Hybrid Arc Palliative Radiation Therapy (HART): A Single Arm Phase II Trial

Inclusion Criteria

• •Histological confirmation of cancer with radiographic (CT, MRI or PET) evidence of metastatic disease
• •Palliative radiotherapy indicated for bone or soft tissue metastases, or primary targets, located in the thorax, abdomen, or pelvis as part of their standard of care treatment plan
• •Age ≥ 18 years.
• •Women of child-bearing potential and men must agree to use adequate contraception prior to study entry, for the duration of study participation, and for 90 days following completion of therapy. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
• •In lieu of a pregnancy test, participants may sign the Pregnancy Attestation Form, a standard form routinely used in clinical practice at UVMCC.
• •Recommended methods of birth control are:
• •The consistent use of an approved hormonal contraception (birth control pill/patches, rings), An intrauterine device (IUD), Contraceptive injection (Depo-Provera), Double barrier methods (Diaphragm with spermicidal gel or condoms with contraceptive foam), Sexual abstinence (no sexual intercourse) or Sterilization.
• •Men must agree to use a condom and not father a child or donate sperm for the duration of the study and for 90 days after completion of therapy.
• •A female of child-bearing potential is any woman (regardless of sexual orientation, having undergone a tubal ligation, or remaining celibate by choice) who meets the following criteria:
• •Has not undergone a hysterectomy or bilateral oophorectomy; or
• •Has not been naturally postmenopausal for at least 12 consecutive months (i.e., has had menses at any time in the preceding 12 consecutive months).
• •Ability to understand and the willingness to sign a written informed consent.