Perioperative blood transfusion does not affect recurrence-free and overall survivals after curative resection for intrahepatic cholangiocarcinoma: a propensity score matching analysis
Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined. Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We con...
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Published in | BMC cancer Vol. 17; no. 1; pp. 762 - 11 |
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Abstract | Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined.
Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT.
After exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 ± 0.104 vs. 0.479 ± 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446-2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221-2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 ± 0.117 VS. 0.193 ± 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756-1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608-1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection.
The present study found that PBT did not affect DFS and OS after curative resection of ICC. |
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AbstractList | Abstract Background Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined. Methods Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT. Results After exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 ± 0.104 vs. 0.479 ± 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446–2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221–2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 ± 0.117 VS. 0.193 ± 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756–1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608–1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection. Conclusions The present study found that PBT did not affect DFS and OS after curative resection of ICC. Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined. Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT. After exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 [+ or -] 0.104 vs. 0.479 [+ or -] 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446-2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221-2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 [+ or -] 0.117 VS. 0.193 [+ or -] 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756-1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608-1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection. The present study found that PBT did not affect DFS and OS after curative resection of ICC. Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined.BACKGROUNDWhether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined.Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT.METHODSOf the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT.After exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 ± 0.104 vs. 0.479 ± 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446-2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221-2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 ± 0.117 VS. 0.193 ± 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756-1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608-1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection.RESULTSAfter exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 ± 0.104 vs. 0.479 ± 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446-2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221-2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 ± 0.117 VS. 0.193 ± 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756-1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608-1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection.The present study found that PBT did not affect DFS and OS after curative resection of ICC.CONCLUSIONSThe present study found that PBT did not affect DFS and OS after curative resection of ICC. Background Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined. Methods Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT. Results After exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 [+ or -] 0.104 vs. 0.479 [+ or -] 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446-2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221-2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 [+ or -] 0.117 VS. 0.193 [+ or -] 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756-1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608-1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection. Conclusions The present study found that PBT did not affect DFS and OS after curative resection of ICC. Keywords: Intrahepatic cholangiocarcinoma, Hepatectomy, Perioperative blood transfusion, Overall survival, Disease-free survival Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative resection remains undetermined. Of the 605 patients who underwent curative liver resection for ICC between 2000 and 2012, 93 received PBT. We conducted Cox regression and variable selection logistic regression analyses to identify confounding factors of PBT. Propensity score matching (PSM) and Cox regression analyses were used to compare the overall survival (OS) and disease-free survival (DFS) between the patients with or without PBT. After exclusion, 93 eligible patients (15.4%) received PBT, compared with 512 (84.6%) who did not receive PBT; the groups were highly biased in terms of the propensity score (PS) analysis (0.096 ± 0.104 vs. 0.479 ± 0.372, p < 0.001). PBT was associated with an increased risk of OS (HR: 1.889, 95% CI: 1.446-2.468, p < 0.001) and DFS (HR: 1.589, 95% CI: 1.221-2.067, p < 0.001) in the entire cohort. After propensity score matching (PSM), no bias was observed between the groups (PS,0.136 ± 0.117 VS. 0.193 ± 0.167, p = 0.785). In the multivariate Cox analysis, PBT was not associated with increased risks of OS (HR: 1.172, 95% CI: 0.756-1.816, p = 0.479) and DFS (HR: 0.944, 95% CI: 0.608-1.466, p = 0.799). After propensity score adjustment, PBT was still not associated with OS or DFS after ICC curative resection. The present study found that PBT did not affect DFS and OS after curative resection of ICC. |
ArticleNumber | 762 |
Audience | Academic |
Author | Zhou, Jian Jiang, Xi-Fei Fan, Jia Liu, Wei-Ren Tang, Zheng Tao, Chen-Yang Dai, Zhi Qiu, Shuang-Jian Shi, Ying-Hong Zhou, Pei-Yun Peng, Yuan-Fei Jin, Lei Tian, Meng-Xin Wang, Han Ding, Zhen-Bin |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29137600$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1186_s12876_019_1109_7 crossref_primary_10_3389_fonc_2021_585808 crossref_primary_10_1007_s00595_020_02192_3 crossref_primary_10_1007_s40140_018_0292_3 crossref_primary_10_1007_s12020_018_1724_z crossref_primary_10_1002_ags3_12266 crossref_primary_10_1016_j_surg_2020_04_015 crossref_primary_10_1038_s41598_024_85020_9 crossref_primary_10_1097_MPA_0000000000001997 |
Cites_doi | 10.1245/s10434-013-3226-9 10.1198/jbes.2009.07333 10.1097/SLA.0b013e318287ab4d 10.3322/caac.21338 10.1007/s00595-017-1553-3 10.3348/kjr.2015.16.2.286 10.1016/j.jhep.2015.10.012 10.1245/s10434-015-4823-6 10.1111/resp.12312 10.1016/0197-2456(90)90005-M 10.1097/00000658-200210000-00001 10.3322/caac.21332 10.5732/cjc.013.10027 10.1097/SLA.0000000000001486 10.1016/S0197-2456(98)00037-3 10.1155/2016/6470857 10.1016/j.amjmed.2013.09.017 10.1097/SLA.0b013e31825b35d5 10.3322/caac.21335 10.1007/s11605-014-2741-8 10.1111/1468-0262.00270 10.1159/000103656 10.1016/j.jamcollsurg.2013.05.021 10.1136/gut.2009.194217 10.1053/j.gastro.2013.10.013 10.1111/jgs.14253 |
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Keywords | Overall survival Disease-free survival Intrahepatic cholangiocarcinoma Hepatectomy Perioperative blood transfusion |
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References | WR Jarnagin (3745_CR23) 2002; 236 A Abadie (3745_CR17) 2011; 29 R Warschkow (3745_CR11) 2014; 259 RL Siegel (3745_CR4) 2016; 66 SA Müller (3745_CR9) 2014; 21 S Baek (3745_CR27) 2015; 16 3745_CR20 N Kimura (3745_CR8) 2015; 19 RM Dodson (3745_CR2) 2013; 217 AG Acheson (3745_CR25) 2012; 256 3745_CR26 EJ Williamson (3745_CR18) 2014; 19 A Abadie (3745_CR15) 2002; 70 SR Salpeter (3745_CR14) 2014; 127 3745_CR6 WD Dupont (3745_CR21) 1990; 11 DH Kim (3745_CR19) 2016; 64 WD Dupont (3745_CR22) 1998; 19 F Mirici-Cappa (3745_CR16) 2010; 59 S Han (3745_CR24) 2016; 264 W Chen (3745_CR3) 2016; 66 3745_CR13 3745_CR10 LA Torre (3745_CR1) 2016; 66 W Chen (3745_CR5) 2013; 32 MN Mavros (3745_CR7) 2015; 22 T Yang (3745_CR12) 2016; 64 |
References_xml | – volume: 21 start-page: 155 issue: 1 year: 2014 ident: 3745_CR9 publication-title: Ann Surg Oncol doi: 10.1245/s10434-013-3226-9 – volume: 29 start-page: 1 issue: 1 year: 2011 ident: 3745_CR17 publication-title: J Bus Econ Stat doi: 10.1198/jbes.2009.07333 – volume: 259 start-page: 131 issue: 1 year: 2014 ident: 3745_CR11 publication-title: Ann Surg doi: 10.1097/SLA.0b013e318287ab4d – volume: 66 start-page: 115 issue: 2 year: 2016 ident: 3745_CR3 publication-title: CA Cancer J Clin doi: 10.3322/caac.21338 – ident: 3745_CR26 doi: 10.1007/s00595-017-1553-3 – volume: 16 start-page: 286 issue: 2 year: 2015 ident: 3745_CR27 publication-title: Korean Soc Radiol doi: 10.3348/kjr.2015.16.2.286 – volume: 64 start-page: 583 year: 2016 ident: 3745_CR12 publication-title: J Hepatol doi: 10.1016/j.jhep.2015.10.012 – volume: 22 start-page: 4382 issue: 13 year: 2015 ident: 3745_CR7 publication-title: Ann Surg Oncol doi: 10.1245/s10434-015-4823-6 – volume: 19 start-page: 625 issue: 5 year: 2014 ident: 3745_CR18 publication-title: Respirology doi: 10.1111/resp.12312 – volume: 11 start-page: 116 issue: 2 year: 1990 ident: 3745_CR21 publication-title: Control Clin Trials doi: 10.1016/0197-2456(90)90005-M – volume: 236 start-page: 397 issue: 4 year: 2002 ident: 3745_CR23 publication-title: Ann Surg doi: 10.1097/00000658-200210000-00001 – volume: 66 start-page: 7 issue: 1 year: 2016 ident: 3745_CR4 publication-title: CA Cancer J Clin doi: 10.3322/caac.21332 – volume: 32 start-page: 162 issue: 4 year: 2013 ident: 3745_CR5 publication-title: Chinese J Cancer doi: 10.5732/cjc.013.10027 – volume: 264 start-page: 339 issue: 2 year: 2016 ident: 3745_CR24 publication-title: Ann Surg doi: 10.1097/SLA.0000000000001486 – volume: 19 start-page: 589 issue: 6 year: 1998 ident: 3745_CR22 publication-title: Control Clin Trials doi: 10.1016/S0197-2456(98)00037-3 – ident: 3745_CR6 doi: 10.1155/2016/6470857 – volume: 127 start-page: 124 issue: 2 year: 2014 ident: 3745_CR14 publication-title: Am J Med doi: 10.1016/j.amjmed.2013.09.017 – volume: 256 start-page: 235 issue: 2 year: 2012 ident: 3745_CR25 publication-title: Ann Surg doi: 10.1097/SLA.0b013e31825b35d5 – volume: 66 start-page: 182 issue: 3 year: 2016 ident: 3745_CR1 publication-title: CA Cancer J Clin doi: 10.3322/caac.21335 – volume: 19 start-page: 866 issue: 5 year: 2015 ident: 3745_CR8 publication-title: J Gastrointest Surg doi: 10.1007/s11605-014-2741-8 – volume: 70 start-page: 91 issue: 1 year: 2002 ident: 3745_CR15 publication-title: Econometrica doi: 10.1111/1468-0262.00270 – ident: 3745_CR10 doi: 10.1159/000103656 – volume: 217 start-page: 736 issue: 4 year: 2013 ident: 3745_CR2 publication-title: J Am Coll Surgeons doi: 10.1016/j.jamcollsurg.2013.05.021 – volume: 59 start-page: 387 issue: 3 year: 2010 ident: 3745_CR16 publication-title: Gut doi: 10.1136/gut.2009.194217 – ident: 3745_CR20 – ident: 3745_CR13 doi: 10.1053/j.gastro.2013.10.013 – volume: 64 start-page: 2065 issue: 10 year: 2016 ident: 3745_CR19 publication-title: J Am Geriatr Soc doi: 10.1111/jgs.14253 |
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Snippet | Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after curative... Background Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients after... Abstract Background Whether perioperative blood transfusions (PBTs) adversely influence oncological outcomes for intrahepatic cholangiocarcinoma (ICC) patients... |
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StartPage | 762 |
SubjectTerms | Biliary tract cancer Blood transfusion Comparative analysis Disease-free survival Hepatectomy Intrahepatic cholangiocarcinoma Liver Overall survival Patient outcomes Perioperative blood transfusion Surgery |
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Title | Perioperative blood transfusion does not affect recurrence-free and overall survivals after curative resection for intrahepatic cholangiocarcinoma: a propensity score matching analysis |
URI | https://www.ncbi.nlm.nih.gov/pubmed/29137600 https://www.proquest.com/docview/1964702971 https://pubmed.ncbi.nlm.nih.gov/PMC5686939 https://doaj.org/article/8bd731dbf34649f69f0771c497be8ce2 |
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