Evidence map›Paper›PMID 37957436›Full record

ArticleCancer chemotherapy and pharmacology2024

Life-threatening toxicities upon Pembrolizumab intake: could pharmacokinetics be the bad guy?

Mourad Hamimed, Raynier Devillier, Pierre-Jean Weiller, Clémence Marin, Jean-Marc Schiano, Nawel Belmecheri, Marie-Christine Etienne-Grimaldi, Joseph Ciccolini, Samia Harbi

Open access · greenAbstract readCase Reports
PubMed Publisher
In one paragraph

Article in Cancer chemotherapy and pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 22% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 1 country.

Mourad HamimedSMARTc Unit, CRCM Inserm U1068, Aix Marseille Univ, Marseille, France.
Raynier DevillierHematology Unit, Paoli Calmettes Institute, Marseille, France.
Pierre-Jean WeillerHematology Unit, Paoli Calmettes Institute, Marseille, France.
Clémence MarinSMARTc Unit, CRCM Inserm U1068, Aix Marseille Univ, Marseille, France.
Jean-Marc SchianoHematology Unit, Paoli Calmettes Institute, Marseille, France.
Nawel BelmecheriHematology Unit, Paoli Calmettes Institute, Marseille, France.
Marie-Christine Etienne-GrimaldiOncopharmacology Unit, Centre Antoine Lacassagne, Nice, France.
Joseph CiccoliniSMARTc Unit, CRCM Inserm U1068, Aix Marseille Univ, Marseille, France. ciccolini.joseph@gmail.com.ORCID 0000-0003-1733-3410
Samia HarbiHematology Unit, Paoli Calmettes Institute, Marseille, France.
Institut Paoli-Calmettes · FRInstitut national de recherche en sciences et technologies du numérique · FRCentre Antoine Lacassagne · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe report the case of an adult patient diagnosed with Hodgkin's lymphoma who was scheduled for Pembrolizumab after failure of standard therapy. After three well-tolerated courses of Pembrolizumab, a PET scan showed a favorable outcome and a fourth course of Pembrolizumab was started. Unexpectedly, extremely severe toxicities (i.e., autoimmune peripheral hypothyroidism, rhabdomyolysis and severe acute renal failure) occurred after this last course, requiring transfer to the intensive care unit.

methodsTherapeutic drug monitoring was performed to measure residual Pembrolizumab levels at intervals from the last dose (i.e., 120 and then 170 days), as well as pharmacogenetics investigations on the FCγR gene.

resultsPembrolizumab plasma concentrations that were still pharmacologically active months after the last administration, suggesting impaired elimination of Pembrolizumab in this patient. Further pharmacokinetic modeling based on the population approach showed that both half-life (47.8 days) and clearance (0.12 L/day) values were significantly different from the standard values usually reported in patients. Further in silico simulations showed that pharmacologically active concentrations of Pembrolizumab were maintained for up to 136 days after the last dose. The search for possible polymorphisms affecting the genes coding for FCγR (i.e., rs1801274 on FCGR2A and rs396991 on FCGR3A gene) was negative. Further TDM showed that Pembrolizumab could be detected up to 263 days after the last administration.

conclusionThis case report suggests that persistent overexposure in plasma could lead to life-threatening toxicities with Pembrolizumab.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalDrug MonitoringHodgkin DiseaseAcute Kidney InjuryAdultHalf-LifeHumansHypothyroidismMaleMiddle AgedReceptors, IgGRhabdomyolysisAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalpembrolizumabReceptors, IgGB lymphomaModelingPembrolizumabPharmacokineticsToxicity

Identifiers

PMID37957436
OpenAlexW4388624854

What OpenQuestion holds

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Registered trials

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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.