scholarly journals The value of restaging CT following neoadjuvant chemotherapy for resectable gastric cancer. A population-based study

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Alina Desiree Sandø ◽  
Reidun Fougner ◽  
Jon Erik Grønbech ◽  
Erling Audun Bringeland

Abstract Background Response evaluation following neoadjuvant chemotherapy (NAC) in gastric cancer is debated. The aim of this study was to investigate the value of UICC-downstaging as mode of response evaluation following a MAGIC-style regimen of NAC. Methods Retrospective, population-based study on consecutive patients with resectable gastric adenocarcinoma receiving NAC from 2007 to 2016. CT-scan was obtained at diagnosis (rTNM) and repeated following NAC (yrTNM) to evaluate response in terms of downstaging. Further, yrTNM stage was crosstabulated to pathologic stage (ypTNM) to depict correlation between radiologic and pathologic assessment. Results Of 171 patients receiving NAC, 169 were available for response evaluation. For TNM-stages, 43% responded, 50% had stable disease and 7% progressed at CT. Crosstabulating yrTNM stage to ypTNM stage, 24% had concordant stages, with CT overstaging 38% and understaging 38% of the tumours, Cohen kappa ƙ = 0,06 (95%CI 0.004–0.12). Similar patterns of discordance were found for T-stages and N-stages separately. For M-category, restaging CT detected 12 patients with carcinomatosis, with an additional 14 diagnosed with carcinomatosis only at operation. No patient developed parenchymal or extra abdominal metastases, and none developed locally non-resectable tumour during delivery of NAC. Restaging CT with response evaluation was not able to stratify patients into groups of different long-term survival rates based on response mode. Conclusions Routine CT-scan following NAC is of limited value. Accuracy of CT staging compared to final pathologic stage is poor, and radiologic downstaging as measure of response evaluation is unreliable and unable to discriminate long-term survival rates based on response mode.

PLoS ONE ◽  
2017 ◽  
Vol 12 (7) ◽  
pp. e0182255 ◽  
Author(s):  
Szu-Chin Li ◽  
Cheng-Hung Lee ◽  
Chung-Lin Hung ◽  
Jin-Chia Wu ◽  
Jian-Han Chen

2021 ◽  
Vol 9 ◽  
Author(s):  
Anika Rath ◽  
Robert Weintraub

Paediatric cardiomyopathies are a heterogenous group of rare disorders, characterised by mechanical and electrical abnormalities of the heart muscle. The overall annual incidence of childhood cardiomyopathies is estimated at about 1 per 100,000 children and is significantly higher during the first 2 years of life. Dilated cardiomyopathies account for approximately half of the cases. Hypertrophic cardiomyopathies form the second largest group, followed by the less common left ventricular non-compaction and restrictive phenotypes. Infectious, metabolic, genetic, and syndromic conditions account for the majority of cases. Congestive heart failure is the typical manifestation in children with dilated cardiomyopathy, whereas presenting symptoms are more variable in other phenotypes. The natural history is largely influenced by the type of cardiomyopathy and its underlying aetiology. Results from a national population-based study revealed 10-year transplant-free survival rates of 80, 62, and 48% for hypertrophic, dilated and left ventricular non-compaction cardiomyopathies, respectively. Long-term survival rates of children with a restrictive phenotype have largely been obscured by early listing for heart transplantation. In general, the majority of adverse events, including death and heart transplantation, occur during the first 2 years after the initial presentation. This review provides an overview of childhood cardiomyopathies with a focus on epidemiology, natural history, and outcomes.


2003 ◽  
Vol 78 (3) ◽  
pp. 278-284 ◽  
Author(s):  
Sergio R. Korndörfer ◽  
Alexander R. Lucas ◽  
Vera J. Suman ◽  
Cynthia S. Crowson ◽  
Lois E. Krahn ◽  
...  

Epilepsia ◽  
1998 ◽  
Vol 39 (1) ◽  
pp. 89-92 ◽  
Author(s):  
Elias Olafsson ◽  
W. Allen Hauser ◽  
Gunnar Gudmundsson

2018 ◽  
Vol 150 (1) ◽  
pp. 44-49 ◽  
Author(s):  
Jill H. Tseng ◽  
Alessia Aloisi ◽  
Yukio Sonoda ◽  
Ginger J. Gardner ◽  
Oliver Zivanovic ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document