Original Article

J Rheum Dis 2017; 24(3): 149-156

Published online June 30, 2017

© Korean College of Rheumatology

Long-term Outcomes of Autologous Peripheral Blood Stem Cell Transplantation for Refractory Rheumatic Diseases

Seung Lee, Sang-Cheol Bae, Jae-Bum Jun, Chan-Bum Choi

Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea

Correspondence to : Chan-Bum Choi, Hanyang University Hospital for Rheumatic Diseases, 222-1 Wangsimni-ro, Seongdong-gu, Seoul 04763, Korea.
E-mail:cbchoi@hanyang.ac.kr

Received: March 15, 2017; Revised: April 27, 2017; Accepted: May 11, 2017

This is an Open Access journal distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Objective. We investigated the long-term outcomes of autologous peripheral blood stem cell transplantation (PBSCT) to treat refractory rheumatic diseases. Methods. Patients who underwent PBSCT for refractory rheumatic diseases at our institution between 2002 and 2005 were assessed for outcomes including treatment response, adverse events, damage accrual, and survival at 6 months and last follow-up. Results. Eleven patients, including six with systemic lupus erythematosus (SLE), four with systemic sclerosis (SSc), and one with Still’s disease were treated with PBSCT. In SLE patients, two showed complete response, two partial response, and two expired. One patient who expired responded completely two months after transplantation but discontinued treatment by choice and expired at six months due to an SLE flare. Long-term, two patients went into remission without organ damage, one patient went into remission with organ damage, and one had low disease activity with organ damage. Of the four patients with SSc, two showed a complete response, one a partial response, and there was one transplantation- related death at six months. At the last record notation, two remained in remission without relapse and one was lost to follow-up. The Still’s disease patient partially responded at six months and was in remission at the last record notation. Conclusion. The ten-year survival rate was 70% with a 40% recurrence rate and 20% treatment-related mortality rate.

Keywords Peripheral blood stem cell transplantation, Systemic lupus erythematosus, Systemic scleroderma, Still disease

Article

Original Article

J Rheum Dis 2017; 24(3): 149-156

Published online June 30, 2017 https://doi.org/10.4078/jrd.2017.24.3.149

Copyright © Korean College of Rheumatology.

Long-term Outcomes of Autologous Peripheral Blood Stem Cell Transplantation for Refractory Rheumatic Diseases

Seung Lee, Sang-Cheol Bae, Jae-Bum Jun, Chan-Bum Choi

Hanyang University Hospital for Rheumatic Diseases, Seoul, Korea

Correspondence to:Chan-Bum Choi, Hanyang University Hospital for Rheumatic Diseases, 222-1 Wangsimni-ro, Seongdong-gu, Seoul 04763, Korea.
E-mail:cbchoi@hanyang.ac.kr

Received: March 15, 2017; Revised: April 27, 2017; Accepted: May 11, 2017

This is an Open Access journal distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Objective. We investigated the long-term outcomes of autologous peripheral blood stem cell transplantation (PBSCT) to treat refractory rheumatic diseases. Methods. Patients who underwent PBSCT for refractory rheumatic diseases at our institution between 2002 and 2005 were assessed for outcomes including treatment response, adverse events, damage accrual, and survival at 6 months and last follow-up. Results. Eleven patients, including six with systemic lupus erythematosus (SLE), four with systemic sclerosis (SSc), and one with Still’s disease were treated with PBSCT. In SLE patients, two showed complete response, two partial response, and two expired. One patient who expired responded completely two months after transplantation but discontinued treatment by choice and expired at six months due to an SLE flare. Long-term, two patients went into remission without organ damage, one patient went into remission with organ damage, and one had low disease activity with organ damage. Of the four patients with SSc, two showed a complete response, one a partial response, and there was one transplantation- related death at six months. At the last record notation, two remained in remission without relapse and one was lost to follow-up. The Still’s disease patient partially responded at six months and was in remission at the last record notation. Conclusion. The ten-year survival rate was 70% with a 40% recurrence rate and 20% treatment-related mortality rate.

Keywords: Peripheral blood stem cell transplantation, Systemic lupus erythematosus, Systemic scleroderma, Still disease

JRD
Jan 01, 2025 Vol.32 No.1, pp. 1~7
COVER PICTURE
Cumulative growth of rheumatology members and specialists (1980~2024). Cumulative distribution of the number of the (A) Korean College of Rheumatology members and (B) rheumatology specialists. (J Rheum Dis 2025;32:63-65)

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