Sunitinib-Induced Elevation of Mean Corpuscular Volume (MCV)-Exploring Its Possible Clinical Relevance in Cancer Patients
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
35735439
PubMed Central
PMC9221843
DOI
10.3390/curroncol29060330
PII: curroncol29060330
Knihovny.cz E-zdroje
- Klíčová slova
- MCV, mean corpuscular volume, sunitinib, toxicity,
- MeSH
- dítě MeSH
- dospělí MeSH
- erytrocytární znaky MeSH
- indoly škodlivé účinky MeSH
- karcinom z renálních buněk * farmakoterapie patologie MeSH
- lidé MeSH
- nádory ledvin * farmakoterapie patologie MeSH
- protinádorové látky * škodlivé účinky MeSH
- pyrroly škodlivé účinky MeSH
- retrospektivní studie MeSH
- sunitinib farmakologie terapeutické užití MeSH
- Check Tag
- dítě MeSH
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- indoly MeSH
- protinádorové látky * MeSH
- pyrroly MeSH
- sunitinib MeSH
Sunitinib is a broad-spectrum multitargeted tyrosine kinase inhibitor mainly used as second-line therapy for non-resectable gastrointestinal stromal or first-line treatment option of metastatic renal cell carcinoma (mRCC), and as an "off-label" option in pediatric oncology. It has been previously reported that sunitinib elevates the mean corpuscular volume of erythrocytes (MCV) in treated subjects. The aim of this study was to assess time-dependent changes of this effect and evaluate its possible clinical relevance. In this study, 179 adult and 21 pediatric patients with solid tumors treated with sunitinib were retrospectively analyzed. The laboratory and treatment-related data were collected for each treatment period. The regression model with a broken-line relationship was used to fit time dependence of the MCV. In the adult group, the MCV was increasing during the first 21.6 weeks (median) of treatment in a median level of 99.8 fL, where it stabilized. MCV increase was faster in the patients who suffered from treatment-related adverse events (21.3 vs. 24.6 weeks, p = 0.010). In the pediatric cohort, the MCV dynamics were similar to adults. In conclusion, MCV changes during sunitinib treatment in pediatric and adult patients may be of clinical utility in monitoring sunitinib treatment course.
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