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Stage IV marginal zone B-cell lymphoma - prognostic factors and the role of rituximab: Consortium for Improving Survival of Lymphoma (CISL) study

Authors
Oh, Sung YongKim, Won SeogKim, Jin SeokKim, Seok JinLee, SueeLee, Dae HoWon, Jong-HoHwang, In GyuKim, Min KyoungLee, Soon IlChae, Yee SooYang, Deok-HwanKang, Hye JinChoi, Chul WonPark, JinnyKim, Hyo JungKwon, Jung HyeLee, Ho SupLee, Gyeong-WonEom, Hyeon SeokKwak, Jae-YongSuh, CheolwonKim, Hyo-Jin
Issue Date
11월-2010
Publisher
WILEY-BLACKWELL
Citation
CANCER SCIENCE, v.101, no.11, pp.2443 - 2447
Indexed
SCIE
SCOPUS
Journal Title
CANCER SCIENCE
Volume
101
Number
11
Start Page
2443
End Page
2447
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/115441
DOI
10.1111/j.1349-7006.2010.01698.x
ISSN
1347-9032
Abstract
Stage IV marginal zone B-cell lymphomas (MZL) are detected in more than 25% of lymphoma patients. In this study, we conducted retrospective analyses of specific cases of stage IV MZL in order to assess their clinical features, as well as the treatments and prognoses of these cases. A total of 94 patients with histological diagnosis of stage IV-MZL from 17 different institutions in Korea were included. Multiple-mucosa-associated lymphoid tissue (MALT)-organs-involved MZL (M-MZL) was detected in 34 patients (36.2%). Bone-marrow-involved stage IV MZL (BM-MZL) was detected in 33 patients (35.1%). Median time to progression (TTP) was 2.4 years (95% CI, 1.9-2.9). Five- and 10-year overall survival rates were 84.5% and 79.8%, respectively. Patients with lymph node involvement in stage IV MZL appeared to have worse prognoses in TTP (P = 0.015). Thirty-one patients were treated with a regimen including rituximab (CTx-R[+]), and 31 with a regimen that did not include rituximab (CTx-R[-]). The CTx-R(+) group showed better responses than the CTx-R(-) group (83.9%versus 54.8%, P = 0.026). However, no differences in TTP duration were detected (P = 0.113). Stage IV MZL tend to follow an indolent disease course. Therefore, lymph node involvement is a more valuable prognostic factor for TTP. Rituximab appears to contribute to better responses, but not in cases of TTP. (Cancer Sci 2010; 101: 2443-2447).
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