The Doorstep to the Temple of Wisdom THE BOTTOM LINE From the Baltim Financial d Correspon Depar Orlea gbvog Received J � 2011 Am 1083-8791 doi:10.101 The Doorstep to the Temple of Wisdom Georgia Vogelsang ‘‘The doorstep to the temple of wisdom is knowl- edge of our own ignorance.’’ Benjamin Franklin. In this issue, Pidala and colleagues report the ap- palling state of ignorance and confusion regarding withdraw of immunosuppression (IS) after allogeneic hematopoietic stem cell transplantation (allo HCT) [1]. The authors document marked variation practice (even within the same transplant group), high esti- mates of graft-vs-host disease (GVHD) emerging in the setting of IS taper, and limited confidence of trans- plant physicians in their therapeutic decisions. The egress from the temple of stem cell transplant is indeed a jumbled muddle. The investigators surveyed the American Society Blood and Marrow Transplantation members using a series of clinical vignettes to explore IS management after allo HCT. Unfortunately, only 21% of physician members participated, which does add a note of con- cern over the validity of the results. Even with this ca- veat, the results are alarming. For example, 25% indicated that they had no consistent strategy for IS ta- pering and half said they had no institutional guidelines for IS tapering. There was marked variation among re- spondents in the taper schedule both in terms of timing and drug dose reduction even in the base case of an un- complicated HLA identical sibling HCT. As the inves- tigators added complexity to the base case (use of peripheral blood, unrelated donor graft, relapse post transplant, and so forth), the variations and uncertainty increased. Moreover, the respondents estimated that the IS approach they used was likely to result in recur- rent acute GVHD (aGVHD) and/or chronic GVHD (cGVHD) in many patients. A total of 41% reported that their current strategy for IS management post- HCT is not adequate, and 26% admitted that they are either uncomfortable or very uncomfortable with making decisions in the management of IS post-HCT. Department of Oncology, Johns Hopkins Hospital, ore, Maryland. isclosure: See Acknowledgment on page 1418. dence and reprint requests: Georgia Vogelsang, MD, tment of Oncology, Johns Hopkins Hospital, 1650 ns Street, Room 2M89, Baltimore, MD 21231 (e-mail: elsang@gmail.com). uly 28, 2011; accepted August 4, 2011 erican Society for Blood and Marrow Transplantation /$36.00 6/j.bbmt.2011.08.004 What happened to create this muddle of uncer- tainty? There are multiple factors. First, transplanta- tion has become more diverse. It has gone from 2 basic transplant types (autologous or identical sibling allogeneic) to almost endless combinations of donor types and stem cell sources. Results from clinical trials are often being applied to patients quite different from the original study group. More concerning, these trials were designed to look at engraftment and GVHD pro- phylaxis, not at effective IS tapering. Although some do report rates of cGVHD, none truly report the bur- den of GVHD occurring on taper or how many pa- tients required reinstitution of IS. Thus, transplant physicians must make their best guess how to adapt the published regimens to their diverse transplant types. Second, the patient population has also changed, expanding to include older patients and pa- tients with multiple medical illnesses, with marginal organ reserves. This group of patients has less immu- nologic plasticity and tolerance induction is likely more difficult. The growth of cord blood transplants has introduced a group with the potential for greater immunologic plasticity. Strikingly, the basic practice of transplantation in many ways has not changed. Care of a patient receiving a transplant is usually trans- ferred to a transplant center for a limited period of time. This care model has long impeded the study and care of patients with cGVHD. It certainly contrib- utes to the lack of research into withdraw of IS. Finally, the few trials of prolonged IS in an attempt to reduce the rates of recurrent aGVHD and cGVHD have produced mixed results with no clear indication that longer standard IS is better [2]. Likewise, attempts to prevent cGVHD using immunomodulatory agents have not proven successful [3]. Indeed, the recent premature closure of the HOVON 76 trial of Lenali- domide after reduced-intensity allogeneic transplanta- tion highlights that the unanticipated (induction of aGVHD) may occur even with agents that have been well tolerated in other posttransplant situations (relapse or progression of multiple myeloma) [4]. Is the situation then a hopeless muddle? Certainly the Pidala paper [1] shows that transplant physicians are extremely uncomfortable with the current state and that there is a wide variation in how patients are managed. The investigators suggest several possible approaches to improve our current state of ignorance. Retrospective studies could examine successful IS 1417 mailto:gbvogelsang@gmail.com http://dx.doi.org/10.1016/j.bbmt.2011.08.004 1418 Biol Blood Marrow Transplant 17:1417-1418, 2011G. Vogelsang discontinuation rates according to tapering schedule. Prospective observational studies could record the IS taper and the associated outcomes. They suggest that this data be used to design prospective randomized trial comparing best approaches for tapering and dis- continuation of IS. My own belief is that the often competing factors listed above that created the muddle make prospective clinical trials comparing the with- draw strategies identified as the ‘‘best’’ extremely com- plicated, time consuming, expensive, and may still produce equivocal results. The investigators suggest another path that is more likely to be fruitful. If vali- dated biomarkers of post-HCT immune tolerance can be developed, these could be used to generate a personalized and informed strategy for IS discontin- uation after allo HCT. Our understanding of the genes regulating tolerance after transplant has improved sig- nificantly in solid organ transplantation. As summa- rized recently in an excellent review in this journal, the current concept is that tolerant solid organ trans- plant patients have a state of immune quiescence with reduced expression of costimulation and immune response genes, and upregulation of cell cycle control genes [5]. CD41CD251FoxP31 regulatory T cells and likely natural killer cells also play important roles in tolerance. Unfortunately, not much is known about the corresponding tolerant stem cell transplant pa- tient, but these same techniques should be able to de- termine the genetic and cellular profile of tolerant patients. Should these markers be validated, this would allow for rationally designed strategies for IS discon- tinuance. This approach has the multiple benefits. IS manipulation could be focused on the nontolerant pa- tients who have the most to gain from success while sparing the cost and toxicity of IS in that group of patients who have already achieved a tolerant state. These IS manipulations could be directed at the iden- tified defect. This approach would also avoid the diffi- culty of having to test IS discontinuance in all the diverse combinations of transplant types. To close with another quote from Benjamin Franklin, ‘‘Being ignorant is not so much a shame, as being unwilling to learn.’’ This paper is a call to all that we have much to learn before we are able to opti- mally manage the final step of the stem cell transplant procedure. ACKNOWLEDGMENTS Financial disclosure: The authors has nothing to de- clare. REFERENCES 1. Pidala J, Lee SJ, Quinn G, Jim H, Kim J, Anasetti C. Variation in management of immune suppression after allogeneic hematopoi- etic cell transplantation. Biol Blood Marrow Transplant. 2001 April 11 [Epup ahead of print]. 2. Kansu E, Gooley T, Flowers ME, et al. Administration of cyclo- sporine for 24 months compared with 6 months for prevention of chronic graft-versus-host disease: a prospective randomized clin- ical trial. Blood. 2001;98:3868-3870. 3. Chao NJ, Parker PM, Niland JC, et al. Paradoxical effect of tha- lidomide prophylaxis on chronic graft-vs.-host disease. Biol Blood Marrow Transplant. 1996;2:86-92. 4. Kneppers E, van der Holt B, Kersten MJ, et al. Lenalidomide maintenance following non-myeloablative allogeneic stem cell transplantation in multiple myeloma is not feasible: results of the HOVON 76 trial. Blood. 2011 June 20. Epub ahead of print]. 5. Pidala J, Bloom GC, Enkemann S, Eschrich S, Lancaster J, Anasetti C. Biomarkers to discern transplantation tolerance after allogeneic hematopoietic cell transplantation. Biol Blood Marrow Transplant. 2010;16:729-738. The Doorstep to the Temple of Wisdom Acknowledgments References