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PMID: 17242397 Published · ppublish English Consensus Development Conference Journal Article Practice Guideline

Use of positron emission tomography for response assessment of lymphoma: consensus of the Imaging Subcommittee of International Harmonization Project in Lymphoma.

Juweid ME, Stroobants S, Hoekstra OS, Mottaghy FM, Dietlein M, Guermazi A, Wiseman GA, Kostakoglu L, Scheidhauer K, Buck A, Naumann R, Spaepen K, Hicks RJ, Weber WA, Reske SN, Schwaiger M, Schwartz LH, Zijlstra JM, Siegel BA, Cheson BD, Imaging Subcommittee of International Harmonization Project in Lymphoma

Abstract

To develop guidelines for performing and interpreting positron emission tomography (PET) imaging for treatment assessment in patients with lymphoma both in clinical practice and in clinical trials. An International Harmonization Project (IHP) was convened to discuss standardization of clinical trial parameters in lymphoma. An imaging subcommittee developed consensus recommendations based on published PET literature and the collective expertise of its members in the use of PET in lymphoma. Only recommendations subsequently endorsed by all IHP subcommittees were adopted. PET after completion of therapy should be performed at least 3 weeks, and preferably at 6 to 8 weeks, after chemotherapy or chemoimmunotherapy, and 8 to 12 weeks after radiation or chemoradiotherapy. Visual assessment alone is adequate for interpreting PET findings as positive or negative when assessing response after completion of therapy. Mediastinal blood pool activity is recommended as the reference background activity to define PET positivity for a residual mass > or = 2 cm in greatest transverse diameter, regardless of its location. A smaller residual mass or a normal sized lymph node (ie, < or = 1 x 1 cm in diameter) should be considered positive if its activity is above that of the surrounding background. Specific criteria for defining PET positivity in the liver, spleen, lung, and bone marrow are also proposed. Use of attenuation-corrected PET is strongly encouraged. Use of PET for treatment monitoring during a course of therapy should only be done in a clinical trial or as part of a prospective registry.

MeSH Terms
Clinical Trials as Topic/standards Humans Image Interpretation, Computer-Assisted International Cooperation Lymphoma/diagnostic imaging,therapy Positron-Emission Tomography/methods Radiopharmaceuticals Time Factors Tomography, X-Ray Computed Treatment Outcome
Chemicals
Radiopharmaceuticals
Authors & Affiliations
21 authors, click to expand affiliations / ORCID
Juweid Malik E
Department of Radiology, University of Iowa, Iowa City, IA 52242, USA. malik-juweid@uiowa.edu
Stroobants Sigrid
Hoekstra Otto S
Mottaghy Felix M
Dietlein Markus
Guermazi Ali
Wiseman Gregory A
Kostakoglu Lale
Scheidhauer Klemens
Buck Andreas
Naumann Ralph
Spaepen Karoline
Hicks Rodney J
Weber Wolfgang A
Reske Sven N
Schwaiger Markus
Schwartz Lawrence H
Zijlstra Josee M
Siegel Barry A
Cheson Bruce D
Imaging Subcommittee of International Harmonization Project in Lymphoma
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
1527-7755
Published
2007-02-10
Epub
2007-00-22
Pages
571-8
Language
English
Region
United States
NLM ID
8309333
Subset
IM
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