Evidence map›Paper›PMID 20423225›Full record

ArticleCancer biotherapy & radiopharmaceuticals2010

Pretargeted radioimmunotherapy for hematologic and other malignancies.

Roland B Walter, Oliver W Press, John M Pagel

Open access · greenAbstract read
In one paragraph

Article in Cancer biotherapy & radiopharmaceuticals, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
  2. Article
  3. Tissue Factor-Targeted ImmunoPET Imaging and Radioimmunotherapy of Anaplastic Thyroid Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  4. Article
  5. Article
  6. Addressing challenges of heterogeneous tumor treatment through bispecific protein-mediated pretargeted drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2015
    Review
  7. Article
  8. Radioimmunotherapy of human tumours.Nature reviews. Cancer · 2015
    Review
  9. Article
  10. Article
  11. Advances in hematopoietic stem cell transplantation in childhood and adolescent lymphomas.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2013
    Review
  12. Chemically modified antibodies as diagnostic imaging agents.Current opinion in chemical biology · 2010
    Review
  13. 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

3 authors at 2 institutions in 1 country.

Roland B WalterClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109-1024, USA. rwalter@fhcrc.org
Oliver W Press
John M Pagel
University of Washington Medical Center · USUniversity of Washington · US

Funding

TREATMENT OF B-CELL LYMPHOMAP01CA044991 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 1988 to 2015
$29.3M
Radioimmunotherapy Combinations for B-cell MalignancyR01CA076287 · NCI · UNIVERSITY OF WASHINGTON · PI GREEN, DAMIAN J. · 1998 to 2025
$8.1M
CD45 Pretargeted Radioimmunotherapy for AMLR01CA109663 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 2004 to 2013
$2.9M
Bispecific Antibody Engineering for AML RITR01CA136639 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 2009 to 2013
$1.6M
Radioimmunotherapy of CD20+ Lymphomas &CD45+LeukemiasK08CA095448 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PAGEL, JOHN M · 2004 to 2008
$668k
AML Stem Cell Heterogeneity: Implications for Gemtuzumab Ozogomicin-based TherapyK23CA137161 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI WALTER, ROLAND BRUNO · 2009 to 2009
$121k
NCI NIH HHS K08-CA95448NCI NIH HHS K23-CA137161NCI NIH HHS P01 CA044991NCI NIH HHS P01-CA44991NCI NIH HHS R01 CA109663NCI NIH HHS R01-CA109663NCI NIH HHS R01-CA136639NCI NIH HHS R01-CA76287
6 · The paper itself

Abstract

Radioimmunotherapy (RIT) has emerged as one of the most promising treatment options, particularly for hematologic malignancies. However, this approach has generally been limited by a suboptimal therapeutic index (target-to-nontarget ratio) and an inability to deliver sufficient radiation doses to tumors selectively. Pretargeted RIT (PRIT) circumvents these limitations by separating the targeting vehicle from the subsequently administered therapeutic radioisotope, which binds to the tumor-localized antibody or is quickly excreted if unbound. A growing number of preclinical proof-of-principle studies demonstrate that PRIT is feasible and safe and provides improved directed radionuclide delivery to malignant cells compared with conventional RIT while sparing normal cells from nonspecific radiotoxicity. Early phase clinical studies corroborate these preclinical findings and suggest better efficacy and lesser toxicities in patients with hematologic and other malignancies. With continued research, PRIT-based treatment strategies promise to become cornerstones to improved outcomes for cancer patients despite their complexities.

Indexed as

RadioimmunotherapyAnimalsAntineoplastic AgentsClinical Trials as TopicHematologic NeoplasmsHumansRadiopharmaceuticalsTreatment OutcomeXenograft Model Antitumor AssaysAntineoplastic AgentsRadiopharmaceuticals

Identifiers

PMID20423225
PMCPMC2936263
OpenAlexW2056177575

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.