Loading…

Immunoprofile of Hodgkin's lymphoma in India

The immunoprofile of the Reed Sternberg cell with respect to immunoreactivity for CD20 and lack of CD15 has been described as a poor prognostic factor. Large scale studies analyzing the immunoprofile of Hodgkin's lymphoma (HL) from India are lacking. The aim of this study was to obtain baseline...

Full description

Saved in:
Bibliographic Details
Published in:Indian journal of cancer 2008-04, Vol.45 (2), p.59-63
Main Authors: Patkar, N, Mehta, J, Kulkarni, B, Pande, R, Advani, S, Borges, A
Format: Article
Language:English
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 63
container_issue 2
container_start_page 59
container_title Indian journal of cancer
container_volume 45
creator Patkar, N
Mehta, J
Kulkarni, B
Pande, R
Advani, S
Borges, A
description The immunoprofile of the Reed Sternberg cell with respect to immunoreactivity for CD20 and lack of CD15 has been described as a poor prognostic factor. Large scale studies analyzing the immunoprofile of Hodgkin's lymphoma (HL) from India are lacking. The aim of this study was to obtain baseline information on relative frequencies and immunoprofiles of the two major types of HL and comparing reports from developed and developing countries. 451 cases of HL were classified as per the WHO into classical (n= 397) HL (cHL) and nodular lymphocyte predominant HL (NLPHL) (n=54). Cases of cHL were divided into 5 immunophenotypic groups; Group A (CD15+,CD30+,CD20-), Group B (CD15-,CD30+,CD20-), Group C (CD15+,CD30+,CD20+), Group D (CD15-,CD30+,CD20+)and Group E (CD15-,CD30-,CD20+). In cases of NLPHL, the immunophenotype of lymphocytes in the background, whether T(CD3) or B(CD20) rich was observed. Most cases of cHL belonged to Group A (44.58%) followed by Group B (40.05%), C(5.54%), D(9.57%) and E(0.25%). Half, (50.89%) the cases of cHL were immunonegative for CD15, whereas CD20 was expressed by 15.61% of the cases. Three (5.55%) cases of NLPHL showed a CD3 (T) cell rich background. Significant differences were also observed with respect to the age distribution of cHL as compared to the west. Our study demonstrates that India has a high number of CD15 negative and a relatively higher number of CD20 positive cHL cases as compared to the western population. Favorable treatment response and good cure rates that one sees in western cHL may not apply to India.
doi_str_mv 10.4103/0019-509X.41772
format article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_69309984</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A181458174</galeid><sourcerecordid>A181458174</sourcerecordid><originalsourceid>FETCH-LOGICAL-g259t-74361ae778ecd699bdc76785d1b6a5ff5d68a80f5242cd537f528b2ed015c7653</originalsourceid><addsrcrecordid>eNptkU1LxDAQhoMouq6evUnxoBe7Jmk-jyJ-LCx4UfBW0ibtRtNkbdqD_94srqKyzGFmmGde3mEAOEFwRhAsriBEMqdQvqSWc7wDJkhKkRPOyS6Y_EwPwGGMrxDiAhOxDw6QYJghCifgct51ow-rPjTWmSw02UPQ7Zv1FzFzH91qGTqVWZ_NvbbqCOw1ykVzvMlT8Hx3-3TzkC8e7-c314u8xVQOOScFQ8pwLkytmZSVrjnjgmpUMUWbhmomlIANxQTXmhY8VaLCRkNEE0mLKTj_0k223kcTh7KzsTbOKW_CGEsmC5jOJAk8-we-hrH3yVuJC0aEFFAmKP-CWuVMaX0Thl7VrfGmVy54sz68vEYCESoQX4vOtvAptOlsvXXh_NfC0ig3LGNw42CDj3_B043dseqMLle97VT_UX6_o_gEF_iIKA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>236489809</pqid></control><display><type>article</type><title>Immunoprofile of Hodgkin's lymphoma in India</title><source>Publicly Available Content Database</source><creator>Patkar, N ; Mehta, J ; Kulkarni, B ; Pande, R ; Advani, S ; Borges, A</creator><creatorcontrib>Patkar, N ; Mehta, J ; Kulkarni, B ; Pande, R ; Advani, S ; Borges, A</creatorcontrib><description>The immunoprofile of the Reed Sternberg cell with respect to immunoreactivity for CD20 and lack of CD15 has been described as a poor prognostic factor. Large scale studies analyzing the immunoprofile of Hodgkin's lymphoma (HL) from India are lacking. The aim of this study was to obtain baseline information on relative frequencies and immunoprofiles of the two major types of HL and comparing reports from developed and developing countries. 451 cases of HL were classified as per the WHO into classical (n= 397) HL (cHL) and nodular lymphocyte predominant HL (NLPHL) (n=54). Cases of cHL were divided into 5 immunophenotypic groups; Group A (CD15+,CD30+,CD20-), Group B (CD15-,CD30+,CD20-), Group C (CD15+,CD30+,CD20+), Group D (CD15-,CD30+,CD20+)and Group E (CD15-,CD30-,CD20+). In cases of NLPHL, the immunophenotype of lymphocytes in the background, whether T(CD3) or B(CD20) rich was observed. Most cases of cHL belonged to Group A (44.58%) followed by Group B (40.05%), C(5.54%), D(9.57%) and E(0.25%). Half, (50.89%) the cases of cHL were immunonegative for CD15, whereas CD20 was expressed by 15.61% of the cases. Three (5.55%) cases of NLPHL showed a CD3 (T) cell rich background. Significant differences were also observed with respect to the age distribution of cHL as compared to the west. Our study demonstrates that India has a high number of CD15 negative and a relatively higher number of CD20 positive cHL cases as compared to the western population. Favorable treatment response and good cure rates that one sees in western cHL may not apply to India.</description><identifier>ISSN: 0019-509X</identifier><identifier>EISSN: 1998-4774</identifier><identifier>DOI: 10.4103/0019-509X.41772</identifier><identifier>PMID: 18626150</identifier><language>eng</language><publisher>India: Medknow Publications and Media Pvt. Ltd</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Antigens, CD20 - analysis ; Cancer cells ; Child ; Child, Preschool ; Development and progression ; Diagnosis ; Health aspects ; Hodgkin Disease - immunology ; Hodgkin's disease ; Humans ; Immunohistochemistry ; Immunophenotyping ; Ki-1 Antigen - analysis ; Lewis X Antigen - analysis ; Middle Aged ; Physiological aspects ; Properties</subject><ispartof>Indian journal of cancer, 2008-04, Vol.45 (2), p.59-63</ispartof><rights>COPYRIGHT 2008 Medknow Publications and Media Pvt. Ltd.</rights><rights>Copyright Medknow Publications 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/236489809?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,37013,44590</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18626150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Patkar, N</creatorcontrib><creatorcontrib>Mehta, J</creatorcontrib><creatorcontrib>Kulkarni, B</creatorcontrib><creatorcontrib>Pande, R</creatorcontrib><creatorcontrib>Advani, S</creatorcontrib><creatorcontrib>Borges, A</creatorcontrib><title>Immunoprofile of Hodgkin's lymphoma in India</title><title>Indian journal of cancer</title><addtitle>Indian J Cancer</addtitle><description>The immunoprofile of the Reed Sternberg cell with respect to immunoreactivity for CD20 and lack of CD15 has been described as a poor prognostic factor. Large scale studies analyzing the immunoprofile of Hodgkin's lymphoma (HL) from India are lacking. The aim of this study was to obtain baseline information on relative frequencies and immunoprofiles of the two major types of HL and comparing reports from developed and developing countries. 451 cases of HL were classified as per the WHO into classical (n= 397) HL (cHL) and nodular lymphocyte predominant HL (NLPHL) (n=54). Cases of cHL were divided into 5 immunophenotypic groups; Group A (CD15+,CD30+,CD20-), Group B (CD15-,CD30+,CD20-), Group C (CD15+,CD30+,CD20+), Group D (CD15-,CD30+,CD20+)and Group E (CD15-,CD30-,CD20+). In cases of NLPHL, the immunophenotype of lymphocytes in the background, whether T(CD3) or B(CD20) rich was observed. Most cases of cHL belonged to Group A (44.58%) followed by Group B (40.05%), C(5.54%), D(9.57%) and E(0.25%). Half, (50.89%) the cases of cHL were immunonegative for CD15, whereas CD20 was expressed by 15.61% of the cases. Three (5.55%) cases of NLPHL showed a CD3 (T) cell rich background. Significant differences were also observed with respect to the age distribution of cHL as compared to the west. Our study demonstrates that India has a high number of CD15 negative and a relatively higher number of CD20 positive cHL cases as compared to the western population. Favorable treatment response and good cure rates that one sees in western cHL may not apply to India.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antigens, CD20 - analysis</subject><subject>Cancer cells</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Health aspects</subject><subject>Hodgkin Disease - immunology</subject><subject>Hodgkin's disease</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunophenotyping</subject><subject>Ki-1 Antigen - analysis</subject><subject>Lewis X Antigen - analysis</subject><subject>Middle Aged</subject><subject>Physiological aspects</subject><subject>Properties</subject><issn>0019-509X</issn><issn>1998-4774</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkU1LxDAQhoMouq6evUnxoBe7Jmk-jyJ-LCx4UfBW0ibtRtNkbdqD_94srqKyzGFmmGde3mEAOEFwRhAsriBEMqdQvqSWc7wDJkhKkRPOyS6Y_EwPwGGMrxDiAhOxDw6QYJghCifgct51ow-rPjTWmSw02UPQ7Zv1FzFzH91qGTqVWZ_NvbbqCOw1ykVzvMlT8Hx3-3TzkC8e7-c314u8xVQOOScFQ8pwLkytmZSVrjnjgmpUMUWbhmomlIANxQTXmhY8VaLCRkNEE0mLKTj_0k223kcTh7KzsTbOKW_CGEsmC5jOJAk8-we-hrH3yVuJC0aEFFAmKP-CWuVMaX0Thl7VrfGmVy54sz68vEYCESoQX4vOtvAptOlsvXXh_NfC0ig3LGNw42CDj3_B043dseqMLle97VT_UX6_o_gEF_iIKA</recordid><startdate>200804</startdate><enddate>200804</enddate><creator>Patkar, N</creator><creator>Mehta, J</creator><creator>Kulkarni, B</creator><creator>Pande, R</creator><creator>Advani, S</creator><creator>Borges, A</creator><general>Medknow Publications and Media Pvt. Ltd</general><general>Medknow Publications &amp; Media Pvt. Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200804</creationdate><title>Immunoprofile of Hodgkin's lymphoma in India</title><author>Patkar, N ; Mehta, J ; Kulkarni, B ; Pande, R ; Advani, S ; Borges, A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g259t-74361ae778ecd699bdc76785d1b6a5ff5d68a80f5242cd537f528b2ed015c7653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antigens, CD20 - analysis</topic><topic>Cancer cells</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Health aspects</topic><topic>Hodgkin Disease - immunology</topic><topic>Hodgkin's disease</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunophenotyping</topic><topic>Ki-1 Antigen - analysis</topic><topic>Lewis X Antigen - analysis</topic><topic>Middle Aged</topic><topic>Physiological aspects</topic><topic>Properties</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Patkar, N</creatorcontrib><creatorcontrib>Mehta, J</creatorcontrib><creatorcontrib>Kulkarni, B</creatorcontrib><creatorcontrib>Pande, R</creatorcontrib><creatorcontrib>Advani, S</creatorcontrib><creatorcontrib>Borges, A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Indian journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Patkar, N</au><au>Mehta, J</au><au>Kulkarni, B</au><au>Pande, R</au><au>Advani, S</au><au>Borges, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunoprofile of Hodgkin's lymphoma in India</atitle><jtitle>Indian journal of cancer</jtitle><addtitle>Indian J Cancer</addtitle><date>2008-04</date><risdate>2008</risdate><volume>45</volume><issue>2</issue><spage>59</spage><epage>63</epage><pages>59-63</pages><issn>0019-509X</issn><eissn>1998-4774</eissn><abstract>The immunoprofile of the Reed Sternberg cell with respect to immunoreactivity for CD20 and lack of CD15 has been described as a poor prognostic factor. Large scale studies analyzing the immunoprofile of Hodgkin's lymphoma (HL) from India are lacking. The aim of this study was to obtain baseline information on relative frequencies and immunoprofiles of the two major types of HL and comparing reports from developed and developing countries. 451 cases of HL were classified as per the WHO into classical (n= 397) HL (cHL) and nodular lymphocyte predominant HL (NLPHL) (n=54). Cases of cHL were divided into 5 immunophenotypic groups; Group A (CD15+,CD30+,CD20-), Group B (CD15-,CD30+,CD20-), Group C (CD15+,CD30+,CD20+), Group D (CD15-,CD30+,CD20+)and Group E (CD15-,CD30-,CD20+). In cases of NLPHL, the immunophenotype of lymphocytes in the background, whether T(CD3) or B(CD20) rich was observed. Most cases of cHL belonged to Group A (44.58%) followed by Group B (40.05%), C(5.54%), D(9.57%) and E(0.25%). Half, (50.89%) the cases of cHL were immunonegative for CD15, whereas CD20 was expressed by 15.61% of the cases. Three (5.55%) cases of NLPHL showed a CD3 (T) cell rich background. Significant differences were also observed with respect to the age distribution of cHL as compared to the west. Our study demonstrates that India has a high number of CD15 negative and a relatively higher number of CD20 positive cHL cases as compared to the western population. Favorable treatment response and good cure rates that one sees in western cHL may not apply to India.</abstract><cop>India</cop><pub>Medknow Publications and Media Pvt. Ltd</pub><pmid>18626150</pmid><doi>10.4103/0019-509X.41772</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0019-509X
ispartof Indian journal of cancer, 2008-04, Vol.45 (2), p.59-63
issn 0019-509X
1998-4774
language eng
recordid cdi_proquest_miscellaneous_69309984
source Publicly Available Content Database
subjects Adolescent
Adult
Aged
Aged, 80 and over
Antigens, CD20 - analysis
Cancer cells
Child
Child, Preschool
Development and progression
Diagnosis
Health aspects
Hodgkin Disease - immunology
Hodgkin's disease
Humans
Immunohistochemistry
Immunophenotyping
Ki-1 Antigen - analysis
Lewis X Antigen - analysis
Middle Aged
Physiological aspects
Properties
title Immunoprofile of Hodgkin's lymphoma in India
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T17%3A29%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immunoprofile%20of%20Hodgkin's%20lymphoma%20in%20India&rft.jtitle=Indian%20journal%20of%20cancer&rft.au=Patkar,%20N&rft.date=2008-04&rft.volume=45&rft.issue=2&rft.spage=59&rft.epage=63&rft.pages=59-63&rft.issn=0019-509X&rft.eissn=1998-4774&rft_id=info:doi/10.4103/0019-509X.41772&rft_dat=%3Cgale_proqu%3EA181458174%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-g259t-74361ae778ecd699bdc76785d1b6a5ff5d68a80f5242cd537f528b2ed015c7653%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=236489809&rft_id=info:pmid/18626150&rft_galeid=A181458174&rfr_iscdi=true