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. Author manuscript; available in PMC: 2017 Dec 19.
Published in final edited form as: Int J Radiat Oncol Biol Phys. 2014 Jan 1;88(1):130–136. doi: 10.1016/j.ijrobp.2013.09.051

Table 1.

Patients inclusion and exclusion criteria.

Inclusion Criteria
  1. Histologically confirmed malignancy with the presence of one or two intraparenchymal brain metastasis.

  2. Age ≥18 years

  3. Karnofsky performance status ≥70

  4. Neurologic function status 0–2

  5. Patients may have extracranial sites of metastatic disease

  6. Adequate bone marrow reserve (hemoglobin ≥8 grams, absolute neutrophil count ≥1000/mm3, platelets ≥50,000/mm3

  7. Patient must sign a study specific informed consent form. If the patient’s mental status precludes his/her giving informed consent, written informed consent may be given to the patient’s legal representative

Exclusion Criteria
  1. Major medical illness including poor cardiac, pulmonary or renal status which would result in patient being a high risk candidate for neurosurgical procedure

  2. Inability to obtain histologic proof of malignancy

  3. Leptomeningeal metastases documented by MRI or CSF evaluation

  4. Metastases within 10 mm of the optic apparatus so that some portion of the optic nerve or chiasm would be included in the high dose SRS boost field

  5. Metastases in the brainstem, midbrain, pons, or medulla

  6. Patients with small cell lung cancer, germ-cell tumors, lymphoma, leukemia and multiple myeloma

  7. Prior history of radiation therapy

  8. Concomitant use of chemotherapy or targeted biological therapy (within a week of SRS treatment)

  9. Patients with ≥3 metastases in the brain

  10. Allergy to both CT and MRI contrast dyes

  11. Platelet count <100,000/mcL or coagulation disorders that cannot be corrected or would render the surgery a high-risk procedure.

Abbreviations: CT: computed tomography, MRI: magnetic resonance imaging.