| Literature DB >> 34217703 |
Daniel Wolff1, Vedran Radojcic2, Robert Lafyatis3, Resat Cinar4, Rachel K Rosenstein5, Edward W Cowen6, Guang-Shing Cheng7, Ajay Sheshadri8, Anne Bergeron9, Kirsten M Williams10, Jamie L Todd11, Takanori Teshima12, Geoffrey D E Cuvelier13, Ernst Holler14, Shannon R McCurdy15, Robert R Jenq16, Alan M Hanash17, David Jacobsohn18, Bianca D Santomasso19, Sandeep Jain20, Yoko Ogawa21, Philipp Steven22, Zhonghui Katie Luo23, Tina Dietrich-Ntoukas24, Daniel Saban25, Ervina Bilic26, Olaf Penack27, Linda M Griffith28, Meredith Cowden29, Paul J Martin7, Hildegard T Greinix30, Stefanie Sarantopoulos31, Gerard Socie32, Bruce R Blazar33, Joseph Pidala34, Carrie L Kitko35, Daniel R Couriel2, Corey Cutler36, Kirk R Schultz37, Steven Z Pavletic38, Stephanie J Lee7, Sophie Paczesny39.
Abstract
Chronic graft-versus-host disease (GVHD) can be associated with significant morbidity, in part because of nonreversible fibrosis, which impacts physical functioning (eye, skin, lung manifestations) and mortality (lung, gastrointestinal manifestations). Progress in preventing severe morbidity and mortality associated with chronic GVHD is limited by a complex and incompletely understood disease biology and a lack of prognostic biomarkers. Likewise, treatment advances for highly morbid manifestations remain hindered by the absence of effective organ-specific approaches targeting "irreversible" fibrotic sequelae and difficulties in conducting clinical trials in a heterogeneous disease with small patient numbers. The purpose of this document is to identify current gaps, to outline a roadmap of research goals for highly morbid forms of chronic GVHD including advanced skin sclerosis, fasciitis, lung, ocular and gastrointestinal involvement, and to propose strategies for effective trial design. The working group made the following recommendations: (1) Phenotype chronic GVHD clinically and biologically in future cohorts, to describe the incidence, prognostic factors, mechanisms of organ damage, and clinical evolution of highly morbid conditions including long-term effects in children; (2) Conduct longitudinal multicenter studies with common definitions and research sample collections; (3) Develop new approaches for early identification and treatment of highly morbid forms of chronic GVHD, especially biologically targeted treatments, with a special focus on fibrotic changes; and (4) Establish primary endpoints for clinical trials addressing each highly morbid manifestation in relationship to the time point of intervention (early versus late). Alternative endpoints, such as lack of progression and improvement in physical functioning or quality of life, may be suitable for clinical trials in patients with highly morbid manifestations. Finally, new approaches for objective response assessment and exploration of novel trial designs for small populations are required.Entities:
Keywords: Allogeneic hematopoietic cell transplantation; Chronic graft-versus-host disease; Consensus; Gastrointestinal tract; Lung; Ocular; Sclerosis; Skin
Mesh:
Year: 2021 PMID: 34217703 PMCID: PMC8478861 DOI: 10.1016/j.jtct.2021.06.001
Source DB: PubMed Journal: Transplant Cell Ther ISSN: 2666-6367