Evidence map›Paper›PMID 24829804›Full record

ReviewLeukemia research and treatment2014

Molecularly targeted therapies in multiple myeloma.

Pilar de la Puente, Barbara Muz, Feda Azab, Micah Luderer, Abdel Kareem Azab

Open access · hybridAbstract readReview
In one paragraph

Review in Leukemia research and treatment, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Immunological Prognostic Factors in Multiple Myeloma.International journal of molecular sciences · 2021
    Review
  6. Article
  7. GANT61 and Valproic Acid Synergistically Inhibited Multiple Myeloma Cell Proliferation via Hedgehog Signaling Pathway.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Enhancing proteasome-inhibitory activity and specificity of bortezomib by CD38 targeted nanoparticles in multiple myeloma.Journal of controlled release : official journal of the Controlled Release Society · 2018
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  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

5 authors at 1 institution in 1 country.

Pilar de la PuenteCancer Biology Division, Department of Radiation Oncology, Washington University in Saint Louis School of Medicine, 4511 Forest Park Avenue, Room 3103, Saint Louis, MO 63108, USA.ORCID 0000-0001-5953-1197
Barbara MuzCancer Biology Division, Department of Radiation Oncology, Washington University in Saint Louis School of Medicine, 4511 Forest Park Avenue, Room 3103, Saint Louis, MO 63108, USA.ORCID 0000-0003-4125-4624
Feda AzabCancer Biology Division, Department of Radiation Oncology, Washington University in Saint Louis School of Medicine, 4511 Forest Park Avenue, Room 3103, Saint Louis, MO 63108, USA.
Micah LudererCancer Biology Division, Department of Radiation Oncology, Washington University in Saint Louis School of Medicine, 4511 Forest Park Avenue, Room 3103, Saint Louis, MO 63108, USA.ORCID 0000-0002-0844-5747
Abdel Kareem AzabCancer Biology Division, Department of Radiation Oncology, Washington University in Saint Louis School of Medicine, 4511 Forest Park Avenue, Room 3103, Saint Louis, MO 63108, USA.ORCID 0000-0002-6371-2780
Washington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma (MM) is a hematological malignancy that remains incurable because most patients will eventually relapse or become refractory to the treatments. Although the treatments have improved, the major problem in MM is the resistance to therapy. Novel agents are currently in development for the treatment of relapsed/refractory MM, including immunomodulatory drugs, proteasome inhibitors, monoclonal antibodies, cell signaling targeted therapies, and strategies targeting the tumor microenvironment. We have previously reviewed in detail the contemporary immunomodulatory drugs, proteasome inhibitors, and monoclonal antibodies therapies for MM. Therefore, in this review, we focused on the role of molecular targeted therapies in the treatment of relapsed/refractory multiple myeloma, including cell signaling targeted therapies (HDAC, PI3K/AKT/mTOR, p38 MAPK, Hsp90, Wnt, Notch, Hedgehog, and cell cycle) and strategies targeting the tumor microenvironment (hypoxia, angiogenesis, integrins, CD44, CXCR4, and selectins). Although these novel agents have improved the therapeutic outcomes for MM patients, further development of new therapeutic agents is warranted.

Identifiers

PMID24829804
PMCPMC4009206
OpenAlexW2158736158

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.