Extracorporeal photopheresis in the management of steroid-refractory chronic graft-versus-host disease after allogeneic stem cell transplantation
Conventional intensified immunosuppressive therapy for refractory chronic graft-versus-host-disease (cGvHD) increases mortality and relapse rates after allogeneic hematopoietic cell transplantation. We retrospectively studied the efficacy and safety of extracorporeal photopheresis (ECP) in 44 patien...
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Veröffentlicht in: | Bone marrow transplantation (Basingstoke) 2009-03, Vol.43 (S1), p.S130 |
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description | Conventional intensified immunosuppressive therapy for refractory chronic graft-versus-host-disease (cGvHD) increases mortality and relapse rates after allogeneic hematopoietic cell transplantation. We retrospectively studied the efficacy and safety of extracorporeal photopheresis (ECP) in 44 patients with corticoid-resistant cGvHD. Thirty-seven patients received grafts from siblings and 7 from matched unrelated donors. Cyclosporine or tacrolimus and methotrexate ± ATG were administered as GvHD prophylaxis. Patients had received 2(1-4) lines of treatment for 13 months (median) before ECP. Ten patients had developed induced cGvHD post immunotherapy. Fifteen patients had mucocutaneous disease only, 9 cutaneous sclerosis manifestations, 13 visceral involvement and 7 patients skin sclerosis and liver. Patients completed a median number of 23 sessions of ECP/patient. The therapeutic schedule included 2 sessions per week for 1 month followed according to the severity of cGvHD, by either a) one session per week for 2 months and 1 per 15 days for 2 months or b) 1 session per 15 days for 4 months, and then both cohorts received 1 session per month for 4-8 months. Response was evaluated at 3 months and at the end of the treatment. Five patients died due to early complications ( |
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We retrospectively studied the efficacy and safety of extracorporeal photopheresis (ECP) in 44 patients with corticoid-resistant cGvHD. Thirty-seven patients received grafts from siblings and 7 from matched unrelated donors. Cyclosporine or tacrolimus and methotrexate ± ATG were administered as GvHD prophylaxis. Patients had received 2(1-4) lines of treatment for 13 months (median) before ECP. Ten patients had developed induced cGvHD post immunotherapy. Fifteen patients had mucocutaneous disease only, 9 cutaneous sclerosis manifestations, 13 visceral involvement and 7 patients skin sclerosis and liver. Patients completed a median number of 23 sessions of ECP/patient. The therapeutic schedule included 2 sessions per week for 1 month followed according to the severity of cGvHD, by either a) one session per week for 2 months and 1 per 15 days for 2 months or b) 1 session per 15 days for 4 months, and then both cohorts received 1 session per month for 4-8 months. Response was evaluated at 3 months and at the end of the treatment. Five patients died due to early complications (<40 days): 2 early deaths occurred due to GvHD or disease progression and 3 deaths due to existing infections before ECP. Response at 3 months was 72% (28/39): 90% in patients with mucocutaneous disease, 62% with skin sclerosis, 58% with visceral disease and 83% with cutaneous sclerosis and liver manifestations. The cGvHD relapsed in 9/28(32%) in 2(1-15) months. Stable response was 48% (19/39) and 15 of 39 patients do not receive any immunosupression. In multivariate analysis only visceral involvement affected the duration of response. Patients with de novo cGvHD seemed to respond better. In terms of immunological reconstitution, a 40% increase of CD4+ cells was observed after 12 months of treatment. Infections (gr? 3 WHO) were seen in 12 patients without any mortality. No relapse of the underlying disease was documented. The 5-year disease free survival from the beginning of ECP was 80% with a median follow-up of 20 months. High response rates with acceptable toxicity and a low incidence of relapse of the underlying disease establishes the role of ECP as a new, reliable therapeutic strategy in the treatment of resistant cGvHD in earlier phase.</description><identifier>ISSN: 0268-3369</identifier><language>eng</language><publisher>Nature Publishing Group</publisher><subject>Apheresis ; Care and treatment ; Complications and side effects ; Graft versus host reaction ; Health aspects ; Immunosuppression ; Patient outcomes ; Risk factors ; Stem cells ; Transplantation</subject><ispartof>Bone marrow transplantation (Basingstoke), 2009-03, Vol.43 (S1), p.S130</ispartof><rights>COPYRIGHT 2009 Nature Publishing Group</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids></links><search><creatorcontrib>Kaloyannidis, P</creatorcontrib><creatorcontrib>Papalexandri, A</creatorcontrib><creatorcontrib>Sakellari, I</creatorcontrib><creatorcontrib>Yannaki, E</creatorcontrib><creatorcontrib>Batsis, I</creatorcontrib><creatorcontrib>Mallouri, D</creatorcontrib><creatorcontrib>Barbouti, A</creatorcontrib><creatorcontrib>Ganidou, M</creatorcontrib><creatorcontrib>Fassas, A</creatorcontrib><creatorcontrib>Anagnostopoulos, A</creatorcontrib><creatorcontrib>Papanicolaou, G</creatorcontrib><title>Extracorporeal photopheresis in the management of steroid-refractory chronic graft-versus-host disease after allogeneic stem cell transplantation</title><title>Bone marrow transplantation (Basingstoke)</title><description>Conventional intensified immunosuppressive therapy for refractory chronic graft-versus-host-disease (cGvHD) increases mortality and relapse rates after allogeneic hematopoietic cell transplantation. We retrospectively studied the efficacy and safety of extracorporeal photopheresis (ECP) in 44 patients with corticoid-resistant cGvHD. Thirty-seven patients received grafts from siblings and 7 from matched unrelated donors. Cyclosporine or tacrolimus and methotrexate ± ATG were administered as GvHD prophylaxis. Patients had received 2(1-4) lines of treatment for 13 months (median) before ECP. Ten patients had developed induced cGvHD post immunotherapy. Fifteen patients had mucocutaneous disease only, 9 cutaneous sclerosis manifestations, 13 visceral involvement and 7 patients skin sclerosis and liver. Patients completed a median number of 23 sessions of ECP/patient. The therapeutic schedule included 2 sessions per week for 1 month followed according to the severity of cGvHD, by either a) one session per week for 2 months and 1 per 15 days for 2 months or b) 1 session per 15 days for 4 months, and then both cohorts received 1 session per month for 4-8 months. Response was evaluated at 3 months and at the end of the treatment. Five patients died due to early complications (<40 days): 2 early deaths occurred due to GvHD or disease progression and 3 deaths due to existing infections before ECP. Response at 3 months was 72% (28/39): 90% in patients with mucocutaneous disease, 62% with skin sclerosis, 58% with visceral disease and 83% with cutaneous sclerosis and liver manifestations. The cGvHD relapsed in 9/28(32%) in 2(1-15) months. Stable response was 48% (19/39) and 15 of 39 patients do not receive any immunosupression. In multivariate analysis only visceral involvement affected the duration of response. Patients with de novo cGvHD seemed to respond better. In terms of immunological reconstitution, a 40% increase of CD4+ cells was observed after 12 months of treatment. Infections (gr? 3 WHO) were seen in 12 patients without any mortality. No relapse of the underlying disease was documented. The 5-year disease free survival from the beginning of ECP was 80% with a median follow-up of 20 months. High response rates with acceptable toxicity and a low incidence of relapse of the underlying disease establishes the role of ECP as a new, reliable therapeutic strategy in the treatment of resistant cGvHD in earlier phase.</description><subject>Apheresis</subject><subject>Care and treatment</subject><subject>Complications and side effects</subject><subject>Graft versus host reaction</subject><subject>Health aspects</subject><subject>Immunosuppression</subject><subject>Patient outcomes</subject><subject>Risk factors</subject><subject>Stem cells</subject><subject>Transplantation</subject><issn>0268-3369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptkM1KAzEUhWehYK2-Q0BwN5LMT5wsS6k_UHDTfckkNzORTDLkpqKP4RuboosW5C4uHL5zLvdcFAta8a6say6uimvEd0pZ09B2UXxvPlOUKsQ5RJCOzGNIYR4hAlok1pM0ApmklwNM4BMJhmCCGKwuI5jsTCF-ETXG4K0iQ5QmlR8Q8YDlGDARbREkAsk6RCKdCwN4yGhOmYgC50i-73F20ieZbPA3xaWRDuH2by-L3dNmt34pt2_Pr-vVthxE15aCs1oY3eqK9Q0TtOoqybg0dSvbijMFvAdGNWu7hmuh-or20IkODK2EFjWvl8Xdb-wgHeytN-HYw2RR7VdMdOyR1k2bqYd_qDwaJquCB2Ozfma4PzGMudI0YnCH42d4Cv4AMpV__Q</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Kaloyannidis, P</creator><creator>Papalexandri, A</creator><creator>Sakellari, I</creator><creator>Yannaki, E</creator><creator>Batsis, I</creator><creator>Mallouri, D</creator><creator>Barbouti, A</creator><creator>Ganidou, M</creator><creator>Fassas, A</creator><creator>Anagnostopoulos, A</creator><creator>Papanicolaou, G</creator><general>Nature Publishing Group</general><scope/></search><sort><creationdate>20090301</creationdate><title>Extracorporeal photopheresis in the management of steroid-refractory chronic graft-versus-host disease after allogeneic stem cell transplantation</title><author>Kaloyannidis, P ; Papalexandri, A ; Sakellari, I ; Yannaki, E ; Batsis, I ; Mallouri, D ; Barbouti, A ; Ganidou, M ; Fassas, A ; Anagnostopoulos, A ; Papanicolaou, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g985-96139fd5d21b4190282a16af35a5261ce6be10d15846d9cb20be898ef029d9363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Apheresis</topic><topic>Care and treatment</topic><topic>Complications and side effects</topic><topic>Graft versus host reaction</topic><topic>Health aspects</topic><topic>Immunosuppression</topic><topic>Patient outcomes</topic><topic>Risk factors</topic><topic>Stem cells</topic><topic>Transplantation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kaloyannidis, P</creatorcontrib><creatorcontrib>Papalexandri, A</creatorcontrib><creatorcontrib>Sakellari, I</creatorcontrib><creatorcontrib>Yannaki, E</creatorcontrib><creatorcontrib>Batsis, I</creatorcontrib><creatorcontrib>Mallouri, D</creatorcontrib><creatorcontrib>Barbouti, A</creatorcontrib><creatorcontrib>Ganidou, M</creatorcontrib><creatorcontrib>Fassas, A</creatorcontrib><creatorcontrib>Anagnostopoulos, A</creatorcontrib><creatorcontrib>Papanicolaou, G</creatorcontrib><jtitle>Bone marrow transplantation (Basingstoke)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kaloyannidis, P</au><au>Papalexandri, A</au><au>Sakellari, I</au><au>Yannaki, E</au><au>Batsis, I</au><au>Mallouri, D</au><au>Barbouti, A</au><au>Ganidou, M</au><au>Fassas, A</au><au>Anagnostopoulos, A</au><au>Papanicolaou, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extracorporeal photopheresis in the management of steroid-refractory chronic graft-versus-host disease after allogeneic stem cell transplantation</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><date>2009-03-01</date><risdate>2009</risdate><volume>43</volume><issue>S1</issue><spage>S130</spage><pages>S130-</pages><issn>0268-3369</issn><abstract>Conventional intensified immunosuppressive therapy for refractory chronic graft-versus-host-disease (cGvHD) increases mortality and relapse rates after allogeneic hematopoietic cell transplantation. We retrospectively studied the efficacy and safety of extracorporeal photopheresis (ECP) in 44 patients with corticoid-resistant cGvHD. Thirty-seven patients received grafts from siblings and 7 from matched unrelated donors. Cyclosporine or tacrolimus and methotrexate ± ATG were administered as GvHD prophylaxis. Patients had received 2(1-4) lines of treatment for 13 months (median) before ECP. Ten patients had developed induced cGvHD post immunotherapy. Fifteen patients had mucocutaneous disease only, 9 cutaneous sclerosis manifestations, 13 visceral involvement and 7 patients skin sclerosis and liver. Patients completed a median number of 23 sessions of ECP/patient. The therapeutic schedule included 2 sessions per week for 1 month followed according to the severity of cGvHD, by either a) one session per week for 2 months and 1 per 15 days for 2 months or b) 1 session per 15 days for 4 months, and then both cohorts received 1 session per month for 4-8 months. Response was evaluated at 3 months and at the end of the treatment. Five patients died due to early complications (<40 days): 2 early deaths occurred due to GvHD or disease progression and 3 deaths due to existing infections before ECP. Response at 3 months was 72% (28/39): 90% in patients with mucocutaneous disease, 62% with skin sclerosis, 58% with visceral disease and 83% with cutaneous sclerosis and liver manifestations. The cGvHD relapsed in 9/28(32%) in 2(1-15) months. Stable response was 48% (19/39) and 15 of 39 patients do not receive any immunosupression. In multivariate analysis only visceral involvement affected the duration of response. Patients with de novo cGvHD seemed to respond better. In terms of immunological reconstitution, a 40% increase of CD4+ cells was observed after 12 months of treatment. Infections (gr? 3 WHO) were seen in 12 patients without any mortality. No relapse of the underlying disease was documented. The 5-year disease free survival from the beginning of ECP was 80% with a median follow-up of 20 months. High response rates with acceptable toxicity and a low incidence of relapse of the underlying disease establishes the role of ECP as a new, reliable therapeutic strategy in the treatment of resistant cGvHD in earlier phase.</abstract><pub>Nature Publishing Group</pub></addata></record> |
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subjects | Apheresis Care and treatment Complications and side effects Graft versus host reaction Health aspects Immunosuppression Patient outcomes Risk factors Stem cells Transplantation |
title | Extracorporeal photopheresis in the management of steroid-refractory chronic graft-versus-host disease after allogeneic stem cell transplantation |
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