Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2012 Aug;39(4):254-262.
doi: 10.1159/000341811. Epub 2012 Jul 26.

Clinical Results of Extracorporeal Photopheresis

Affiliations

Clinical Results of Extracorporeal Photopheresis

Nina Worel et al. Transfus Med Hemother. 2012 Aug.

Abstract

Extracorporeal photopheresis (ECP) is a combination of leukapheresis and photodynamic therapy in which blood is treated with photoactivable drugs which are then activated with ultraviolet light and re-infused to the patient. It has been used successfully for more than 30 years in the treatment of erythrodermic cutaneous T-cell lymphoma (CTCL) and over 20 years for chronic graft-versus-host disease (GVHD). ECP has also shown promising results in the treatment of acute GVHD and other T-cell-mediated diseases, including systemic sclerosis, treatment and prevention of solid organ rejection, and more recently Crohn's disease. The use of ECP may allow a significant reduction or even discontinuation of corticosteroids and/or other immunosuppressants, thus leading to reduced long-term morbidity and mortality and improved overall survival. ECP is a well-tolerated therapy. No significant side effects have been reported during the last 30 years. It has been shown that ECP is not associated with an increased incidence of infections, malignancies, or recurrence of underlying malignant disease, neither during short-term nor during long-term therapy.

Die extrakorporale Photopherese (ECP) ist eine Kombination aus Leukapherese und photodynamischer Therapie, bei der Blut mit photoaktiven Substanzen behandelt, mit ultraviolettem Licht bestrahlt und reinfundiert wird. Die ECP-Therapie wird seit 30 Jahren erfolgreich in der Behandlung von erythrodermen kutanen T-Zell-Lymphomen und seit 20 Jahren in der Behandlung von chronischer Graft-versus-Host-Erkrankung (GVHD) eingesetzt. Darüber hinaus konnten vielversprechende Ergebnisse in der Behandlung der akuten GVHD und anderer T-Zell-mediierter Erkrankungen einschließlich Systemischer Sklerose, Behandlung und Prävention von Abstoßungsreaktion nach Transplantation solider Organe und kürzlich auch bei Therapie des Morbus Crohn gezeigt werden. Der Einsatz von ECP erlaubt eine signifikante Reduktion oder sogar das Absetzen von Steroiden und/oder anderen immunsuppressiven Medikamenten, was zu einer Reduktion der Morbidität und Mortalität und zu einem verbesserten Gesamtüberleben führt. In den letzten 30 Jahren wurden keine signifikanten Nebenwirkungen der ECP berichtet. Es konnte gezeigt werden, dass die ECP weder bei kurzer, noch bei langer Anwendungsdauer mit einem erhöhten Risiko für das Auftreten von Infekten, Malignomen oder Rezidiv der zugrunde liegenden malignen Erkrankung vergesellschaftet ist.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
During ECP whole blood is drawn from the patient and separated in plasma and different cell fractions. MNCs are collected, incubated with 8-MOP, photoactivated with UVA light and re-infused to the patient.
Fig. 2
Fig. 2
Kaplan-Meier probability of overall survival among patients with steroid-refractory and-dependent acute GVHD was significantly higher among those showing complete response (CR) to ECP (black line) compared with those with no CR to ECP (grey line). This figure was published in Greinix, et al: The effect of intensified extra-corporeal photochemotherapy on long-term survival in patients with severe acute graft-versus-host disease. Haematologica 2006;91:405–408, Copyright © 2006 Ferrata Storti Foundation.
Fig. 3
Fig. 3
Cumulative incidence of complete or partial response of skin was higher among patients with steroid-refractory/-dependent/-intolerant chronic GVHD treated with ECP than in the control group. This figure was originally published in Flowers et al: A multicenter prospective phase 2 randomized study of extracorporeal photopheresis for treatment of chronic graft-versus-host disease. Blood 2008;112:2593–2594, Copyright © 2008 The American Society of Hematology.

Similar articles

Cited by

References

    1. Edelson R, Berger C, Gasparro F, Jegasothy B, Heald P, Wintroub B, Vonderheid E, Knobler R, Wolff K, Plewig G, et al. Treatment of cutaneous T-cell lymphoma by extracorporeal photochemotherapy. Preliminary results. N Engl J Med. 1987;316:297–303. - PubMed
    1. Ward DM. Extracorporeal photopheresis: how, when, and why. J Clin Apher. 2011;26:276–285. - PubMed
    1. Xia CQ, Campbell KA, Clare-Salzler MJ. Extracorporeal photopheresis-induced immune tolerance: a focus on modulation of antigen-presenting cells and induction of regulatory T cells by apoptotic cells. Curr Opin Organ Transplant. 2009;14:338–343. - PMC - PubMed
    1. Schmitt S, Johnson TS, Karakhanova S, Naher H, Mahnke K, Enk AH. Extracorporeal photophoresis augments function of CD4+CD25+FoxP3+ regulatory T cells by triggering adenosine production. Transplantation. 2009;88:411–416. - PubMed
    1. Perseghin P, Dassi M, Balduzzi A, Rovelli A, Bonanomi S, Uderzo C. Mononuclear cell collection in patients undergoing extra-corporeal photo-chemotherapy for acute and chronic graft-vs.-host-disease (GvHD): comparison between COBE Spectra version 4.7 and 6.0 (AutoPBSC). J Clin Apher. 2002;17:65–71. - PubMed