Evidence map›Paper›PMID 35333967›Full record

ReviewCancer chemotherapy and pharmacology2022

Anti-drug antibodies in the current management of cancer.

Miguel Borregón, Katherine Martínez, Alba Ramos, Irene Ramos, Beatriz Berzal, Manuel Mazariegos, Elia Martínez, Tatiana Hernández, Bernard Doger, Víctor Moreno

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cancer chemotherapy and pharmacology, 2022. 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
2.2field-weighted citation impact, top 13% 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, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Long-term safety and efficacy of the fully human CAR-T therapy CT103A in relapsed/refractory multiple myeloma.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  6. Sequencing of Targeted Therapy in Psoriasis: Does it Matter?American journal of clinical dermatology · 2024
    Review
  7. Observational
  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

10 authors at 4 institutions in 1 country.

Miguel BorregónMedical Oncology, Hospital Virgen de la Salud de Toledo, Toledo, Spain.
Katherine MartínezMedical Oncology, Hospital General de Segovia, Segovia, Spain.
Alba RamosMedical Oncology, Hospital Virgen de la Salud de Toledo, Toledo, Spain.
Irene RamosMedical Oncology, Hospital Virgen de la Salud de Toledo, Toledo, Spain.
Beatriz BerzalMedical Oncology, Hospital Virgen de la Salud de Toledo, Toledo, Spain.
Manuel MazariegosMedical Oncology, Hospital Virgen de la Salud de Toledo, Toledo, Spain.
Elia MartínezMedical Oncology, Hospital Universitario de Fuenlabrada, Madrid, Spain.
Tatiana HernándezSTART Madrid-FJD, Early Phase Clinical Trials Unit, Hospital Universitario Fundación Jiménez Díaz, Avda. de los Reyes Católicos, 2, 28040, Madrid, Spain.
Bernard DogerSTART Madrid-FJD, Early Phase Clinical Trials Unit, Hospital Universitario Fundación Jiménez Díaz, Avda. de los Reyes Católicos, 2, 28040, Madrid, Spain.
Víctor MorenoSTART Madrid-FJD, Early Phase Clinical Trials Unit, Hospital Universitario Fundación Jiménez Díaz, Avda. de los Reyes Católicos, 2, 28040, Madrid, Spain. victor.moreno@startmadrid.com.ORCID http://orcid.org/0000-0001-6099-4236
Hospital Virgen de la Salud · ESHospital Universitario Fundación Jiménez Díaz · ESHospital General De Segovia · ESHospital Universitario de Fuenlabrada · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monoclonal antibodies (mAbs) have become one of the main therapeutic weapons in modern oncology, mainly as targeted therapies, and immune checkpoint inhibitors. The generation of anti-drug antibodies (ADAs) after their administration can alter their pharmacokinetic, pharmacodynamic, efficacy and safety profile causing infusion-related reactions. Several risk factors have been associated with ADAs development, notably host genetics and immune status, comorbidity, concomitant medications, mAbs molecular structure, dose and route of administration. ADAs are not usually tested on daily clinical practice, being their analysis generally placed in early stages of drug development. ELISA-type assay the most common method. ADAs detection can involve important implications for treatment strategies of cancer patients, guiding therapeutic adjustment. In oncology, some studies about ADAs synthesis related to targeted therapies and immune checkpoint inhibitors have been recently published. Several strategies are proposed to reduce mAbs immunogenicity, such as different schedules, routes of administration or even the use of immunosuppressants. Another question that arises in relation to ADAs generation is the need to measure the concentration levels of active drug to guide the administration schedule. In this review, we will discuss all the aspects that are currently under discussion in relation with ADAs in oncology.

Indexed as

Antineoplastic Agents, ImmunologicalNeoplasmsAntibodies, MonoclonalEnzyme-Linked Immunosorbent AssayHumansImmune Checkpoint InhibitorsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsAnti-drug antibodies (ADAs)Immune checkpoint inhibitorsImmunogenicityMonoclonal antibodies (mAbs)

Identifiers

PMID35333967
OpenAlexW4220774869

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.