TY - JOUR
T1 - Streptozocin/5-fluorouracil chemotherapy is associated with durable response in patients with advanced pancreatic neuroendocrine tumours
AU - Dilz, Lisa Marie
AU - Denecke, Timm
AU - Steffen, Ingo G.
AU - Prasad, Vikas
AU - Von Weikersthal, Ludwig Fischer
AU - Pape, Ulrich Frank
AU - Wiedenmann, Bertram
AU - Pavel, Marianne
N1 - Publisher Copyright:
© 2015 Elsevier Ltd.
PY - 2015/7/1
Y1 - 2015/7/1
N2 - Background The role of systemic chemotherapy for pancreatic neuroendocrine tumours (pNET) is controversially discussed. Objective response rates (RR) reported for streptozocin (STZ)-based chemotherapy are variable and novel targeted drugs have recently been approved. However, the sequence of treatment remains unclear. We aimed to evaluate the efficacy of STZ plus 5-fluorouracil (STZ/5-FU) in a large pNET cohort. Methods Data from 96 pNET patients treated with STZ/5-FU were analysed retrospectively. Endpoints of the study were RR, time to tumour progression (TTP) and overall survival (OS). Results Mean age of patients at the start of chemotherapy was 57.6 years (range, 32.1-80.4). STZ/5-FU was the 1st line treatment in 56.3%. 11.5% had G1, 79.2% G2 and 6.3% G3 neoplasms. Baseline progression was evident in 74%. Objective response rate was 42.7%. 40.6% of patients showed stable disease as best response while 16.7% showed progressive disease. Treatment was discontinued due to toxicity in 16 patients. Median TTP and OS were 19.4 (95% confidence interval (CI), 13.6-25.2) and 54.8 months (95% CI, 34.7-74.9), respectively. In Cox regression analysis, Ki67 > 15% was the only negative prognostic factor for TTP (hazard ratio (HR), 3.3; P < 0.001), confirmed by multivariate analysis (HR, 6.7; P = 0.001). Conclusions STZ/5-FU was associated with considerable RR. Treatment was associated with durable TTP especially in patients with Ki67-index of ≤15%. These findings along with good tolerability strengthen the value of this two-drug chemotherapy for the management of unresectable pNET.
AB - Background The role of systemic chemotherapy for pancreatic neuroendocrine tumours (pNET) is controversially discussed. Objective response rates (RR) reported for streptozocin (STZ)-based chemotherapy are variable and novel targeted drugs have recently been approved. However, the sequence of treatment remains unclear. We aimed to evaluate the efficacy of STZ plus 5-fluorouracil (STZ/5-FU) in a large pNET cohort. Methods Data from 96 pNET patients treated with STZ/5-FU were analysed retrospectively. Endpoints of the study were RR, time to tumour progression (TTP) and overall survival (OS). Results Mean age of patients at the start of chemotherapy was 57.6 years (range, 32.1-80.4). STZ/5-FU was the 1st line treatment in 56.3%. 11.5% had G1, 79.2% G2 and 6.3% G3 neoplasms. Baseline progression was evident in 74%. Objective response rate was 42.7%. 40.6% of patients showed stable disease as best response while 16.7% showed progressive disease. Treatment was discontinued due to toxicity in 16 patients. Median TTP and OS were 19.4 (95% confidence interval (CI), 13.6-25.2) and 54.8 months (95% CI, 34.7-74.9), respectively. In Cox regression analysis, Ki67 > 15% was the only negative prognostic factor for TTP (hazard ratio (HR), 3.3; P < 0.001), confirmed by multivariate analysis (HR, 6.7; P = 0.001). Conclusions STZ/5-FU was associated with considerable RR. Treatment was associated with durable TTP especially in patients with Ki67-index of ≤15%. These findings along with good tolerability strengthen the value of this two-drug chemotherapy for the management of unresectable pNET.
KW - 5-Fluorouracil
KW - Chemotherapy
KW - Ki-67
KW - Neuroendocrine tumour
KW - Objective response
KW - Pancreas
KW - Pancreatic neuroendocrine tumour
KW - Streptozocin
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=84930047325&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2015.04.005
DO - 10.1016/j.ejca.2015.04.005
M3 - Article
C2 - 25935542
AN - SCOPUS:84930047325
SN - 0959-8049
VL - 51
SP - 1253
EP - 1262
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 10
ER -