Sarcopenia as a predictor of poor surgical and oncologic outcomes after abdominal surgery for digestive tract cancer: A prospective cohort study

2019 ◽  
Vol 38 (6) ◽  
pp. 2881-2888 ◽  
Author(s):  
Shuze Zhang ◽  
Shanjun Tan ◽  
Yi Jiang ◽  
Qiulei Xi ◽  
Qingyang Meng ◽  
...  
2014 ◽  
Vol 26 (2) ◽  
pp. 297-301 ◽  
Author(s):  
Harindra Jayasekara ◽  
Robert J. MacInnis ◽  
Allison M. Hodge ◽  
John L. Hopper ◽  
Graham G. Giles ◽  
...  

BMJ Open ◽  
2014 ◽  
Vol 4 (10) ◽  
pp. e006239 ◽  
Author(s):  
Aneel Bhangu ◽  
J Edward Fitzgerald ◽  
Stuart Fergusson ◽  
Chetan Khatri ◽  
Hampus Holmer ◽  
...  

IntroductionEmergency abdominal surgery outcomes represent an internationally important marker of healthcare quality and capacity. In this study, a novel approach to investigating global surgical outcomes is proposed, involving collaborative methodology using ‘snapshot’ clinical data collection over a 2-week period. The primary aim is to identify internationally relevant, modifiable surgical practices (in terms of modifiable process, equipment and clinical management) associated with best care for emergency abdominal surgery.Methods and analysisThis is a multicentre, international, prospective cohort study. Any hospital in the world performing acute surgery can participate, and any patient undergoing emergency intraperitoneal surgery is eligible to enter the study. Centres will collect observational data on patients for a 14-day period during a 5-month window and required data points will be limited to ensure practicality for collaborators collecting data. The primary outcome measure is the 24 h perioperative mortality, with 30-day perioperative mortality as a secondary outcome measure. During registration, participants will undertake a survey of available resources and capacity based on the WHO Tool for Situational Analysis.Ethics and disseminationThe study will not affect clinical care and has therefore been classified as an audit by the South East Scotland Research Ethics Service in Edinburgh, Scotland. Baseline outcome measurement in relation to emergency abdominal surgery has not yet been undertaken at an international level and will provide a useful indicator of surgical capacity and the modifiable factors that influence this. This novel methodological approach will facilitate delivery of a multicentre study at a global level, in addition to building international audit and research capacity.Trial registration numberThe study has been registered with ClinicalTrials.gov (Identifier: NCT02179112).


2018 ◽  
Vol 61 (1) ◽  
pp. 42-49 ◽  
Author(s):  
Line Rokkedal Jønsson ◽  
Lina Holm Ingelsrud ◽  
Line Toft Tengberg ◽  
Thomas Bandholm ◽  
Nicolai Bang Foss ◽  
...  

2019 ◽  
Vol 37 (15_suppl) ◽  
pp. 4082-4082 ◽  
Author(s):  
Junho Kang ◽  
Changhoon Yoo ◽  
Jae Ho Jeong ◽  
Boyeong Kang ◽  
YunJin Hong ◽  
...  

4082 Background: For patients with advanced BTC, standard chemotherapy has limited benefit and no molecular targeted agents have been approved. Pembrolizumab is an anti PD-1 immune checkpoint inhibitor which has shown modest activity for advanced BTC patients in prior single-arm phase I/II studies. Considering the heterogeneity of BTC, more data are needed to evaluate the clinical outcomes of pembrolizumab in unresectable or metastatic BTC. Methods: In this prospective cohort study, 39 patients with PD-L1 positive BTC who received pembrolizumab in Asan Medical Center, Seoul, Korea were included (ClinicalTrials.gov identifier, NCT03695952). PD-L1 expression was assessed using immunohistochemistry and PD-L1 positive tumors were defined as the expression of PD-L1 in ≥ 1% of tumor cells. Pembrolizumab was given at a fixed dose of 200 mg intravenously, every 3 weeks. Results: The median age was 61 years old (range, 41-76) and 22 (56.4%) patients were male. Intrahepatic cholangiocarcinoma (CCA) was the most common type (n = 18, 46.2%), followed by gallbladder cancer (n = 12, 30.8%) and extrahepatic CCA (n = 9, 23.1%). Most of the patients had distant metastasis (n = 37, 94.9%). Pembrolizumab was administered as 2nd-, 3rd- and 4th or greater line chemotherapy in 18 (46.2%), 16 (41.0%) and 5 (12.8%) patients, respectively, and median 2 cycles (range 1-10) of pembrolizumab were given. In 36 patients whose response was assessable, partial response (PR) and stable disease were achieved in 4 (11.1%) and 13 (36.1%), respectively. In 19 (52.8%) patients, progressive disease was the best response. In patients with PR, the median time to response was 2.1 months (95% confidence interval (CI), 0.4 – 3.9). With a median follow-up duration of 4.4 months (95% CI, 2.4 – 6.4), median progression-free survival and overall survival was 1.5 months (95% CI, 0.4 – 2.6) and 4.3 months (95% CI, 2.6 – 6.1), respectively. No grade 3/4 adverse events (AEs) were reported and grade 1/2 fatigue (n = 4, 10.3%) was the most common AE. Conclusions: In PD-L1 positive BTC, pembrolizumab showed modest efficacy with 11.1% of response rates although our patients were heavily pretreated. Considering the limited therapeutic options and poor survival for these patients, further evaluation of immunotherapy including biomarker analysis is needed.


2011 ◽  
Vol 37 (9) ◽  
Author(s):  
María E. Ochoa-Ardila ◽  
Ana García-Cañas ◽  
Karen Gómez-Mediavilla ◽  
Ana González-Torralba ◽  
Inmaculada Alía ◽  
...  

2019 ◽  
Vol 62 (2) ◽  
pp. 111-117 ◽  
Author(s):  
Aroub Alkaaki ◽  
Osman O. Al-Radi ◽  
Ahmad Khoja ◽  
Anfal Alnawawi ◽  
Abrar Alnawawi ◽  
...  

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