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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: Curr Opin Hematol. 2011 Nov;18(6):414–420. doi: 10.1097/MOH.0b013e32834ba87d

Table 2.

Secondary treatment for chronic GVHD

Treatment Study type No. of patients % Overall Response Overall Survival Reference
Therapies reported during the two years review period
 Extracorporeal photopheresis (ECP) Phase II 23 70 78% [27]
Retrospective 43 65 70%/1-yr [28]
Retrospective 9 67 [29]
 Rituximab Phase II 37 86 72%/1-yr [31]
Meta-analysis 111 66 [33]
 Imatinib Phase I/II 19 79 84%/1.5-yr [11]
Phase I/II 9 22 78%/1.5-yr [12]
Retrospective 14 50 75%/1.5-yr [13]
 Pentostatin Phase II 51 53 60%/3-yr [34]
Retrospective 18 56 34%/1-yr [35]
 Mesenchymal stem cells infusions (MSC) Phase I/II 19 74 78%/2-yr [37]
Phase I/II 8 50 [38]
 Mycophenolate mofetil Retrospective 23 26a 96%/1-yr [39]
Retrospective 11 64 67%/1-yr [40]
 mTOR inhibitor Retrospective 34 76 72%/3-yr [42]
Other therapies summarized in recent reviews [17,25,46]
 Calcineurin inhibitor graphic file with name nihms348481t1.jpg 20 – 82% overall response rates reported
 High-dose methylprednisolone
 Methotrexate
 Thalidomide
 Hydroxychloroquine
 Clofazimine
 Thoracoabdominal irradiation
 Alefacept
 Infliximab

mTOR, mammalian target of rapamycin.

a

Response was defined as discontinuation of all immunosuppressive treatment by 3 years.

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