# Tandem autologous hematopoietic stem cell transplantation in multiple myeloma: A historical perspective and current challenges

**Authors:** Xueting Wang, Yushan Cui, Yaomei Wang, Baijun Fang

PMC · DOI: 10.1007/s00277-025-06563-z · 2025-09-15

## TL;DR

This paper reviews the role of tandem autologous stem cell transplants in treating multiple myeloma, comparing it with other treatments and discussing its challenges.

## Contribution

The paper critically evaluates the efficacy and challenges of tandem autologous hematopoietic stem cell transplantation in the context of emerging therapies for multiple myeloma.

## Key findings

- Tandem autologous HSCT improves progression-free and overall survival in high-risk multiple myeloma.
- Allogeneic HSCT offers potential cure but is limited by transplant-related mortality and GVHD.
- Emerging therapies challenge the role of tandem autologous HSCT in MM treatment.

## Abstract

Multiple myeloma (MM) is a heterogeneous and relapse-prone hematologic malignancy that remains incurable. For newly diagnosed patients aged 70 years or younger, who are eligible for transplantation, autologous hematopoietic stem cell transplantation (auto-HSCT) is the preferred first-line treatment. In patients with high-risk multiple myeloma (HRMM), some studies have demonstrated that tandem auto-HSCT provides notable benefits over single auto-HSCT, particularly in extending progression-free survival (PFS) and overall survival (OS). Although allogeneic hematopoietic stem cell transplantation (allo-HSCT) currently offers the only potential for long-term cure in MM, its application is limited by high transplant-related mortality (TRM) and the risk of graft-versus-host disease (GVHD). In recent years, the emergence of novel therapies, including proteasome inhibitors, immunomodulatory drugs, monoclonal antibodies, and chimeric antigen receptor T-cell (CAR-T) therapy, has posed new challenges to the role of tandem auto-HSCT in MM treatment. This review aims to critically examine the efficacy differences between tandem and single auto-HSCT, and sequential allo-HSCT following auto-HSCT. Furthermore, it will rigorously evaluate the role and challenges of tandem auto-HSCT within the evolving therapeutic landscape.

## Linked entities

- **Diseases:** multiple myeloma (MONDO:0009693)

## Full-text entities

- **Diseases:** hematologic malignancy (MESH:D019337), HRMM (MESH:D009101), GVHD (MESH:D006086)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12552249/full.md

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Source: https://tomesphere.com/paper/PMC12552249