Chinese Medicine Yishen Jiangu Granules () on Aromatase Inhibitor-Associated Musculoskeletal Symptoms.
- Author:
Xing ZHANG
1
;
Nan PENG
1
;
Ming-Wei YU
1
;
Gan-Lin ZHANG
1
;
Xu SUN
1
;
Guo-Wang YANG
1
;
Chen LI
1
;
Lin YANG
1
;
Xiao-Min WANG
2
Author Information
- Publication Type:Journal Article
- Keywords: Chinese medicine; Yishen Jiangu Granules; aromatase inhibitors; breast cancer; musculoskeletal symptoms
- From:Chinese journal of integrative medicine 2018;24(11):867-872
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo assess the effectiveness of Yishen Jiangu Granules (, YSJGG) on aromatase inhibitor-associated musculoskeletal symptoms (AIMSS).
METHODSA single-arm, open-label study was conducted in 34 postmenopausal women with breast cancer who experienced AIMSS. Patients were treated with YSJGG for 12 weeks (12.4 g orally twice daily). The primary outcome was a change in the mean worst pain score of Brief Pain Inventory-Short Form (BPI-SF) over 12 weeks, and the second outcomes included changes in pain severity and pain-related interference of BPI-SF and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), Modified Score for the Assessment of Chronic Rheumatoid Affections of the Hands (M-SACRAH), the Functional Assessment of Cancer Therapy-Breast (FACT-B), bone mineral density (BMD) and blood indices such as calcium (Ca), phosphate (P), and alkaline phosphatase (ALP).
RESULTSOf 37 women recruited, 30 initiated the therapy and 24 were evaluable at 12 weeks. The primary outcome (BPI-SF worst pain scores) achieved a 2.17-point reduction compared with baseline (5.75±1.87 vs 3.58±2.15, P<0.01). There were reductions in pain severity (decreased 1.65, P<0.01) and pain-related interference (decreased 2.55, P<0.01). The changes in WOMAC and M-SACRAH scores were similar to BPI-SF (P<0.05). In the FACT-B, only physical well-being and functional well-being were improved compared with baseline (P<0.05). No clinical differences were found in BMD, Ca, P and ALP.
CONCLUSIONYSJGG is an effective and well-tolerated agent to reduce AIMSS.