Evidence map›Paper›PMID 30006739›Full record

ReviewSeminars in immunopathology2019

Cancer immune therapy for lymphoid malignancies: recent advances.

Uffe Klausen, Nicolai Grønne Dahlager Jørgensen, Jacob Handlos Grauslund, Morten Orebo Holmström, Mads Hald Andersen

Abstract readReview
PubMed Publisher
In one paragraph

Review in Seminars in immunopathology, 2019. 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
1.3field-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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. How to Train Your T Cells: Overcoming Immune Dysfunction in Multiple Myeloma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2020
    Review
  10. Humanized mouse models of immunological diseases and precision medicine.Mammalian genome : official journal of the International Mammalian Genome Society · 2019
    Review
  11. T cell-redirecting bispecific antibodies in cancer immunotherapy: recent advances.Journal of cancer research and clinical oncology · 2019
    Review
  12. Article
  13. Genetically engineered T cells for cancer immunotherapy.Signal transduction and targeted therapy
    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

5 authors at 3 institutions in 1 country.

Uffe KlausenCenter for Cancer Immunotherapy, Department of hematology, Herlev Hospital, Herlev, Denmark. uffe.klausen@regionh.dk.ORCID http://orcid.org/0000-0001-8932-0374
Nicolai Grønne Dahlager JørgensenCenter for Cancer Immunotherapy, Department of hematology, Herlev Hospital, Herlev, Denmark.
Jacob Handlos GrauslundCenter for Cancer Immunotherapy, Department of hematology, Herlev Hospital, Herlev, Denmark.
Morten Orebo HolmströmCenter for Cancer Immunotherapy, Department of hematology, Herlev Hospital, Herlev, Denmark.
Mads Hald AndersenCenter for Cancer Immunotherapy, Department of hematology, Herlev Hospital, Herlev, Denmark.
Herlev Hospital · DKRoskilde Sygehus · DKUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has played an important part in improving the life of patients with lymphoproliferative diseases especially since the addition of rituximab to chemotherapy in the CD20-positive neoplasms in the 1990s. While this field of passive immunotherapy is continuously evolving, several breakthroughs will expand the treatment modalities to include more active immunotherapy. With the approval of immune checkpoint-blocking antibodies for Hodgkin lymphoma and bispecific antibodies for acute lymphoblastic leukemia (ALL), activation of endogenous T cells already plays a role in several lymphoid malignancies. With the approval of cellular therapies with CAR-T cells for ALL and diffuse large B cell lymphoma, the impact of the manipulation of immune responses is taken even further. Vaccines are cellular therapies in the opposite end of the spectrum in terms of side effects, and while the big breakthrough is still to come, the prospect of a very low-toxic immunotherapy which could be applicable also in premalignant states or in frail patients drives a considerable research activity in the area. In this review, we summarize the mechanisms of action and clinical data on trials in the lymphoid neoplasms with chimeric antigen receptor T cells, bispecific antibodies, immune checkpoint-blocking antibodies, and antineoplastic vaccination therapy.

Indexed as

ImmunotherapyAnimalsAntibodies, BispecificAntineoplastic Agents, ImmunologicalBiomarkers, TumorCancer VaccinesHumansImmunotherapy, AdoptiveLeukemia, LymphoidLymphomaReceptors, Chimeric AntigenT-Lymphocyte SubsetsVaccinationAntibodies, BispecificAntineoplastic Agents, ImmunologicalBiomarkers, TumorCancer VaccinesReceptors, Chimeric AntigenBispecific antibodiesCAR-T cellsImmune checkpoint inhibitorsImmunotherapyLeukemiaLymphomaMultiple myelomaVaccination therapy

Identifiers

PMID30006739
OpenAlexW2883776170

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.