Evidence map›Paper›PMID 23860529›Full record

Trial reportBritish journal of cancer2013

Development of an imaging-guided CEA-pretargeted radionuclide treatment of advanced colorectal cancer: first clinical results.

R Schoffelen, O C Boerman, D M Goldenberg, R M Sharkey, C M L van Herpen, G M Franssen, W J McBride, C-H Chang, E A Rossi, W T A van der Graaf and 1 more

Open access · hybridAbstract readClinical Trial
In one paragraph

Trial report in British journal of cancer, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

46 citing papers in PubMed, 86 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Current landscape and clinical progress of targeted alpha radioimmunotherapy.American journal of nuclear medicine and molecular imaging · 2025
    Review
  4. Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Review
  10. Pretargeting: A Path Forward for Radioimmunotherapy.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2022
    Review
  11. A proof-of-concept study on the use of a fluorescein-basedEJNMMI radiopharmacy and chemistry · 2022
    Article
  12. Article
  13. Review
  14. Current Landscape in Clinical Pretargeted Radioimmunoimaging and Therapy.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Review
  15. Review
  16. Pancreatic Ductal Adenocarcinoma: The Dawn of the Era of Nuclear Medicine?International journal of molecular sciences · 2021
    Review
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 4 institutions in 2 countries.

R SchoffelenRadboud University Nijmegen Medical Centre, PO Box 9101, Nijmegen, The Netherlands.
O C Boerman
D M Goldenberg
R M Sharkey
C M L van Herpen
G M Franssen
W J McBride
C-H Chang
E A Rossi
W T A van der Graaf
W J G Oyen
Radboud University Medical Center · NLImmunomedics (United States) · USCenter for Molecular Medicine and Immunology · USRadboud University Nijmegen · NL

Funding

F-18 FDG Peptides for Pretargeted PET Imaging of PancreaR43EB003751 · NIBIB · IMMUNOMEDICS, INC. · PI MCBRIDE, WILLIAM JOHN · 2005 to 2005
$134k
NIBIB NIH HHS 1 R43 EB003751NIBIB NIH HHS R43 EB003751
6 · The paper itself

Abstract

backgroundRadiolabelled antibody targeting of cancer is limited by slow blood clearance. Pretargeting with a non-radiolabelled bispecific monoclonal antibody (bsMAb) followed by a rapidly clearing radiolabelled hapten peptide improves tumour localisation. The primary goals of this first pretargeting study in patients with the anti-CEACAM5 × anti-hapten (HSG) bsMAb, TF2, and the radiolabelled hapten-peptide, IMP288, were to assess optimal pretargeting conditions and safety in patients with metastatic colorectal cancer (CRC).

methodsDifferent dose schedules were studied in four cohorts of five patients: (1) shortening the interval between the bsMAb and peptide administration (5 days vs 1 day), (2) escalating the TF2 dose (from 75 to 150 mg), and (3) reducing the peptide dose (from 100 to 25 μg). After confirmation of tumour targeting by (111)In-IMP288, patients were treated with a bsMAb/(177)Lu-IMP288 cycle.

resultsRapid and selective tumour targeting of the radiolabelled peptide was visualised within 1 h, with high tumour-to-tissue ratios (>20 at 24 h). Improved tumour targeting was achieved with a 1-day interval between the administration of the bsMAb and the peptide and with the 25-μg peptide dose. High (177)Lu-IMP288 doses (2.5-7.4 GBq) were well tolerated, with some manageable TF2 infusion reactions, and transient grades 3-4 thrombocytopaenia in 10% of the patients who received (177)Lu-IMP288.

conclusionThis phase I study demonstrates for the first time that pretargeting with bsMAb TF2 and radiolabelled IMP288 in patients with CEA-expressing CRC is feasible and safe. With this pretargeting method, tumours are specifically and rapidly targeted.

Indexed as

AdultAgedAntibodies, BispecificCarcinoembryonic AntigenCohort StudiesColorectal NeoplasmsFemaleGPI-Linked ProteinsHaptensHeterocyclic Compounds, 1-RingHumansMaleMiddle AgedOligopeptidesRadioimmunotherapyAntibodies, BispecificCarcinoembryonic AntigenCEACAM5 protein, humanDOTA-tyrosyl-lysyl(histaminyl-succinyl-glycyl)-glutamyl-lysyl(histaminyl-succinyl-glycyl)amideGPI-Linked ProteinsHaptensHeterocyclic Compounds, 1-RingOligopeptides

Identifiers

PMID23860529
PMCPMC3749562
OpenAlexW2014187441

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.