scholarly journals Prospective cohort study of neoadjuvant therapy toxicity in the treatment of oesophageal adenocarcinoma

2018 ◽  
Vol 52 ◽  
pp. 126-130
Author(s):  
David Bunting ◽  
Richard Berrisford ◽  
Tim Wheatley ◽  
Lee Humphreys ◽  
Arun Ariyarathenam ◽  
...  
2015 ◽  
Vol 1 ◽  
pp. 10-13
Author(s):  
Shai Libson ◽  
Vadim Koshenkov ◽  
Steven Rodgers ◽  
Judith Hurley ◽  
Eli Avisar

BMC Cancer ◽  
2015 ◽  
Vol 15 (1) ◽  
Author(s):  
Kathrin Halfter ◽  
◽  
Nina Ditsch ◽  
Hans-Christian Kolberg ◽  
Holger Fischer ◽  
...  

2017 ◽  
Vol 35 (15_suppl) ◽  
pp. 3610-3610 ◽  
Author(s):  
Jin Gu ◽  
Changzheng Du ◽  
Ming Li ◽  
Yifan Peng ◽  
Yunfeng Yao ◽  
...  

3610 Background: It has been reported that non-operative treatment (wait and see) is feasible for the selected rectal cancer cases with a complete clinical response (cCR) following neoadjuvant therapy (NT). The aim of this study is to determine whether "wait and see" policy is efficient for the cCR patients in China. Methods: We designed a prospective cohort study in China (ChiCTR-TRC-12002488). From Jul 2012 to August 2016, totally 45 patients with locally advanced rectal cancer who were cCR following NT were enrolled in the study; within whom, 32 patients were assigned to wait and see group, and the remaining 13 patients were assigned to surgery group (intent-to-treat grouping). Results: The median follow-up time was 24 months (range: 3-51). Of the patients who were followed up more than 12 months (n=37), 8 patients developed tumor progression (7 in wait and see group and 1 in surgery group, respectively). In the wait and see group, the local regrowth took an account of 23.1% (6/26), while the distant metastasis rate was 3.8% (1/26). In the surgery group, there were 23.1% (3/13) of patients who has residual cancer confirmed by postoperative pathological assessment. All the patients with tumor regrowth underwent radical surgery and no body died of cancer. Conclusions: Wait and see policy has an acceptable safety and efficiency, it may become an alternative treatment for the patients who were cCR following NT. Clinical trial information: ChiCTR-TRC-12002488. [Table: see text]


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