Impact of sarcopenia on outcomes following intra-arterial therapy of hepatic malignancies.

Impact of sarcopenia on outcomes following intra-arterial therapy of hepatic malignancies.
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DOI:
10.1007/s11605-013-2348-5
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发表时间:
2013-12
影响因子:
3.2
通讯作者:
Pawlik, Timothy M.
Pawlik, Timothy M.
中科院分区:
医学3区
文献类型:
--
作者:
Dodson, Rebecca M.;Firoozmand, Amin;Hyder, Omar;Tacher, Vania;Cosgrove, David P.;Bhagat, Nikhil;Herman, Joseph M.;Wolfgang, Christopher L.;Geschwind, Jean-Francois H.;Kamel, Ihab R.;Pawlik, Timothy M.

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Assessment of patient performance status is often subjective. Sarcopenia—measurement of muscle wasting—may be a more objective means to assess performance status and therefore mortality risk following intra-arterial therapy (IAT). Total psoas area (TPA) was measured on cross-sectional imaging in 216 patients undergoing IATof hepatic malignancies between 2002 and 2012. Sarcopenia was defined as TPA in the lowest sex-specific quartile. Impact of sarcopenia was assessed relative to other clinicopathological factors. Indications for IAT included hepatocellular carcinoma (51 %), intrahepatic cholangiocarcinoma (13 %), colorectal liver metastasis (7 %), or other metastatic disease (30 %). Median TPA among men (568 mm2/m2) was greater than women (413 mm2/m2). IAT involved conventional chemoembolization (54 %), drug-eluting beads (40 %), or yttrium-90 (6 %). Median tumor size was 5.8 cm; most patients had multiple lesions (74 %). Ninety-day mortality was 9.3 %; 3-year survival was 39 %. Factors associated with risk of death were tumor size (HR=1.84) and Child's score (HR=2.15) (all P <0.05). On multivariate analysis, sarcopenia remained independently associated with increased risk of death (lowest vs. highest TPA quartile, HR=1.84; P =0.04). Sarcopenic patients had a 3-year survival of 28 vs. 44 % for non-sarcopenic patients. Sarcopenia was an independent predictor of mortality following IAT with sarcopenic patients having a twofold increased risk of death. Sarcopenia is an objective measure of frailty that can help clinical decision-making regarding IAT for hepatic malignancies.
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