Evidence map›Paper›PMID 20010170›Full record

ReviewCancer journal (Sudbury, Mass.)

Novel immunotherapies.

Qing Yi

Open access · greenAbstract readReview
In one paragraph

Review in Cancer journal (Sudbury, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. B-cell maturation antigen is a promising target for adoptive T-cell therapy of multiple myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2013
    Article
  6. Article
  7. Article
  8. 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

1 author at 1 institution in 1 country.

Qing YiDivision of Cancer Medicine, Department of Lymphoma and Myeloma, Center for Cancer Immunology Research, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA. qyi@mdanderson.org
The University of Texas MD Anderson Cancer Center · US

Funding

Targeting Plasmacytoid Dendritic Cells to Treat Human MyelomaR01CA163881 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2012 to 2016
$2.0M
C-reactive protein promotes myeloma cell-mediated bone destructionR01CA138398 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2010 to 2014
$1.6M
Idiotype-specific effector T cells in multiple myelomaR01CA096569 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2002 to 2006
$1.5M
Optimizing Dendritic Cell Immunotherapy in MyelomaR01CA103978 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2004 to 2008
$1.4M
Targeting surface b2M for myeloma and bone therapyR01CA138402 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI YI, QING · 2009 to 2013
$1.3M
NCI NIH HHS CA138402NCI NIH HHS R01 CA096569NCI NIH HHS R01 CA103978NCI NIH HHS R01 CA138398NCI NIH HHS R01 CA138402NCI NIH HHS R01 CA163881NCI NIH HHS R01 CA96569
6 · The paper itself

Abstract

Multiple myeloma is still a fatal disease. Despite advances in high-dose chemotherapy and stem-cell transplantation and the development of novel therapeutics, relapse of the underlying disease remains the primary cause of treatment failure. Strategies for posttransplantation immunomodulation are desirable for eradication of remaining tumor cells. To this end, immunotherapy aimed at inducing myeloma-specific immunity in patients has been explored. Idiotype protein, secreted by myeloma cells, has been the primary target for immunotherapy as it is the best defined tumor-specific antigen. This chapter focuses on novel immunotherapies that are being developed to treat patients with myeloma. I will discuss potential myeloma antigens, antigen-specific T cells, and their function on myeloma tumor cells, and T-cell-based and antibody-based immunotherapies for myeloma. Furthermore, clinical studies of T-cell-based immunotherapy in the form of vaccination, allogeneic stem-cell transplantation and donor lymphocyte infusions, with or without donor vaccination using patient-derived idiotype, and future application of donor-derived or patient-derived, antigen-specific T-cell infusion in this disease are also discussed. Based on the specificity of the immune effector molecules and cells, immunotherapies with specific T cells or therapeutic antibodies may represent novel strategies for the treatment of multiple myeloma in the near future.

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, Neoplasmbeta 2-MicroglobulinCancer VaccinesHumansImmunoglobulin IdiotypesImmunotherapyImmunotherapy, AdoptiveIntercellular Signaling Peptides and ProteinsLymphokinesMultiple MyelomaReceptors, ImmunologicSignaling Lymphocytic Activation Molecule FamilyStem Cell TransplantationT-Lymphocytes, CytotoxicAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedAntigens, Neoplasmantigen-specific helper factorsbeta 2-MicroglobulinCancer VaccinesDKK1 protein, humanelotuzumabImmunoglobulin IdiotypesIntercellular Signaling Peptides and ProteinsLymphokinesReceptors, ImmunologicSignaling Lymphocytic Activation Molecule FamilySLAMF7 protein, humanVaccines, DNA

Identifiers

PMID20010170
PMCPMC2862628
OpenAlexW4211152882

What OpenQuestion holds

Textmetadata
LicenceTDM
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.