Predictive value of technetium-99m sestamibi in patients with multiple myeloma and potential role in the follow-up

Technetium-99m 2-methoxyisobutylisonitrile (99mTc-MIBI or setamibi) has recently been proposed for use in the evaluation of multiple myeloma (MM). The aims of this study were to investigate its potential predictive value in patients with MM and its possible role in the follow-up. Thirty patients wit...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European Journal of Nuclear Medicine 2001-03, Vol.28 (3), p.304-312
Hauptverfasser: PACE, Leonardo, CATALANO, Lucio, SALVATORE, Marco, DEL VECCHIO, Silvana, DI GENNARO, Francesca, DE RENZO, Amalia, SICA, Giulia, CALIFANO, Catello, TEDESCO, Nicolina, BORRELLI, Giovanni, ROTOLI, Bruno
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 312
container_issue 3
container_start_page 304
container_title European Journal of Nuclear Medicine
container_volume 28
creator PACE, Leonardo
CATALANO, Lucio
SALVATORE, Marco
DEL VECCHIO, Silvana
DI GENNARO, Francesca
DE RENZO, Amalia
SICA, Giulia
CALIFANO, Catello
TEDESCO, Nicolina
BORRELLI, Giovanni
ROTOLI, Bruno
description Technetium-99m 2-methoxyisobutylisonitrile (99mTc-MIBI or setamibi) has recently been proposed for use in the evaluation of multiple myeloma (MM). The aims of this study were to investigate its potential predictive value in patients with MM and its possible role in the follow-up. Thirty patients with MM who had undergone two 99mTc-MIBI scintigraphic studies at least 2 months apart constituted the study group; 22 of them received chemotherapy in the interval between the two scans. The scans were classified as showing pattern N when only physiological uptake was present, pattern D when diffuse bone marrow uptake was observed, pattern F when areas of focal uptake of the tracer were evident, and pattern F + D when both D and F patterns were observed. Comparative 99mTc-MIBI scintigraphy was considered indicative of disease progression when there was a worsening of the pattern (i.e. from N to D, or from N or D to F or to F + D) or an increase in the pattern D semiquantitative score. It was considered indicative of disease improvement when the opposite trend was observed; otherwise, it was considered to document a stable condition. A significant association was observed between the baseline scintigraphic pattern and clinical status at follow-up in the group of patients evaluated after chemotherapy (chi 2 = 16.7, P < 0.05). A negative baseline 99mTc-MIBI scintigram showed a high predictive accuracy (100%) for remission, while the presence of pattern F or F + D was often associated with a less favourable outcome. A multivariate analysis showed that 99mTc-MIBI uptake pattern has an added value in relation to known prognostic variables such as C-reactive protein. 99mTc-MIBI scintigraphy patterns at follow-up were significantly associated with the clinical status evaluated after chemotherapy (chi 2 = 32.6, P < 0.0001). Considering pattern N as indicating remission, pattern D stable condition, and pattern F or F + D progressive disease, a high concordance between scintigraphic findings and clinical status was found in the 22 patients undergoing chemotherapy (91%). Variation in 99mTc-MIBI findings comparing baseline and follow-up evaluations was significantly associated with clinical status both in patients undergoing chemotherapy (chi 2 = 26.5, P < 0.0005) and in those not undergoing chemotherapy (chi 2 = 8.0, P < 0.005). In conclusion, the results of this study suggest a prognostic value of 99mTc-MIBI scintigraphy in patients with MM and a potential role during the fo
doi_str_mv 10.1007/s002590000440
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1026702240</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>77076452</sourcerecordid><originalsourceid>FETCH-LOGICAL-c345t-4158f93fa2369c75143675672b6cb2f586f0e8bbf65ff2f153012992bd81e3d93</originalsourceid><addsrcrecordid>eNpd0ctvFiEQAHBiauxn9ejVkDTxtsqb5WgaX0kTPeh5w7JDPhpYVmDb9L8X7Rdfc-EwP4YZBqEXlLymhOg3lRAmDekhBHmEDlRRM2gymjN0IFyQQRmjz9HTWm9-GS6foHNKOZXS6AMqXwoswbVwC_jWxh1w9riBO67Qwp4GYxKuUJtNYQ44rHizLcDaKr4L7YjTHlvYIuB0DzEni-264C23LoKNuOSe6pfaEbDPMea7Yd-eocfexgrPT-cF-vb-3derj8P15w-frt5eD44L2QZB5egN95ZxZZyWVHClpdJsVm5mXo7KExjn2SvpPfNUckKZMWxeRgp8MfwCvXqou5X8fe8zTClUBzHaFfJeJ62JVkKyDi__gzd5L2vvbaKEKU0YE6Sr4UG5kmst4KethGTLfUfTz1VM_6yi-5enqvucYPmjT3__17O2Oht9sasL9bczVGhO-Q9SUY_A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1026702240</pqid></control><display><type>article</type><title>Predictive value of technetium-99m sestamibi in patients with multiple myeloma and potential role in the follow-up</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>PACE, Leonardo ; CATALANO, Lucio ; SALVATORE, Marco ; DEL VECCHIO, Silvana ; DI GENNARO, Francesca ; DE RENZO, Amalia ; SICA, Giulia ; CALIFANO, Catello ; TEDESCO, Nicolina ; BORRELLI, Giovanni ; ROTOLI, Bruno</creator><creatorcontrib>PACE, Leonardo ; CATALANO, Lucio ; SALVATORE, Marco ; DEL VECCHIO, Silvana ; DI GENNARO, Francesca ; DE RENZO, Amalia ; SICA, Giulia ; CALIFANO, Catello ; TEDESCO, Nicolina ; BORRELLI, Giovanni ; ROTOLI, Bruno</creatorcontrib><description>Technetium-99m 2-methoxyisobutylisonitrile (99mTc-MIBI or setamibi) has recently been proposed for use in the evaluation of multiple myeloma (MM). The aims of this study were to investigate its potential predictive value in patients with MM and its possible role in the follow-up. Thirty patients with MM who had undergone two 99mTc-MIBI scintigraphic studies at least 2 months apart constituted the study group; 22 of them received chemotherapy in the interval between the two scans. The scans were classified as showing pattern N when only physiological uptake was present, pattern D when diffuse bone marrow uptake was observed, pattern F when areas of focal uptake of the tracer were evident, and pattern F + D when both D and F patterns were observed. Comparative 99mTc-MIBI scintigraphy was considered indicative of disease progression when there was a worsening of the pattern (i.e. from N to D, or from N or D to F or to F + D) or an increase in the pattern D semiquantitative score. It was considered indicative of disease improvement when the opposite trend was observed; otherwise, it was considered to document a stable condition. A significant association was observed between the baseline scintigraphic pattern and clinical status at follow-up in the group of patients evaluated after chemotherapy (chi 2 = 16.7, P &lt; 0.05). A negative baseline 99mTc-MIBI scintigram showed a high predictive accuracy (100%) for remission, while the presence of pattern F or F + D was often associated with a less favourable outcome. A multivariate analysis showed that 99mTc-MIBI uptake pattern has an added value in relation to known prognostic variables such as C-reactive protein. 99mTc-MIBI scintigraphy patterns at follow-up were significantly associated with the clinical status evaluated after chemotherapy (chi 2 = 32.6, P &lt; 0.0001). Considering pattern N as indicating remission, pattern D stable condition, and pattern F or F + D progressive disease, a high concordance between scintigraphic findings and clinical status was found in the 22 patients undergoing chemotherapy (91%). Variation in 99mTc-MIBI findings comparing baseline and follow-up evaluations was significantly associated with clinical status both in patients undergoing chemotherapy (chi 2 = 26.5, P &lt; 0.0005) and in those not undergoing chemotherapy (chi 2 = 8.0, P &lt; 0.005). In conclusion, the results of this study suggest a prognostic value of 99mTc-MIBI scintigraphy in patients with MM and a potential role during the follow-up.</description><identifier>ISSN: 0340-6997</identifier><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s002590000440</identifier><identifier>PMID: 11315597</identifier><identifier>CODEN: EJNMD9</identifier><language>eng</language><publisher>Berlin: Springer</publisher><subject>Aged ; Biological and medical sciences ; Disease Progression ; Female ; Follow-Up Studies ; Humans ; Immunodeficiencies. Immunoglobulinopathies ; Immunoglobulinopathies ; Immunopathology ; Investigative techniques, diagnostic techniques (general aspects) ; Male ; Medical sciences ; Middle Aged ; Miscellaneous. Technology ; Multiple Myeloma - diagnostic imaging ; Multiple Myeloma - drug therapy ; Predictive Value of Tests ; Radionuclide Imaging ; Radionuclide investigations ; Radiopharmaceuticals ; Technetium Tc 99m Sestamibi ; Whole-Body Counting</subject><ispartof>European Journal of Nuclear Medicine, 2001-03, Vol.28 (3), p.304-312</ispartof><rights>2001 INIST-CNRS</rights><rights>Springer-Verlag 2001</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c345t-4158f93fa2369c75143675672b6cb2f586f0e8bbf65ff2f153012992bd81e3d93</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=914731$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11315597$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PACE, Leonardo</creatorcontrib><creatorcontrib>CATALANO, Lucio</creatorcontrib><creatorcontrib>SALVATORE, Marco</creatorcontrib><creatorcontrib>DEL VECCHIO, Silvana</creatorcontrib><creatorcontrib>DI GENNARO, Francesca</creatorcontrib><creatorcontrib>DE RENZO, Amalia</creatorcontrib><creatorcontrib>SICA, Giulia</creatorcontrib><creatorcontrib>CALIFANO, Catello</creatorcontrib><creatorcontrib>TEDESCO, Nicolina</creatorcontrib><creatorcontrib>BORRELLI, Giovanni</creatorcontrib><creatorcontrib>ROTOLI, Bruno</creatorcontrib><title>Predictive value of technetium-99m sestamibi in patients with multiple myeloma and potential role in the follow-up</title><title>European Journal of Nuclear Medicine</title><addtitle>Eur J Nucl Med</addtitle><description>Technetium-99m 2-methoxyisobutylisonitrile (99mTc-MIBI or setamibi) has recently been proposed for use in the evaluation of multiple myeloma (MM). The aims of this study were to investigate its potential predictive value in patients with MM and its possible role in the follow-up. Thirty patients with MM who had undergone two 99mTc-MIBI scintigraphic studies at least 2 months apart constituted the study group; 22 of them received chemotherapy in the interval between the two scans. The scans were classified as showing pattern N when only physiological uptake was present, pattern D when diffuse bone marrow uptake was observed, pattern F when areas of focal uptake of the tracer were evident, and pattern F + D when both D and F patterns were observed. Comparative 99mTc-MIBI scintigraphy was considered indicative of disease progression when there was a worsening of the pattern (i.e. from N to D, or from N or D to F or to F + D) or an increase in the pattern D semiquantitative score. It was considered indicative of disease improvement when the opposite trend was observed; otherwise, it was considered to document a stable condition. A significant association was observed between the baseline scintigraphic pattern and clinical status at follow-up in the group of patients evaluated after chemotherapy (chi 2 = 16.7, P &lt; 0.05). A negative baseline 99mTc-MIBI scintigram showed a high predictive accuracy (100%) for remission, while the presence of pattern F or F + D was often associated with a less favourable outcome. A multivariate analysis showed that 99mTc-MIBI uptake pattern has an added value in relation to known prognostic variables such as C-reactive protein. 99mTc-MIBI scintigraphy patterns at follow-up were significantly associated with the clinical status evaluated after chemotherapy (chi 2 = 32.6, P &lt; 0.0001). Considering pattern N as indicating remission, pattern D stable condition, and pattern F or F + D progressive disease, a high concordance between scintigraphic findings and clinical status was found in the 22 patients undergoing chemotherapy (91%). Variation in 99mTc-MIBI findings comparing baseline and follow-up evaluations was significantly associated with clinical status both in patients undergoing chemotherapy (chi 2 = 26.5, P &lt; 0.0005) and in those not undergoing chemotherapy (chi 2 = 8.0, P &lt; 0.005). In conclusion, the results of this study suggest a prognostic value of 99mTc-MIBI scintigraphy in patients with MM and a potential role during the follow-up.</description><subject>Aged</subject><subject>Biological and medical sciences</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>Immunoglobulinopathies</subject><subject>Immunopathology</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Miscellaneous. Technology</subject><subject>Multiple Myeloma - diagnostic imaging</subject><subject>Multiple Myeloma - drug therapy</subject><subject>Predictive Value of Tests</subject><subject>Radionuclide Imaging</subject><subject>Radionuclide investigations</subject><subject>Radiopharmaceuticals</subject><subject>Technetium Tc 99m Sestamibi</subject><subject>Whole-Body Counting</subject><issn>0340-6997</issn><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpd0ctvFiEQAHBiauxn9ejVkDTxtsqb5WgaX0kTPeh5w7JDPhpYVmDb9L8X7Rdfc-EwP4YZBqEXlLymhOg3lRAmDekhBHmEDlRRM2gymjN0IFyQQRmjz9HTWm9-GS6foHNKOZXS6AMqXwoswbVwC_jWxh1w9riBO67Qwp4GYxKuUJtNYQ44rHizLcDaKr4L7YjTHlvYIuB0DzEni-264C23LoKNuOSe6pfaEbDPMea7Yd-eocfexgrPT-cF-vb-3derj8P15w-frt5eD44L2QZB5egN95ZxZZyWVHClpdJsVm5mXo7KExjn2SvpPfNUckKZMWxeRgp8MfwCvXqou5X8fe8zTClUBzHaFfJeJ62JVkKyDi__gzd5L2vvbaKEKU0YE6Sr4UG5kmst4KethGTLfUfTz1VM_6yi-5enqvucYPmjT3__17O2Oht9sasL9bczVGhO-Q9SUY_A</recordid><startdate>20010301</startdate><enddate>20010301</enddate><creator>PACE, Leonardo</creator><creator>CATALANO, Lucio</creator><creator>SALVATORE, Marco</creator><creator>DEL VECCHIO, Silvana</creator><creator>DI GENNARO, Francesca</creator><creator>DE RENZO, Amalia</creator><creator>SICA, Giulia</creator><creator>CALIFANO, Catello</creator><creator>TEDESCO, Nicolina</creator><creator>BORRELLI, Giovanni</creator><creator>ROTOLI, Bruno</creator><general>Springer</general><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20010301</creationdate><title>Predictive value of technetium-99m sestamibi in patients with multiple myeloma and potential role in the follow-up</title><author>PACE, Leonardo ; CATALANO, Lucio ; SALVATORE, Marco ; DEL VECCHIO, Silvana ; DI GENNARO, Francesca ; DE RENZO, Amalia ; SICA, Giulia ; CALIFANO, Catello ; TEDESCO, Nicolina ; BORRELLI, Giovanni ; ROTOLI, Bruno</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c345t-4158f93fa2369c75143675672b6cb2f586f0e8bbf65ff2f153012992bd81e3d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Aged</topic><topic>Biological and medical sciences</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>Immunoglobulinopathies</topic><topic>Immunopathology</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Miscellaneous. Technology</topic><topic>Multiple Myeloma - diagnostic imaging</topic><topic>Multiple Myeloma - drug therapy</topic><topic>Predictive Value of Tests</topic><topic>Radionuclide Imaging</topic><topic>Radionuclide investigations</topic><topic>Radiopharmaceuticals</topic><topic>Technetium Tc 99m Sestamibi</topic><topic>Whole-Body Counting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PACE, Leonardo</creatorcontrib><creatorcontrib>CATALANO, Lucio</creatorcontrib><creatorcontrib>SALVATORE, Marco</creatorcontrib><creatorcontrib>DEL VECCHIO, Silvana</creatorcontrib><creatorcontrib>DI GENNARO, Francesca</creatorcontrib><creatorcontrib>DE RENZO, Amalia</creatorcontrib><creatorcontrib>SICA, Giulia</creatorcontrib><creatorcontrib>CALIFANO, Catello</creatorcontrib><creatorcontrib>TEDESCO, Nicolina</creatorcontrib><creatorcontrib>BORRELLI, Giovanni</creatorcontrib><creatorcontrib>ROTOLI, Bruno</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>ProQuest Central (Corporate)</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies &amp; Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Advanced Technologies &amp; Aerospace Database</collection><collection>ProQuest Advanced Technologies &amp; Aerospace Collection</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>MEDLINE - Academic</collection><jtitle>European Journal of Nuclear Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PACE, Leonardo</au><au>CATALANO, Lucio</au><au>SALVATORE, Marco</au><au>DEL VECCHIO, Silvana</au><au>DI GENNARO, Francesca</au><au>DE RENZO, Amalia</au><au>SICA, Giulia</au><au>CALIFANO, Catello</au><au>TEDESCO, Nicolina</au><au>BORRELLI, Giovanni</au><au>ROTOLI, Bruno</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Predictive value of technetium-99m sestamibi in patients with multiple myeloma and potential role in the follow-up</atitle><jtitle>European Journal of Nuclear Medicine</jtitle><addtitle>Eur J Nucl Med</addtitle><date>2001-03-01</date><risdate>2001</risdate><volume>28</volume><issue>3</issue><spage>304</spage><epage>312</epage><pages>304-312</pages><issn>0340-6997</issn><issn>1619-7070</issn><eissn>1619-7089</eissn><coden>EJNMD9</coden><abstract>Technetium-99m 2-methoxyisobutylisonitrile (99mTc-MIBI or setamibi) has recently been proposed for use in the evaluation of multiple myeloma (MM). The aims of this study were to investigate its potential predictive value in patients with MM and its possible role in the follow-up. Thirty patients with MM who had undergone two 99mTc-MIBI scintigraphic studies at least 2 months apart constituted the study group; 22 of them received chemotherapy in the interval between the two scans. The scans were classified as showing pattern N when only physiological uptake was present, pattern D when diffuse bone marrow uptake was observed, pattern F when areas of focal uptake of the tracer were evident, and pattern F + D when both D and F patterns were observed. Comparative 99mTc-MIBI scintigraphy was considered indicative of disease progression when there was a worsening of the pattern (i.e. from N to D, or from N or D to F or to F + D) or an increase in the pattern D semiquantitative score. It was considered indicative of disease improvement when the opposite trend was observed; otherwise, it was considered to document a stable condition. A significant association was observed between the baseline scintigraphic pattern and clinical status at follow-up in the group of patients evaluated after chemotherapy (chi 2 = 16.7, P &lt; 0.05). A negative baseline 99mTc-MIBI scintigram showed a high predictive accuracy (100%) for remission, while the presence of pattern F or F + D was often associated with a less favourable outcome. A multivariate analysis showed that 99mTc-MIBI uptake pattern has an added value in relation to known prognostic variables such as C-reactive protein. 99mTc-MIBI scintigraphy patterns at follow-up were significantly associated with the clinical status evaluated after chemotherapy (chi 2 = 32.6, P &lt; 0.0001). Considering pattern N as indicating remission, pattern D stable condition, and pattern F or F + D progressive disease, a high concordance between scintigraphic findings and clinical status was found in the 22 patients undergoing chemotherapy (91%). Variation in 99mTc-MIBI findings comparing baseline and follow-up evaluations was significantly associated with clinical status both in patients undergoing chemotherapy (chi 2 = 26.5, P &lt; 0.0005) and in those not undergoing chemotherapy (chi 2 = 8.0, P &lt; 0.005). In conclusion, the results of this study suggest a prognostic value of 99mTc-MIBI scintigraphy in patients with MM and a potential role during the follow-up.</abstract><cop>Berlin</cop><pub>Springer</pub><pmid>11315597</pmid><doi>10.1007/s002590000440</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0340-6997
ispartof European Journal of Nuclear Medicine, 2001-03, Vol.28 (3), p.304-312
issn 0340-6997
1619-7070
1619-7089
language eng
recordid cdi_proquest_journals_1026702240
source MEDLINE; SpringerLink Journals - AutoHoldings
subjects Aged
Biological and medical sciences
Disease Progression
Female
Follow-Up Studies
Humans
Immunodeficiencies. Immunoglobulinopathies
Immunoglobulinopathies
Immunopathology
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Middle Aged
Miscellaneous. Technology
Multiple Myeloma - diagnostic imaging
Multiple Myeloma - drug therapy
Predictive Value of Tests
Radionuclide Imaging
Radionuclide investigations
Radiopharmaceuticals
Technetium Tc 99m Sestamibi
Whole-Body Counting
title Predictive value of technetium-99m sestamibi in patients with multiple myeloma and potential role in the follow-up
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-04T19%3A47%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Predictive%20value%20of%20technetium-99m%20sestamibi%20in%20patients%20with%20multiple%20myeloma%20and%20potential%20role%20in%20the%20follow-up&rft.jtitle=European%20Journal%20of%20Nuclear%20Medicine&rft.au=PACE,%20Leonardo&rft.date=2001-03-01&rft.volume=28&rft.issue=3&rft.spage=304&rft.epage=312&rft.pages=304-312&rft.issn=0340-6997&rft.eissn=1619-7089&rft.coden=EJNMD9&rft_id=info:doi/10.1007/s002590000440&rft_dat=%3Cproquest_cross%3E77076452%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1026702240&rft_id=info:pmid/11315597&rfr_iscdi=true