Evidence map›Paper›PMID 26877783›Full record

ArticleTheranostics2016

11C-Methionine-PET in Multiple Myeloma: Correlation with Clinical Parameters and Bone Marrow Involvement.

Constantin Lapa, Stefan Knop, Martin Schreder, Martina Rudelius, Markus Knott, Gerhard Jörg, Samuel Samnick, Ken Herrmann, Andreas K Buck, Hermann Einsele and 1 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Theranostics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.5field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 86 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Imaging of Multiple Myeloma: Present and Future.Journal of clinical medicine · 2024
    Review
  5. Head-to-Head Comparison between FDG andDiagnostics (Basel, Switzerland) · 2023
    Review
  6. Prognostic value of semi-quantitative parameters ofAnnals of nuclear medicine · 2023
    Article
  7. Comparison of [Molecular imaging and biology · 2022
    Article
  8. International journal of molecular sciences · 2022
    Article
  9. First Experience ofTurkish journal of haematology : official journal of Turkish Society of Haematology · 2022
    Article
  10. Review
  11. Review
  12. Reduced splenic uptake onTheranostics · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Constantin Lapa1. University Hospital Würzburg, Department of Nuclear Medicine, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Stefan Knop2. University Hospital Würzburg, Department of Hematology and Oncology, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Martin Schreder2. University Hospital Würzburg, Department of Hematology and Oncology, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Martina Rudelius3. Institute for Pathology, University of Würzburg, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Markus Knott2. University Hospital Würzburg, Department of Hematology and Oncology, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Gerhard Jörg1. University Hospital Würzburg, Department of Nuclear Medicine, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Samuel Samnick1. University Hospital Würzburg, Department of Nuclear Medicine, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Ken Herrmann1. University Hospital Würzburg, Department of Nuclear Medicine, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Andreas K Buck1. University Hospital Würzburg, Department of Nuclear Medicine, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Hermann Einsele2. University Hospital Würzburg, Department of Hematology and Oncology, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Katharina Lückerath1. University Hospital Würzburg, Department of Nuclear Medicine, Würzburg, Germany; 4. Comprehensive Cancer Center Mainfranken, Würzburg, Germany.
Comprehensive Cancer Center Mainfranken · DEUniversitätsklinikum Würzburg · DEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) remains an essentially incurable hematologic malignancy originating from clonal plasma cells. This study evaluated the usefulness of the radiotracers (11)C-methionine (MET) and (18)F-2`-deoxy-2`-fluorodeoxyglucose (FDG) for staging and re-staging in MM. 43 patients with MM underwent both MET- and FDG-PET/CT for staging or re-staging within 3±2 days. Scans were compared on a patient and on a lesion basis. Tracer uptake was correlated with the degree of bone marrow (BM) involvement and standard clinical parameters of disease activity. Additionally, BM samples were stained for L-type amino acid transporter 1 (LAT1) expression in 15 patients. MET-PET detected focal lesions (FL) in 39/43 subjects (90.7%), whereas 10 patients were missed in FDG-PET/CT (detection rate, 33/43; 76.7%; p<0.05). MET depicted more FL in 28/43 patients (65.1%; p<0.001), whereas in the remainder (34.9%, n=15) both tracers yielded comparable results. LAT1 was highly expressed on the cell surface of myeloma cells. Both FDG and MET uptake correlated significantly with biopsy-proven BM involvement (p<0.001), with MET demonstrating a stronger correlation (SUVmean, r=0.9 vs r=0.6; SUVmax, r=0.88 vs r=0.58). Abnormal beta-2-microglobulin and free light chain levels correlated with the presence of focal intramedullary lesions detected in MET- or FDG-PET/CT (MET, p=0.006 and p=0.01, respectively; FDG, p=0.02 and p=0.01). MET appears to be superior to FDG for staging and re-staging of both intra- and extramedullary MM lesions. Tracer uptake correlates with BM involvement, β2m and FLC levels and appears to be a more accurate marker of tumor burden and disease activity.

Indexed as

MethioninePositron-Emission TomographyRadiopharmaceuticalsAdultAgedAged, 80 and overBiomarkers, TumorBone MarrowFemaleFluorodeoxyglucose F18HumansMaleMiddle AgedMultimodal ImagingMultiple MyelomaTomography, X-Ray ComputedBiomarkers, Tumorcarbon-11 methionineFluorodeoxyglucose F18MethionineRadiopharmaceuticals11C-methionineFDGmultiple myelomaPET/CT

Identifiers

PMID26877783
PMCPMC4729773
OpenAlexW2396014655

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.