scholarly journals Role of adjuvant therapy in resected stage IA subcentimeter (T1a/T1b) pancreatic cancer

Cancer ◽  
2018 ◽  
Vol 125 (1) ◽  
pp. 57-67 ◽  
Author(s):  
Walid L. Shaib ◽  
Amit Surya Narayan ◽  
Jeffrey M. Switchenko ◽  
Sujata R. Kane ◽  
Christina Wu ◽  
...  
2005 ◽  
Vol 39 ◽  
pp. 223-244 ◽  
Author(s):  
Dan Laheru ◽  
Charles J. Yeo

2015 ◽  
Vol 139 (3) ◽  
pp. 589
Author(s):  
Michel Prefontaine ◽  
Vikram Velker ◽  
David D'Souza ◽  
Eric Leung

2019 ◽  
Vol 6 (3) ◽  
pp. MMT28 ◽  
Author(s):  
Evangeline Samuel ◽  
Maggie Moore ◽  
Mark Voskoboynik ◽  
Mark Shackleton ◽  
Andrew Haydon

There is a global increase in the incidence of melanoma, with approximately 300,000 new cases in 2018 worldwide, according to statistics from the International Agency for Research on Cancer. With this rising incidence, it is important to optimize treatment strategies in all stages of the disease to provide better patient outcomes. The role of adjuvant therapy in patients with resected stage 3 melanoma is a rapidly evolving field. Interferon was the first agent shown to have any utility in this space, however, recent advances in both targeted therapies and immunotherapies have led to a number of practice changing adjuvant trials in resected stage 3 disease.


2018 ◽  
Vol 149 (2) ◽  
pp. 283-290 ◽  
Author(s):  
X. Melody Qu ◽  
Vikram M. Velker ◽  
Eric Leung ◽  
Janice S. Kwon ◽  
Mohamed A. Elshaikh ◽  
...  

2019 ◽  
Vol 105 (1) ◽  
pp. E240-E241
Author(s):  
S.J. Ma ◽  
O.T. Oladeru ◽  
J.A. Miccio ◽  
A.J. Iovoli ◽  
G.M. Hermann ◽  
...  

2016 ◽  
Vol 26 (3) ◽  
pp. 491-496 ◽  
Author(s):  
Vikram Velker ◽  
David D’Souza ◽  
Michel Prefontaine ◽  
Jacob McGee ◽  
Eric Leung

Cancers ◽  
2021 ◽  
Vol 13 (15) ◽  
pp. 3892
Author(s):  
Kaisa Lehtomäki ◽  
Harri Mustonen ◽  
Pirkko-Liisa Kellokumpu-Lehtinen ◽  
Heikki Joensuu ◽  
Kethe Hermunen ◽  
...  

In colorectal cancer (CRC), 20–50% of patients relapse after curative-intent surgery with or without adjuvant therapy. We investigated the lead times and prognostic value of post-adjuvant (8 months from randomisation to adjuvant treatment) serum CEA, CA19-9, IL-6, CRP, and YKL-40. We included 147 radically resected stage II–IV CRC treated with 24 weeks of adjuvant 5-fluorouracil-based chemotherapy in the phase III LIPSYT-study (ISRCTN98405441). All 147 were included in lead time analysis, but 12 relapsing during adjuvant therapy were excluded from post-adjuvant analysis. Elevated post-adjuvant CEA, IL-6, and CRP were associated with impaired disease-free survival (DFS) with hazard ratio (HR) 5.21 (95% confidence interval 2.32–11.69); 3.72 (1.99–6.95); 2.58 (1.18–5.61), respectively, and elevated IL-6 and CRP with impaired overall survival (OS) HR 3.06 (1.64–5.73); 3.41 (1.55–7.49), respectively. Elevated post-adjuvant IL-6 in CEA-normal patients identified a subgroup with impaired DFS. HR 3.12 (1.38–7.04) and OS, HR 3.20 (1.39–7.37). The lead times between the elevated biomarker and radiological relapse were 7.8 months for CEA and 10.0–53.1 months for CA19-9, IL-6, CRP, and YKL-40, and the lead time for the five combined was 27.3 months. Elevated post-adjuvant CEA, IL-6, and CRP were associated with impaired DFS. The lead time was shortest for CEA.


2002 ◽  
Vol 11 (1) ◽  
pp. 87-107 ◽  
Author(s):  
Mark Hartley ◽  
Paula Ghaneh ◽  
Robert Sutton ◽  
John P Neoptolemos ◽  
Conor J Magee

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