• Subject must have histologically confirmed adenoid cystic carcinoma (ACC) of any primary site with distant metastases detected clinically or on imaging (biopsy of metastatic disease preferred, but not required)

• Cohort 1

‣ One to five detectable sites of metastatic disease at any organ or site (including bone and CNS involvement)

• Maximum size of 3 cm for brain lesions.

∙ Note: Measurable disease is not required

∙ Note: Patients with isolated intracranial disease for whom SRS would be the preferred standard of care are not eligible.

∙ Note: Patients may have additional sites of disease for which radiation is not feasible or indicated provided this disease is: 1) Less than 1 cm in maximum diameter on most recent imaging; or 2) Stable over the last 3 months as determined by the investigator

• Cohort 2

‣ At least 1 site of non-osseous disease

• Cohort 1

‣ All (up to 5) metastatic foci should be amenable to SBRT as per review by a radiation oncologist based on protocol specified dose / dose constraints (there is no prespecified minimum or maximum size)

• Cohort 2

‣ At least one metastatic focus amenable to local ablative treatment with any of the following: radiation therapy; radiofrequency, microwave, or cryoablation; bland or chemoembolization

• Cohort 1

‣ Primary tumor either controlled, or amenable for local treatment with SBRT

⁃ Defined as no evidence of progression at primary or local site of disease (if known) within 6 months prior to enrollment

• Age 18 years or older

• ECOG performance status of 0-2

• Prior systemic therapy is allowed but no therapy (cytotoxic or molecularly targeted agents) 2 weeks prior to the first fraction of radiotherapy, and until after the last fraction of SBRT.

• Cohort 1

‣ For patients with metastases that have been previously treated (prior resection, radiotherapy, radiofrequency or cryoablation):

• If the previously treated site is controlled based on imaging, the patient is eligible for this trial and does not need further treatment of the controlled site

∙ If the previously treated site is not controlled based on imaging, the patient is eligible for this trial as long as the site is amenable to SBRT

• Ability to understand and the willingness to sign a written informed consent document.

• Women of childbearing potential must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 72 hours prior to the start of (chemo)radiation therapy.

⁃ Women of childbearing potential (WOCBP) is defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy or bilateral oophorectomy) or who is not postmenopausal. Menopause is defined clinically as 12 months of amenorrhea in a woman over 45 in the absence of other biological or physiological causes. In addition, women under the age of 55 must have a documented serum follicle stimulating hormone (FSH) level less than 40 mIU/mL.

• Men who are sexually active with WOCBP must agree to use any contraceptive method with a failure rate of less than 1% per year. Men who are sexually active with WOCBP will be instructed to adhere to contraception for a period of 1 month after treatment. Women who are not of childbearing potential (i.e., who are postmenopausal or surgically sterile as well as azoospermic men) do not require contraception. See Appendix B for further guidance on contraception.