Long-term control of extensive refractory chronic graft versus host disease in a multiple myeloma relapsing after allogeneic transplant. A case report

2017 ◽  
Vol 58 (11) ◽  
pp. 2770-2771 ◽  
Author(s):  
Federica Cocito ◽  
Silvia Mangiacavalli ◽  
Paolo Bernasconi ◽  
Anna A. Colombo ◽  
Daniela Caldera ◽  
...  
2021 ◽  
Vol 9 (5) ◽  
Author(s):  
Joe Truong Nguyen ◽  
Clint T. Allen ◽  
Joshua T. Dodge ◽  
Koenraad Van Doorslaer ◽  
Alison A. McBride ◽  
...  

1988 ◽  
Vol 50 (4) ◽  
pp. 626-630
Author(s):  
Naoko KATO ◽  
Riri ADACHI ◽  
Takashi AOYAGI ◽  
Akira OHKAWARA ◽  
Takehiro TOGASHI ◽  
...  

Blood ◽  
1998 ◽  
Vol 91 (7) ◽  
pp. 2581-2587 ◽  
Author(s):  
Cong Yu ◽  
Kristy Seidel ◽  
Richard A. Nash ◽  
H. Joachim Deeg ◽  
Brenda M. Sandmaier ◽  
...  

Abstract Mycophenolate mofetil (MMF) was evaluated either alone or combined with cyclosporine (CSP) for preventing graft-versus-host disease (GVHD) in dogs given 9.2 Gy total body irradiation and DLA-nonidentical unrelated marrow grafts. Marrow autograft studies showed gut toxicity as limiting MMF side effects. Four groups were studied for GVHD prevention: six dogs in group 1 received MMF 10 mg/kg twice daily subcutaneously (SC) on days 0 to 27. They died between 8 to 28 days from infection or GVHD; survival was better than that of 72 controls given no immunosuppression (P = .04), but not different from 19 dogs given CSP. Four dogs in group 2 received MMF as described, along with CSP at 10 to 15 mg/kg twice daily on days 0 to 27. They died at 6 to 98 days from CSP-associated toxicity, weight loss, or infection. Nine dogs in group 3 received MMF SC twice daily 6 mg/kg/d for 3 days, followed by 10 mg/kg twice daily until day 27, along with CSP as described; four died between 7 to 106 days with intussusception, infection, or GVHD, and five became long-term survivors. Six dogs in group 4 received shortened MMF (21 days) and reduced doses of CSP given through day 100. Three died with GVHD or infection between days 38 to 119, and three became long-term survivors. Results support the notion of synergism between MMF and CSP, as evidenced by stable graft-host tolerance in greater than 50% of dogs.


Author(s):  
Marjorie Das Posses Bridi ◽  
Renata Caroline Wanderley Nobre ◽  
Rosany Larissa Brito De Oliveira ◽  
Valtuir Barbosa Felix ◽  
Andréia Barbosa Da Silva ◽  
...  

Blood ◽  
2014 ◽  
Vol 124 (3) ◽  
pp. 363-373 ◽  
Author(s):  
Shernan G. Holtan ◽  
Marcelo Pasquini ◽  
Daniel J. Weisdorf

Abstract Over the past 5 years, many novel approaches to early diagnosis, prevention, and treatment of acute graft-versus-host disease (aGVHD) have been translated from the bench to the bedside. In this review, we highlight recent discoveries in the context of current aGVHD care. The most significant innovations that have already reached the clinic are prophylaxis strategies based upon a refinement of our understanding of key sensors, effectors, suppressors of the immune alloreactive response, and the resultant tissue damage from the aGVHD inflammatory cascade. In the near future, aGVHD prevention and treatment will likely involve multiple modalities, including small molecules regulating immunologic checkpoints, enhancement of suppressor cytokines and cellular subsets, modulation of the microbiota, graft manipulation, and other donor-based prophylaxis strategies. Despite long-term efforts, major challenges in treatment of established aGVHD still remain. Resolution of inflammation and facilitation of rapid immune reconstitution in those with only a limited response to corticosteroids is a research arena that remains rife with opportunity and urgent clinical need.


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