Adjuvant rituximab therapy of pemphigus: a single-center experience with 31 patients.
Adjuvant rituximab therapy of pemphigus: a single-center experience with 31 patients.
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DOI:
10.1001/archdermatol.2012.1522
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发表时间:
2012-09
影响因子:
--
通讯作者:
Payne AS
中科院分区:
文献类型:
--
作者:
Lunardon L;Tsai KJ;Propert KJ;Fett N;Stanley JR;Werth VP;Tsai DE;Payne AS
We conducted a retrospective study of pemphigus vulgaris (n=24) and foliaceus (n=7) patients treated with adjuvant rituximab to determine efficacy and adverse events. The endpoint for efficacy was complete remission of disease on no or minimal therapy. 18 patients (58%) achieved the study endpoint. Of these, 13 patients achieved complete remission off systemic therapy. Patients achieving the study endpoint had a median disease duration prior to rituximab of 19 months, versus 86 months in those not achieving the endpoint (p=0.01). For the 18 patients achieving the endpoint, the median duration of remission was 19 +/− 2 months. Eight (44%) of these 18 patients relapsed 6–17 months after treatment. Serious adverse events attributed to rituximab (osteomyelitis, phlegmon) occurred in two patients (6%). In paired serum samples from 10 patients before and after rituximab, the percent change in serum desmoglein index value (median −80%) was unrelated to the percent change in pneumococcal antibodies (median +8%) (Spearman rank correlation coefficient r=−0.2). Our experience suggests that patients treated with rituximab earlier in the course of disease may have better outcomes. A discussion of rituximab mechanism of action supports the rationale for early therapy. Prospective clinical studies are necessary to substantiate this observation.
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