Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography for Interim Response Assessment of Advanced-Stage Hodgkin's Lymphoma and Diffuse Large B-Cell Lymphoma: A Systematic Review
To systematically review the prognostic accuracy of fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) for interim response assessment of patients with untreated advanced-stage Hodgkin's lymphoma (HL) or diffuse large B-cell lymphoma (DLBCL). MEDLINE, EMBASE, SCOPUS, and Biol...
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Veröffentlicht in: | Journal of clinical oncology 2009-04, Vol.27 (11), p.1906-1914 |
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container_issue | 11 |
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container_title | Journal of clinical oncology |
container_volume | 27 |
creator | TERASAWA, Teruhiko LAU, Joseph BARDET, Stéphane COUTURIER, Olivier HOTTA, Tomomitsu HUTCHINGS, Martin NIHASHI, Takashi NAGAI, Hirokazu |
description | To systematically review the prognostic accuracy of fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) for interim response assessment of patients with untreated advanced-stage Hodgkin's lymphoma (HL) or diffuse large B-cell lymphoma (DLBCL).
MEDLINE, EMBASE, SCOPUS, and Biologic Abstracts were searched for relevant studies. Two assessors independently reviewed studies for inclusion and extracted data. Relevant unpublished data were requested from the investigators if unavailable from publications. A meta-analysis of the prognostic accuracy was performed.
Thirteen studies involving 360 advanced-stage HL patients and 311 DLBCL patients met our inclusion criteria. Advanced-stage HL studies included few unfavorable-risk patients. DLBCL studies were heterogeneous. FDG-PET had an overall sensitivity of 0.81 (95% CI, 0.72 to 0.89) and a specificity of 0.97 (95% CI, 0.94 to 0.99) for advanced-stage HL, and a sensitivity of 0.78 (95% CI, 0.64 to 0.87) and a specificity of 0.87 (95% CI, 0.75 to 0.93) for DLBCL. Meta-regression and subgroup analyses did not identify factors that affect prognostic accuracy.
For low- to intermediate-risk advanced-stage HL, FDG-PET performed after a few cycles of standard chemotherapy seems to be a reliable prognostic test to identify poor responders, warranting prospective studies to assess PET-based treatment strategies. For DLBCL, no reliable conclusions can be drawn due to heterogeneity. Interim PET remains an unproven test for routine clinical practice. Its use should be reserved for research settings where treatment regimens and imaging conditions are standardized. |
doi_str_mv | 10.1200/JCO.2008.16.0861 |
format | Article |
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MEDLINE, EMBASE, SCOPUS, and Biologic Abstracts were searched for relevant studies. Two assessors independently reviewed studies for inclusion and extracted data. Relevant unpublished data were requested from the investigators if unavailable from publications. A meta-analysis of the prognostic accuracy was performed.
Thirteen studies involving 360 advanced-stage HL patients and 311 DLBCL patients met our inclusion criteria. Advanced-stage HL studies included few unfavorable-risk patients. DLBCL studies were heterogeneous. FDG-PET had an overall sensitivity of 0.81 (95% CI, 0.72 to 0.89) and a specificity of 0.97 (95% CI, 0.94 to 0.99) for advanced-stage HL, and a sensitivity of 0.78 (95% CI, 0.64 to 0.87) and a specificity of 0.87 (95% CI, 0.75 to 0.93) for DLBCL. Meta-regression and subgroup analyses did not identify factors that affect prognostic accuracy.
For low- to intermediate-risk advanced-stage HL, FDG-PET performed after a few cycles of standard chemotherapy seems to be a reliable prognostic test to identify poor responders, warranting prospective studies to assess PET-based treatment strategies. For DLBCL, no reliable conclusions can be drawn due to heterogeneity. Interim PET remains an unproven test for routine clinical practice. Its use should be reserved for research settings where treatment regimens and imaging conditions are standardized.</description><identifier>ISSN: 0732-183X</identifier><identifier>EISSN: 1527-7755</identifier><identifier>DOI: 10.1200/JCO.2008.16.0861</identifier><identifier>PMID: 19273713</identifier><language>eng</language><publisher>Alexandria, VA: American Society of Clinical Oncology</publisher><subject>Adolescent ; Adult ; Biological and medical sciences ; Child ; Disease Progression ; Fluorodeoxyglucose F18 ; Hematologic and hematopoietic diseases ; Hodgkin Disease - diagnostic imaging ; Humans ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Life Sciences ; Lymphoma, Large B-Cell, Diffuse - diagnostic imaging ; Medical sciences ; Positron-Emission Tomography ; Predictive Value of Tests ; Prognosis ; Radiopharmaceuticals ; Tumors</subject><ispartof>Journal of clinical oncology, 2009-04, Vol.27 (11), p.1906-1914</ispartof><rights>2009 INIST-CNRS</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-77102bd3ddc95ae8670349e34b7304fca4201e19d1171165bb42976efc03ba6a3</citedby><cites>FETCH-LOGICAL-c459t-77102bd3ddc95ae8670349e34b7304fca4201e19d1171165bb42976efc03ba6a3</cites><orcidid>0000-0002-1881-8674</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,3729,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21397465$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19273713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-angers.hal.science/hal-03171896$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>TERASAWA, Teruhiko</creatorcontrib><creatorcontrib>LAU, Joseph</creatorcontrib><creatorcontrib>BARDET, Stéphane</creatorcontrib><creatorcontrib>COUTURIER, Olivier</creatorcontrib><creatorcontrib>HOTTA, Tomomitsu</creatorcontrib><creatorcontrib>HUTCHINGS, Martin</creatorcontrib><creatorcontrib>NIHASHI, Takashi</creatorcontrib><creatorcontrib>NAGAI, Hirokazu</creatorcontrib><title>Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography for Interim Response Assessment of Advanced-Stage Hodgkin's Lymphoma and Diffuse Large B-Cell Lymphoma: A Systematic Review</title><title>Journal of clinical oncology</title><addtitle>J Clin Oncol</addtitle><description>To systematically review the prognostic accuracy of fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) for interim response assessment of patients with untreated advanced-stage Hodgkin's lymphoma (HL) or diffuse large B-cell lymphoma (DLBCL).
MEDLINE, EMBASE, SCOPUS, and Biologic Abstracts were searched for relevant studies. Two assessors independently reviewed studies for inclusion and extracted data. Relevant unpublished data were requested from the investigators if unavailable from publications. A meta-analysis of the prognostic accuracy was performed.
Thirteen studies involving 360 advanced-stage HL patients and 311 DLBCL patients met our inclusion criteria. Advanced-stage HL studies included few unfavorable-risk patients. DLBCL studies were heterogeneous. FDG-PET had an overall sensitivity of 0.81 (95% CI, 0.72 to 0.89) and a specificity of 0.97 (95% CI, 0.94 to 0.99) for advanced-stage HL, and a sensitivity of 0.78 (95% CI, 0.64 to 0.87) and a specificity of 0.87 (95% CI, 0.75 to 0.93) for DLBCL. Meta-regression and subgroup analyses did not identify factors that affect prognostic accuracy.
For low- to intermediate-risk advanced-stage HL, FDG-PET performed after a few cycles of standard chemotherapy seems to be a reliable prognostic test to identify poor responders, warranting prospective studies to assess PET-based treatment strategies. For DLBCL, no reliable conclusions can be drawn due to heterogeneity. Interim PET remains an unproven test for routine clinical practice. Its use should be reserved for research settings where treatment regimens and imaging conditions are standardized.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Disease Progression</subject><subject>Fluorodeoxyglucose F18</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hodgkin Disease - diagnostic imaging</subject><subject>Humans</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Life Sciences</subject><subject>Lymphoma, Large B-Cell, Diffuse - diagnostic imaging</subject><subject>Medical sciences</subject><subject>Positron-Emission Tomography</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Radiopharmaceuticals</subject><subject>Tumors</subject><issn>0732-183X</issn><issn>1527-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkUGP0zAQhSMEYsvCnRPyBVYcUjxxYid7K2WXLoq0iF0kbpbjTFovSVzspEt_GX8Pl0blNCPre89686LoNdA5JJR--LK8nYeZz4HPac7hSTSDLBGxEFn2NJpRwZIYcvbjLHrh_QOlkOYsex6dQZEIJoDNoj_X7Wid6TFw8b_d1mh_79ftqK1H8tV6Mzjbk6vOeG_Ccm87u3Zqu9mTxjpy0w_oTEe-od_aPigW3qP3HfYDsQ1Z1DvVa6zju0Gtkaxsvf5p-gtPyn233dhOEdXX5JNpmjFoS-UC9DFeYtueiEuyIHd7P2CnBqPDRzuDjy-jZ41qPb6a5nn0_frqfrmKy9vPN8tFGes0K4ZwCKBJVbO61kWmMOeCsrRAllaC0bTRKk0oIBQ1gADgWVWlSSE4NpqySnHFzqP3R9-NauU2BFVuL60ycrUo5eGNsqDMC76DwL47sltnf43oBxlupkMU1aMdveQilJbnB5AeQe2s9w6bkzNQeShWhmLloVgJXB6KDZI3k_dYdVj_F0xNBuDtBCivVdu4cHbjT1wCrBApzwJ3MQUy682jcSh9p9o22CbyQdtESIDgSjn7C_Q3ukk</recordid><startdate>20090410</startdate><enddate>20090410</enddate><creator>TERASAWA, Teruhiko</creator><creator>LAU, Joseph</creator><creator>BARDET, Stéphane</creator><creator>COUTURIER, Olivier</creator><creator>HOTTA, Tomomitsu</creator><creator>HUTCHINGS, Martin</creator><creator>NIHASHI, Takashi</creator><creator>NAGAI, Hirokazu</creator><general>American Society of Clinical Oncology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-1881-8674</orcidid></search><sort><creationdate>20090410</creationdate><title>Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography for Interim Response Assessment of Advanced-Stage Hodgkin's Lymphoma and Diffuse Large B-Cell Lymphoma: A Systematic Review</title><author>TERASAWA, Teruhiko ; LAU, Joseph ; BARDET, Stéphane ; COUTURIER, Olivier ; HOTTA, Tomomitsu ; HUTCHINGS, Martin ; NIHASHI, Takashi ; NAGAI, Hirokazu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-77102bd3ddc95ae8670349e34b7304fca4201e19d1171165bb42976efc03ba6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Disease Progression</topic><topic>Fluorodeoxyglucose F18</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Hodgkin Disease - diagnostic imaging</topic><topic>Humans</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Life Sciences</topic><topic>Lymphoma, Large B-Cell, Diffuse - diagnostic imaging</topic><topic>Medical sciences</topic><topic>Positron-Emission Tomography</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Radiopharmaceuticals</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TERASAWA, Teruhiko</creatorcontrib><creatorcontrib>LAU, Joseph</creatorcontrib><creatorcontrib>BARDET, Stéphane</creatorcontrib><creatorcontrib>COUTURIER, Olivier</creatorcontrib><creatorcontrib>HOTTA, Tomomitsu</creatorcontrib><creatorcontrib>HUTCHINGS, Martin</creatorcontrib><creatorcontrib>NIHASHI, Takashi</creatorcontrib><creatorcontrib>NAGAI, Hirokazu</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TERASAWA, Teruhiko</au><au>LAU, Joseph</au><au>BARDET, Stéphane</au><au>COUTURIER, Olivier</au><au>HOTTA, Tomomitsu</au><au>HUTCHINGS, Martin</au><au>NIHASHI, Takashi</au><au>NAGAI, Hirokazu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography for Interim Response Assessment of Advanced-Stage Hodgkin's Lymphoma and Diffuse Large B-Cell Lymphoma: A Systematic Review</atitle><jtitle>Journal of clinical oncology</jtitle><addtitle>J Clin Oncol</addtitle><date>2009-04-10</date><risdate>2009</risdate><volume>27</volume><issue>11</issue><spage>1906</spage><epage>1914</epage><pages>1906-1914</pages><issn>0732-183X</issn><eissn>1527-7755</eissn><abstract>To systematically review the prognostic accuracy of fluorine-18-fluorodeoxyglucose positron emission tomography (FDG-PET) for interim response assessment of patients with untreated advanced-stage Hodgkin's lymphoma (HL) or diffuse large B-cell lymphoma (DLBCL).
MEDLINE, EMBASE, SCOPUS, and Biologic Abstracts were searched for relevant studies. Two assessors independently reviewed studies for inclusion and extracted data. Relevant unpublished data were requested from the investigators if unavailable from publications. A meta-analysis of the prognostic accuracy was performed.
Thirteen studies involving 360 advanced-stage HL patients and 311 DLBCL patients met our inclusion criteria. Advanced-stage HL studies included few unfavorable-risk patients. DLBCL studies were heterogeneous. FDG-PET had an overall sensitivity of 0.81 (95% CI, 0.72 to 0.89) and a specificity of 0.97 (95% CI, 0.94 to 0.99) for advanced-stage HL, and a sensitivity of 0.78 (95% CI, 0.64 to 0.87) and a specificity of 0.87 (95% CI, 0.75 to 0.93) for DLBCL. Meta-regression and subgroup analyses did not identify factors that affect prognostic accuracy.
For low- to intermediate-risk advanced-stage HL, FDG-PET performed after a few cycles of standard chemotherapy seems to be a reliable prognostic test to identify poor responders, warranting prospective studies to assess PET-based treatment strategies. For DLBCL, no reliable conclusions can be drawn due to heterogeneity. Interim PET remains an unproven test for routine clinical practice. Its use should be reserved for research settings where treatment regimens and imaging conditions are standardized.</abstract><cop>Alexandria, VA</cop><pub>American Society of Clinical Oncology</pub><pmid>19273713</pmid><doi>10.1200/JCO.2008.16.0861</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1881-8674</orcidid></addata></record> |
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subjects | Adolescent Adult Biological and medical sciences Child Disease Progression Fluorodeoxyglucose F18 Hematologic and hematopoietic diseases Hodgkin Disease - diagnostic imaging Humans Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Life Sciences Lymphoma, Large B-Cell, Diffuse - diagnostic imaging Medical sciences Positron-Emission Tomography Predictive Value of Tests Prognosis Radiopharmaceuticals Tumors |
title | Fluorine-18-Fluorodeoxyglucose Positron Emission Tomography for Interim Response Assessment of Advanced-Stage Hodgkin's Lymphoma and Diffuse Large B-Cell Lymphoma: A Systematic Review |
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