scholarly journals Palliative Resection of the Primary Tumour is Associated with Increased Survival in Patients with Synchronous Metastatic Colorectal Cancer: A Nationwide Population-Based Study from the Netherlands

2014 ◽  
Vol 25 ◽  
pp. ii110
Author(s):  
J. 't Lam -Boer ◽  
L. Van derGeest ◽  
C. Verhoef ◽  
M. Koopman ◽  
M. Elferink ◽  
...  
2020 ◽  
Vol 59 (4) ◽  
pp. 395-403
Author(s):  
Lotte Keikes ◽  
Miriam Koopman ◽  
Martijn M. Stuiver ◽  
Valery E. P. P. Lemmens ◽  
Martijn G. H. van Oijen ◽  
...  

Author(s):  
Anne-Marie Bouvier ◽  
Valérie Jooste ◽  
Maria José Sanchez-Perez ◽  
Maria José Bento ◽  
Jessica Rocha Rodrigues ◽  
...  

HPB ◽  
2021 ◽  
Vol 23 ◽  
pp. S742
Author(s):  
Y. Meyer ◽  
P. Olthof ◽  
D. Grünhagen ◽  
C. Verhoef ◽  
I. de Hingh ◽  
...  

2007 ◽  
Vol 25 (18_suppl) ◽  
pp. 4077-4077 ◽  
Author(s):  
H. J. Lim ◽  
C. Fitzgerald ◽  
S. Gill ◽  
B. Melosky ◽  
C. Speers ◽  
...  

4077 Background: Over the past 10 years, chemotherapeutic options for MCRC has significantly expanded from 5-FU based therapy, to include irinotecan and oxaliplatin. The effect of the availability of these treatments on overall survival is evaluated among patients in 3 time cohorts referred to the British Columbia Cancer Agency (BCCA). Methods: Patients with newly diagnosed or relapsed metastatic colorectal cancer referred to the BCCA in 1995/96, 2000 and 2003/04 were included. In 1995/96, 5-FU was the only palliative chemotherapy agent available at BCCA and irinotecan and oxaliplatin were available in 2000 and 2003, respectively. A one year period was used for the irinotecan cohort to minimize overlap between groups. Overall survival estimates were generated using the Kaplan Meier method. Survival was calculated from time of diagnosis of distant metastatic disease to either death or last contact date. Results: Cohorts were generally similar, however, a significantly higher proportion of patients received chemotherapy in more recent eras ( Table 1 ). Only 25% of patients received both irinotecan and oxaliplatin in 2003/4 and only 10 % received biologic therapies. An improvement in median survival of 3.6 months was observed. The improvement in the treated subgroup was 4.2 months. Outcomes of patients untreated with chemotherapy were unchanged between cohorts. Conclusions: In this population based study, the proportion of patients with MCRC treated with chemotherapy significantly increased between 1995/6 and 2000/2003/4. Patients treated with chemotherapy experienced a 4.2 month increase in median survival in 2003/4 compared to 1995/6. Survival improvements were only significant in the time period when all three effective chemotherapies (5FU, irinotecan and oxaliplatin) were available. As bevacizumab was not available until 2006, its survival impact in this population is not yet known. [Table: see text] No significant financial relationships to disclose.


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