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Factors associated with pulmonary toxicity after myeloablative conditioning using fractionated total body irradiation

Authors :
Chang Ok Suh
Won Hee Lee
Byung Min Lee
Jin Seok Kim
Andrew Jihoon Yang
Chuhl Joo Lyu
Hong In Yoon
June-Won Cheong
J.H. Lee
Jaeho Cho
Hyo Sun Kim
Yoo Hong Min
Ki Jung Ahn
Hwa Kyung Byun
Hyun-Ju Kim
Soo Jeong Kim
Source :
Radiation Oncology Journal
Publication Year :
2017
Publisher :
Korean Society for Therapeutic Radiology and Oncology, 2017.

Abstract

Purpose Pulmonary toxicities, including infectious pneumonia (IP) and idiopathic pneumonia syndrome (IPS), are serious side effects of total body irradiation (TBI) used for myeloablative conditioning. This study aimed to evaluate clinical factors associated with IP and IPS following TBI. Materials and methods Fifty-eight patients with hematologic malignancies who underwent TBI before allogeneic hematopoietic stem cell transplantation between 2005 and 2014 were reviewed. Most patients (91%) received 12 Gy in 1.5 Gy fractions twice a day. Pulmonary toxicities were diagnosed based on either radiographic evidence or reduced pulmonary function, and were subdivided into IP and IPS based on the presence or absence of concurrent infection. Results Pulmonary toxicities developed in 36 patients (62%); 16 (28%) had IP and 20 (34%) had IPS. IP was significantly associated with increased treatment-related mortality (p = 0.028) and decreased survival (p = 0.039). Multivariate analysis revealed that the risk of developing IPS was significantly higher in patients who received stem cells from a matched unrelated donor than from a matched sibling donor (p = 0.021; hazard ratio [HR] = 12.67; 95% confidence interval [CI], 1.46-110.30). Combining other conditioning agents with cyclophosphamide produced a higher tendency to develop IP (p = 0.064; HR = 6.19; 95% CI, 0.90-42.56). Conclusion IP and IPS involve different risk factors and distinct pathogeneses that should be considered when planning treatments before and after TBI.

Details

ISSN :
22343156 and 22341900
Volume :
35
Database :
OpenAIRE
Journal :
Radiation Oncology Journal
Accession number :
edsair.doi.dedup.....90136ce735d6a3aaaae825d0092989b8