About this trial
Chemotherapy-induced febrile neutropenia (CIFN) is a dangerous complication of many chemotherapy drugs, with current treatment with granulocyte colony-stimulating factors (G-CSFs) accompanied by adverse effects, primarily muscle and bone pain. Adult patients with sarcoma treated with doxorubicin-based chemotherapy have a high risk (\>40%) for developing CIFN. Acupuncture has been shown to have a potentially myelo-protective effect on bone marrow during chemotherapy, though its effect on the incidence of CIFN-related hospitalization has yet to be examined. In the proposed study, patients with sarcoma will be randomly allocated (in a ratio of 1:1) to Group A, receiving acupuncture during cycles 1, 3, and 5; or Group B, during cycles 2, 4, and 6, with the study oncologist blinded regarding allocation. Acupuncture will be administered on the first day (d1) and the 8th day (d8) of the chemotherapy cycles, with press-tack needles on d1 to d8, and patients will be taught to self-treat with acupressure from d8 to the next cycle. The incidence and duration of hospitalization due to CIFN will be examined, as will adherence to the chemotherapy regimen; G-CSF-related pain; and other outcomes using 3 quality-of-life-focused questionnaires. The study findings will have important implications regarding the role of acupuncture in the treatment of patients treated with chemotherapy drugs with a high risk for CIFN, such as those used in the treatment of sarcoma.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
age 18-65 years
diagnosed with sarcoma of any stage
scheduled for doxorubicin-based chemotherapy
function ECOG status score of 0-1
Disqualifiers
not fulfilling all inclusion criteria
unwilling or unable to provide written informed consent for study participation
Trial design
Crossover
Treatments tested in this trial
Acupuncture
DeviceAcupuncture will be administered bilaterally on points PC6, LI 4, CV6, SP6, SP10 and ST36 on the first day of each cycle (d1), prior to administration of chemotherapy; and on d8, each session lasting between 30 to 45 minutes. Patients will continue from d1 to d8 with press-tack acupuncture needles on points PC 6, LI4, SP 6 and ST 36. On d8, patients will again undergo acupuncture, and continue with self-acupressure on the same points as the press-tack needles, until the next chemotherapy cycle.
Treatment groups
Trial outcomes
Primary outcomes
Incidence of chemotherapy-induced febrile neutropenia-related hospitalization
Duration of chemotherapy-induced febrile neutropenia-related hospitalization
Secondary outcomes
Relative Dose Intensity of Chemotherapy Regimen
Actual vs. planned dosage and interval between cycles
G-CSF-related muscle and bone pain
Patient-reported outcome measures
Quality of life-related outcomes: Quantitative Assessment
Patient-reported outcome measures
Quality of life-related outcomes: Qualitative Assessment
MYCaW narratives
Sponsors and contacts
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