Follow-up of patients with refractory or relapsed multiple myeloma after allogeneic hematopoietic cell transplantation

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Follow-up of patients with refractory or relapsed multiple myeloma after allogeneic hematopoietic cell transplantation. / Schneidawind, Corina; Duerr-Stoerzer, Silke; Faul, Christoph; Kanz, Lothar; Weisel, Katja; Bethge, Wolfgang; Schneidawind, Dominik.

in: CLIN TRANSPLANT, Jahrgang 31, Nr. 7, 07.2017.

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@article{8d4c959c1aee4af1bd5ccf073f720ddd,
title = "Follow-up of patients with refractory or relapsed multiple myeloma after allogeneic hematopoietic cell transplantation",
abstract = "BACKGROUND: The role of allogeneic hematopoietic cell transplantation (HCT) for the treatment of multiple myeloma is controversial. However, the introduction of proteasome inhibitors and immunomodulatory drugs might influence outcomes in case of relapse or refractory disease after allogeneic HCT.METHODS: We report 41 consecutive patients that underwent allogeneic HCT for the treatment of relapsed or refractory multiple myeloma.RESULTS: Three-year event-free survival (EFS) and overall survival (OS) of the whole cohort were 15% and 51%, respectively. In a subgroup analysis, allogeneic HCT after a second high-dose chemotherapy with autologous stem cell support was associated with a decreased 3-year EFS (6% vs 24%, P=.04) and OS (35% vs 64%, P=.09). In case of relapse or refractory disease after allogeneic HCT, the treatment with proteasome inhibitors or immunomodulatory drugs significantly improved survival (1-year OS 79% vs 29%, P=.001).CONCLUSION: The incorporation of proteasome inhibitors and immunomodulatory drugs into transplant protocols has the potential to improve outcomes and refine the role of allogeneic HCT for the treatment of multiple myeloma as a platform for long-term disease control.",
keywords = "Adult, Aged, Female, Follow-Up Studies, Graft Rejection, Graft Survival, Graft vs Host Disease, Hematopoietic Stem Cell Transplantation, Humans, Immunomodulation, Male, Middle Aged, Multiple Myeloma, Neoplasm Recurrence, Local, Prognosis, Proteasome Inhibitors, Retrospective Studies, Risk Factors, Transplantation Conditioning, Transplantation, Homologous, Journal Article",
author = "Corina Schneidawind and Silke Duerr-Stoerzer and Christoph Faul and Lothar Kanz and Katja Weisel and Wolfgang Bethge and Dominik Schneidawind",
note = "{\textcopyright} 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.",
year = "2017",
month = jul,
doi = "10.1111/ctr.12994",
language = "English",
volume = "31",
journal = "CLIN TRANSPLANT",
issn = "0902-0063",
publisher = "Wiley-Blackwell",
number = "7",

}

RIS

TY - JOUR

T1 - Follow-up of patients with refractory or relapsed multiple myeloma after allogeneic hematopoietic cell transplantation

AU - Schneidawind, Corina

AU - Duerr-Stoerzer, Silke

AU - Faul, Christoph

AU - Kanz, Lothar

AU - Weisel, Katja

AU - Bethge, Wolfgang

AU - Schneidawind, Dominik

N1 - © 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

PY - 2017/7

Y1 - 2017/7

N2 - BACKGROUND: The role of allogeneic hematopoietic cell transplantation (HCT) for the treatment of multiple myeloma is controversial. However, the introduction of proteasome inhibitors and immunomodulatory drugs might influence outcomes in case of relapse or refractory disease after allogeneic HCT.METHODS: We report 41 consecutive patients that underwent allogeneic HCT for the treatment of relapsed or refractory multiple myeloma.RESULTS: Three-year event-free survival (EFS) and overall survival (OS) of the whole cohort were 15% and 51%, respectively. In a subgroup analysis, allogeneic HCT after a second high-dose chemotherapy with autologous stem cell support was associated with a decreased 3-year EFS (6% vs 24%, P=.04) and OS (35% vs 64%, P=.09). In case of relapse or refractory disease after allogeneic HCT, the treatment with proteasome inhibitors or immunomodulatory drugs significantly improved survival (1-year OS 79% vs 29%, P=.001).CONCLUSION: The incorporation of proteasome inhibitors and immunomodulatory drugs into transplant protocols has the potential to improve outcomes and refine the role of allogeneic HCT for the treatment of multiple myeloma as a platform for long-term disease control.

AB - BACKGROUND: The role of allogeneic hematopoietic cell transplantation (HCT) for the treatment of multiple myeloma is controversial. However, the introduction of proteasome inhibitors and immunomodulatory drugs might influence outcomes in case of relapse or refractory disease after allogeneic HCT.METHODS: We report 41 consecutive patients that underwent allogeneic HCT for the treatment of relapsed or refractory multiple myeloma.RESULTS: Three-year event-free survival (EFS) and overall survival (OS) of the whole cohort were 15% and 51%, respectively. In a subgroup analysis, allogeneic HCT after a second high-dose chemotherapy with autologous stem cell support was associated with a decreased 3-year EFS (6% vs 24%, P=.04) and OS (35% vs 64%, P=.09). In case of relapse or refractory disease after allogeneic HCT, the treatment with proteasome inhibitors or immunomodulatory drugs significantly improved survival (1-year OS 79% vs 29%, P=.001).CONCLUSION: The incorporation of proteasome inhibitors and immunomodulatory drugs into transplant protocols has the potential to improve outcomes and refine the role of allogeneic HCT for the treatment of multiple myeloma as a platform for long-term disease control.

KW - Adult

KW - Aged

KW - Female

KW - Follow-Up Studies

KW - Graft Rejection

KW - Graft Survival

KW - Graft vs Host Disease

KW - Hematopoietic Stem Cell Transplantation

KW - Humans

KW - Immunomodulation

KW - Male

KW - Middle Aged

KW - Multiple Myeloma

KW - Neoplasm Recurrence, Local

KW - Prognosis

KW - Proteasome Inhibitors

KW - Retrospective Studies

KW - Risk Factors

KW - Transplantation Conditioning

KW - Transplantation, Homologous

KW - Journal Article

U2 - 10.1111/ctr.12994

DO - 10.1111/ctr.12994

M3 - SCORING: Journal article

C2 - 28470884

VL - 31

JO - CLIN TRANSPLANT

JF - CLIN TRANSPLANT

SN - 0902-0063

IS - 7

ER -