Ec. Vonderheid et al., METHOTREXATE IS EFFECTIVE THERAPY FOR LYMPHOMATOID PAPULOSIS AND OTHER PRIMARY CUTANEOUS CD30-POSITIVE LYMPHOPROLIFERATIVE DISORDERS, Journal of the American Academy of Dermatology, 34(3), 1996, pp. 470-481
Background: The spectrum of primacy cutaneous CD30(+) lymphoprolifenti
ve disease consists of lymphomatoid papulosis (LyP) at one extreme and
CD30+ peripheral T-cell lymphoma (Ki-1(+) lymphoma) presenting in the
skin at the other extreme. Methotrexate has been reported to be effec
tive in LyP, but the experience has been Limited to single case report
s or small series. Objective: The objective was to determine the effec
tiveness of methotrexate in the treatment of primary cutaneous CD30+ l
ymphoproliferative disease. Methods: We reviewed our 20-year experienc
e with the use of methotrexate in 45 patients with relatively severe L
yP, Ki-1(+) lymphoma, and interface presentations. Results: During ind
uction of methotrexate therapy patient received maximum doses ranging
from 10 to 60 mg/week (median, 20 mg/week). Clinical improvement usual
ly occurred quickly, typically at doses of 15 to 20 mg weekly, and sat
isfactory long-term control was achieved in 39 patients (87%) with mai
ntenance doses given at 10- to 14-day intervals (range, 7 to 28 days).
After methotrexate was discontinued, 10 patients remained free of CD3
0(+) lesions from more than 24 months to more than 227 months (median,
more than 127 months). The median total duration of methotrexate ther
apy for all patients exceeded 39 months (range, 2 to 205 months). Adve
rse effects were generally mild and transient and included fatigue (47
%), nausea (22%), weight loss (13%), diarrhea or gastrointestinal cram
ping (10%), increased serum hepatic transaminase levels (27%), anemia
(11%), or leukopenia (9%). Early hepatic fibrosis was found in 5 of 10
patients, all of wham had been treated for more than 3 years (range,
38 to 111 months). Conclusion: Low-dose methotrexate (25 mg or less gi
ven at 1- to 4-week intervals) is an effective and well-tolerated trea
tment of selected patients with primary cutaneous CD30(+) lymphoprolif
erative disease.