Journal article
Partial splenic embolization to permit continuation of systemic chemotherapy
Cancer medicine (Malden, MA), Vol.5(10), pp.2715-2720
10/2016
DOI: 10.1002/cam4.856
PMID: 27611010
Abstract
Systemic chemotherapy treatments, commonly those that comprise oxaliplatin, have been linked to the appearance of distinctive liver lesions that evolves to portal hypertension, spleen enlargement, platelets sequestration, and thrombocytopenia. This outcome can interrupt treatment or force dosage reduction, decreasing efficiency of cancer therapy. We conducted a prospective phase II study for the evaluation of partial splenic embolization in patients with thrombocytopenia that impeded systemic chemotherapy continuation. From August 2014 through July 2015, 33 patients underwent partial splenic embolization to increase platelets count and allow their return to treatment. Primary endpoint was the accomplishment of a thrombocyte level superior to 130 × 10
/L and the secondary endpoints were the return to chemotherapy and toxicity. Partial splenic embolization was done 36 times in 33 patients. All patients presented gastrointestinal cancer and colorectal malignancy was the commonest primary site. An average of 6.4 cycles of chemotherapy was done before splenic embolization and the most common regimen was Folfox. Mean platelet count prior to embolization was 69 × 10
/L. A total of 94% of patients achieved primary endpoint. All patients in need reinitiated treatment and median time to chemotherapy return was 14 days. No grade 3 or above adverse events were identified. Aiming for a 50% to 70% infarction area may be sufficient to achieve success without the complications associated with more extensive infarction. Combined with the better safety profile, partial splenic embolization is an excellent option in the management of thrombocytopenia, enabling the resumption of systemic chemotherapy with minimal procedure-related morbidity.
Details
- Title: Subtitle
- Partial splenic embolization to permit continuation of systemic chemotherapy
- Creators
- Jose Hugo M Luz - Hospital do Câncer IIIPaula M Luz - Instituto Evandro ChagasEdson Marchiori - Universidade Federal do Rio de JaneiroLeonardo A Rodrigues - Hospital do Câncer IIIHugo R Gouveia - Hospital do Câncer IIIHenrique S Martin - Hospital do Câncer IIIIgor M Faria - Hospital do Câncer IIIRoberto R Souza - Department of Interventional Radiology, Radiology Division, National Cancer Institute, INCA, Rio de Janeiro, BrazilRoberto de Almeida Gil - Department of Clinical Oncology, National Cancer Institute, INCA, Rio de Janeiro, BrazilAlexandre de M Palladino - Department of Clinical Oncology, National Cancer Institute, INCA, Rio de Janeiro, BrazilKarina B Pimenta - Hospital do Câncer IIIHenrique S de Souza - Hospital do Câncer III
- Resource Type
- Journal article
- Publication Details
- Cancer medicine (Malden, MA), Vol.5(10), pp.2715-2720
- DOI
- 10.1002/cam4.856
- PMID
- 27611010
- ISSN
- 2045-7634
- eISSN
- 2045-7634
- Grant note
- UM1 AI069476 / NIAID NIH HHS
- Language
- English
- Date published
- 10/2016
- Academic Unit
- Radiology
- Record Identifier
- 9985177933602771
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