Volume 98, Issue 2 pp. 408-412
Full Access

Complementarity determining region-III is a useful molecular marker for the evaluation of minimal residual disease in mantle cell lymphoma

Toshiro Kurokawa

Toshiro Kurokawa

First Department of Internal Medicine,

Search for more papers by this author
Tomohiro Kinoshita

Tomohiro Kinoshita

First Department of Internal Medicine,

Search for more papers by this author
Takashi Murate

Takashi Murate

First Department of Internal Medicine,

Search for more papers by this author
Tetsuro Nagasaka

Tetsuro Nagasaka

Department of Laboratory Medicine, Nagoya University School of Medicine, Showa-ku, Nagoya,

Search for more papers by this author
Yoshitoyo Kagami

Yoshitoyo Kagami

Haematology and Chemotherapy,

Search for more papers by this author
Michinori Ogura

Michinori Ogura

Haematology and Chemotherapy,

Search for more papers by this author
Shigeo Nakamura

Shigeo Nakamura

Department of Pathology and Clinical Laboratories, Aichi Cancer Centre Hospital,

Search for more papers by this author
Masao Seto

Masao Seto

Laboratory of Chemotherapy, Aichi Cancer Centre Research Institute, Chikusa-ku, Nagoya,,

Search for more papers by this author
Tomomitsu Hotta

Tomomitsu Hotta

Fourth Department of Internal Medicine, Tokai University School of Medicine, Boseidai, Isehara-city, Kanagawa, Japan

Search for more papers by this author
Hidehiko Saito

Hidehiko Saito

First Department of Internal Medicine,

Search for more papers by this author
First published: 29 October 2003
Citations: 13
Dr Tomohiro Kinoshita First Department of Internal Medicine, Nagoya University School of Medicine, 65 Tsurumai-cho, Showa-ku, Nagoya 466, Japan.

Abstract

Bone marrow (BM) and peripheral blood (PB) involvement in 10 patients with mantle cell lymphoma (MCL) was analysed by a polymerase chain reaction (PCR)-mediated RNase protection assay. The complementarity determining regions (CDR)-III of all 10 MCLs examined was amplified efficiently with consensus VH and JH primers by PCR, and BM and/or PB involvement was evaluated by RNase protection assay in all 10 patients examined. Our assay showed BM and/or PB of the entire group to have neoplastic cells at presentation, despite the fact that eight patients were found to have BM and/or PB involvement on the basis of morphological examination and/or surface marker analysis. We also examined minimal residual disease (MRD) after conventional chemotherapy, and detected MRD in a patient in complete remission (CR). Although previous studies have shown that t(11;14) breakpoint amplification by PCR was only applicable to about 30–40% of cases, the present study indicates that CDR-III is a useful molecular marker and the PCR-mediated RNase protection assay is a good tool for the evaluation of MRD in MCL. It is suggested that BM and PB of MCL patients are quite frequently involved at presentation and even after conventional chemotherapy at the molecular level.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.