ARTICLE
ejd.2011.1567
Auteur(s) : Alexandra Maria Giovanna Brunasso1,2 giovanna.brunasso@gmail.com,
Matteo Puntoni3, Chiara Delfino4, Cesare Massone5
1 Department of Enviromental Dermatology and
Venereology,
Medical University of Graz,
Auenbruggerplatz 8,
A-8036 Graz-Austria
2 Department of Dermatology,
Galliera Hospital,
Genoa,
Italy
3 Department of Oncology and Biostatistical research,
Galliera Hospital,
Genoa,
Italy
4 Department of Dermatological Sciences,
Florence,
Italy
5 Department of Dermatology,
Medical University of Graz,
Auenbruggerplatz 8,
A-8036 Graz-Austria
We performed a retrospective study of patients affected by
severe plaque psoriasis (PASI>20) with palmoplantar involvement
(PPI) who underwent infliximab therapy for more than 24 weeks, in
order to describe and compare the clinical response of PPI
vs that of plaque psoriasis elsewhere on the body. Clinical
charts were reviewed for: demographics, psoriasis severity
(Psoriasis Area Severity Index [PASI], m-PPPASI [modified
PalmoPlantar Psoriasis Area Severity Index]), treatment (duration,
dosages, adverse events) and concomitant treatments (duration and
dosages) [1-3]. We used the Mann Whitney test to compare PASI and
m-PPPASI improvements.
Five patients treated with infliximab, 3 males and 2 females,
with a mean age of 41.4 years, affected by severe plaque psoriasis
(mean baseline-PASI: 34) with PPI (mean baseline m-PPPASI: 31.7)
were followed for an average of 87.6 weeks. Demographics, severity
indexes, adverse events and therapy schedules are reported in table 1.
Table 1 Clinical and therapy summary, evolution measures
and adverse events.
| Patient # |
Age-sex |
PsA |
Previous systemic therapies |
Inflixi-mab dose |
Number of infusions |
Weeks of treatment |
Associated therapy |
PASI Day-0 |
PASI Week-14 |
PASI Week-30 |
m-PPPASI Day-0 |
m-PPPASI Week-14 |
m-PPPASI Week-30 |
Adverse events |
| Patient #1 |
40-M |
No |
CsA, Mtx, efalizumab |
5 mg/kg* |
7 |
38 weeks |
Mtx, local emollients |
40.2 |
6.2 |
3.2 |
37.2 |
32.6 |
26.2 |
No |
| Patient #2 |
43-M |
No |
CsA, Mtx, PUVA |
5 mg/kg* |
7 |
38 weeks |
Mtx, local emollients |
36.8 |
5.2 |
2.8 |
38.4 |
28.6 |
18.2 |
Mild infusion reaction |
| Patient #3 |
24-M |
No |
CsA, Mtx, PUVA, etanercept |
5 mg/kg* |
6 |
30 weeks |
Mtx, local emollients |
34.8 |
4.2 |
1.8 |
32.6 |
18.2 |
10.8 |
No |
| Patient #4 |
39-F |
No |
CsA, Mtx, PUVA, efalizumab, |
5 mg/kg* |
13 |
86 weeks |
Local emollients |
36.2 |
3.8 |
4.8 |
36 |
22.8 |
23.2 |
No |
| Patient #5 |
61-F |
Yes |
CsA, adalimumab, etanercept, Mtx |
5 mg/kg* |
33 |
246 weeks |
Mtx, local emollients |
21.8 |
3.2 |
4.2 |
14.2 |
12.2 |
14.8 |
No |
Sex: M: male, F: female; PsA: confirmed psoriatic arthritis;
CsA: cyclosporine A; Mtx: methotrexate; PUVA: Psoralen +
ultraviolet A photo-therapy. Associated therapy: Mtx: methotrexate
(5 mg/weekly in patients #1, #2 and #3 and 10 mg/weekly in patient
#5).
At week 0, 2, 6 and every 8 weeks thereafter.
At week-14, the mean PASI improvement was 86.8% and the mean
m-PPPASI improvement was 27.69% (p: 0.008). At week-30, the mean
PASI improvement was 89.11% and the mean m-PPPASI improvement was
41.2% (p: 0.008). Comparative PASI and m-PPPASI score evolutions
are shown in figure
1. Mean PASI and m-PPPASI improvements at the last
follow-up visit were 80.8% and 44.8% respectively (p:0.03).
We decided to conduct this retrospective study because of the
continuous complaints of two patients (patients #4 and #5) who were
not satisfied, even if their PASI scores were significantly lower
compared to baseline. The patients referred a lower efficacy in the
palmoplantar area compared with the rest of the body response, not
only for functional and cosmetic reasons but also because the
psoriasis stigmata were always visible. Our results confirmed the
patients’ theory, the palm and sole improvements were less
encouraging than those of the rest of the body. It's worth
noticing, that there was no statistically significant difference
between the severity of PPI and the severity of diffuse psoriasis
involvement comparing PASI and m-PPASI scores at baseline (p:0.8)
but when we compared the efficacy at week-14 and week-30, the mean
PASI improvements were 86.8% and 89.11% respectively, while the
mean m-PPPASI improvements were only 27.69% and 41.2%
(p:0.008).
Our knowledge of the use of infliximab in palmoplantar plaque
psoriasis is confined to the experience of 27 patients and data
comparing the palmoplantar response vs the rest of the body
response are lacking [3, 4]. In contrast with our results, Di
Lernia et al., published 3 cases affected by diffuse plaque
psoriasis with PPI who reported an excellent response (PPPASI: 63-
100%) after 24 weeks of infliximab [4]. A randomized controlled
trial (RCT) with 24 patients revealed that only 33.3% of patients
achieved an m-PPPASI 75 at week-14, not reaching the primary
endpoint of the study [3]. This response of PPI is lower if
compared to trials where 75.5- 87.9% of patients with moderate to
severe plaque psoriasis achieved a PASI-75 at week-14 [5].
Unfortunately the severity and the response-rate for the diffuse
psoriasis were not available in these 27 patients [3, 4].
This report is the first attempt to evaluate and compare the
palmoplantar response with the rest of the body response in
patients who followed biological therapy. These data become
important if we consider that QOL impairment is higher in patients
affected by palmoplantar psoriasis compared to psoriasis vulgaris
[6].
Our data, together with the efficacy rates shown in the
previously mentioned RCT, suggest that, even if infliximab is one
of the most effective treatments for severe plaque psoriasis, the
effect on the PPI of patients affected by severe diffuse plaque
psoriasis seems to be less dramatic [3].
Disclosure
Financial support: none. Conflicts of interest:
none.
References
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patients. J Eur Acad Dermatol Venereol 2009; 23: 415-9.
3. Bissonnette R, Poulin Y, Guenther L, et al.
Treatment of palmoplantar psoriasis with infliximab: a randomized,
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6. Pettey AA, Balrishnan R, Rapp SR, et al.
Patients with palmo-plantar psoriasis have more physical disability
and discomfort than patients with other forms of psoriasis:
implications for clinical practice. J Am Acad Dermatol 2003;
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