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. 2019 Aug 6;9:733. doi: 10.3389/fonc.2019.00733

Table 5.

Results of recent scalp-cooling studies.

References N Study design Scalp-cooling method Cancer type Chemotherapy agents Observation period Hair preservation % of hair preservation (controls)
Nangia et al. (6) 182 Randomized control Paxman cooling system Early-stage breast cancer Taxane and/or anthracycline based During chemotherapy CTCAE grade ≦ 1 assessed by independent clinicians 51% (0%)
Smetanay et al. (15) 79 Randomized control Dignicap cooling system Breast cancer (stages 1–3) Taxane and/or anthracycline based 6 months after chemotherapy Dean grade ≤ 2 assessed by patients 39% (0%)
Rugo et al. (7) 122 Non-randomized controlled Dignicap cooling system Early-stage breast cancer Taxane based 4 weeks after completion of chemotherapy Dean grade ≤ 2 assessed by patients 66% (0%)
Betticher et al. (16) 238 Non-randomized controlled Paxman cooling system/Cold Cap Breast, lung, prostate cancer, etc. Docetaxel During chemotherapy WHO grade ≤ 2 assessed by physician, and no wig required 82% (36%)
Chan et al. (17) 60 No control Dignicap cooling system Breast cancer (stages 1–3) Taxane and/or anthracycline based 2–4 weeks after completion of chemotherapy Dean grade ≤ 2 assessed by patients 33%
Vasconcelos et al. (18) 131 No control Paxman cooling system Breast cancer (stages 1–3) Taxane and/or anthracycline based During chemotherapy Visual evaluation ≤ 50% hair loss assessed by nurse and no wig required 71%
Rice et al. (19) 103 Registry Penguin Cold Caps Early or advanced stage breast cancer Taxane and/or anthracycline based 4 weeks after completion of chemotherapy VAS ≤ 50% hair loss assessed by patients 61%
Van den Hurk et al. (14) 1411 Registry Paxman cooling system Breast, female genital, gastrointestinal/colorectal, lung, prostate cancer, etc. Various During chemotherapy No wig required 50%
Present study 48 Non-randomized controlled Paxman cooling system Early-stage breast cancer Taxane or anthracycline based 3 months after chemotherapy CTCAE grade ≤ 1 assessed by two independent clinicians 27% (0%)

VAS, Visual analog scale; WHO, World Health Organization.