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OtherClinical Investigations

Whole-Body 18F-FDG PET Identifies High-Risk Myeloma

Brian G.M. Durie, Alan D. Waxman, Allesandro D’Agnolo and Cindy M. Williams
Journal of Nuclear Medicine November 2002, 43 (11) 1457-1463;
Brian G.M. Durie
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Alan D. Waxman
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Allesandro D’Agnolo
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Cindy M. Williams
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  • FIGURE 1.
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    FIGURE 1.

    Patient with IgA λ-chain myeloma, stage IIIA. Radiographs revealed multiple lytic lesions in areas that showed positive findings on 18F-FDG PET imaging (e.g., spine, pelvis, and hips). Plasmacytoma in left lung was confirmed on biopsy. Plasmacytomas were noted in left apex and hilar regions on CT scanning. Splenic myeloma was also suspected but not directly confirmed.

  • FIGURE 2.
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    FIGURE 2.

    Patient with Bence Jones protein λ-chain myeloma. Extensive disease is seen in spine, and plasmacytomas are seen in right lower lung and left upper abdomen.

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    FIGURE 3.

    Patient with relapse after stem cell transplantation. Dysphagia developed and was associated with positive finding in distal esophagus. Direct biopsy showed plasma cells with local amyloid deposition. This responded well to local irradiation.

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    TABLE 1

    Study Population

    No. per groupDisease statusTotal
    MGUSActive myelomaRemissionRelapse
    18F-FDG PET scans2024203498*
    Patients1416102666
    • ↵* 25 patients had serial scans.

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    TABLE 2

    Whole-Body 18F-FDG PET Scan Results

    Disease statusResult of baseline studyResult of follow-up study
    MGUS14/14 (100%) negative; followed 3–43+ moIn 1/14 (7%), myeloma developed at 8 mo; in 1 patient, focal plasmacytoma with amyloid developed*
    Active myeloma16/16 (100%) positive; 4/16 (25%) had negative radiography results but multiple focal lesions on scanIn 1 patient, disease was upstaged from stage I to III: Multiple new disease sites were identified
    4/16 (25%) had extramedullary diseasePoor outcome with extramedullary disease
    RemissionIn 6/10 (60%), new lesions developed over 6–42+ moLocal irradiation used for focal relapse; nonsecretory relapse detected and treated
    Relapse21/26 (81%) had new sites of diseaseAnatomic distribution of lesions documented
    6/26 (23%) had extramedullary diseaseVery poor survival with extramedullary disease: median, 7 mo
    • View popup
    TABLE 3

    Potential Role for 18F-FDG PET Scan Evaluation Based on Current Data

    Suspected disease statusClinical questionPotential role of 18F-FDG PET
    MGUS*How likely is progression?If 18F-FDG PET results are negative, stable MGUS is likely
    Active myeloma*Is disease smoldering or active?If 18F-FDG PET results are positive, active disease is likely, even if radiography results are negative
    What is prognosis?Extramedullary disease indicates poor prognosis
    RemissionIs there true complete remission?Positive scan findings after transplantation indicate persistent disease or relapse and poorer outcome
    Is there new disease?New focal disease (especially nonsecretory) can be documented and treated
    RelapseIs there unsuspected new disease?Can detect clinically important disease requiring unanticipated therapy (e.g., ureteral obstruction)
    What is baseline restaging at relapse?Can establish baseline for ongoing monitoring in clinical trials
    • ↵* Working definitions for MGUS vs. active myeloma are currently under review by International Prognostic Index Study Group. It is possible that 18F-FDG PET scanning can contribute to diagnostic or discriminatory criteria.

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Journal of Nuclear Medicine
Vol. 43, Issue 11
November 1, 2002
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Whole-Body 18F-FDG PET Identifies High-Risk Myeloma
Brian G.M. Durie, Alan D. Waxman, Allesandro D’Agnolo, Cindy M. Williams
Journal of Nuclear Medicine Nov 2002, 43 (11) 1457-1463;

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Whole-Body 18F-FDG PET Identifies High-Risk Myeloma
Brian G.M. Durie, Alan D. Waxman, Allesandro D’Agnolo, Cindy M. Williams
Journal of Nuclear Medicine Nov 2002, 43 (11) 1457-1463;
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