BEAC induction regimen and prior thoracic radiotherapy increases the risk of ASCT associated pneumonitis.

High-dose chemotherapy (HDT) followed by autologous stem cell transplant (ASCT) has been standard of care in the treatment of relapsed and refractory lymphoma. Some severe toxicities are associated with this treatment modality. Pulmonary toxicity is one of these significant adverse effects and a potential cause of treatment related mortality. In this retrospective study we report the incidence, risk factors and outcome of treatment-induced pneumonitis in 286 lymphoma patients receiving HDT followed by ASCT. The cumulative incidence of treatment-induced pneumonitis was 4,6 % and occurred in 11/286 patients. 3 months incidence rate was 2,6 %. Most of the patients diagnosed with treatment-induced pneumonitis had received BEAC as HDT regimen. The risk of treatment-induced pneumonitis was higher if HDT-ASCT was given in later treatment lines. Also, a prior thoracic radiotherapy as part of first line treatment was associated with higher risk for pneumonitis after HDT-ASCT. In two patients the pneumonitis did not response to high dose steroid treatment. This study is providing new information about the incidence of pneumonitis associated with HDT-ASCT and its risk factors, which might be useful to take into consideration during and after treatment with HDT-ASCT.

Authors

Publication Details

Journal
Acta Haematologica
Published
2026-03-09
DOI
https://doi.org/10.1159/000551311
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

BEAC induction regimen and prior thoracic radiotherapy increases the risk of ASCT associated pneumonitis.

Outi Kuittinen, Anna Jokimäki, Hanne Kuitunen, Elina Kaprio et al.
Acta Haematologica
Lymphoma Diagnosis and Treatment
article

BEAC induction regimen and prior thoracic radiotherapy increases the risk of ASCT associated pneumonitis.

Outi Kuittinen, Anna Jokimäki, Hanne Kuitunen, Elina Kaprio, Tuomas Selander, Taina Turpeenniemi-Hujanen, Joel Kontiainen
article en

Abstract

High-dose chemotherapy (HDT) followed by autologous stem cell transplant (ASCT) has been standard of care in the treatment of relapsed and refractory lymphoma. Some severe toxicities are associated with this treatment modality. Pulmonary toxicity is one of these significant adverse effects and a potential cause of treatment related mortality. In this retrospective study we report the incidence, risk factors and outcome of treatment-induced pneumonitis in 286 lymphoma patients receiving HDT followed by ASCT. The cumulative incidence of treatment-induced pneumonitis was 4,6 % and occurred in 11/286 patients. 3 months incidence rate was 2,6 %. Most of the patients diagnosed with treatment-induced pneumonitis had received BEAC as HDT regimen. The risk of treatment-induced pneumonitis was higher if HDT-ASCT was given in later treatment lines. Also, a prior thoracic radiotherapy as part of first line treatment was associated with higher risk for pneumonitis after HDT-ASCT. In two patients the pneumonitis did not response to high dose steroid treatment. This study is providing new information about the incidence of pneumonitis associated with HDT-ASCT and its risk factors, which might be useful to take into consideration during and after treatment with HDT-ASCT.

Acta Haematologica
Good health and well-being
Openalex Percentile: Top 30%
Lymphoma Diagnosis and Treatment
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

BEAC induction regimen and prior thoracic radiotherapy increases the risk of ASCT associated pneumonitis. — Outi Kuittinen, Anna Jokimäki, et al. · Acta Haematologica (2026) | TGRS Research Map | TGRS