About this trial
The phase II trial evaluates the effectiveness of cryocompression therapy alone or in combination with cilostazol in preventing paclitaxel-induced peripheral neuropathy (numbness, pain or tingling in the feet and hands) for patients with gynecologic cancers. Peripheral neuropathy is a common side effect of many chemotherapeutic agents, including paclitaxel. Paclitaxel is in a class of medications called antimicrotubule agents. It stops cancer cells from growing and dividing and may kill them. Cryocompression is a therapy that combines compression garments or dressings with cooling of the treated area. Cilostazol is in a class of medications called platelet-aggregation inhibitors (antiplatelet medications). It works by improving blood flow to the legs. Giving cilostazol together with cryocompression may be safe and tolerable in treating patients with gynecological cancers.
Eligibility criteria
Qualifiers
Age 18 years or older
Diagnosis of uterine, ovarian/fallopian tube/primary peritoneal, cervical, or vulvar cancer and planned chemotherapy regimen of 6-9 cycles of paclitaxel and carboplatin or cisplatin with or without VEGF inhibition, with or without immunotherapy, and with or without HER2-directed therapy
Eastern Cooperative Oncology Group performance status from 0 to 2
ARM C: Age 18 years or older
Disqualifiers
Any patient unable and/or unwilling to cooperate with all study protocols
Previous treatment with paclitaxel
Patients with baseline pre-chemotherapy neuropathy requiring pharmacologic treatment
Diabetes mellitus with hemoglobin A1c >7.0
Trial design
Treatments tested in this trial
- Best Practice
- Cilostazol
- Cryocompression Therapy
- Paclitaxel
- Quality-of-Life Assessment
Treatment groups
Sponsors and collaborators
Emory University
Lead sponsor
National Cancer Institute (NCI)
Collaborator