Evidence map›Paper›PMID 24578502›Full record

ReviewBlood2014

Advances in the treatment of hematologic malignancies using immunoconjugates.

Maria Corinna Palanca-Wessels, Oliver W Press

Open access · greenAbstract readReview
In one paragraph

Review in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
6.4field-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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Tissue Factor-Targeted ImmunoPET Imaging and Radioimmunotherapy of Anaplastic Thyroid Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  6. Article
  7. Article
  8. Novel agents in follicular lymphoma: choosing the best target.Hematology. American Society of Hematology. Education Program · 2016
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Immune-based therapies for childhood cancer.Nature reviews. Clinical oncology · 2014
    Review
  15. Bortezomib for the treatment of non-Hodgkin's lymphoma.Expert opinion on pharmacotherapy · 2014
    Review
  16. Review
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

2 authors at 1 institution in 1 country.

Maria Corinna Palanca-WesselsClinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA; and.
Oliver W Press
Fred Hutch Cancer Center · US

Funding

Vaccinating against IGFBP-2 to prevent ovarian cancer relapseP50CA083636 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI DRESCHER, CHARLES, URBAN, NICOLE DENISE · 1999 to 2015
$35.1M
TREATMENT OF B-CELL LYMPHOMAP01CA044991 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RAJENDRAN, JOSEPH G · 1988 to 2015
$29.3M
Radioimmunotherapy Combinations for B-cell MalignancyR01CA076287 · NCI · UNIVERSITY OF WASHINGTON · PI GREEN, DAMIAN J. · 1998 to 2025
$8.1M
Biofunctional Polymers for Intracellular Drug DeliveryR01EB002991 · NIBIB · UNIVERSITY OF WASHINGTON · PI STAYTON, PATRICK S. · 2003 to 2011
$3.9M
CD45 Pretargeted Radioimmunotherapy for AMLR01CA109663 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 2004 to 2013
$2.9M
CD38 Pretargeted Radioimmunotherapy for MyelomaR01CA154897 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI GREEN, DAMIAN J. · 2011 to 2015
$1.8M
Bispecific Antibody Engineering for AML RITR01CA136639 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PRESS, OLIVER W. · 2009 to 2013
$1.6M
Antibody directed delivery of short interfering RNA for the treatment of ovarianK08CA163603 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PALANCA-WESSELS, MARIA CORINNA · 2012 to 2013
$341k
NCI NIH HHS K08 CA163603NCI NIH HHS K08CA163603NCI NIH HHS P01 CA044991NCI NIH HHS P50 CA083636NCI NIH HHS P50CA083636NCI NIH HHS R01 CA076287NCI NIH HHS R01 CA109663NCI NIH HHS R01 CA136639NCI NIH HHS R01 CA154897NIBIB NIH HHS R01 EB002991NIBIB NIH HHS R01EB002991
6 · The paper itself

Abstract

Monoclonal antibody therapy has revolutionized cancer treatment by significantly improving patient survival both in solid tumors and hematologic malignancies. Recent technological advances have increased the effectiveness of immunotherapy leading to its broader application in diverse treatment settings. Immunoconjugates (ICs) consist of a cytotoxic effector covalently linked to a monoclonal antibody that enables the targeted delivery of its therapeutic payload to tumors based on cell-surface receptor recognition. ICs are classified into 3 groups based on their effector type: immunotoxins (protein toxin), radioimmunoconjugates (radionuclide), and antibody drug conjugates (small-molecule drug). Optimization of each individual component of an IC (antibody, linker, and effector) is essential for therapeutic efficacy. Clinical trials have been conducted to investigate the effectiveness of ICs in hematologic malignancies both as monotherapy and in multiagent regimens in relapsed/refractory disease as well as frontline settings. These studies have yielded encouraging results particularly in lymphoma. ICs comprise an exciting group of therapeutics that promise to play an increasingly important role in the management of hematologic malignancies.

Indexed as

AntibodiesHematologic NeoplasmsHumansImmunoconjugatesImmunotherapyAntibodiesImmunoconjugates

Identifiers

PMID24578502
PMCPMC3983610
OpenAlexW2028244943

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.