This version was published on 1 November 2008
Ann Clin Biochem 2008;
45:560-566
doi:10.1258/acb.2008.008033
© 2008 Association for Clinical Biochemistry
A rapid rise in circulating pancreastatin in response to somatostatin analogue therapy is associated with poor survival in patients with neuroendocrine tumours
R L Stronge1,
G B Turner2,
B T Johnston3,
D R McCance3,
A McGinty4,
C C Patterson5 and
J E S Ardill3
1 St George's Hospital Medical School, University of London;
2 Altnagelvin Hospital, Londonderry;
3 Neuroendocrine Tumour Group, Royal Victoria Hospital;
4 School of Medicine;
5 Medical Statistics, Queen's University, Belfast, UK

View larger version (15K):
[in this window]
[in a new window]
|
Figure 1 Change in circulating pancreastatin pre- to during-treatment with somatostatin analogues (SST)
|
|

View larger version (10K):
[in this window]
[in a new window]
|
Figure 2 Kaplan-Meier plot of cumulative survival against the change in pancreastatin (during-treatment:pre-treatment pancreastatin ratio). Solid line denotes reduced or no change; dashed line denotes 1.5-fold to five-fold increase; dotted line denotes >five-fold increase: (blot denotes censored). 2 = 24.364 (P < 0.001)
|
|

View larger version (10K):
[in this window]
[in a new window]
|
Figure 3 Kaplan-Meier plot of cumulative survival against primary tumour site. Solid line denotes midgut carcinoid tumours; dashed line denotes broncho-pulmonary tumours and dotted line denotes pancreatic tumours (blot = censored). 2 = 10.36 (P = 0.006)
|
|

CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?