Literature DB >> 2140855

Immunobiologic factors predictive of clinical outcome in diffuse large-cell lymphoma.

D J Slymen1, T P Miller, S M Lippman, C M Spier, D P Kerrigan, J A Rybski, C S Rangel, L C Richter, T M Grogan.   

Abstract

The prognostic importance of immunobiologic factors in diffuse large-cell lymphoma (DLCL) is studied in 105 consecutive DLCL patients. Multivariate results using the Cox proportional hazards model clearly indicate that the Ki-67 index (P = .002), a marker of cell proliferation activity, and the presence or absence of human leukocyte antigen-DR (HLA-DR) (P = .007) are strong predictors of survival even in the presence of established clinical factors of stage (P = .015) and symptoms (P = .050). Using these four variables, prognostic groups were formed identifying patient groups with varying degrees of risk. The group of patients with three or four risk factors present at the time of diagnosis had a median survival of 4 months compared with a median survival of 59 months for the group with no risk factors. Similarly, prognostic groups for disease-free survival (DFS) were constructed based on the proportional hazards model that involved B versus T phenotype (P = .035) and HLA-DR (P = .054). Median DFS for the patient group with one or two risk factors present was 11 months compared with 43 months with no risk factors present. This study suggests immunobiologic parameters are important predictors of clinical outcome in DLCL patients and are of value in identifying subgroups of patients who have not responded to currently available therapy. The practical significance of this study is to identify parameters that may suggest specific changes in therapy of patient subgroups.

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Year:  1990        PMID: 2140855     DOI: 10.1200/JCO.1990.8.6.986

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  6 in total

1.  Prognostic significance of T cell subsets in peripheral blood of B cell non-Hodgkin's lymphoma patients.

Authors:  Mehdi Dehghani; Shokouh Sharifpour; Zahra Amirghofran; Hamid Reza Zare
Journal:  Med Oncol       Date:  2012-02-04       Impact factor: 3.064

2.  Microarray analysis of B-cell lymphoma cell lines with the t(14;18).

Authors:  Ryan S Robetorye; Sandra D Bohling; John W Morgan; G Chris Fillmore; Megan S Lim; Kojo S J Elenitoba-Johnson
Journal:  J Mol Diagn       Date:  2002-08       Impact factor: 5.568

3.  Absence of tumor-specific over-expression of Polo-like kinase 1 (Plk1) in major non-Hodgkin lymphoma and relatively low expression of Plk1 in nasal NK/T cell lymphoma.

Authors:  Hidenori Imai; Koichi Sugimoto; Yasushi Isobe; Makoto Sasaki; Hajime Yasuda; Kengo Takeuchi; Shinji Nakamura; Yuko Kojima; Junichi Tomomatsu; Kazuo Oshimi
Journal:  Int J Hematol       Date:  2009-05-19       Impact factor: 2.490

4.  p27KIP1 is abnormally expressed in Diffuse Large B-cell Lymphomas and is associated with an adverse clinical outcome.

Authors:  A Sáez; E Sánchez; M Sánchez-Beato; M A Cruz; I Chacón; E Muñoz; F I Camacho; J C Martínez-Montero; M Mollejo; J F García; M A Piris
Journal:  Br J Cancer       Date:  1999-07       Impact factor: 7.640

5.  Ki-67 is a valuable prognostic predictor of lymphoma but its utility varies in lymphoma subtypes: evidence from a systematic meta-analysis.

Authors:  Xin He; Zhigang Chen; Tao Fu; Xueli Jin; Teng Yu; Yun Liang; Xiaoying Zhao; Liansheng Huang
Journal:  BMC Cancer       Date:  2014-03-05       Impact factor: 4.430

6.  The clinicopathologic features and response to treatment of patients with Nonhodgkin Lymphoma: A single-center experiment in Turkey.

Authors:  Rahsan Yildirim; Gulden Sincan
Journal:  Pak J Med Sci       Date:  2019 Jan-Feb       Impact factor: 1.088

  6 in total

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