Pub Date : 2026-04-01Epub Date: 2025-09-01DOI: 10.1097/SLA.0000000000006916
Shahin Ayazi, John C Lipham, Brian E Louie
{"title":"Why the BOSS Trial Falls Short of Guiding Clinical Practice in Barrett's Esophagus.","authors":"Shahin Ayazi, John C Lipham, Brian E Louie","doi":"10.1097/SLA.0000000000006916","DOIUrl":"10.1097/SLA.0000000000006916","url":null,"abstract":"","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":" ","pages":"562-563"},"PeriodicalIF":6.4,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978727/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144939802","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2025-09-25DOI: 10.1097/SLA.0000000000006955
Caitlin J Cain-Trivette
{"title":"How She Was Born.","authors":"Caitlin J Cain-Trivette","doi":"10.1097/SLA.0000000000006955","DOIUrl":"10.1097/SLA.0000000000006955","url":null,"abstract":"","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":" ","pages":"567-568"},"PeriodicalIF":6.4,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145136329","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2024-07-23DOI: 10.1097/SLA.0000000000006449
Aurélien Lambert, Julia Salleron, Alexandre Harlé, James J Biagi, Agnès Leroux, Jacques Thomas, Laure Monard, Jérôme Cros, Frédéric Marchal, Ahmet Ayav, Thierry Conroy
Objective: To investigate the correlation between positive resection margins and outcomes in patients with pancreatic ductal adenocarcinoma who underwent surgery and adjuvant chemotherapy according to the pivotal trial PRODIGE 24-CCTG PA-6.
Background: The primary focus is on elucidating the prognostic significance of specific resection margins, including those associated with the superior-mesenteric vein, medial, and posterior pancreas.
Methods: The analysis involved 400 patients across multiple centers in France and Canada. Surgical resection and subsequent adjuvant chemotherapy were core interventions. This study assessed the prognostic impact of resection margins, highlighting the significance of standardized pathology assessments. In addition, the influence of chemotherapy regimen choice, comparing gemcitabine to mFOLFIRINOX, on the implications of positive resection margins was examined.
Results: Only 3 margins, superior-mesenteric vein [hazard ratio (HR) = 1.48 (95% CI: 1.11; 1.96); P < 0.001], medial [HR = 1.92 (95% CI: 1.36; 2.73); P < 0.001] and posterior [HR = 1.65 (95% CI: 1.21; 2.24); P = 0.002], had a significant prognostic impact on disease-free survival and were sufficient compared with the 7 recommended margins (Kappa = 0.90; 95% CI: 0.87; 0.94). R1 status was a significant independent prognostic factor for poorer survival in gemcitabine-treated patients [HR = 1.97 (95% CI: 1.23; 3.16); P = 0.005] but lost its significance with mFOLFIRINOX [HR = 1.46 (95% CI: 0.91; 2.35); P = 0.114].
Conclusions: All efforts should be made to evaluate the 3 margins of the highest prognostic value, with the others being secondary. A key finding of this study is the likely effect of mFOLFIRINOX on local invasion in operated patients, which seems to correct the impairment related to margin involvement, probably explaining the improvements in disease-free survival and overall survival.
研究目的本研究调查了根据关键性试验 PRODIGE 24-CCTG PA-6 接受手术和辅助化疗的胰腺导管腺癌患者的阳性切除边缘与预后之间的相关性:主要重点是阐明特定切除边缘的预后意义,包括与肠系膜上静脉(SMV)、胰腺内侧和后方相关的切除边缘:分析涉及法国和加拿大多个中心的 400 名患者。手术切除和随后的辅助化疗是核心干预措施。该研究评估了切除边缘对预后的影响,强调了标准化病理评估的重要性。此外,研究还比较了吉西他滨和 mFOLFIRINOX 化疗方案的选择对阳性切除边缘的影响:结果:只有三个切缘为SMV(HR=1.48 95% CI [1.11;1.96],PC结论:应竭尽全力评估预后价值最高的三个切缘,其他切缘应作为次要切缘。本研究的一个重要发现是 mFOLFIRINOX 可能会对手术患者的局部浸润产生影响,这似乎纠正了与边缘受累相关的损害,可能是 DFS 和 OS 改善的原因。
{"title":"Impact of Positive Resection Margins on Recurrence and Survival After Resection and Adjuvant Chemotherapy in Pancreatic Cancer: Results of the PRODIGE 24-CCTG PA-6 Randomized Controlled Trial.","authors":"Aurélien Lambert, Julia Salleron, Alexandre Harlé, James J Biagi, Agnès Leroux, Jacques Thomas, Laure Monard, Jérôme Cros, Frédéric Marchal, Ahmet Ayav, Thierry Conroy","doi":"10.1097/SLA.0000000000006449","DOIUrl":"10.1097/SLA.0000000000006449","url":null,"abstract":"<p><strong>Objective: </strong>To investigate the correlation between positive resection margins and outcomes in patients with pancreatic ductal adenocarcinoma who underwent surgery and adjuvant chemotherapy according to the pivotal trial PRODIGE 24-CCTG PA-6.</p><p><strong>Background: </strong>The primary focus is on elucidating the prognostic significance of specific resection margins, including those associated with the superior-mesenteric vein, medial, and posterior pancreas.</p><p><strong>Methods: </strong>The analysis involved 400 patients across multiple centers in France and Canada. Surgical resection and subsequent adjuvant chemotherapy were core interventions. This study assessed the prognostic impact of resection margins, highlighting the significance of standardized pathology assessments. In addition, the influence of chemotherapy regimen choice, comparing gemcitabine to mFOLFIRINOX, on the implications of positive resection margins was examined.</p><p><strong>Results: </strong>Only 3 margins, superior-mesenteric vein [hazard ratio (HR) = 1.48 (95% CI: 1.11; 1.96); P < 0.001], medial [HR = 1.92 (95% CI: 1.36; 2.73); P < 0.001] and posterior [HR = 1.65 (95% CI: 1.21; 2.24); P = 0.002], had a significant prognostic impact on disease-free survival and were sufficient compared with the 7 recommended margins (Kappa = 0.90; 95% CI: 0.87; 0.94). R1 status was a significant independent prognostic factor for poorer survival in gemcitabine-treated patients [HR = 1.97 (95% CI: 1.23; 3.16); P = 0.005] but lost its significance with mFOLFIRINOX [HR = 1.46 (95% CI: 0.91; 2.35); P = 0.114].</p><p><strong>Conclusions: </strong>All efforts should be made to evaluate the 3 margins of the highest prognostic value, with the others being secondary. A key finding of this study is the likely effect of mFOLFIRINOX on local invasion in operated patients, which seems to correct the impairment related to margin involvement, probably explaining the improvements in disease-free survival and overall survival.</p>","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":" ","pages":"651-658"},"PeriodicalIF":6.4,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141747258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2025-09-03DOI: 10.1097/SLA.0000000000006930
Syed Shahyan Bakhtiyar
{"title":"Leadership in Surgery: Insights From the Helm of Academic Medicine.","authors":"Syed Shahyan Bakhtiyar","doi":"10.1097/SLA.0000000000006930","DOIUrl":"10.1097/SLA.0000000000006930","url":null,"abstract":"","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":" ","pages":"564-566"},"PeriodicalIF":6.4,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144939862","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-04-01Epub Date: 2024-09-06DOI: 10.1097/SLA.0000000000006527
Rudolf van den Berg, Louis Matthijs van den Dop, Lucas Timmermans, Michiel van den Berg, Robert E G J M Pierik, Willem A R Zwaans, Daniel Reim, Steven E Buijk, Jerome P van Brussel, Johan F Lange, Johannes J Jeekel, Pieter J Tanis
Objective: To evaluate all mesh-related problems during reoperations after mesh reinforcement of the abdominal wall 15 years after the start of the PRIMA trial.
Background: Prophylactic mesh reinforcement during closure of a midline laparotomy has proven to reduce the incidence of incisional hernia, especially in high-risk patients, but long-term mesh-related morbidity is largely unknown.
Methods: Patients receiving a prophylactic onlay or retrorectus mesh in the PRIMA trial between 2009 and 2012 were included on an as-treated basis from participating centers that made reoperation notes available. The main outcomes were the incidences of complications requiring mesh explantation, mesh-related ileus, and mesh-related problems during laparotomy for other diagnoses.
Results: Out of 373 patients randomized to prophylactic mesh reinforcement, 242 were included: 127 with onlay and 115 patients with retrorectus mesh. Median follow-up is 27 months (interquartile range: 12-78). Thirty-four patients underwent reoperation for any reason during the entire follow-up, 22 after onlay (17.3%), and 12 after retrorectus mesh (10.4%). The reoperation rate for complications that required mesh explantation was 4/127 (3.1%) after onlay and 0/115 (0%) after retrorectus mesh. Mesh-related ileus occurred in none of the onlay group, and 3/115 (2.6%) in the retrorectus group. During subsequent laparotomies for other primary diagnoses, adhesions to the mesh were noted in 3/10 patients in the onlay group and 1/5 patients in the retrorectus group. Overall, the mesh was removed in 10/127 (7.9%) in the onlay group and 7/115 (6.1%) patients in the retrorectus group.
Conclusions: In high-risk patients receiving a prophylactic mesh during midline laparotomy closure, low incidences of mesh-related complications requiring reoperation and mesh-related problems during unrelated subsequent laparotomies were found, for both the onlay and retrorectus techniques.
{"title":"Prophylactic Mesh-related Reoperations and Mesh-related Problems During Subsequent Relaparotomies: Long-term Results From the PRIMA Trial.","authors":"Rudolf van den Berg, Louis Matthijs van den Dop, Lucas Timmermans, Michiel van den Berg, Robert E G J M Pierik, Willem A R Zwaans, Daniel Reim, Steven E Buijk, Jerome P van Brussel, Johan F Lange, Johannes J Jeekel, Pieter J Tanis","doi":"10.1097/SLA.0000000000006527","DOIUrl":"10.1097/SLA.0000000000006527","url":null,"abstract":"<p><strong>Objective: </strong>To evaluate all mesh-related problems during reoperations after mesh reinforcement of the abdominal wall 15 years after the start of the PRIMA trial.</p><p><strong>Background: </strong>Prophylactic mesh reinforcement during closure of a midline laparotomy has proven to reduce the incidence of incisional hernia, especially in high-risk patients, but long-term mesh-related morbidity is largely unknown.</p><p><strong>Methods: </strong>Patients receiving a prophylactic onlay or retrorectus mesh in the PRIMA trial between 2009 and 2012 were included on an as-treated basis from participating centers that made reoperation notes available. The main outcomes were the incidences of complications requiring mesh explantation, mesh-related ileus, and mesh-related problems during laparotomy for other diagnoses.</p><p><strong>Results: </strong>Out of 373 patients randomized to prophylactic mesh reinforcement, 242 were included: 127 with onlay and 115 patients with retrorectus mesh. Median follow-up is 27 months (interquartile range: 12-78). Thirty-four patients underwent reoperation for any reason during the entire follow-up, 22 after onlay (17.3%), and 12 after retrorectus mesh (10.4%). The reoperation rate for complications that required mesh explantation was 4/127 (3.1%) after onlay and 0/115 (0%) after retrorectus mesh. Mesh-related ileus occurred in none of the onlay group, and 3/115 (2.6%) in the retrorectus group. During subsequent laparotomies for other primary diagnoses, adhesions to the mesh were noted in 3/10 patients in the onlay group and 1/5 patients in the retrorectus group. Overall, the mesh was removed in 10/127 (7.9%) in the onlay group and 7/115 (6.1%) patients in the retrorectus group.</p><p><strong>Conclusions: </strong>In high-risk patients receiving a prophylactic mesh during midline laparotomy closure, low incidences of mesh-related complications requiring reoperation and mesh-related problems during unrelated subsequent laparotomies were found, for both the onlay and retrorectus techniques.</p>","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":" ","pages":"642-650"},"PeriodicalIF":6.4,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12978706/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142139067","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-18DOI: 10.1097/sla.0000000000007050
Christina L Roland
{"title":"Not all Sarcomas are Created Equal: Getting it Right the First-Time Matters.","authors":"Christina L Roland","doi":"10.1097/sla.0000000000007050","DOIUrl":"https://doi.org/10.1097/sla.0000000000007050","url":null,"abstract":"","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":"50 1","pages":""},"PeriodicalIF":9.0,"publicationDate":"2026-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147471446","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
OBJECTIVEWe evaluated the prognostic significance and implications of a major pathologic response (MPR) after preoperative treatment for pancreatic ductal adenocarcinoma (PDAC).SUMMARY BACKGROUND DATAPreoperative treatment is increasingly used for PDAC to improve oncologic outcomes. The pathologic response represents a potential indicator of treatment efficacy; however, its prognostic value in PDAC remains unclear.METHODSWe retrospectively analyzed 739 patients who underwent pancreatectomy for PDAC after preoperative treatment at 21 institutions in Japan. The pathologic response was graded using Evans' classification, with MPR defined as Evans grade III/IV. Survival outcomes and prognostic factors were evaluated, and factors associated with achieving MPR were analyzed to develop a predictive model.RESULTSMPR was achieved in 11.5% of patients. The MPR group had a significantly longer median overall survival (71.5 vs. 40.9 mo) and recurrence-free survival (55.5 vs. 15.2 mo) than the non-MPR group. Multivariate analysis identified MPR as an independent prognostic factor for overall survival. In the MPR subgroup, neither overall nor recurrence-free survival differed according to adjuvant chemotherapy administration; multivariate analysis did not identify adjuvant therapy as an independent prognostic factor. Predictive factors for achieving MPR included chemoradiotherapy, preoperative duration ≥6 months, normal carbohydrate antigen 19-9 after preoperative treatment, and complete or partial radiologic response. Finally, we developed a simplified predictive model for achieving MPR.CONCLUSIONSMPR was independently associated with favorable survival in PDAC. The prognostic impact of adjuvant chemotherapy was not observed among patients who achieved MPR, suggesting that MPR may inform individualized postoperative management and warrants prospective validation.
{"title":"Prognostic Impact of Major Pathologic Response After Preoperative Treatment in Resected Pancreatic Ductal Adenocarcinoma: A Multi-Institutional Retrospective Study of 739 Cases.","authors":"Kei Yamane,Kazuyuki Nagai,Takayuki Anazawa,Yosuke Kasai,Asahi Sato,Yu Hidaka,Yumiko Ibi,Toshihiko Masui,Yuichiro Uchida,Kazuhiko Kitaguchi,Shintaro Yagi,Yusuke Okamura,Takafumi Machimoto,Kohta Iguchi,Toshiyuki Hata,Masato Narita,Kentaro Yasuchika,Koji Doi,Akira Mori,Koji Kitamura,Kenya Yamanaka,Takashi Komatsubara,Yusuke Uemoto,Yukihiro Okuda,Naoya Sasaki,Kunihiko Tsuboi,Rei Toda,Etsuro Hatano","doi":"10.1097/sla.0000000000007052","DOIUrl":"https://doi.org/10.1097/sla.0000000000007052","url":null,"abstract":"OBJECTIVEWe evaluated the prognostic significance and implications of a major pathologic response (MPR) after preoperative treatment for pancreatic ductal adenocarcinoma (PDAC).SUMMARY BACKGROUND DATAPreoperative treatment is increasingly used for PDAC to improve oncologic outcomes. The pathologic response represents a potential indicator of treatment efficacy; however, its prognostic value in PDAC remains unclear.METHODSWe retrospectively analyzed 739 patients who underwent pancreatectomy for PDAC after preoperative treatment at 21 institutions in Japan. The pathologic response was graded using Evans' classification, with MPR defined as Evans grade III/IV. Survival outcomes and prognostic factors were evaluated, and factors associated with achieving MPR were analyzed to develop a predictive model.RESULTSMPR was achieved in 11.5% of patients. The MPR group had a significantly longer median overall survival (71.5 vs. 40.9 mo) and recurrence-free survival (55.5 vs. 15.2 mo) than the non-MPR group. Multivariate analysis identified MPR as an independent prognostic factor for overall survival. In the MPR subgroup, neither overall nor recurrence-free survival differed according to adjuvant chemotherapy administration; multivariate analysis did not identify adjuvant therapy as an independent prognostic factor. Predictive factors for achieving MPR included chemoradiotherapy, preoperative duration ≥6 months, normal carbohydrate antigen 19-9 after preoperative treatment, and complete or partial radiologic response. Finally, we developed a simplified predictive model for achieving MPR.CONCLUSIONSMPR was independently associated with favorable survival in PDAC. The prognostic impact of adjuvant chemotherapy was not observed among patients who achieved MPR, suggesting that MPR may inform individualized postoperative management and warrants prospective validation.","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":"12 1","pages":""},"PeriodicalIF":9.0,"publicationDate":"2026-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147471478","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-10DOI: 10.1097/sla.0000000000007049
David Simon,Michael K Paasche-Orlow,Hooman Noorchashm
{"title":"How FDA Device Regulation Shapes Medical (Mal)Practice.","authors":"David Simon,Michael K Paasche-Orlow,Hooman Noorchashm","doi":"10.1097/sla.0000000000007049","DOIUrl":"https://doi.org/10.1097/sla.0000000000007049","url":null,"abstract":"","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":"193 1","pages":""},"PeriodicalIF":9.0,"publicationDate":"2026-03-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147381281","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-03-09DOI: 10.1097/sla.0000000000007046
Jordan Nantais,Refik Saskin,Andrew Calzavara,Joseph Kim,David Gomez,Nancy N Baxter
OBJECTIVEWe aimed to determine if treatment at non-transplant centers was associated with worse outcomes for patients with solid-organ transplants and an emergency general surgery condition.SUMMARY BACKGROUND DATAEmergency general surgery diagnoses are common and hazardous in patients with solid-organ transplants. The ideal hospital for their treatment is controversial.METHODSWe performed a retrospective population-based cohort study using linked administrative data in Ontario, Canada. Adults with a solid-organ transplant and emergency general surgery condition hospitalized April 1, 2002-December 31, 2021 were included. Treatment at a transplant center was compared to other center types. The primary outcome was 30-day mortality. Secondary outcomes included 90-day mortality, a composite of 30-day complications or mortality, and 30-day readmission. Adjusted analyses used multivariable logistic regression with generalized estimating equations accounting for repeat events.RESULTSAmongst 2,679 hospitalizations in this population, 111 (4%) died at 30-days and 821 (31%) suffered complications or mortality. The adjusted association between 30-day mortality and center depended on transplant type and was higher at academic centers compared to transplant centers (aOR 3.52, 95%CI:1.43-8.65, p=0.006) for patients with kidney transplants. There was no association between center and mortality for non-kidney transplants. Regardless of transplant type, the composite of complications or mortality was significantly higher for most center types compared to transplant centers.CONCLUSIONSNon-transplant centers were associated with higher mortality for patients with kidney transplants, and our composite measure was increased in non-transplant centers for all organs. Emergency general surgery care for these groups should be preferentially offered at transplant centers.
{"title":"Transplant Center Treatment in Emergency General Surgery Patients with a Solid-Organ Transplant.","authors":"Jordan Nantais,Refik Saskin,Andrew Calzavara,Joseph Kim,David Gomez,Nancy N Baxter","doi":"10.1097/sla.0000000000007046","DOIUrl":"https://doi.org/10.1097/sla.0000000000007046","url":null,"abstract":"OBJECTIVEWe aimed to determine if treatment at non-transplant centers was associated with worse outcomes for patients with solid-organ transplants and an emergency general surgery condition.SUMMARY BACKGROUND DATAEmergency general surgery diagnoses are common and hazardous in patients with solid-organ transplants. The ideal hospital for their treatment is controversial.METHODSWe performed a retrospective population-based cohort study using linked administrative data in Ontario, Canada. Adults with a solid-organ transplant and emergency general surgery condition hospitalized April 1, 2002-December 31, 2021 were included. Treatment at a transplant center was compared to other center types. The primary outcome was 30-day mortality. Secondary outcomes included 90-day mortality, a composite of 30-day complications or mortality, and 30-day readmission. Adjusted analyses used multivariable logistic regression with generalized estimating equations accounting for repeat events.RESULTSAmongst 2,679 hospitalizations in this population, 111 (4%) died at 30-days and 821 (31%) suffered complications or mortality. The adjusted association between 30-day mortality and center depended on transplant type and was higher at academic centers compared to transplant centers (aOR 3.52, 95%CI:1.43-8.65, p=0.006) for patients with kidney transplants. There was no association between center and mortality for non-kidney transplants. Regardless of transplant type, the composite of complications or mortality was significantly higher for most center types compared to transplant centers.CONCLUSIONSNon-transplant centers were associated with higher mortality for patients with kidney transplants, and our composite measure was increased in non-transplant centers for all organs. Emergency general surgery care for these groups should be preferentially offered at transplant centers.","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":"85 1","pages":""},"PeriodicalIF":9.0,"publicationDate":"2026-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147373892","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: Complications after esophagectomy are associated with poor long-term outcomes; however, the prognostic impacts of postoperative complications in patients receiving intensive neoadjuvant chemotherapy remain unclear. This study aimed to investigate the association between postoperative complications and the prognosis of patients receiving intensive neoadjuvant treatment.
Summary background data: This study is a supplementary analysis of JCOG1109, which is a phase III randomized trial that assessed the efficacy of neoadjuvant doublet chemotherapy (cisplatin plus 5-fluorouracil [CF]), triplet chemotherapy (docetaxel plus cisplatin plus 5-FU [DCF]), and chemoradiotherapy (radiation with CF [CF-RT]) in patients with locally advanced esophageal cancer.
Methods: Patients were randomly assigned to one of the three preoperative therapies, followed by open esophagectomy (OE) or thoracoscopic esophagectomy (TE) with regional lymphadenectomy. Postoperative complications (Grade ≥2) and their impacts on overall survival (OS) and progression-free survival (PFS) were assessed within each arm.
Results: A total of 601 patients were randomized (CF/DCF/CF-RT: 199/202/200) and 541 underwent esophagectomy (CF/DCF/CF-RT: 183/181/177) between 2012 and 2018. Postoperative complications, including pneumonia, anastomotic leakage, recurrent laryngeal nerve paralysis, and infectious complications, exhibited no significant impact on OS in any treatment arm. TE introduction appeared to attenuate the prognostic impact of complications: hazard ratios for OS shifted from 1.557 to 0.802, from 1.151 to 0.703, and from 1.548 to 1.186 in the CF, DCF, and CF-RT arms, when comparing OE with TE, respectively.
Conclusion: In this exploratory analysis of JCOG1109, postoperative complications were not significantly associated with prognosis. Minimally invasive esophagectomy, such as TE and intensified neoadjuvant therapy, may reduce the negative prognostic impact of complications.
{"title":"Prognostic Impact of Postoperative Complications After Neoadjuvant Therapy Followed by Esophagectomy for Esophageal Cancer: An Exploratory Analysis of Phase III Trial JCOG1109.","authors":"Eisuke Booka, Ken Kato, Yoshinori Ito, Hiroyuki Daiko, Kazuo Koyanagi, Miho Yamamoto, Takashi Ogata, Takashi Fukuda, Takeo Fujita, Tetsuya Abe, Masanobu Takahashi, Masayuki Watanabe, Hiroshi Ichikawa, Jun Hihara, Mitsuro Kanda, Yoichi Hamai, Takahiro Tsushima, Ryunosuke Machida, Keita Sasaki, Hiroya Takeuchi","doi":"10.1097/SLA.0000000000007045","DOIUrl":"https://doi.org/10.1097/SLA.0000000000007045","url":null,"abstract":"<p><strong>Objective: </strong>Complications after esophagectomy are associated with poor long-term outcomes; however, the prognostic impacts of postoperative complications in patients receiving intensive neoadjuvant chemotherapy remain unclear. This study aimed to investigate the association between postoperative complications and the prognosis of patients receiving intensive neoadjuvant treatment.</p><p><strong>Summary background data: </strong>This study is a supplementary analysis of JCOG1109, which is a phase III randomized trial that assessed the efficacy of neoadjuvant doublet chemotherapy (cisplatin plus 5-fluorouracil [CF]), triplet chemotherapy (docetaxel plus cisplatin plus 5-FU [DCF]), and chemoradiotherapy (radiation with CF [CF-RT]) in patients with locally advanced esophageal cancer.</p><p><strong>Methods: </strong>Patients were randomly assigned to one of the three preoperative therapies, followed by open esophagectomy (OE) or thoracoscopic esophagectomy (TE) with regional lymphadenectomy. Postoperative complications (Grade ≥2) and their impacts on overall survival (OS) and progression-free survival (PFS) were assessed within each arm.</p><p><strong>Results: </strong>A total of 601 patients were randomized (CF/DCF/CF-RT: 199/202/200) and 541 underwent esophagectomy (CF/DCF/CF-RT: 183/181/177) between 2012 and 2018. Postoperative complications, including pneumonia, anastomotic leakage, recurrent laryngeal nerve paralysis, and infectious complications, exhibited no significant impact on OS in any treatment arm. TE introduction appeared to attenuate the prognostic impact of complications: hazard ratios for OS shifted from 1.557 to 0.802, from 1.151 to 0.703, and from 1.548 to 1.186 in the CF, DCF, and CF-RT arms, when comparing OE with TE, respectively.</p><p><strong>Conclusion: </strong>In this exploratory analysis of JCOG1109, postoperative complications were not significantly associated with prognosis. Minimally invasive esophagectomy, such as TE and intensified neoadjuvant therapy, may reduce the negative prognostic impact of complications.</p>","PeriodicalId":8017,"journal":{"name":"Annals of surgery","volume":" ","pages":""},"PeriodicalIF":6.4,"publicationDate":"2026-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147363762","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}