Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients
Immuno-PET is an appealing concept in the detection of tumors and planning of antibody-based therapy. For this purpose, the long-lived positron emitter (89)Zr (half-life, 78.4 h) recently became available. The aim of the present first-in-humans (89)Zr immuno-PET study was to assess safety, biodistri...
Gespeichert in:
Veröffentlicht in: | The Journal of nuclear medicine (1978) 2009-11, Vol.50 (11), p.1828 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 11 |
container_start_page | 1828 |
container_title | The Journal of nuclear medicine (1978) |
container_volume | 50 |
creator | Borjesson, Pontus K.E Jauw, Yvonne W.S de Bree, Remco Roos, Jan C Castelijns, Jonas A Leemans, C. Rene van Dongen, Guus A.M.S Boellaard, Ronald |
description | Immuno-PET is an appealing concept in the detection of tumors and planning of antibody-based therapy. For this purpose, the long-lived positron emitter (89)Zr (half-life, 78.4 h) recently became available. The aim of the present first-in-humans (89)Zr immuno-PET study was to assess safety, biodistribution, radiation dose, and quantification of the (89)Zr-labeled chimeric monoclonal antibody (cmAb) U36 in patients with head and neck squamous cell carcinoma (HNSCC). In addition, the performance of immuno-PET for detecting lymph node metastases was evaluated, as described previously.
Twenty HNSCC patients, scheduled to undergo surgical tumor resection, received 75 MBq of (89)Zr-cmAb U36 (10 mg). Immuno-PET scans were acquired at 1, 24, 72, or 144 h after injection. The biodistribution of the radioimmunoconjugate was evaluated by ex vivo radioactivity measurement in blood and in biopsies from the surgical specimen obtained at 168 h after injection. Uptake levels and residence times in blood, tumors, and organs of interest were derived from quantitative immuno-PET studies, and absorbed doses were calculated using OLINDA/EXM 1.0. The red marrow dose was calculated using the residence time for blood.
(89)Zr-cmAb U36 was well tolerated by all subjects. PET quantification of blood-pool activity in the left ventricle of the heart showed a good agreement with sampled blood activity (difference equals 0.2% +/- 16.9% [mean +/- SD]) except for heavy-weight patients (>100 kg). A good agreement was also found for the assessment of mAb uptake in primary tumors (mean deviation, -8.4% +/- 34.5%). The mean absorbed red marrow dose was 0.07 +/- 0.02 mSv/MBq and 0.09 +/- 0.01 mSv/MBq in men and women, respectively. The normal organ with the highest absorbed dose was the liver (mean dose, 1.25 +/- 0.27 mSv/MBq in men and 1.35 +/- 0.21 mSv/MBq in women), thereafter followed by kidneys, thyroid, lungs, and spleen. The mean effective dose was 0.53 +/- 0.03 mSv/MBq in men and 0.66 +/- 0.03 mSv/MBq in women. Measured excretion via the urinary tract was less than 3% during the first 72 h.
(89)Zr immuno-PET can be safely used to quantitatively assess biodistribution, uptake, organ residence times, and radiation dose, justifying its further clinical exploitation in the detection of tumors and planning of mAb-based therapy. |
doi_str_mv | 10.2967/jnumed.109.065862 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_highw</sourceid><recordid>TN_cdi_pubmed_primary_19837762</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>19837762</sourcerecordid><originalsourceid>FETCH-LOGICAL-h1972-3c007615cf6f2bea001658a370245232d6deb8fb440d9b932d166533d85dbf2e3</originalsourceid><addsrcrecordid>eNo1kE9Lw0AUxBdRbK1-AC_yjl5S9093szmWWK1QtUh78RI22Y3ZmuyWTYIU_PBGqqeBmR_zeIPQNcFTmoj4buf6xugpwckUCy4FPUFjwhmPuBDxKRpjIkjEOeYjdNG2O4yxkFKeoxFJJItjQcfo-01pqzrrHdz71jamCwfwJcjkPUQrlZvaaEirIQi2gGfvfFF7p2qYu87mXh9gywSoFrbtAJY-wFPT9M5H68UGrIOlURqU0_Biik9IlStMgPVw0LiuvURnpapbc_WnE7R9WGzSZbR6fXxK56uoIklMI1ZgHAvCi1KUNDcKD39xqViM6YxTRrXQJpdlPpthneTJYBAhOGNacp2X1LAJujn27vt8GCzbB9uocMj-ZxiA2yNQ2Y_qywaTub6ojQq_9M41HGeEZERSyX4AhSBtLQ</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients</title><source>MEDLINE</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Borjesson, Pontus K.E ; Jauw, Yvonne W.S ; de Bree, Remco ; Roos, Jan C ; Castelijns, Jonas A ; Leemans, C. Rene ; van Dongen, Guus A.M.S ; Boellaard, Ronald</creator><creatorcontrib>Borjesson, Pontus K.E ; Jauw, Yvonne W.S ; de Bree, Remco ; Roos, Jan C ; Castelijns, Jonas A ; Leemans, C. Rene ; van Dongen, Guus A.M.S ; Boellaard, Ronald</creatorcontrib><description>Immuno-PET is an appealing concept in the detection of tumors and planning of antibody-based therapy. For this purpose, the long-lived positron emitter (89)Zr (half-life, 78.4 h) recently became available. The aim of the present first-in-humans (89)Zr immuno-PET study was to assess safety, biodistribution, radiation dose, and quantification of the (89)Zr-labeled chimeric monoclonal antibody (cmAb) U36 in patients with head and neck squamous cell carcinoma (HNSCC). In addition, the performance of immuno-PET for detecting lymph node metastases was evaluated, as described previously.
Twenty HNSCC patients, scheduled to undergo surgical tumor resection, received 75 MBq of (89)Zr-cmAb U36 (10 mg). Immuno-PET scans were acquired at 1, 24, 72, or 144 h after injection. The biodistribution of the radioimmunoconjugate was evaluated by ex vivo radioactivity measurement in blood and in biopsies from the surgical specimen obtained at 168 h after injection. Uptake levels and residence times in blood, tumors, and organs of interest were derived from quantitative immuno-PET studies, and absorbed doses were calculated using OLINDA/EXM 1.0. The red marrow dose was calculated using the residence time for blood.
(89)Zr-cmAb U36 was well tolerated by all subjects. PET quantification of blood-pool activity in the left ventricle of the heart showed a good agreement with sampled blood activity (difference equals 0.2% +/- 16.9% [mean +/- SD]) except for heavy-weight patients (>100 kg). A good agreement was also found for the assessment of mAb uptake in primary tumors (mean deviation, -8.4% +/- 34.5%). The mean absorbed red marrow dose was 0.07 +/- 0.02 mSv/MBq and 0.09 +/- 0.01 mSv/MBq in men and women, respectively. The normal organ with the highest absorbed dose was the liver (mean dose, 1.25 +/- 0.27 mSv/MBq in men and 1.35 +/- 0.21 mSv/MBq in women), thereafter followed by kidneys, thyroid, lungs, and spleen. The mean effective dose was 0.53 +/- 0.03 mSv/MBq in men and 0.66 +/- 0.03 mSv/MBq in women. Measured excretion via the urinary tract was less than 3% during the first 72 h.
(89)Zr immuno-PET can be safely used to quantitatively assess biodistribution, uptake, organ residence times, and radiation dose, justifying its further clinical exploitation in the detection of tumors and planning of mAb-based therapy.</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><identifier>DOI: 10.2967/jnumed.109.065862</identifier><identifier>PMID: 19837762</identifier><language>eng</language><publisher>United States: Soc Nuclear Med</publisher><subject>Aged ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal - chemistry ; Antibodies, Monoclonal - pharmacokinetics ; Bone Marrow - radiation effects ; Carcinoma, Squamous Cell - diagnostic imaging ; Carcinoma, Squamous Cell - immunology ; Carcinoma, Squamous Cell - metabolism ; Clinical Trials as Topic ; Drug-Related Side Effects and Adverse Reactions ; Female ; Head and Neck Neoplasms - diagnostic imaging ; Head and Neck Neoplasms - immunology ; Head and Neck Neoplasms - metabolism ; Humans ; Isotope Labeling ; Male ; Middle Aged ; Positron-Emission Tomography ; Radiation Dosage ; Radioisotopes ; Radiometry ; Recombinant Fusion Proteins - adverse effects ; Recombinant Fusion Proteins - chemistry ; Recombinant Fusion Proteins - pharmacokinetics ; Tissue Distribution ; Zirconium - chemistry</subject><ispartof>The Journal of nuclear medicine (1978), 2009-11, Vol.50 (11), p.1828</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19837762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borjesson, Pontus K.E</creatorcontrib><creatorcontrib>Jauw, Yvonne W.S</creatorcontrib><creatorcontrib>de Bree, Remco</creatorcontrib><creatorcontrib>Roos, Jan C</creatorcontrib><creatorcontrib>Castelijns, Jonas A</creatorcontrib><creatorcontrib>Leemans, C. Rene</creatorcontrib><creatorcontrib>van Dongen, Guus A.M.S</creatorcontrib><creatorcontrib>Boellaard, Ronald</creatorcontrib><title>Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients</title><title>The Journal of nuclear medicine (1978)</title><addtitle>J Nucl Med</addtitle><description>Immuno-PET is an appealing concept in the detection of tumors and planning of antibody-based therapy. For this purpose, the long-lived positron emitter (89)Zr (half-life, 78.4 h) recently became available. The aim of the present first-in-humans (89)Zr immuno-PET study was to assess safety, biodistribution, radiation dose, and quantification of the (89)Zr-labeled chimeric monoclonal antibody (cmAb) U36 in patients with head and neck squamous cell carcinoma (HNSCC). In addition, the performance of immuno-PET for detecting lymph node metastases was evaluated, as described previously.
Twenty HNSCC patients, scheduled to undergo surgical tumor resection, received 75 MBq of (89)Zr-cmAb U36 (10 mg). Immuno-PET scans were acquired at 1, 24, 72, or 144 h after injection. The biodistribution of the radioimmunoconjugate was evaluated by ex vivo radioactivity measurement in blood and in biopsies from the surgical specimen obtained at 168 h after injection. Uptake levels and residence times in blood, tumors, and organs of interest were derived from quantitative immuno-PET studies, and absorbed doses were calculated using OLINDA/EXM 1.0. The red marrow dose was calculated using the residence time for blood.
(89)Zr-cmAb U36 was well tolerated by all subjects. PET quantification of blood-pool activity in the left ventricle of the heart showed a good agreement with sampled blood activity (difference equals 0.2% +/- 16.9% [mean +/- SD]) except for heavy-weight patients (>100 kg). A good agreement was also found for the assessment of mAb uptake in primary tumors (mean deviation, -8.4% +/- 34.5%). The mean absorbed red marrow dose was 0.07 +/- 0.02 mSv/MBq and 0.09 +/- 0.01 mSv/MBq in men and women, respectively. The normal organ with the highest absorbed dose was the liver (mean dose, 1.25 +/- 0.27 mSv/MBq in men and 1.35 +/- 0.21 mSv/MBq in women), thereafter followed by kidneys, thyroid, lungs, and spleen. The mean effective dose was 0.53 +/- 0.03 mSv/MBq in men and 0.66 +/- 0.03 mSv/MBq in women. Measured excretion via the urinary tract was less than 3% during the first 72 h.
(89)Zr immuno-PET can be safely used to quantitatively assess biodistribution, uptake, organ residence times, and radiation dose, justifying its further clinical exploitation in the detection of tumors and planning of mAb-based therapy.</description><subject>Aged</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal - chemistry</subject><subject>Antibodies, Monoclonal - pharmacokinetics</subject><subject>Bone Marrow - radiation effects</subject><subject>Carcinoma, Squamous Cell - diagnostic imaging</subject><subject>Carcinoma, Squamous Cell - immunology</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Clinical Trials as Topic</subject><subject>Drug-Related Side Effects and Adverse Reactions</subject><subject>Female</subject><subject>Head and Neck Neoplasms - diagnostic imaging</subject><subject>Head and Neck Neoplasms - immunology</subject><subject>Head and Neck Neoplasms - metabolism</subject><subject>Humans</subject><subject>Isotope Labeling</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Positron-Emission Tomography</subject><subject>Radiation Dosage</subject><subject>Radioisotopes</subject><subject>Radiometry</subject><subject>Recombinant Fusion Proteins - adverse effects</subject><subject>Recombinant Fusion Proteins - chemistry</subject><subject>Recombinant Fusion Proteins - pharmacokinetics</subject><subject>Tissue Distribution</subject><subject>Zirconium - chemistry</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE9Lw0AUxBdRbK1-AC_yjl5S9093szmWWK1QtUh78RI22Y3ZmuyWTYIU_PBGqqeBmR_zeIPQNcFTmoj4buf6xugpwckUCy4FPUFjwhmPuBDxKRpjIkjEOeYjdNG2O4yxkFKeoxFJJItjQcfo-01pqzrrHdz71jamCwfwJcjkPUQrlZvaaEirIQi2gGfvfFF7p2qYu87mXh9gywSoFrbtAJY-wFPT9M5H68UGrIOlURqU0_Biik9IlStMgPVw0LiuvURnpapbc_WnE7R9WGzSZbR6fXxK56uoIklMI1ZgHAvCi1KUNDcKD39xqViM6YxTRrXQJpdlPpthneTJYBAhOGNacp2X1LAJujn27vt8GCzbB9uocMj-ZxiA2yNQ2Y_qywaTub6ojQq_9M41HGeEZERSyX4AhSBtLQ</recordid><startdate>200911</startdate><enddate>200911</enddate><creator>Borjesson, Pontus K.E</creator><creator>Jauw, Yvonne W.S</creator><creator>de Bree, Remco</creator><creator>Roos, Jan C</creator><creator>Castelijns, Jonas A</creator><creator>Leemans, C. Rene</creator><creator>van Dongen, Guus A.M.S</creator><creator>Boellaard, Ronald</creator><general>Soc Nuclear Med</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>200911</creationdate><title>Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients</title><author>Borjesson, Pontus K.E ; Jauw, Yvonne W.S ; de Bree, Remco ; Roos, Jan C ; Castelijns, Jonas A ; Leemans, C. Rene ; van Dongen, Guus A.M.S ; Boellaard, Ronald</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h1972-3c007615cf6f2bea001658a370245232d6deb8fb440d9b932d166533d85dbf2e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Aged</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - chemistry</topic><topic>Antibodies, Monoclonal - pharmacokinetics</topic><topic>Bone Marrow - radiation effects</topic><topic>Carcinoma, Squamous Cell - diagnostic imaging</topic><topic>Carcinoma, Squamous Cell - immunology</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Clinical Trials as Topic</topic><topic>Drug-Related Side Effects and Adverse Reactions</topic><topic>Female</topic><topic>Head and Neck Neoplasms - diagnostic imaging</topic><topic>Head and Neck Neoplasms - immunology</topic><topic>Head and Neck Neoplasms - metabolism</topic><topic>Humans</topic><topic>Isotope Labeling</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Positron-Emission Tomography</topic><topic>Radiation Dosage</topic><topic>Radioisotopes</topic><topic>Radiometry</topic><topic>Recombinant Fusion Proteins - adverse effects</topic><topic>Recombinant Fusion Proteins - chemistry</topic><topic>Recombinant Fusion Proteins - pharmacokinetics</topic><topic>Tissue Distribution</topic><topic>Zirconium - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Borjesson, Pontus K.E</creatorcontrib><creatorcontrib>Jauw, Yvonne W.S</creatorcontrib><creatorcontrib>de Bree, Remco</creatorcontrib><creatorcontrib>Roos, Jan C</creatorcontrib><creatorcontrib>Castelijns, Jonas A</creatorcontrib><creatorcontrib>Leemans, C. Rene</creatorcontrib><creatorcontrib>van Dongen, Guus A.M.S</creatorcontrib><creatorcontrib>Boellaard, Ronald</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borjesson, Pontus K.E</au><au>Jauw, Yvonne W.S</au><au>de Bree, Remco</au><au>Roos, Jan C</au><au>Castelijns, Jonas A</au><au>Leemans, C. Rene</au><au>van Dongen, Guus A.M.S</au><au>Boellaard, Ronald</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><addtitle>J Nucl Med</addtitle><date>2009-11</date><risdate>2009</risdate><volume>50</volume><issue>11</issue><spage>1828</spage><pages>1828-</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><abstract>Immuno-PET is an appealing concept in the detection of tumors and planning of antibody-based therapy. For this purpose, the long-lived positron emitter (89)Zr (half-life, 78.4 h) recently became available. The aim of the present first-in-humans (89)Zr immuno-PET study was to assess safety, biodistribution, radiation dose, and quantification of the (89)Zr-labeled chimeric monoclonal antibody (cmAb) U36 in patients with head and neck squamous cell carcinoma (HNSCC). In addition, the performance of immuno-PET for detecting lymph node metastases was evaluated, as described previously.
Twenty HNSCC patients, scheduled to undergo surgical tumor resection, received 75 MBq of (89)Zr-cmAb U36 (10 mg). Immuno-PET scans were acquired at 1, 24, 72, or 144 h after injection. The biodistribution of the radioimmunoconjugate was evaluated by ex vivo radioactivity measurement in blood and in biopsies from the surgical specimen obtained at 168 h after injection. Uptake levels and residence times in blood, tumors, and organs of interest were derived from quantitative immuno-PET studies, and absorbed doses were calculated using OLINDA/EXM 1.0. The red marrow dose was calculated using the residence time for blood.
(89)Zr-cmAb U36 was well tolerated by all subjects. PET quantification of blood-pool activity in the left ventricle of the heart showed a good agreement with sampled blood activity (difference equals 0.2% +/- 16.9% [mean +/- SD]) except for heavy-weight patients (>100 kg). A good agreement was also found for the assessment of mAb uptake in primary tumors (mean deviation, -8.4% +/- 34.5%). The mean absorbed red marrow dose was 0.07 +/- 0.02 mSv/MBq and 0.09 +/- 0.01 mSv/MBq in men and women, respectively. The normal organ with the highest absorbed dose was the liver (mean dose, 1.25 +/- 0.27 mSv/MBq in men and 1.35 +/- 0.21 mSv/MBq in women), thereafter followed by kidneys, thyroid, lungs, and spleen. The mean effective dose was 0.53 +/- 0.03 mSv/MBq in men and 0.66 +/- 0.03 mSv/MBq in women. Measured excretion via the urinary tract was less than 3% during the first 72 h.
(89)Zr immuno-PET can be safely used to quantitatively assess biodistribution, uptake, organ residence times, and radiation dose, justifying its further clinical exploitation in the detection of tumors and planning of mAb-based therapy.</abstract><cop>United States</cop><pub>Soc Nuclear Med</pub><pmid>19837762</pmid><doi>10.2967/jnumed.109.065862</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0161-5505 |
ispartof | The Journal of nuclear medicine (1978), 2009-11, Vol.50 (11), p.1828 |
issn | 0161-5505 1535-5667 |
language | eng |
recordid | cdi_pubmed_primary_19837762 |
source | MEDLINE; EZB-FREE-00999 freely available EZB journals |
subjects | Aged Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal - chemistry Antibodies, Monoclonal - pharmacokinetics Bone Marrow - radiation effects Carcinoma, Squamous Cell - diagnostic imaging Carcinoma, Squamous Cell - immunology Carcinoma, Squamous Cell - metabolism Clinical Trials as Topic Drug-Related Side Effects and Adverse Reactions Female Head and Neck Neoplasms - diagnostic imaging Head and Neck Neoplasms - immunology Head and Neck Neoplasms - metabolism Humans Isotope Labeling Male Middle Aged Positron-Emission Tomography Radiation Dosage Radioisotopes Radiometry Recombinant Fusion Proteins - adverse effects Recombinant Fusion Proteins - chemistry Recombinant Fusion Proteins - pharmacokinetics Tissue Distribution Zirconium - chemistry |
title | Radiation Dosimetry of 89Zr-Labeled Chimeric Monoclonal Antibody U36 as Used for Immuno-PET in Head and Neck Cancer Patients |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T04%3A12%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_highw&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Radiation%20Dosimetry%20of%2089Zr-Labeled%20Chimeric%20Monoclonal%20Antibody%20U36%20as%20Used%20for%20Immuno-PET%20in%20Head%20and%20Neck%20Cancer%20Patients&rft.jtitle=The%20Journal%20of%20nuclear%20medicine%20(1978)&rft.au=Borjesson,%20Pontus%20K.E&rft.date=2009-11&rft.volume=50&rft.issue=11&rft.spage=1828&rft.pages=1828-&rft.issn=0161-5505&rft.eissn=1535-5667&rft_id=info:doi/10.2967/jnumed.109.065862&rft_dat=%3Cpubmed_highw%3E19837762%3C/pubmed_highw%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/19837762&rfr_iscdi=true |