Evidence map›Paper›PMID 30736842›Full record

ReviewJournal of hematology & oncology2019

Clinical trial update on bispecific antibodies, antibody-drug conjugates, and antibody-containing regimens for acute lymphoblastic leukemia.

Delong Liu, Juanjuan Zhao, Yongping Song, Xiaofeng Luo, Ting Yang

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. VNAR development through antigen immunization of Japanese topeshark (Frontiers in bioengineering and biotechnology · 2023
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Targeting a Radiosensitizing Antibody-Drug Conjugate to a Radiation-Inducible Antigen.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  10. Review
  11. Review
  12. Review
  13. CAR T cells better than BiTEs.Blood advances · 2021
    Article
  14. Article
  15. BCMA-targeted immunotherapy for multiple myeloma.Journal of hematology & oncology · 2020
    Review
  16. Review
  17. Review
  18. Review
  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 3 institutions in 1 country.

Delong LiuDepartment of Oncology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China. DELONG_LIU@NYMC.EDU.ORCID 0000-0003-4502-4949
Juanjuan ZhaoDepartment of Hematology, The Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital, Zhengzhou, China.
Yongping SongDepartment of Hematology, The Affiliated Cancer Hospital of Zhengzhou University and Henan Cancer Hospital, Zhengzhou, China.
Xiaofeng LuoDepartment of Hematology, Fujian Institute of Hematology, Fujian Provincial Key Laboratory of Hematology, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Ting YangDepartment of Hematology, Fujian Institute of Hematology, Fujian Provincial Key Laboratory of Hematology, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian, China.
Fujian Medical University · CNZhengzhou University · CNFirst Affiliated Hospital of Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The relapse rate remains high after chemotherapy for adult patients with acute lymphoblastic leukemia (ALL). With better molecular diagnosis and classification as well as better assessment for minimal residual disease, major progress in the treatment for refractory and/or relapsed ALL is being made. In addition to the tyrosine kinase inhibitors (TKIs) for Philadelphia chromosome-positive ALL, immunotherapeutic agents, blinatumomab, inotuzumab ozogamicin (INO), and chimeric antigen receptor (CAR) T cells, are changing the treatment paradigm for ALL. Blinatumomab and INO are being incorporated into induction chemotherapy regimens and combined with TKIs for ALL therapy. A novel low-intensity regimen, miniHCVD-INO-blinatumomab, appears to be less toxic and more effective than conventional intensive chemotherapy regimens. This review summarized new therapeutic researches of ALL and updated latest progress in clinical trials on bispecific antibodies, antibody-drug conjugates, and new regimens incorporating these novel antibodies.

Indexed as

AdultAntibodies, BispecificAntigens, CD19Antineoplastic Combined Chemotherapy ProtocolsCD3 ComplexClinical Trials as TopicFemaleHumansImmunoconjugatesInotuzumab OzogamicinMaleMolecular Targeted TherapyNeoplasm, ResidualPrecursor Cell Lymphoblastic Leukemia-LymphomaProtein Kinase InhibitorsSialic Acid Binding Ig-like Lectin 2Antibodies, BispecificAntigens, CD19blinatumomabCD19 molecule, humanCD22 protein, humanCD3 ComplexImmunoconjugatesInotuzumab OzogamicinProtein Kinase InhibitorsSialic Acid Binding Ig-like Lectin 2Acute lymphoblastic leukemiaAntibody-drug conjugateBispecific antibodyChimeric antigen receptorHyper-CVAD

Identifiers

PMID30736842
PMCPMC6368716
OpenAlexW2921153822

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.