Acupuncture as add-on to G-CSF for Febrile Neutropenia-related Hospitalization in Doxorubicin-treated Patients With Sarcoma

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorShaare Zedek Medical Center

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 volunteers

Qualifiers

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

Design model

Crossover

Treatments tested in this trial

  • Acupuncture

    Device

    Acupuncture 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

60 Participants
are divided into 2 treatment groups
Group A: Group AActive comparator 1 intervention
Group B: Group BActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Incidence of chemotherapy-induced febrile neutropenia-related hospitalization

Time frame
3 weeks
2

Duration of chemotherapy-induced febrile neutropenia-related hospitalization

Time frame
3 weeks

Secondary outcomes

1

Relative Dose Intensity of Chemotherapy Regimen

Actual vs. planned dosage and interval between cycles

Time frame
3 weeks
2

G-CSF-related muscle and bone pain

Patient-reported outcome measures

Time frame
3 wseks
3

Quality of life-related outcomes: Quantitative Assessment

Patient-reported outcome measures

Time frame
3 weeks
4

Quality of life-related outcomes: Qualitative Assessment

MYCaW narratives

Time frame
3 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: