{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,10]],"date-time":"2026-09-10T03:35:04Z","timestamp":1789011304993,"version":"build-2803163510"},"reference-count":72,"publisher":"Archives of Pathology and Laboratory Medicine","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2013,5]]},"abstract":"<jats:p>\n                    <jats:italic>Context<\/jats:italic>\n                    .\u2014Methods for plasma cell enrichment of bone marrow (BM) specimens can increase the sensitivity of fluorescence in situ hybridization (FISH) for detecting cytogenomic abnormalities. There are no published reports using these methods to evaluate high-risk cytogenomic abnormalities in patients with plasma cell neoplasms (PCNs) after therapy.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:italic>Objective<\/jats:italic>\n                    .\u2014To evaluate the utility of plasma cell enrichment combined with FISH for detection of high-risk cytogenomic abnormalities in patients with PCNs after therapy.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:italic>Design<\/jats:italic>\n                    .\u2014Twenty-eight patients with PCNs, of whom 22 received treatment, were included in this study. Plasma cells were enriched in BM aspirates by using a magnetic cell-sorting procedure to select CD138\n                    <jats:sup>+<\/jats:sup>\n                    cells. Probes were chosen to assess for del(17p13\/\n                    <jats:italic>TP53<\/jats:italic>\n                    ), del(13q14\/\n                    <jats:italic>RB1<\/jats:italic>\n                    ), 1q21\/\n                    <jats:italic>CKS1B<\/jats:italic>\n                    gain,\n                    <jats:italic>IgH\/FGFR3<\/jats:italic>\n                    , and\n                    <jats:italic>IgH\/MAF<\/jats:italic>\n                    . Clinicopathologic data were collected during clinical follow-up after plasma cell enrichment.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:italic>Results<\/jats:italic>\n                    .\u2014Plasma cells in nonenriched BM specimens ranged from 1% to 28% (median, 8%) compared with 28% to 96% (median, 73%) in enriched BM specimens (\n                    <jats:italic>P<\/jats:italic>\n                    &lt; .001). In a subset of treated patients in clinical remission, FISH detected high-risk cytogenomic abnormalities only in plasma cell\u2013enriched samples. This approach also detected abnormalities in cases of solitary plasmacytoma and monoclonal gammopathy of undetermined significance.\n                  <\/jats:p>\n                  <jats:p>\n                    <jats:italic>Conclusions<\/jats:italic>\n                    .\u2014Plasma cell enrichment of BM specimens increases FISH sensitivity for detecting high-risk cytogenomic abnormalities, particularly in treated patients, and these results, in combination with clinical follow-up data, can be of value to improve risk stratification and patient management.\n                  <\/jats:p>","DOI":"10.5858\/arpa.2012-0209-oa","type":"journal-article","created":{"date-parts":[[2013,4,29]],"date-time":"2013-04-29T14:08:53Z","timestamp":1367244533000},"page":"625-631","source":"Crossref","is-referenced-by-count":29,"title":["Plasma Cell Enrichment Enhances Detection of High-Risk Cytogenomic Abnormalities by Fluorescence In Situ Hybridization and Improves Risk Stratification of Patients With Plasma Cell Neoplasms"],"prefix":"10.5858","volume":"137","author":[{"given":"Gary","family":"Lu","sequence":"first","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ramya","family":"Muddasani","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Robert Z.","family":"Orlowski","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lynne V.","family":"Abruzzo","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Muzaffar H.","family":"Qazilbash","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M. James","family":"You","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yaping","family":"Wang","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ming","family":"Zhao","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Su","family":"Chen","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Isabella Claudia","family":"Glitza","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"L. Jeffrey","family":"Medeiros","sequence":"additional","affiliation":[{"name":"From the Departments of Hematopathology (Drs Lu, Abruzzo, You, Chen, and Medeiros, and Ms Muddasani), Myeloma (Dr Orlowski), and Stem Cell Transplantation (Drs Qazilbash and Glitza) and the Cytogenetic Technology Program (Dr Zhao), The University of Texas MD Anderson Cancer Center, Houston, Texas; and the Division of Biostatistics, The University of Texas School of Public Health, Houston, Texas (Mr Wang)."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"3906","reference":[{"issue":"11","key":"i1543-2165-137-5-625-b01","series-title":"Eur J Cancer","first-page":"1520","article-title":"Cytogenetics and molecular cytogenetics in multiple myeloma","volume":"42","author":"Liebisch\n              P,","year":"2006","unstructured":"Liebisch\n              P, \n            \n              Dohner\n              H. \n          \n          Cytogenetics and molecular cytogenetics in multiple myeloma. 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Am J Clin Pathol. 2006;125(6):895\u2013904."},{"issue":"2","key":"i1543-2165-137-5-625-b29","series-title":"Cancer Genet Cytogenet","first-page":"99","article-title":"Targeting plasma cells improves detection of cytogenetic aberrations in multiple myeloma: phenotype\/genotype fluorescence in situ hybridization","volume":"158","author":"Slovak\n              ML,","year":"2005","unstructured":"Slovak\n              ML, \n            \n              Bedell\n              V, \n            \n              Pagel\n              K, \n            et al\n          . Targeting plasma cells improves detection of cytogenetic aberrations in multiple myeloma: phenotype\/genotype fluorescence in situ hybridization. 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