Literature DB >> 20406923

Oxaliplatin-mediated increase in spleen size as a biomarker for the development of hepatic sinusoidal injury.

Michael J Overman1, Dipen M Maru, Chusilp Charnsangavej, Evelyn M Loyer, Huamin Wang, Priyanka Pathak, Cathy Eng, Paulo M Hoff, Jean-Nicolas Vauthey, Robert A Wolff, Scott Kopetz.   

Abstract

PURPOSE: Oxaliplatin-based chemotherapy can cause hepatic sinusoidal injury, with resultant sinusoidal damage and portal hypertension. We sought to explore the relationship between oxaliplatin induced hepatic sinusoidal injury, increases in spleen size, and the subsequent development of thrombocytopenia. PATIENTS AND METHODS: We retrospectively assessed the relationship between chemotherapy exposure, changes in spleen size (determined by volumetric measurements), and platelet counts in 136 patients treated with adjuvant fluorouracil and oxaliplatin (FOLFOX) or fluoropyrimidine for stage II or III colorectal adenocarcinoma. Hepatic sinusoidal injury and changes in spleen size were graded in a separate population of 63 patients with metastatic colorectal cancer receiving fluoropyrimidine and oxaliplatin before liver resection.
RESULTS: Spleen size increased in 86% of patients treated with adjuvant FOLFOX (P < .001), with a > or = 50% increase in 24% of patients. Spleen size did not significantly increase in patients treated with adjuvant fluoropyrimidine. Increases in spleen size correlated with cumulative oxaliplatin dose (P = .003). Patients with splenic enlargement > or = 50% had higher rates of thrombocytopenia in the first year after completion of chemotherapy (27% v 5%; P = .003). In patients with hepatic metastases treated with preoperative fluoropyrimidine and oxaliplatin, increases in spleen size was a predictor of higher histologic grades of sinusoidal injury in both univariate (P = .03) and multivariate (P = .02) analyses.
CONCLUSION: Increases in spleen size correlate with increasing grade of hepatic sinusoidal injury and can serve as a simple method for identifying patients at risk for this toxicity. Oxaliplatin-induced increases in spleen size should be recognized as a potential etiology of persistent thrombocytopenia after oxaliplatin treatment.

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Year:  2010        PMID: 20406923     DOI: 10.1200/JCO.2009.27.5701

Source DB:  PubMed          Journal:  J Clin Oncol        ISSN: 0732-183X            Impact factor:   44.544


  71 in total

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2.  Sinusoidal obstruction syndrome after oxaliplatin-based chemotherapy.

Authors:  An Na Seo; Haeryoung Kim
Journal:  Clin Mol Hepatol       Date:  2014-03

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4.  Assessing splenic enlargement on CT by unidimensional measurement changes in patients with colorectal liver metastases.

Authors:  Breanna J Joiner; Amber L Simpson; Julie N Leal; Michael I D'Angelica; Richard K G Do
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5.  A 39-year-old female patient with metastatic rectal cancer develops thrombocytopenia.

Authors:  Haifaa Dbouk; Simon Mentha; Deborah Mukherji; Jean Lee; Ali Haydar; Ali Shamseddine; Eileen M O'Reilly; Leonard Saltz; Ghassan K Abou-Alfa
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8.  Efficacy and safety of oxaliplatin, bevacizumab and oral S-1 for advanced recurrent colorectal cancer.

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9.  Sinusoidal obstruction syndrome (SOS) related to chemotherapy for colorectal liver metastases: factors predictive of severe SOS lesions and protective effect of bevacizumab.

Authors:  Catherine Hubert; Christine Sempoux; Yves Humblet; Marc van den Eynde; Francis Zech; Isabelle Leclercq; Jean-François Gigot
Journal:  HPB (Oxford)       Date:  2013-01-18       Impact factor: 3.647

10.  Magnetic resonance imaging flowmetry demonstrates portal vein dilatation subsequent to oxaliplatin therapy in patients with colorectal liver metastasis.

Authors:  Jozef Urdzik; Tomas Bjerner; Alkwin Wanders; Frans Duraj; Ulf Haglund; Agneta Norén
Journal:  HPB (Oxford)       Date:  2012-08-20       Impact factor: 3.647

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