Solid Tumors (mRECIST) and alpha-fetoprotein (AFP) behavior was reviewed for 306 patients within the Milan criteria (MC-IN) and 116 patients outside the Milan criteria (MC-OUT) who underwent LRTand LT between January 1999 and March 2010. A prospectively collected database originating from 6 collaborating European centers was used for the study. Sixty-one patients (14.5%) developed HCC recurrence. For both MC-IN and MC-OUT patients, an AFP slope > 15 ng/mL/month and mRECIST progression were unique independent risk factors for HCC recurrence and patient death. When the radiological Milan criteria (MC) status was combined with radiological and biological progression, MC-IN and MC-OUT patients without risk factors had similarly excellent 5- year tumor-free and patient survival rates. MC-IN patients with at least 1 risk factor had worse outcomes, and MC-OUT patients with at least 1 risk factor had the poorest survival (P < 0.001). In conclusion, both radiological and biological modifications permit documentation of the response to LRT in patients waiting for LT. According to these 2 parameters, tumor progression significantly increases the risk of recurrence and patient death not only forMC-OUT patients but also for MC-IN patients. Themonitoring of both parameters in combination with the initial radiological MC status is an essential element for further refining the selection criteria for potential liver recipients with HCC

Alpha-Fetoprotein and Modified Response Evaluation Criteria in Solid Tumors Progression After Locoregional Therapy as Predictors of Hepatocellular Cancer Recurrence and Death After Transplantation / Lai, Quirino; Avolio, Aw; Graziadei, I; Otto, G; Rossi, Massimo; Tisone, G; Goffette, P; Vogel, W; Pitton, Mb; Lerut, J.. - In: LIVER TRANSPLANTATION. - ISSN 1527-6465. - STAMPA. - 10:19(2013), pp. 1108-1118. [10.1002/lt.23706]

Alpha-Fetoprotein and Modified Response Evaluation Criteria in Solid Tumors Progression After Locoregional Therapy as Predictors of Hepatocellular Cancer Recurrence and Death After Transplantation

LAI, QUIRINO;ROSSI, MASSIMO;
2013

Abstract

Solid Tumors (mRECIST) and alpha-fetoprotein (AFP) behavior was reviewed for 306 patients within the Milan criteria (MC-IN) and 116 patients outside the Milan criteria (MC-OUT) who underwent LRTand LT between January 1999 and March 2010. A prospectively collected database originating from 6 collaborating European centers was used for the study. Sixty-one patients (14.5%) developed HCC recurrence. For both MC-IN and MC-OUT patients, an AFP slope > 15 ng/mL/month and mRECIST progression were unique independent risk factors for HCC recurrence and patient death. When the radiological Milan criteria (MC) status was combined with radiological and biological progression, MC-IN and MC-OUT patients without risk factors had similarly excellent 5- year tumor-free and patient survival rates. MC-IN patients with at least 1 risk factor had worse outcomes, and MC-OUT patients with at least 1 risk factor had the poorest survival (P < 0.001). In conclusion, both radiological and biological modifications permit documentation of the response to LRT in patients waiting for LT. According to these 2 parameters, tumor progression significantly increases the risk of recurrence and patient death not only forMC-OUT patients but also for MC-IN patients. Themonitoring of both parameters in combination with the initial radiological MC status is an essential element for further refining the selection criteria for potential liver recipients with HCC
2013
Alpha-Fetoprotein, locoregional therapy, liver transplantation
01 Pubblicazione su rivista::01a Articolo in rivista
Alpha-Fetoprotein and Modified Response Evaluation Criteria in Solid Tumors Progression After Locoregional Therapy as Predictors of Hepatocellular Cancer Recurrence and Death After Transplantation / Lai, Quirino; Avolio, Aw; Graziadei, I; Otto, G; Rossi, Massimo; Tisone, G; Goffette, P; Vogel, W; Pitton, Mb; Lerut, J.. - In: LIVER TRANSPLANTATION. - ISSN 1527-6465. - STAMPA. - 10:19(2013), pp. 1108-1118. [10.1002/lt.23706]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/785619
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