Partial splenic embolization to manage thrombocytopenia in cancer patients: Case series and review of the literature
Notice bibliographique
Résumé
Abstract Introduction Thrombocytopenia is a common complication of cancer and its management (Liebman, 2014). Alleviating thrombocytopenia in cancer patients is essential to avoid dose-reduction or delay of chemotherapy (Soff et al., 2024). Partial splenic embolization (PSE) is a procedure that can increase their platelet count, allowing for initiation/resumption of chemotherapy. We present two cases of cancer patients that had a PSE, but had different experiences/outcomes. Using this case series, we aim to provide some insight on enhancing the procedure's effectiveness and safety for this patient population. Methods A search of the PubMed and Ovid databases for articles that discussed PSEs performed on cancer patients was completed. After excluding irrelevant articles, data was extracted from the remaining papers and organized into tables to support the discussion. Two case reports were written based on up-to-date information from the patients' charts. Data from hematology, oncology and interventional radiology consult notes, lab work and imaging reports were used to present the clinical cases. Results The first case was a patient with metastatic colorectal cancer that had been on palliative chemotherapy, which was repeatedly delayed due to thrombocytopenia. They underwent a PSE that resulted in about 30-35% embolization of the spleen. The PSE increased their platelet count, allowing them to re-initiate chemotherapy. However, their thrombocytopenia worsened 18 months later, such that a second PSE was necessary to return to treatment. The second patient had breast cancer that required adjuvant combined chemoradiation therapy. They had thrombocytopenia, so to improve this and proceed with treatment, they underwent a PSE. After the procedure, the patient was found to have infarction of the whole spleen, severe necrotizing pancreatitis, and splenic and portal vein thrombosis. Although their platelet count increased post-PSE, they were not deemed a candidate for chemotherapy due to delays and complications. Discussion These cases present potential room for improvement of the effectiveness and safety of the PSEs performed. In the first case, the patient had a recurrence of thrombocytopenia after their first PSE, during which 30-35% of the spleen was embolized. The percentage of spleen embolized may partially explain the re-emergence of thrombocytopenia, as one study suggests that a minimum of 50% splenic infarction is associated with long-term improvements in platelet count (up to 5 years post-PSE) in cirrhotic patients with hypersplenism (Zhu et al., 2009). However, the increase in platelet count post-PSE is multifactorial, and this patient also experienced an increase in their chemotherapy dose that could have had an impact. Moreover, in the second case, excessive embolization of the spleen occurred (complete as opposed to partial), likely the result of unintentional non-target embolization. Understanding how to prevent non-target embolization is important to minimize complications. Estimating the volume of spleen that has been infarcted intraprocedurally is a difficult task and most methods strongly rely on operator experience (Koizumi et al., 2013; Ou et al., 2013). Being able to use imaging intraprocedurally for this purpose has the potential to decrease the likelihood of excessive embolization and associated complications (Koizumi et al., 2013). Acquiring a deeper understanding of a patient's splenic anatomy could also help guide a safer embolization. Overall, these cases demonstrate that although a PSE can benefit a cancer patient, there can be serious complications associated with the procedure. Understanding how to enhance the effectiveness and safety of PSEs in cancer patients is key to successful and durable outcomes.
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Comment cette classification a été obtenuedéplier
Prédiction machine sur la base complète
Imitation des enseignantsNi prévalence calibrée, ni vérité terrain. Validation humaine à venir. Le volet Gemma est une étiquette directe du modèle pour chaque travail de la base, lue sur la notice réduite au titre. Le volet Codex est un classifieur appris des 10 348 étiquettes directes de Codex et calibré sur les taux pondérés de l'échantillon; les champs sans appui suffisant ne portent aucun appel Codex. Le mode candidate est l'union des deux volets; le consensus est leur intersection. Ces sorties portent le statut machine_predicted_unvalidated et ne sont pas des étiquettes humaines.
Scores du classifieur distillé par catégorie (deux têtes)
| Catégorie | Codex | Gemma |
|---|---|---|
| Métarecherche | 0,001 | 0,003 |
| Méta-épidémiologie (sens strict) | 0,001 | 0,000 |
| Méta-épidémiologie (sens large) | 0,001 | 0,001 |
| Bibliométrie | 0,005 | 0,006 |
| Études des sciences et des technologies | 0,001 | 0,001 |
| Communication savante | 0,001 | 0,002 |
| Science ouverte | 0,001 | 0,001 |
| Intégrité de la recherche | 0,002 | 0,001 |
| Charge utile insuffisante (le modèle a refusé de juger) | 0,002 | 0,001 |
Scores machine (provisoires)
Les deux têtes enseignantes du modèle étudiant, lues sur ce travail. Un score ordonne la base pour la relecture; il n'affirme jamais une catégorie, et le statut de validation accompagne chaque rangée tel quel.
Scores de référence d'un modèle non mature (critères de maturité non atteints, 7 itérations). Un score ordonne; il n'affirme jamais une catégorie.
score_only:v0-immature-baseline · tel quel depuis la passe de notation : score_only signifie que le nombre peut ordonner les travaux, et qu'aucune étiquette de catégorie n'en découleClassification
machine, non validéePrédiction automatique; un appel candidat d’une seule source (Gemma direct ou Codex distillé), pas un consensus.
Le détail, modèle par modèle et score par score, se trouve en fin de page sous « Comment cette classification a été obtenue ».