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. 2019 Dec 9;47(3):241–250. doi: 10.1111/cup.13615

Table 1.

Clinical characteristics of 40 patients with plaque stage folliculotropic mycosis fungoides

Total group (n = 40) NP‐FMF (n = 20) P‐FMF (n = 20) P‐value
Median age at diagnosis (range; months) 56 (19‐82) 51 (19‐68) 62 (29‐82) <0.01
Male‐female (ratio) 29‐11 (2.6) 15‐5 (3.0) 14‐6 (2.3) 0.72
Median time from first skin lesion to diagnosis (months) 24 (3‐300) 10 (2‐360) 36 (3‐300) 0.19
Extent of skin lesions 0.11
Solitary 2 (5%) 2 (10%) 0
Localized 2 (5%) 2 (10%) 0
Generalized 36 (90%) 16 (80%) 20 (100%)
Predominant head/neck involvement 32 (80%) 16 (80%) 16 (80%) 1.0
Pruritus 0.34
Yes 30 (75%) 13 (65%) 17 (85%)
No 8 (20%) 5 (25%) 3 (15%)
Unknown 2 (5%) 2 (10%)
Type of initial treatment 0.61
Topical steroids 4 (10%) 3 (15%) 1 (5%)
Narrow‐band UVB 2 (5%) 0 (0%) 2 (10%)
PUVA 16 (40%) 9 (45%) 7 (35%)
PUVA + local radiotherapy 6 (15%) 2 (10%) 4 (20%)
Local radiotherapy 6 (15%) 3 (15%) 3 (15%)
Total skin radiotherapy 6 (15%) 3 (15%) 3(15%)
Result initial treatment 0.03
Complete remission 15 (37%) 12 (60%) 3 (15%)
Partial remission 13 (32%) 3 (15%) 10 (50%)
Stable disease 10 (25%) 4 (20%) 6 (30%)
Progressive disease 2 (5%) 1 (5%) 1 (5%)
Median duration follow‐up (range) (months) 80 (6‐320) 104 (38‐320) 59 (6‐241) 0.05
Status at last follow‐up <0.01
Alive without disease 7 (17%) 7 (35%) 0 (0%)
Alive with ongoing disease 14 (35%) 10 (50%) 4 (20%)
Died of lymphoma 15 (37%) 0 (0%) 15 (75%)
Died of unrelated disease 4 (10%) 3 (15%) 1 (5%)
Disease‐specific survival at 5/10 years 72%/57% 100%/100% 45%/24% <0.01
Overall survival at 5/10 years 68%/54% 90%/90% 45%/24% <0.01

Abbreviations: NP‐FMF: non‐progressive folliculotropic mycosis fungoides; P‐FMF, progressive folliculotropic mycosis fungoides; PUVA: psoralen plus ultraviolet A therapy; UVB: ultraviolet B therapy.