2015
DOI: 10.1016/s0959-8049(16)31118-2
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2201 Peri-operative chemotherapy ± bevacizumab for resectable gastro-oesophageal adenocarcinoma: Results from the UK Medical Research Council randomised ST03 trial (ISRCTN 46020948)

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Cited by 30 publications
(19 citation statements)
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“…In the substantive part of this ST03 trial, patients with esophageal and junctional adenocarcinoma of stomach or junction were randomised to ECX chemotherapy or ECX in combination with the VEGF inhibitor bevacizumab, for 3 cycles before and after surgery, with a further 6 maintenance doses in the bevacizumab arm. Although no differences in survival were reported, a high anastomotic leak rate (23%) in patients undergoing esophageal surgery on the experimental arm, compared with 9% in the ECX arm, with 30 day mortalities of 11% and 5%, respectively, resulting in closure of recruitment to patients with esophageal and junctional tumors in 2013 (33) With respect to immunotherapy, an industry sponsored phase III trial will randomise patients who have undergone neoadjuvant chemoradiotherapy and surgery to adjuvant nivolumab or placebo (Checkmate 577, NCT02743494) (34). Nivolumab is a human IGG4 anti-PD-1 monoclonal antibody which acts as a checkpoint inhibitor which prevents inactivation of anti-tumour T cells (35).…”
Section: Question 2: Trials Of Targeted Therapies and Immune Based Apmentioning
confidence: 94%
“…In the substantive part of this ST03 trial, patients with esophageal and junctional adenocarcinoma of stomach or junction were randomised to ECX chemotherapy or ECX in combination with the VEGF inhibitor bevacizumab, for 3 cycles before and after surgery, with a further 6 maintenance doses in the bevacizumab arm. Although no differences in survival were reported, a high anastomotic leak rate (23%) in patients undergoing esophageal surgery on the experimental arm, compared with 9% in the ECX arm, with 30 day mortalities of 11% and 5%, respectively, resulting in closure of recruitment to patients with esophageal and junctional tumors in 2013 (33) With respect to immunotherapy, an industry sponsored phase III trial will randomise patients who have undergone neoadjuvant chemoradiotherapy and surgery to adjuvant nivolumab or placebo (Checkmate 577, NCT02743494) (34). Nivolumab is a human IGG4 anti-PD-1 monoclonal antibody which acts as a checkpoint inhibitor which prevents inactivation of anti-tumour T cells (35).…”
Section: Question 2: Trials Of Targeted Therapies and Immune Based Apmentioning
confidence: 94%
“…The addition of the anti-VEGF antibody bevacizumab to perioperative ECX revealed to be feasible but failed to improve survival in the United Kingdom STO-3 study [35,36]. This negative study result highlights the need to better understand the role and function of treatment targets in the adjuvant treatment of gastric cancer.…”
Section: Accepted Manuscriptmentioning
confidence: 99%
“…A follow up British trial that added bevacizumab to preoperative chemotherapy failed to demonstrate any benefit in OS and complication rates were substantial. 2830 Currently, we recommend to consider perioperative chemotherapy in patients who have clinical ≥T2 any N primary. Similarly, all GAC patients considered appropriate for perioperative therapy, should also be considered for a staging laparoscopy before initiation of therapy.…”
Section: Gastric Adenocarcinomamentioning
confidence: 99%