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Autologous stem cell transplantation for post-transplant lymphoproliferative disorders after solid organ transplantation: a retrospective analysis from the Lymphoma Working Party of the EBMT
by
Kerre Tessa
, Bachy Emmanuel
, Eyre, Toby A
, Bargetzi Mario
, Tholouli Eleni
, Montoto, Silvia
, Zimmermann Heiner
, Gandhi, Damaj
, Hilgendorf Inken
, Boumendil Ariane
, De Wilde Virginie
, Crawley, Charles
, Kanfer, Edward
, Kozák Tomáš
, Caillard Sophie
, Kothari Jaimal
, Trappe, Ralf Ulrich
, Trněný Marek
, Broom, Angus
, Robinson, Stephen
, Finel Herve
in
Autografts
/ Case reports
/ Confidence intervals
/ Disorders
/ Immunoproliferative diseases
/ Lymphatic diseases
/ Lymphocytes
/ Lymphoma
/ Melphalan
/ Plasmacytoma
/ Posttransplant lymphoproliferative disorders
/ Remission
/ Stem cell transplantation
/ Stem cells
/ Toxicity
/ Transplantation
/ Transplants & implants
2021
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Autologous stem cell transplantation for post-transplant lymphoproliferative disorders after solid organ transplantation: a retrospective analysis from the Lymphoma Working Party of the EBMT
by
Kerre Tessa
, Bachy Emmanuel
, Eyre, Toby A
, Bargetzi Mario
, Tholouli Eleni
, Montoto, Silvia
, Zimmermann Heiner
, Gandhi, Damaj
, Hilgendorf Inken
, Boumendil Ariane
, De Wilde Virginie
, Crawley, Charles
, Kanfer, Edward
, Kozák Tomáš
, Caillard Sophie
, Kothari Jaimal
, Trappe, Ralf Ulrich
, Trněný Marek
, Broom, Angus
, Robinson, Stephen
, Finel Herve
in
Autografts
/ Case reports
/ Confidence intervals
/ Disorders
/ Immunoproliferative diseases
/ Lymphatic diseases
/ Lymphocytes
/ Lymphoma
/ Melphalan
/ Plasmacytoma
/ Posttransplant lymphoproliferative disorders
/ Remission
/ Stem cell transplantation
/ Stem cells
/ Toxicity
/ Transplantation
/ Transplants & implants
2021
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Autologous stem cell transplantation for post-transplant lymphoproliferative disorders after solid organ transplantation: a retrospective analysis from the Lymphoma Working Party of the EBMT
by
Kerre Tessa
, Bachy Emmanuel
, Eyre, Toby A
, Bargetzi Mario
, Tholouli Eleni
, Montoto, Silvia
, Zimmermann Heiner
, Gandhi, Damaj
, Hilgendorf Inken
, Boumendil Ariane
, De Wilde Virginie
, Crawley, Charles
, Kanfer, Edward
, Kozák Tomáš
, Caillard Sophie
, Kothari Jaimal
, Trappe, Ralf Ulrich
, Trněný Marek
, Broom, Angus
, Robinson, Stephen
, Finel Herve
in
Autografts
/ Case reports
/ Confidence intervals
/ Disorders
/ Immunoproliferative diseases
/ Lymphatic diseases
/ Lymphocytes
/ Lymphoma
/ Melphalan
/ Plasmacytoma
/ Posttransplant lymphoproliferative disorders
/ Remission
/ Stem cell transplantation
/ Stem cells
/ Toxicity
/ Transplantation
/ Transplants & implants
2021
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Autologous stem cell transplantation for post-transplant lymphoproliferative disorders after solid organ transplantation: a retrospective analysis from the Lymphoma Working Party of the EBMT
Journal Article
Autologous stem cell transplantation for post-transplant lymphoproliferative disorders after solid organ transplantation: a retrospective analysis from the Lymphoma Working Party of the EBMT
2021
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Overview
Published data describing the efficacy and safety of autologous stem-cell transplantation (autoSCT) in post-transplant lymphoproliferative disorders (PTLD) is limited to case reports. This is a retrospective analysis of 21 patients reported to the EBMT registry who received an autoSCT for PTLD post solid organ transplant (SOT). Median age at autoSCT was 47 (range: 22–71) years. The commonest SOTs were kidney (48%) and liver (24%). Commonest histologies included DLBCL-type PTLD (14/21) and plasmacytoma-like PTLD (3/21). Patients received a median of two lines of therapy (range: 1–4) pre-autoSCT. ECOG performance status pre-autoSCT was 0 in 14% and 1 in 86%. Remission status pre-autoSCT was CR 47% and PR 38%. BEAM conditioning was used in 57% and high-dose melphalan in 10%. The median follow-up post-autoSCT was 64 months for alive patients. 3-year PFS was 62% [95% confidence interval (CI) 44–87%] and 3-year OS was 61% [95% CI:43–86]. There were 12 deaths, including four related to autoSCT. 100-day non-relapse-mortality (NRM) was 14% and 1-year NRM was 24%. This study suggests that autoSCT, although feasible and with potential therapeutic activity, is associated with a high NRM, primarily driven by infectious toxicity. A multi-disciplinary approach, expert microbiological input and stringent patient selection are required to optimise outcomes.
Publisher
Nature Publishing Group
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