Table 1. Characteristics of the included studies.
study | country | patients | Interventions | outcomes | |||||
number | age average | gender | cancer type | chemotherapy drug | T | C | |||
Chalermchai 2010[13] | Thailand | 56 | 56.7(range,26–82) | female(57%) male(43%) | breast cancer:17 colorectal cancer:39 | capecitabine | 400 mg/d po | 200 mg/d po | (2),(3),(4),(5) |
Corrie 2012[10] | UK | 106 | 73(range,42–87) | female(64%) male(36%) | colorectal cancer:68 breast cancer:38 | capecitabine | 150 mg/d po | placebo | (1),(2),(5),(6),(7),(8) |
Fang 2010[14] | China | 56 | 61(range,38–78) | female(48%) male(52%) | breast cancer:18 colorectal cancer:28 stomach cancer:10 | capecitabine | 300 mg/d po | - | (1),(2) |
Gruenigen 2010[12] | USA | 34 | 64(range,45–81) | female(100%) | ovarian/peritoneal cancer:25 endometrial cancer:8 breast cancer:1 | pegylated liposomal doxorubicin | 200 mg/d po | placebo | (1),(2), (6), (9) |
Kang 2010[11] | Korea | 360 | 56(range,20–75) | female(37.5%) male(62.5%) | stomach cancer:132 colon cancer:215 biliary tract cancer:12 duodenum cancer:1 | capecitabine | 200 mg/d po | placebo | (1),(2),(4) |
Total | 612 | 62.1(range,20–87) |
Abbreviation: T, treatment group; C, control group; –, no treatment; po. per os.
Outcomes reported:(1)Incidence of all grades HFS; (2)Incidence of grade 2 or worse HFS; (3)Time to development of grade 2 or worse HFS; (4)Factors affecting development of HFS;(5)Tumor response;(6)Quality of life;(7)Chemotherapy drug dose modification;(8)Progression-free survival;(9)Incidence of Adverse Events excluding HFS.