Ruxolitinib in refractory acute and chronic graft-versus-host disease: a multicenter survey study.
Virginia Escamilla GómezValentín García-GutiérrezLucía López CorralGarcía-Cadenas IreneAriadna Pérez MartínezFrancisco J Márquez MalaverTeresa Caballero-VelázquezPedro A González SierraMaría C Viguria AlegríaIngrid M Parra SalinasCristina Calderón CabreraMarta González VicentNancy Rodríguez TorresRocío Parody PorrasChristelle Ferra CollGuillermo OrtiDavid Valcárcel FerreirasRafael De la Cámara LLanzáPaula MolésKyra Velázquez-KennedyMaría João MendeDolores Caballero BarrigónEstefanía PérezRodrigo Martino BofarullSilvanna Saavedra GerosaJorge SierraMarc PochMaría T Zudaire RipaMiguel A Díaz PérezBlanca Molina AnguloIsabel Sánchez OrtegaJaime Sanz CaballerJuan Montoro GómezIldefonso Espigado TocinoJosé A Pérez-Simónnull nullPublished in: Bone marrow transplantation (2019)
Graft-versus-host disease is the main cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation. First-line treatment is based on the use of high doses of corticosteroids. Unfortunately, second-line treatment for both acute and chronic graft-versus-host disease, remains a challenge. Ruxolitinib has been shown as an effective and safe treatment option for these patients. Seventy-nine patients received ruxolitinib and were evaluated in this retrospective and multicenter study. Twenty-three patients received ruxolitinib for refractory acute graft-versus-host disease after a median of 3 (range 1-5) previous lines of therapy. Overall response rate was 69.5% (16/23) which was obtained after a median of 2 weeks of treatment, and 21.7% (5/23) reached complete remission. Fifty-six patients were evaluated for refractory chronic graft-versus-host disease. The median number of previous lines of therapy was 3 (range 1-10). Overall response rate was 57.1% (32/56) with 3.5% (2/56) obtaining complete remission after a median of 4 weeks. Tapering of corticosteroids was possible in both acute (17/23, 73%) and chronic graft-versus-host disease (32/56, 57.1%) groups. Overall survival was 47% (CI: 23-67%) at 6 months for patients with aGVHD (62 vs 28% in responders vs non-responders) and 81% (CI: 63-89%) at 1 year for patients with cGVHD (83 vs 76% in responders vs non-responders). Ruxolitinib in the real life setting is an effective and safe treatment option for GVHD, with an ORR of 69.5% and 57.1% for refractory acute and chronic graft-versus-host disease, respectively, in heavily pretreated patients.
Keyphrases
- end stage renal disease
- ejection fraction
- newly diagnosed
- liver failure
- chronic kidney disease
- prognostic factors
- allogeneic hematopoietic stem cell transplantation
- drug induced
- peritoneal dialysis
- clinical trial
- acute lymphoblastic leukemia
- rheumatoid arthritis
- intensive care unit
- acute myeloid leukemia
- mesenchymal stem cells
- replacement therapy
- combination therapy