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Pancreatic Atrophy in Hepatocellular Carcinoma Patients Receiving Long-Term Treatment with Sorafenib
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<b><i>Objective:</i></b> To date, sorafenib is the only approved systemic therapy for advanced hepatocellular carcinoma (HCC). Pancreatic atrophy has recently been reported in 2 patients as a novel side effect after long-term sorafenib treatment. <b><i>Methods:</i></b> We retrospectively analyzed clinical and radiological data of patients with advanced HCC with long-term treatment of sorafenib (median 279 days, range 153-826 days). Pancreata were semi-manually segmented section by section to calculate the pancreas volumes before and under sorafenib treatment. <b><i>Results:</i></b> Sorafenib reduced pancreatic volume in 18/19 (95%) HCC patients with a mean pancreatic volume loss of 25% (p = 0.002). Pancreatic volume loss depended on the dose (r = 0.36) and exposure time of sorafenib (r = 0.35) and was detectable as early as after 3 months of sorafenib treatment and already after a cumulative sorafenib dose of <100 g. Median overall survival was 13.2 months (range 7.8-31.3 months) but did not correlate with sorafenib-induced pancreatic volume reduction (hazard ratio 1.002, 95% confidence interval 0.981-1.060, p = 0.24). <b><i>Conclusion:</i></b> We could confirm pancreatic atrophy as a novel adverse event of sorafenib therapy in HCC patients, correlating with sorafenib dose and exposure time.
Title: Pancreatic Atrophy in Hepatocellular Carcinoma Patients Receiving Long-Term Treatment with Sorafenib
Description:
<b><i>Objective:</i></b> To date, sorafenib is the only approved systemic therapy for advanced hepatocellular carcinoma (HCC).
Pancreatic atrophy has recently been reported in 2 patients as a novel side effect after long-term sorafenib treatment.
<b><i>Methods:</i></b> We retrospectively analyzed clinical and radiological data of patients with advanced HCC with long-term treatment of sorafenib (median 279 days, range 153-826 days).
Pancreata were semi-manually segmented section by section to calculate the pancreas volumes before and under sorafenib treatment.
<b><i>Results:</i></b> Sorafenib reduced pancreatic volume in 18/19 (95%) HCC patients with a mean pancreatic volume loss of 25% (p = 0.
002).
Pancreatic volume loss depended on the dose (r = 0.
36) and exposure time of sorafenib (r = 0.
35) and was detectable as early as after 3 months of sorafenib treatment and already after a cumulative sorafenib dose of <100 g.
Median overall survival was 13.
2 months (range 7.
8-31.
3 months) but did not correlate with sorafenib-induced pancreatic volume reduction (hazard ratio 1.
002, 95% confidence interval 0.
981-1.
060, p = 0.
24).
<b><i>Conclusion:</i></b> We could confirm pancreatic atrophy as a novel adverse event of sorafenib therapy in HCC patients, correlating with sorafenib dose and exposure time.
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