Evidence map›Paper›PMID 37644709›Full record

ArticleThe American journal of case reports2023

Bevacizumab-Associated Thrombotic Microangiopathy Treated with Eculizumab: A Case Report.

Wallace Stwart Carvalho Padilha, Bruno Nogueira Cesar, Samara Theodoro Pacheco, Alessandra Alves De Sousa, Felipe Lourenço Ledesma, Denise Maria Avancini Costa Malheiros, Marcela Crosara Alves Teixeira

Open access · hybridAbstract readCase Reports
In one paragraph

Article in The American journal of case reports, 2023. 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
1.5field-weighted citation impact, top 17% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. When is A Kidney Biopsy Indicated During the Treatment of Brain Cancer?European journal of case reports in internal medicine · 2025
    Article
  7. Review
  8. 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

7 authors at 2 institutions in 1 country.

Wallace Stwart Carvalho PadilhaDepartment of Nephrology, Hospital DFStar Rede D'Or São Luiz, Brasília, DF, Brazil.ORCID 0000-0003-3716-6058
Bruno Nogueira CesarDepartment of Nephrology, Hospital DFStar Rede D'Or São Luiz, Brasília, DF, Brazil.ORCID 0000-0002-6584-6985
Samara Theodoro PachecoDepartment of Oncology, Hospital DFStar Rede D'Or São Luiz, Brasília, DF, Brazil.
Alessandra Alves De SousaDepartment of Nephrology, Hospital DFStar Rede D'Or São Luiz, Brasília, DF, Brazil.
Felipe Lourenço LedesmaDepartment of Pathology, University of Sao Paulo, São Paulo, SP, Brazil.
Denise Maria Avancini Costa MalheirosDepartment of Pathology, University of Sao Paulo, São Paulo, SP, Brazil.
Marcela Crosara Alves TeixeiraDepartment of Oncology, Hospital DFStar Rede D'Or São Luiz, Brasília, DF, Brazil.
D’Or Institute for Research and Education · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Bevacizumab is an approved targeted therapy for metastatic cancer treatment. It can have adverse effects on multiple organs. Despite its low incidence, thrombotic microangiopathy (TMA) is the most severe complication. TMA has been associated with complement dysregulation, and treatment with eculizumab can be effective, despite the paucity of literature on eculizumab therapy for bevacizumab-associated TMA. To date, 10 cases have been reported, with less than half of them including a kidney biopsy. We present a new case of bevacizumab-associated TMA successfully treated with eculizumab, along with kidney biopsy records and an overview of mechanisms underlying TMA development in bevacizumab-treated patients. CASE REPORT A female patient diagnosed with metastatic breast cancer who was treated with bevacizumab in conjunction with chemotherapy was admitted to the hospital for acute kidney injury requiring hemodialysis, microangiopathic hemolytic anemia, and thrombocytopenia. TMA was diagnosed and was later confirmed by a kidney biopsy. Primary causes for TMA, such as ADAMTS13 deficiency and shiga toxin associated hemolytic-uremic syndrome, were ruled out, and the patient's condition was ultimately found to be triggered by exposure to bevacizumab. After discontinuing bevacizumab and receiving 4 weekly doses of eculizumab, kidney function and hematological parameters improved. CONCLUSIONS Bevacizumab-associated TMA can be reversed or attenuated in some patients with the use of eculizumab (inhibiting complement system overactivation), possibly reducing time to recovery, with fewer long-term sequelae. This additional case encourages future clinical trials to evaluate the safety and efficacy of eculizumab in cases of TMA associated with bevacizumab.

Indexed as

Purpura, Thrombotic ThrombocytopenicThrombotic MicroangiopathiesAntibodies, Monoclonal, HumanizedBevacizumabFemaleHumansAntibodies, Monoclonal, HumanizedBevacizumabeculizumab

Identifiers

PMID37644709
PMCPMC10474846
OpenAlexW4385269383

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.