Detail
Article
Online article
FT
Medvik - BMC
  • Something wrong with this record ?

Microsatellite Instability as a Prognostic Factor in Stage II Colon Cancer Patients, a Meta-Analysis of Published Literature

I. Gkekas, J. Novotny, L. Pecen, K. Strigård, R. Palmqvist, U. Gunnarsson,

. 2017 ; 37 (12) : 6563-6574.

Language English Country Greece

Document type Journal Article, Meta-Analysis, Review

BACKGROUND/AIM: The prognostic role of microsatellite instability (MSI) in stage II colon cancer patients remains controversial despite the fact that it has been investigated in a number of studies. Hazard ratios differ considerably among these studies. We performed a meta-analysis to define the significance of MSI in this group of patients. MATERIALS AND METHODS: Studies indexed in PubMed presenting separate data on MSI status and survival outcomes for stage II colon cancer patients have been analyzed using fixed-effect meta-analysis of hazard ratio (HR) according to the method of Peto. RESULTS: Analysis was performed on 19 studies including 5,998 patients. A 47.3% of patients received postoperative chemotherapy and included 52.8% males and 47.2% females. Eight studies included some rectal cancer patients although this cohort was not clearly defined in 3 of these. MSI observed in 20.8% (mean) of patients (median 19.9%). HR for overall survival (OS) of MSI vs. microsatellite stable (MSS) tumors for the entire population: 0.73 (95% confidence interval (CI)=0.33-1.65); HR for disease-free survival (DFS):0.60 (95%CI=0.27-1.32). No statistical significant difference was found when studies analyzing MSI with genotyping (MG) and immunohistochemistry (IHC) were compared separately (MG vs. IHC: HR OS 0.45, 95%CI=0.10-2.05 vs. 0.95, 95%CI=0.57-1.58; HR DFS 0.51, 95%CI=0.14-1.85 vs. 0.67, 95%CI=0.26-1.70). However, numerically MSI determination with genotyping shows significantly lower hazard ratios for both DFS and OS. Separate analysis of studies describing colon cancer patients only showed HR OS 0.72 (95%CI=0.31-1.71); HR DFS 0.60 (95%CI=0.27-1.31). CONCLUSION: No significant relation was found between MSI status and OS or DFS. Routine determination of MSI status to guide postoperative management of stage II colon cancer patients cannot be recommended. New large scale high quality studies are needed to answer this question definitively, since currently analyzed studies vary considerably.

References provided by Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18016218
003      
CZ-PrNML
005      
20180515104016.0
007      
ta
008      
180515s2017 gr f 000 0|eng||
009      
AR
024    7_
$a 10.21873/anticanres.12113 $2 doi
035    __
$a (PubMed)29187431
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gr
100    1_
$a Gkekas, Ioannis $u Department of Surgical and Perioperative Sciences, Umea University, Umea, Sweden ioannis.gkekas@nll.se. Department of Surgery, Sunderby hospital Lulea, Lulea, Sweden.
245    10
$a Microsatellite Instability as a Prognostic Factor in Stage II Colon Cancer Patients, a Meta-Analysis of Published Literature / $c I. Gkekas, J. Novotny, L. Pecen, K. Strigård, R. Palmqvist, U. Gunnarsson,
520    9_
$a BACKGROUND/AIM: The prognostic role of microsatellite instability (MSI) in stage II colon cancer patients remains controversial despite the fact that it has been investigated in a number of studies. Hazard ratios differ considerably among these studies. We performed a meta-analysis to define the significance of MSI in this group of patients. MATERIALS AND METHODS: Studies indexed in PubMed presenting separate data on MSI status and survival outcomes for stage II colon cancer patients have been analyzed using fixed-effect meta-analysis of hazard ratio (HR) according to the method of Peto. RESULTS: Analysis was performed on 19 studies including 5,998 patients. A 47.3% of patients received postoperative chemotherapy and included 52.8% males and 47.2% females. Eight studies included some rectal cancer patients although this cohort was not clearly defined in 3 of these. MSI observed in 20.8% (mean) of patients (median 19.9%). HR for overall survival (OS) of MSI vs. microsatellite stable (MSS) tumors for the entire population: 0.73 (95% confidence interval (CI)=0.33-1.65); HR for disease-free survival (DFS):0.60 (95%CI=0.27-1.32). No statistical significant difference was found when studies analyzing MSI with genotyping (MG) and immunohistochemistry (IHC) were compared separately (MG vs. IHC: HR OS 0.45, 95%CI=0.10-2.05 vs. 0.95, 95%CI=0.57-1.58; HR DFS 0.51, 95%CI=0.14-1.85 vs. 0.67, 95%CI=0.26-1.70). However, numerically MSI determination with genotyping shows significantly lower hazard ratios for both DFS and OS. Separate analysis of studies describing colon cancer patients only showed HR OS 0.72 (95%CI=0.31-1.71); HR DFS 0.60 (95%CI=0.27-1.31). CONCLUSION: No significant relation was found between MSI status and OS or DFS. Routine determination of MSI status to guide postoperative management of stage II colon cancer patients cannot be recommended. New large scale high quality studies are needed to answer this question definitively, since currently analyzed studies vary considerably.
650    _2
$a nádory tračníku $x farmakoterapie $x genetika $x chirurgie $7 D003110
650    _2
$a přežití bez známek nemoci $7 D018572
650    _2
$a lidé $7 D006801
650    12
$a mikrosatelitní nestabilita $7 D053842
650    _2
$a staging nádorů $7 D009367
650    _2
$a hodnocení výsledků zdravotní péče $x metody $x statistika a číselné údaje $7 D017063
650    _2
$a prognóza $7 D011379
650    _2
$a proporcionální rizikové modely $7 D016016
655    _2
$a časopisecké články $7 D016428
655    _2
$a metaanalýza $7 D017418
655    _2
$a přehledy $7 D016454
700    1_
$a Novotny, Jan $u Department of Surgery, Sunderby hospital Lulea, Lulea, Sweden.
700    1_
$a Pecen, Ladislav $u Faculty Hospital Pilsen, Charles University, Prague, Czech Republic.
700    1_
$a Strigård, Karin $u Department of Surgical and Perioperative Sciences, Umea University, Umea, Sweden.
700    1_
$a Palmqvist, Richard $u Department of Medical Biosciences/Pathology, Umea University, Umea, Sweden.
700    1_
$a Gunnarsson, Ulf $u Department of Surgical and Perioperative Sciences, Umea University, Umea, Sweden.
773    0_
$w MED00000478 $t Anticancer research $x 1791-7530 $g Roč. 37, č. 12 (2017), s. 6563-6574
856    41
$u https://pubmed.ncbi.nlm.nih.gov/29187431 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180515 $b ABA008
991    __
$a 20180515104149 $b ABA008
999    __
$a ok $b bmc $g 1299842 $s 1013058
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2017 $b 37 $c 12 $d 6563-6574 $i 1791-7530 $m Anticancer research $n Anticancer Res $x MED00000478
LZP    __
$a Pubmed-20180515

Find record

Citation metrics

Loading data ...

Archiving options

Loading data ...