Evidence map›Paper›PMID 28747219›Full record

ArticleJournal of medical case reports2017

Role of eculizumab in a pediatric refractory gemcitabine-induced thrombotic microangiopathy: a case report.

Ludovica Facchini, Maurizio Lucchesi, Alessia Stival, Rosa Maria Roperto, Francesca Melosi, Marco Materassi, Silvia Farina, Veronica Tintori, Maurizio de Martino, Iacopo Sardi

Open access · goldAbstract readCase Reports
In one paragraph

Article in Journal of medical case reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

5 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Complement in Secondary Thrombotic Microangiopathy.Kidney international reports · 2021
    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 2 institutions in 1 country.

Ludovica FacchiniNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, Viale G. Pieraccini 24, 50139, Florence, Italy.
Maurizio LucchesiNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, Viale G. Pieraccini 24, 50139, Florence, Italy.
Alessia StivalNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, Viale G. Pieraccini 24, 50139, Florence, Italy.
Rosa Maria RopertoNephrology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
Francesca MelosiIntensive Care Unit, Meyer Children's Hospital, Florence, Italy.
Marco MaterassiNephrology Unit, Meyer Children's Hospital, University of Florence, Florence, Italy.
Silvia FarinaNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, Viale G. Pieraccini 24, 50139, Florence, Italy.
Veronica TintoriTransplantation Unit, Department of Pediatric Oncology, Meyer Children's Hospital, Florence, Italy.
Maurizio de MartinoDepartment of Health Sciences, University of Florence, Meyer Children's Hospital, Florence, Italy.
Iacopo SardiNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, Viale G. Pieraccini 24, 50139, Florence, Italy. iacopo.sardi@meyer.it.
Meyer Children's Hospital · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of gemcitabine-induced hemolytic uremic syndrome has already been described in adults. Several approaches have been employed in the treatment of gemcitabine-induced hemolytic uremic syndrome with different outcomes. One of the most promising agents is eculizumab, which is a monoclonal antibody directed against C5 complement protein. CASE PRESENTATION: We reported the case of a 3-year-old white boy with medulloblastoma who underwent high-dose chemotherapy and craniospinal irradiation. Afterwards he started maintenance chemotherapy with gemcitabine and oxaliplatin. After five courses he presented a progressive clinical worsening, which resulted in a systemic thrombotic microangiopathy. Initially he was treated with rituximab without clinical improvement. Therefore he started therapy with repeated cycles of eculizumab. After seven infusions he showed a gradual improvement and finally a complete remission of gemcitabine-induced hemolytic uremic syndrome.

conclusionsEculizumab prevents serious complement-mediated vascular damage for chemotherapy-induced thrombotic microangiopathy in pediatric cases.

Indexed as

Antibodies, Monoclonal, HumanizedAntimetabolites, AntineoplasticCerebellar NeoplasmsChild, PreschoolComplement Inactivating AgentsDeoxycytidineFatal OutcomeGemcitabineHemolytic-Uremic SyndromeHumansMaleMedulloblastomaAntibodies, Monoclonal, HumanizedAntimetabolites, AntineoplasticComplement Inactivating AgentsDeoxycytidineeculizumabGemcitabineBrain tumorsCase reportEculizumabGemcitabineMedulloblastomaMicroangiopathyRadiotherapy

Identifiers

PMID28747219
PMCPMC5530476
OpenAlexW2736614321

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.