Aug 2026· Journal of Clinical Medicine· Vol 15, pp. 6520· 0 citations· 251 references
Medicine
TL;DR
This narrative review synthesizes current indications for autologous (auto-HSCT) and allogeneic (allo-HSCT) transplantations in adults, and flags areas of persistent controversy where randomized data are still maturing.
Abstract
Hematopoietic stem-cell transplantation (HSCT) has evolved from a salvage procedure for otherwise-fatal leukemia into a curative modality spanning nearly every hematological malignancy and several non-malignant disorders. The contemporary landscape has been reshaped by three converging forces: the refinement of disease-specific risk stratification (European LeukemiaNet [ELN] 2022 for acute myeloid leukemia, Molecular International Prognostic Scoring System [IPSS-M] for myelodysplastic syndromes, Mutation-Enhanced International Prognostic Scoring System [MIPSS70+ v2.0], and Myelofibrosis Transplant Scoring System [MTSS] for myelofibrosis); the integration of measurable residual disease (MRD) into dynamic, response-adapted transplant decisions; and the approval of immune effector cell therapies that have displaced transplantation from several long-standing indications while creating new ones (bridge-to-transplant, post-CAR-T consolidation). In parallel, post-transplant cyclophosphamide (PTCy) has largely equalized outcomes across matched sibling, matched unrelated, and mismatched alternative donors, and novel agents (ruxolitinib, belumosudil, axatilimab) have materially reduced graft-versus-host disease (GVHD) morbidity. This narrative review synthesizes current indications for autologous (auto-HSCT) and allogeneic (allo-HSCT) transplantations in adults, and flags areas of persistent controversy where randomized data are still maturing. Across all indications, the clinician’s question is shifting from “transplant or not?” towards “which donor, which conditioning, which bridge, and which post-transplant maintenance?”, each tailored to disease biology, MRD trajectory, and patient fitness.
PreDLI is a safe and effective intervention in pediatric transplantation, particularly as repeated, escalating doses, while acknowledging that standardization remains challenging and outcome depends on center experience and indication.
Carmen Junk, Sebastian U. Michaelis, M. Döring et al.· Pediatric Blood & Cancer· 0 citations
This review synthesizes contemporary breakthroughs in HSCT biology, technology, and clinical application, critically examines unresolved barriers, and highlights future directions, including Artificial Intelligence (AI)-driven predictive analytics, universal donor platforms, and equitable global access strategies.
M. Abah, Ovwigho Ugbede, Oghenetejiri C et al.· DS Reviews of Research in Li...· 0 citations
Adult T-cell leukemia/lymphoma (ATL) is associated with a dismal prognosis in aggressive subtypes, with a median overall survival (OS) of less than one year. In Japan, first line chemotherapy followed by allogeneic stem cell transplantation (allo-SCT) is recommended for eligible patients, yet this strategy is scarcely...
A. Marçais, L. Lhermitte, V. Avettand-Fenoel et al.· Blood Advances· 0 citations
Background. Multiple myeloma (MM) remains a chronic hematologic malignancy. However, treatment outcomes have improved significantly due to the introduction of new targeted agents and high-dose therapy with autologous hematopoietic stem cell transplantation (auto-HSCT) into clinical practice. Several researchers have de...
M. Solovev, L. Mendeleeva, M. V. Solov'eva· Oncohematology· 0 citations
A GVL Failure Framework is proposed that organizes posttransplant relapse into three biologically defined categories of immune escape, aligns matched cellular therapies with each, and overlays a separate clinical transplant-eligibility axis that sets the therapeutic goal.
Naif I. Aljohani, Ahlam Almasari, Zayed Alzahrani et al.· Frontiers in Immunology· 0 citations
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