Clinical Research Details

Descriptive Information
Oxaliplatin-Induced Increase in Spleen Volume; Accurate Detection and Correlation with Other Oxaliplatin Adverse Events

Ali Shamseddine
as04@aub.edu.lb

IM.AS.27
Completed- Has Results

Observational  


No
Conditions and Keywords
Liver increase in size
Oxliplatin,spleen volume,liver fibrosis
Study Design
Eligibility and IRB
Both
Min: 18
Max:
Yes
No

 

The objective of this study is to measure the splenic volume of patients on oxaliplatin therapy, using AUBMC’s new software (ISP upgrade), before and during chemotherapy to detect any increase in splenic size as a biomarker for early oxaliplatin toxicity. Also, we will measure liver scarring/fibrosis through transient elastography (FibroScan machine) as a way to assess oxaliplatin induced liver injury. These two techniques will then be compared to determine if liver injury detected by FibroScan precedes that detected by measuring an increase in spleen size Other clinical indicators of oxaliplatin toxicity will also be measured to study any possible correlation between the grading of adverse events like peripheral neuropathy or increase in transaminases and the occurrence and severity of oxaliplatin-mediated increase in splenic size.

·         Measure the splenic volume of patients on oxaliplatin therapy, using AUBMC’s new software (ISP upgrade), before and during chemotherapy to detect any increase in splenic size as a biomarker for early oxaliplatin toxicity.

·         Using liver FibroScan, measure liver elasticity and controlled attenuated parameter (CAP) before and during chemotherapy to detect liver fibrosis as a potential biomarker for early Oxaliplatin toxicity.

·         Measure splenic volume after discontinuation of oxaliplatin chemotherapy to assess for reversibility of oxaliplatin- induced increase in splenic size, if any.

·         Measure other clinical indicators of oxaliplatin toxicity to study any possible correlation between the grading of adverse events like peripheral neuropathy or increase in transaminases and the occurrence and severity of oxaliplatin-mediated increase in spleen size.

·         Measure synthetic liver functions (PT, PTT, albumin…), before, during, and after Oxaliplatin therapy

·         Measure liver elasticity and CAP after discontinuation of Oxaliplatin to assess reversibility of Oxaliplatin-induced liver fibrosis, if already present.

·         In case of patients undergoing surgery:

-Measure portal venous pressure through transhepatic or transvenous catheterization of    the portal vein.

-Examine liver for oxaliplatin induced injury (fibrosis/cirrhosis) by immunohistochemistry.