ID | 114570 |
Author |
Ohnuma, Hiroyuki
Sapporo Medical University
Hayasaka, Naotaka
Sapporo Medical University
Matsuno, Teppei
Sapporo Medical University
Fujita, Chisa
Sapporo Medical University
Sato, Masanori
Sapporo Medical University
Osuga, Takahiro
Sapporo Medical University
Hirakawa, Masahiro
Sapporo Medical University
Miyanishi, Koji
Sapporo Medical University
Sagawa, Tamotsu
Hokkaido Cancer Center
Fujikawa, Koshi
Hokkaido Cancer Center
Ohi, Motoh
Sapporo Kyoritsu Gorinbashi Hospital
Okagawa, Yutaka
Tonan Hospital
Tsuji, Yasushi
Tonan Hospital
Hirayama, Michiaki
Tonan Hospital
Ito, Tatsuya
Sapporo Medical University
Nobuoka, Takayuki
Sapporo Medical University
Takemasa, Ichiro
Sapporo Medical University
Kobune, Masayoshi
Sapporo Medical University
Kato, Junji
Sapporo Medical University
|
Keywords | docetaxel
esophageal cancer
esophageal squamous cell carcinoma
nedaplatin
neoadjuvant chemotherapy
|
Content Type |
Journal Article
|
Description | Cisplatin plus 5‐fluorouracil is regarded as standard neoadjuvant chemotherapy for esophageal squamous cell carcinoma (ESCC) in Japan, but the prognosis remains poor. We have previously described how definitive chemoradiotherapy with docetaxel, nedaplatin, and 5‐fluorouracil (DNF) led to a very high response rate and promising survival times. We therefore undertook a phase II trial to evaluate the feasibility and efficacy of neoadjuvant DNF. The study included patients with clinical stage Ib‐III ESCC. Chemotherapy consisted of i.v. docetaxel (30 mg/m2) and nedaplatin (50 mg/m2) on days 1 and 8, and a continuous infusion of 5‐fluorouracil (400 mg/m2/day) on days 1‐5 and 8‐12, every 3 weeks. After three courses of chemotherapy, esophagectomy was carried out. The primary end‐point was the completion rate of the protocol treatment. Twenty‐eight patients were enrolled (cStage Ib/II/III, 2/3/23) and all received at least two cycles of chemotherapy. Twenty‐five patients underwent surgery, all of whom achieved an R0 resection, leading to a completion rate of 89.3%. The overall response rate was 87.0%. A pathological complete response was confirmed in eight (32.0%) cases. Grade 3/4 adverse events included leukopenia (32.1%), neutropenia (39.3%), febrile neutropenia (10.7%), thrombocytopenia (10.7%), and diarrhea (14.3%), but were manageable. Treatment‐related deaths and major surgical complications did not occur. Estimated 2‐year progression‐free and overall survival rates were 70.4% and 77.2%, respectively. Thus, DNF therapy was well tolerated and deemed feasible, with a strong tumor response in a neoadjuvant setting for ESCC. This trial is registered with the University Hospital Medical Information Network (UMIN ID: 000014305).
|
Journal Title |
Cancer Science
|
ISSN | 13497006
|
Publisher | Japanese Cancer Association|John Wiley & Sons
|
Volume | 109
|
Issue | 11
|
Start Page | 3554
|
End Page | 3563
|
Published Date | 2018-08-23
|
Rights | © 2018 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. (https://creativecommons.org/licenses/by-nc/4.0/) |
EDB ID | |
DOI (Published Version) | |
URL ( Publisher's Version ) | |
FullText File | |
language |
eng
|
TextVersion |
Publisher
|
departments |
Medical Sciences
|