Evidence map›Paper›PMID 29421983›Full record

SynthesisImmunotherapy2018

Emerging immune targets for the treatment of multiple myeloma.

Atif Sohail, Adeela Mushtaq, Ahmad Iftikhar, Zabih Warraich, Sandra E Kurtin, Pavan Tenneti, Ali McBride, Faiz Anwer

Abstract readSystematic Review
In one paragraph

Synthesis in Immunotherapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Article
  4. Syndecan-1 (CD138), Carcinomas and EMT.International journal of molecular sciences · 2021
    Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Article
  14. Pancreatic Extramedullary Plasmacytoma Presenting as a Pancreatic Mass.Clinical medicine insights. Gastroenterology · 2018
    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

8 authors.

Atif SohailDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.
Adeela MushtaqDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.
Ahmad IftikharDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.
Zabih WarraichDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.
Sandra E KurtinDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.
Pavan TennetiDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.
Ali McBrideCollege of Pharmacy, The University of Arizona, Tucson, AZ 85719, USA.
Faiz AnwerDepartment of Medicine, Division of Hematology/Oncology, The University of Arizona, Tucson, AZ 85724, USA.

Funding

VITAMIN AP30CA023074 · NCI · UNIVERSITY OF ARIZONA · PI Teri L Bankhead · 1985 to 2026
$110.2M
NCI NIH HHS P30 CA023074
6 · The paper itself

Abstract

We reviewed emerging immune strategies for multiple myeloma (MM) therapy excluding US FDA approved drugs. In relapsed refractory MM, isatuximab (anti-CD38) monotherapy achieved overall response (OR) of 24%. Other monoclonal antibodies that have shown efficacy in combination therapy include siltuximab (OR: 66%), indatuximab (OR: 78%), isatuximab (OR: 64.5%), pembrolizumab (OR: 60%), bevacizumab (OR: 70%), dacetuzumab (OR: 39%) and lorvotuzumab (OR: 56.4%). No OR was observed with monotherapy using BI-505, siltuximab, bevacizumab, AVE-1642, figitumumab, atacicept, milatuzumab, dacetuzumab, lucatumumab, IPH2101, lorvotuzumab, BT062 and nivolumab. We included seven clinical trials on chimeric antigen receptor (CAR) T cells. CAR T-cell targets include BCMA, CD19, KLC and CD138. A recent experience of CAR T-cell (B-cell maturation antigen) therapy in advanced MM has shown global response of 100%. The future of monoclonal antibodies and adoptive T cells for MM treatment seems promising.

Indexed as

HumansImmunotherapyMultiple Myelomaadoptive cell therapyantibodiesantibody therapeuticschimeric antigen T cellsimmunotherapymultiple myeloma

Identifiers

PMID29421983
PMCPMC5810847

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.