeks to the whole brain with a simultaneous integrated boost of 40 Gy in 10 fractions to metastatic lesions. Hippocampal regions were limited to 16 Gy. Cognitive performance and cancer outcomes were evaluated. Results A total of 50 patients, median age 60 years (interquartile range, 54–65), were enrolled. Median progression-free survival was 2.9 months (95% CI: 1.5–4.0) and overall survival was 9 months. As expected, poor survival and end-of-life considerations resulted in a high exclusion rate from cognitive testing. Nevertheless, mean decline in Hopkins Verbal Learning Test–Revised delayed recall (HVLT-R DR) at 3 months after HSIB-WBRT was only 10.6% (95% CI: −36.5‒15.3%). Cumulative incidence of local and intracranial failure with death as a competing risk was 8.8% (95% CI: 2.7‒19.6%) and 21.3% (95% CI: 10.7‒34.2%) at 1 year, respectively. Three grade 3 toxicities consisting of nausea, vomiting, and necrosis or headache were observed in 3 patients. Scores on the Multidimensional Fatigue Inventory 20 remained stable for evaluable patients at 3 months. Conclusions HVLT-R DR after HSIB-WBRT was significantly improved compared with historical outcomes in patients treated with traditional WBRT, while achieving intracranial control similar to patients treated with WBRT plus stereotactic radiosurgery (SRS). This technique can be considered in select patients with multiple brain metastases who cannot otherwise receive SRS.

Funder

University of Texas Southwestern Medical Center

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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