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Tumor necrosis could reflect advanced disease status in patients with diffuse large B cell lymphoma treated with R-CHOP therapy

Authors
Song, Moo-KonChung, Joo-SeopShin, Dong-YeopLim, Sung-NamLee, Gyeong-wonChoi, Jae-CheolPark, Won-YoungOh, So-Yeon
Issue Date
Jan-2017
Publisher
Springer Verlag
Keywords
Tumor necrosis; Diffuse large B cell lymphoma; Ann Arbor stage; Survival
Citation
Annals of Hematology, v.96, no.1, pp 17 - 23
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Annals of Hematology
Volume
96
Number
1
Start Page
17
End Page
23
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153066
DOI
10.1007/s00277-016-2822-8
ISSN
0939-5555
1432-0584
Abstract
Tumor necrosis (TN) can lower responsiveness to chemotherapy and confer basic resistance to anti-cancer therapy. We investigated the association of TN with poor clinical features and outcome in diffuse large B cell lymphoma (DLBCL). We examined the presence or absence of TN in 476 DLBCL patients of who received rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) therapy. Eighty-nine (18.7 %) patients had TN at diagnosis. Patients with TN had a progression-free survival (PFS) and overall survival (OS) of 39.3 and 46.7 %, whereas patients without TN had a PFS and OS of 73.4 and 82.6 %. Adverse clinical factors of poor Eastern Cooperative Oncology Group performance status ≥ grade 2 (p = 0.005), elevated lactate dehydrogenase ratio >1 (p < 0.001), advanced Ann Arbor stage (p = 0.002), and bulky disease (p = 0.026) were more prevalent in the TN group than the non-TN group. Cox regression model analysis revealed TN as an independent prognostic factor for PFS and OS in DLBCL (PFS, hazard ratio [HR] = 1.967, 95 % confidence interval [CI] = 1.399–2.765, p < 0.001; OS, HR = 2.445, 95 % CI = 1.689–3.640, p < 0.001). The results indicate that TN could reflect adverse clinical features and worse prognosis in DLBCL patients receiving R-CHOP therapy.
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