• Je něco špatně v tomto záznamu ?

Impact of multiple primary cancers on overall survival of patients with hepatocellular carcinoma

P. Hříbek, S. Fraňková, J. Klasová, K. Chmelová, L. Miková, J. Šperl, P. Urbánek

. 2024 ; 71 (3) : 289-296. [pub] -

Jazyk angličtina Země Slovensko

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc24019984

The increasing occurrence of multiple primary cancers (MPC) is a long-term trend, but the prevalence of MPC in patients with hepatocellular carcinoma (HCC) and its impact on overall survival (OS) remains unknown. We retrospectively analyzed 497 patients with HCC treated at two tertiary centers. The cohort was divided into two subgroups - liver transplant (LT, 324 patients) and non-liver transplant (non-LT, 173 patients). We analyzed MPC occurrence, its impact on survival, and identified variables predicting unfavorable outcomes. The MPC were detected in 88 patients (18%). The most common MPC were prostate (17%), skin (15.9%), kidney (12.5%), and lung (10.2%). The median OS of the whole cohort and the LT and non-LT subgroups were 70, 116, and 17 months, respectively (p<0.0001). The median OS in patients with HCC only and HCC with another cancer was 77 (95% CI, 67-96) and 50 months (95% CI, 37-62), respectively (p=0.25). The OS of LT patients was significantly better than that of those in whom LT had been contraindicated owing to concomitant MPC (116 vs. 35 months, p<0.0009). Autoimmune etiology, non-alcoholic steatohepatitis (NASH), HCC as the first diagnosed malignancy, and male sex were identified as factors significantly influencing the patients' outcomes (HR 0.43, 3.2326, 0.70, and 1.43, respectively). The MPC frequency was 18%. The impact of MPC on OS was not significant, except for individuals contraindicated for LT because of MPC. A better prognosis is associated with the autoimmune etiology of cirrhosis, and when HCC is diagnosed as the first malignancy. Male sex and NASH worsened the outcomes.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc24019984
003      
CZ-PrNML
005      
20250402152542.0
007      
ta
008      
241015s2024 xo f 000 0|eng||
009      
AR
024    7_
$a 10.4149/neo_2024_231217N649 $2 doi
035    __
$a (PubMed)38958713
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xo
100    1_
$a Hříbek, Petr $u Department of Medicine, 1st Faculty of Medicine Charles University and Military University Hospital Prague, Military University Hospital Prague, Prague, Czech Republic $u Department of Internal Medicine, University of Defense, Faculty of Military Health Sciences in Hradec Kralove, Hradec Kralove, Czech Republic
245    10
$a Impact of multiple primary cancers on overall survival of patients with hepatocellular carcinoma / $c P. Hříbek, S. Fraňková, J. Klasová, K. Chmelová, L. Miková, J. Šperl, P. Urbánek
520    9_
$a The increasing occurrence of multiple primary cancers (MPC) is a long-term trend, but the prevalence of MPC in patients with hepatocellular carcinoma (HCC) and its impact on overall survival (OS) remains unknown. We retrospectively analyzed 497 patients with HCC treated at two tertiary centers. The cohort was divided into two subgroups - liver transplant (LT, 324 patients) and non-liver transplant (non-LT, 173 patients). We analyzed MPC occurrence, its impact on survival, and identified variables predicting unfavorable outcomes. The MPC were detected in 88 patients (18%). The most common MPC were prostate (17%), skin (15.9%), kidney (12.5%), and lung (10.2%). The median OS of the whole cohort and the LT and non-LT subgroups were 70, 116, and 17 months, respectively (p<0.0001). The median OS in patients with HCC only and HCC with another cancer was 77 (95% CI, 67-96) and 50 months (95% CI, 37-62), respectively (p=0.25). The OS of LT patients was significantly better than that of those in whom LT had been contraindicated owing to concomitant MPC (116 vs. 35 months, p<0.0009). Autoimmune etiology, non-alcoholic steatohepatitis (NASH), HCC as the first diagnosed malignancy, and male sex were identified as factors significantly influencing the patients' outcomes (HR 0.43, 3.2326, 0.70, and 1.43, respectively). The MPC frequency was 18%. The impact of MPC on OS was not significant, except for individuals contraindicated for LT because of MPC. A better prognosis is associated with the autoimmune etiology of cirrhosis, and when HCC is diagnosed as the first malignancy. Male sex and NASH worsened the outcomes.
650    _2
$a lidé $7 D006801
650    12
$a hepatocelulární karcinom $x mortalita $x patologie $7 D006528
650    12
$a nádory jater $x mortalita $x patologie $7 D008113
650    _2
$a mužské pohlaví $7 D008297
650    _2
$a ženské pohlaví $7 D005260
650    12
$a mnohočetné primární nádory $x mortalita $x patologie $7 D009378
650    _2
$a retrospektivní studie $7 D012189
650    _2
$a lidé středního věku $7 D008875
650    12
$a transplantace jater $x mortalita $7 D016031
650    _2
$a senioři $7 D000368
650    _2
$a prognóza $7 D011379
650    _2
$a dospělí $7 D000328
655    _2
$a časopisecké články $7 D016428
700    1_
$a Fraňková, Soňa $u Institute for Clinical and Experimental Medicine, Prague, Czech Republic $7 xx0329475
700    1_
$a Klasová, Johana $u Department of Medicine, 1st Faculty of Medicine Charles University and Military University Hospital Prague, Military University Hospital Prague, Prague, Czech Republic
700    1_
$a Chmelová, Klára $u Institute for Clinical and Experimental Medicine, Prague, Czech Republic
700    1_
$a Miková, Lucie $u Department of Medicine, 1st Faculty of Medicine Charles University and Military University Hospital Prague, Military University Hospital Prague, Prague, Czech Republic
700    1_
$a Šperl, Jan $u Institute for Clinical and Experimental Medicine, Prague, Czech Republic
700    1_
$a Urbánek, Petr $u Department of Medicine, 1st Faculty of Medicine Charles University and Military University Hospital Prague, Military University Hospital Prague, Prague, Czech Republic
773    0_
$w MED00003470 $t Neoplasma $x 0028-2685 $g Roč. 71, č. 3 (2024), s. 289-296
856    41
$u https://pubmed.ncbi.nlm.nih.gov/38958713 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y - $z 0
990    __
$a 20241015 $b ABA008
991    __
$a 20250402152538 $b ABA008
999    __
$a ok $b bmc $g 2202303 $s 1231957
BAS    __
$a 3
BAS    __
$a PreBMC-MEDLINE
BMC    __
$a 2024 $b 71 $c 3 $d 289-296 $e - $i 0028-2685 $m Neoplasma $n Neoplasma $x MED00003470
LZP    __
$a Pubmed-20241015

Najít záznam

Citační ukazatele

Nahrávání dat ...

    Možnosti archivace