Bleiker T O, Nicolaou N, Traulsen J, Hutchinson P E
Department of Dermatology, Leicester Royal Infirmary, Leicester LE1 5WW, UK.
Br J Dermatol. 2005 Jul;153(1):103-12. doi: 10.1111/j.1365-2133.2005.06608.x.
Hair loss from cytotoxic drugs is classically ascribed to the loss of fractured hairs (anagen effluvium). Telogen hair loss has also been described but some authors have denied any effect on the hair cycle. There are conflicting reports on a protective effect of pretreatment with a vitamin D analogue on cytotoxic drug-induced hair loss in rodents.
To investigate the process of cytotoxic hair loss and any protective effect on the hair of pretreatment with topical calcipotriol.
Breast cancer patients who were about to receive cycles of chemotherapy with cyclophosphamide 600 mg m(-2), methotrexate 40 mg m(-2) and 5-fluorouracil 600 mg m(-2) were recruited and randomized to receive calcipotriol scalp solution 50 microg mL(-1) or vehicle. The solution was applied twice daily from 4 days prior to chemotherapy and continued for 14 days in each treatment cycle. Shed, plucked and cut hairs were sampled. Absolute shed rates, the proportion of major hair types, the presence of proximal hair shaft changes, regrowth (using the new anagen hair count) and hair density were assessed.
Ten patients receiving calcipotriol and 14 receiving vehicle completed three treatment cycles and nine from both groups completed six cycles. There was no detectable effect of calcipotriol on the proportion of patients experiencing minimal hair loss from chemotherapy, shed rates, plucked telogen and fractured hair counts, the morphology of shed and plucked hair, hair regrowth or hair density. Combining results of the treatment groups, there was a large variation in the impact of chemotherapy on hair loss, from total loss in five patients to no obvious loss in five. Excluding the latter, during chemotherapy shed telogen hairs (mean 81% of shed hairs) predominated over fractured (12%) and anagen hairs (6%) (P = 0.0002). The major pathological change was proximal hair shaft tapering, baseline mean 3% of shed hairs rising to 48% (P = 0.0005) during treatment, and there was a consequent decrease in normal telogen hairs, baseline mean 98% of all telogen hairs falling to 55% (P = 0.0005) during treatment. The pathological tapered telogen hairs had normal or small, sometimes diminutive, bulbs. Fracturing of hairs with diminutive bulbs produced typical 'exclamation mark' hairs.
The cardinal effects of cytotoxic drugs found in this study were tapering of the proximal hair shaft and premature entry of the follicle into telogen, conflicting with the conventional view that affected hair follicles continue in anagen. There was a resulting effluvium of a mixture of tapering telogen hairs and fractured hairs. As entry into telogen is an integral part of the process, cytotoxic hair loss may be regarded as a variant of the conventional 'telogen effluvium' and we propose the term 'atrophic telogen effluvium'. There was no obvious protective effect on the hair loss of prior treatment with topical calcipotriol.
细胞毒性药物导致的脱发传统上归因于断裂毛发的脱落(生长期脱发)。休止期脱发也有相关描述,但一些作者否认其对毛发周期有任何影响。关于维生素D类似物预处理对啮齿动物细胞毒性药物诱导脱发的保护作用,存在相互矛盾的报道。
研究细胞毒性脱发的过程以及外用卡泊三醇预处理对毛发的任何保护作用。
招募即将接受环磷酰胺600mg/m²、甲氨蝶呤40mg/m²和5-氟尿嘧啶600mg/m²化疗周期的乳腺癌患者,并随机分为接受50μg/mL卡泊三醇头皮溶液或赋形剂组。从化疗前4天开始,每天两次涂抹溶液,每个治疗周期持续14天。对脱落、拔除和剪断的毛发进行采样。评估绝对脱落率、主要毛发类型的比例、近端毛干变化的存在情况、再生情况(使用新生长期毛发计数)和毛发密度。
10名接受卡泊三醇治疗的患者和14名接受赋形剂治疗的患者完成了三个治疗周期,两组各有9名患者完成了六个周期。卡泊三醇对经历化疗后脱发最少的患者比例、脱落率、拔除的休止期毛发和断裂毛发计数、脱落和拔除毛发的形态、毛发再生或毛发密度均无明显影响。综合治疗组的结果,化疗对脱发的影响差异很大,从5名患者完全脱发到5名患者无明显脱发。排除后者,化疗期间脱落的休止期毛发(平均占脱落毛发的81%)占主导地位,超过断裂毛发(12%)和生长期毛发(6%)(P = 0.0002)。主要病理变化是近端毛干变细,治疗期间基线时平均3%的脱落毛发增至48%(P = 0.0005),随之正常休止期毛发减少,基线时所有休止期毛发平均98%降至治疗期间的55%(P = 0.0005)。病理上变细的休止期毛发毛囊正常或较小,有时微小。带有微小毛囊的毛发断裂产生典型的“感叹号”毛发。
本研究中发现细胞毒性药物的主要作用是近端毛干变细和毛囊过早进入休止期,这与受影响毛囊继续处于生长期的传统观点相矛盾。由此导致变细的休止期毛发和断裂毛发混合脱落。由于进入休止期是该过程的一个组成部分,细胞毒性脱发可被视为传统“休止期脱发”的一种变体,我们提出“萎缩性休止期脱发”这一术语。外用卡泊三醇预处理对脱发无明显保护作用。