TY - JOUR
T1 - Clinical and pathological features of B-cell non-Hodgkin lymphomas lacking the surface expression of immunoglobulin light chains
AU - Matsushita, Hiromichi
AU - Nakamura, Naoya
AU - Tanaka, Yuzo
AU - Ohgiya, Daisuke
AU - Tanaka, Yumiko
AU - Damdinsuren, Anar
AU - Asai, Satomi
AU - Yabe, Miharu
AU - Kawada, Hiroshi
AU - Ogawa, Yoshiaki
AU - Ando, Kiyoshi
AU - Miyachi, Hayato
PY - 2012/9
Y1 - 2012/9
N2 - Background: The flow cytometric analysis of surface immunoglobulin light chains (sIgL) is used as a simple method for evaluating monoclonal B-cell proliferation. However, the sIgL expression, κ or λ, is occasionally undetectable in cases with B-cell non-Hodgkin lymphomas (B-NHL). The purpose of this study was to investigate the clinical and pathological characteristics of these B-NHL cases. Methods: We retrospectively analyzed 50 cases with previously untreated sIgL-negative B-NHL. All of these cases had been diagnosed at Tokai University Hospital between January 2001 and February 2011. Their medical charts were reviewed. Results: These cases had several clinical features: diffuse large B-cell lymphoma (DLBCL) (72 %), a high serum lactate dehydrogenase level (66 %), clinical stage III and IV (68 %), and complex karyotypes (58 %). Seven out of eight evaluated patients (87 %) did not express cytoplasmic IgL, and the DNA rearrangement pattern of IgL showed diversity in 10 analyzed patients. The 5-year event-free survival of all the sIgL-negative B-NHL cases was significantly better with rituximabcontaining chemotherapies in comparison to the regimens without it (57.9 % vs. 17.9 %, p = 0.0207), although there was no statistical significance when the DLBCL cases were analyzed (56.6 % vs. 22.2 %, p = 0.1530). Conclusions: These findings suggest that sIgL-negative B-NHL cases predominantly developed DLBCL in advanced disease, but were heterogeneous at the molecular level.
AB - Background: The flow cytometric analysis of surface immunoglobulin light chains (sIgL) is used as a simple method for evaluating monoclonal B-cell proliferation. However, the sIgL expression, κ or λ, is occasionally undetectable in cases with B-cell non-Hodgkin lymphomas (B-NHL). The purpose of this study was to investigate the clinical and pathological characteristics of these B-NHL cases. Methods: We retrospectively analyzed 50 cases with previously untreated sIgL-negative B-NHL. All of these cases had been diagnosed at Tokai University Hospital between January 2001 and February 2011. Their medical charts were reviewed. Results: These cases had several clinical features: diffuse large B-cell lymphoma (DLBCL) (72 %), a high serum lactate dehydrogenase level (66 %), clinical stage III and IV (68 %), and complex karyotypes (58 %). Seven out of eight evaluated patients (87 %) did not express cytoplasmic IgL, and the DNA rearrangement pattern of IgL showed diversity in 10 analyzed patients. The 5-year event-free survival of all the sIgL-negative B-NHL cases was significantly better with rituximabcontaining chemotherapies in comparison to the regimens without it (57.9 % vs. 17.9 %, p = 0.0207), although there was no statistical significance when the DLBCL cases were analyzed (56.6 % vs. 22.2 %, p = 0.1530). Conclusions: These findings suggest that sIgL-negative B-NHL cases predominantly developed DLBCL in advanced disease, but were heterogeneous at the molecular level.
KW - Diffuse large B-cell lymphoma
KW - Non-Hodgkin lymphoma
KW - Rituximab
KW - Southern blotting analysis
KW - Surface immunoglobulin light chains
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U2 - 10.1515/cclm-2011-1854
DO - 10.1515/cclm-2011-1854
M3 - Article
C2 - 23100378
AN - SCOPUS:84867795098
SN - 1434-6621
VL - 50
SP - 1665
EP - 1670
JO - Zeitschrift fur klinische Chemie und klinische Biochemie
JF - Zeitschrift fur klinische Chemie und klinische Biochemie
IS - 9
ER -