Skip to main content

Main menu

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI

User menu

  • Subscribe
  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Nuclear Medicine
  • SNMMI
    • JNM
    • JNMT
    • SNMMI Journals
    • SNMMI
  • Subscribe
  • My alerts
  • Log in
  • My Cart
Journal of Nuclear Medicine

Advanced Search

  • Home
  • Content
    • Current
    • Ahead of print
    • Past Issues
    • JNM Supplement
    • SNMMI Annual Meeting Abstracts
    • Continuing Education
    • JNM Podcasts
  • Subscriptions
    • Subscribers
    • Institutional and Non-member
    • Rates
    • Journal Claims
    • Corporate & Special Sales
  • Authors
    • Submit to JNM
    • Information for Authors
    • Assignment of Copyright
    • AQARA requirements
  • Info
    • Reviewers
    • Permissions
    • Advertisers
  • About
    • About Us
    • Editorial Board
    • Contact Information
  • More
    • Alerts
    • Feedback
    • Help
    • SNMMI Journals
  • View or Listen to JNM Podcast
  • Visit JNM on Facebook
  • Join JNM on LinkedIn
  • Follow JNM on Twitter
  • Subscribe to our RSS feeds
OtherClinical Investigations

18F-FDG PET for the Diagnosis and Grading of Soft-Tissue Sarcoma: A Meta-Analysis

John P.A. Ioannidis and Joseph Lau
Journal of Nuclear Medicine May 2003, 44 (5) 717-724;
John P.A. Ioannidis
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Joseph Lau
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • FIGURE 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    FIGURE 1.

    SROC curves for (A) qualitative visualization, (B) standard uptake value (cutoff, 2.0), (C) standard uptake value (cutoff, 3.0), and (D) metabolic rate of glucose (cutoff, 6.0 μmol/100 g/min). Curves show trade-off between true-positive rate (sensitivity) and false-positive rate (100 − specificity) across all pertinent studies. Each study is shown by eclipse with diameters approximately proportional to number of subjects evaluated for sensitivity (vertical dimension) and specificity (horizontal dimension) of study. Two SROC curves are shown based on weighted (bold line) and unweighted (thin line) calculations. SROC curves should be used for inferences of diagnostic accuracy preferably within range of sensitivity and specificity values of studies that are included in their calculations. X = random effects estimates of sensitivity and specificity; horizontal and vertical dimensions of rectangle = corresponding 95% confidence intervals.

Tables

  • Figures
    • View popup
    TABLE 1

    Characteristics of Studies Evaluating 18F-FDG PET for Diagnosis or Grading of STS

    StudyMean age (range)Patients with STLEvaluable patients* (lesions)Malignant (%)Inclusion/exclusion criteriaPrimary/recurrentDesign
    Schwarzbach 200054 (16–78)5047 (56)35 (63)Consecutive patients suspected of STS from clinical symptoms and MRI or CT19/37Prospective
    Watanabe 200047 (12–77)3737 (37)7 (19)Patients referred for STM evaluation after CT, MRI, or angiography33/4Unclear
    Griffeth 199250 (16–84)2119 (20)10 (50)Patients referred for STM evaluation after CT or MRI10/10?Unclear
    Schulte 199949 (1–89)102102 (102)66 (65)Patients with STL suggestive of benign or malignant tumor on US or MRI88/14Prospective
    Lucas 199951 (6–85)3030 (31)19 (61)Consecutive patients with suspected STS from clinical symptoms and MRI31/0Unclear
    Nieweg 199650 (18–82)2222 (22)18 (82)Patients suspected of STS from clinical findings22/0Prospective
    Hain 199939 (11–81)1616 (16)2 (13)Patients after amputation for STS, evaluated for recurrence0/16Retrospective
    Kern 198830 (12–63)44 (4)3 (75)Patients referred with STM4/0Unclear
    Lucas 199851 (3–84)6262 (72)19 (26)STS patients evaluated for local recurrence0/72Retrospective
    Lodge 199950 (18–76)2929 (29)12 (41)STM suspected to be malignant based on clinical examination and MRI29/0Prospective
    van Ginkel 199649 (18–80)207 (7)7 (100)Patients with biopsy-proven recurrent STS, assessed before HILP therapy0/7Prospective
    Kole 199754 (32–83)1717 (17)15 (88)Patients with proven or suspected local recurrence of STS0/17Prospective
    Ferner 200026 (12–62)1515 (19)5 (26)Patients with neurofibromatosis with symptomatic visible neurofibromas19/0Unclear
    Adler 1990ND (41–85)55 (5)5 (100)Patients with liposarcoma of the thigh5/0Prospective?
    Jones 199654 (46–65)44 (4)4 (100)Histologically confirmed STS with planned radiotherapy/hyperthermia4/0Unclear
    • ↵* In Schwarzbach et al. (2000), 3 patients were excluded because of no biopsy or technical failure; in Griffeth et al. (1992), 2 patients were excluded because of no diagnostic documentation or follow-up; in van Ginkel et al. (1996), 20 patients with STS were assessed, but those with primary lesions overlapped with patients included in Nieweg et al. (1996). Thus, only the 7 recurrent lesions were considered in all analyses and are listed in table.

    • STL = soft-tissue lesion; STM = soft-tissue mass; US = ultrasound; HILP = hyperthermic isolated limb perfusion; ND = no data.

    • Whenever both soft-tissue lesions and other lesions were included (Watanabe, Kern, Ferner, Jones), only data on soft-tissue lesions are presented in table. Median age is provided in Schwarzbach et al. (2000) and in Schulte et al. (1999).

    • View popup
    TABLE 2

    Characteristics of 18F-FDG PET Imaging and of Reference Standards

    Study18F-FDG dose (MBq)MeasuresReference standardPotential verification bias
    Schwarzbach 2000370–440Visualization, SUVBiopsy, except for 7 patients followed clinically and radiologically for 4–27 moLimited
    Watanabe 2000185–350Visualization, SUVBiopsy, surgical excision or postmortem, except for 1 patient (clinical and radiologic criteria)Very limited
    Griffeth 1992370Visualization (TBR), SUVBiopsy or surgical excision, except for 1 patient (clinical and radiologic criteria)Very limited
    Schulte 1999120–300Visualization (TBR)Excisional, incisional, or needle biopsy followed by surgical resection when indicatedNo
    Lucas 1999350Visualization, SUVOpen biopsy, followed by surgical excision when appropriateNo
    Nieweg 1996187–407Visualization, SUV, MRGBiopsy (no details)No
    Hain 1999320VisualizationUnclear, presumably biopsy performed only when indicatedConsiderable
    Kern 1988185Visualization, MRGBiopsy and tumor resectionNo
    Lucas 1998350VisualizationBiopsy (and operative diagnosis), when PET or MRI suggested recurrence, otherwise clinical and imaging follow-upConsiderable
    Lodge 1999350SUV (at 60, 120, 255 min),* MRGBiopsy followed by appropriate surgical excisionNo
    Van Ginkel 1996370Visualization, MRGBiopsy of irresectable tumorsNo
    Kole 1997370Visualization, MRGBiopsy (no details)No
    Ferner 2000350Visualization, SUVBiopsy, except for 9 patients assessed clinically and radiologicallyConsiderable
    Adler 1990148–278Visualization (TBR), SUVBiopsy presumably (no details)No?
    Jones 1996370Visualization, SUVNeedle or incisional biopsy followed by surgical resectionNo
    • ↵* SUV data at 60 min are used in quantitative synthesis.

    • View popup
    TABLE 3

    Summary Diagnostic Performance of 18F-FDG PET for Diagnosing Malignant vs. Benign Soft-Tissue Lesions

    Diagnostic parameterCase series (subjects)Independent estimates (95% CI)*Typical SROC estimates (sensitivity, specificity)†
    SensitivitySpecificityUnweightedWeighted
    Qualitative visualization13 (398)88% (81–93)73% (56–86)(90%, 73%)(92%, 73%)
     Primary lesions7 (231)95% (89–98)59% (38–78)(95%, 59%)(96%, 59%)
     Recurrent lesions5 (146)81% (69–89)91% (81–96)(74%, 91%)(81%, 91%)
    SUV ≥ 2.010 (208)76% (64–85)79% (71–86)(92%, 79%)(87%, 92%)
     Primary lesions7 (157)79% (67–88)77% (67–85)(93%, 77%)(91%, 77%)
     Recurrent lesions3 (51)63% (44–78)91% (71–98)(70%, 91%)(72%, 91%)
    SUV ≥ 3.010 (208)58% (48–67)87% (79–92)(90%, 87%)(70%, 87%)
     Primary lesions7 (157)60% (48–72)86% (77–92)(82%, 86%)(66%, 86%)
     Recurrent lesions3 (51)52% (35–69)91% (71–98)(62%, 91%)(62%, 91%)
    MRG ≥ 6.0 μmol/100 g/min4 (66)70% (54–82)73% (53–87)(72%, 73%)(74%, 73%)
     Primary lesions3 (52)75% (57–87)72% (50–87)(76%, 72%)(76%, 72%)
     Recurrent lesions1 (14)58% (29–83)100% (16–100)NENE
    • ↵* Independent random effects pooling of sensitivity and specificity across studies.

    • ↵† Pairs of sensitivity and specificity from SROC curves; specificity values are selected from random-effects estimates.

    • NE = not estimable.

PreviousNext
Back to top

In this issue

Journal of Nuclear Medicine
Vol. 44, Issue 5
May 1, 2003
  • Table of Contents
  • Index by author
Print
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for your interest in spreading the word on Journal of Nuclear Medicine.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
18F-FDG PET for the Diagnosis and Grading of Soft-Tissue Sarcoma: A Meta-Analysis
(Your Name) has sent you a message from Journal of Nuclear Medicine
(Your Name) thought you would like to see the Journal of Nuclear Medicine web site.
Citation Tools
18F-FDG PET for the Diagnosis and Grading of Soft-Tissue Sarcoma: A Meta-Analysis
John P.A. Ioannidis, Joseph Lau
Journal of Nuclear Medicine May 2003, 44 (5) 717-724;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
18F-FDG PET for the Diagnosis and Grading of Soft-Tissue Sarcoma: A Meta-Analysis
John P.A. Ioannidis, Joseph Lau
Journal of Nuclear Medicine May 2003, 44 (5) 717-724;
Twitter logo Facebook logo LinkedIn logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Bookmark this article

Jump to section

  • Article
    • Abstract
    • MATERIALS AND METHODS
    • RESULTS
    • DISCUSSION
    • CONCLUSION
    • Acknowledgments
    • Footnotes
    • REFERENCES
  • Figures & Data
  • Info & Metrics
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • Comparison of [68Ga]Ga-Fibroblast Activation Protein Inhibitor-04 and [18F]FDG PET Imaging for Solitary Fibrous Tumor and Preliminary Application of FAP-Targeted Radiopharmaceutical Therapy
  • Diagnostic Accuracy of 68Ga-FAPI Versus 18F-FDG PET in Patients with Various Malignancies
  • 68Ga-FAPI as a Diagnostic Tool in Sarcoma: Data from the 68Ga-FAPI PET Prospective Observational Trial
  • Simulation of Tracer Dose Reduction in 18F-FDG PET/MRI: Effects on Oncologic Reading, Image Quality, and Artifacts
  • Imaging in Sarcoma
  • Correlation Between Glycolytic Phenotype and Tumor Grade in Soft-Tissue Sarcomas by 18F-FDG PET
  • Contemporary Imaging in Sarcoma
  • 11C-Methionine vs. 18F-FDG PET in Soft Tissue Sarcoma Patients Treated with Neoadjuvant Therapy: Preliminary Results
  • Imaging Bone and Soft Tissue Tumors with the Proliferation Marker [18F]Fluorodeoxythymidine
  • 18F-FDG PET for Evaluation of Bone Marrow Infiltration in Staging of Lymphoma: A Meta-Analysis
  • Detection and Grading of Soft Tissue Sarcomas of the Extremities with 18F-3'-Fluoro-3'-Deoxy-L-Thymidine
  • Google Scholar

More in this TOC Section

  • Feasibility of Ultra-Low-Activity 18F-FDG PET/CT Imaging Using a Long–Axial-Field-of-View PET/CT System
  • Cardiac Presynaptic Sympathetic Nervous Function Evaluated by Cardiac PET in Patients with Chronotropic Incompetence Without Heart Failure
  • Validation and Evaluation of a Vendor-Provided Head Motion Correction Algorithm on the uMI Panorama PET/CT System
Show more Clinical Investigations

Similar Articles

SNMMI

© 2025 SNMMI

Powered by HighWire