Literature DB >> 28711321

Importance of positron emission tomography for assessing the response of primary and metastatic lesions to induction treatments in T4 esophageal cancer.

Tomoki Makino1, Makoto Yamasaki2, Koji Tanaka2, Mitsuaki Tatsumi3, Shuji Takiguchi2, Jun Hatazawa3, Masaki Mori2, Yuichiro Doki2.   

Abstract

BACKGROUND: There is no consensus strategy for treatment of T4 esophageal cancer, and because of this, a better evaluation of treatment response is crucial to establish personalized therapies. This study aimed to establish a useful system for evaluating treatment response in T4 esophageal cancer.
METHODS: This study included 130 patients with cT4 esophageal cancer without distant metastasis who underwent 18F-fluorodeoxyglucose-positron emission tomography before and after a series of induction treatments comprising chemoradiation or chemotherapy. We evaluated the maximal standardized uptake value and treatment response.
RESULTS: The mean ± standard deviation of standardized uptake value in the primary tumor before and after induction treatments were 13.8 ± 4.4 and 5.4 ± 4.1, respectively, and the mean standardized uptake value decrease was 58.4%. The most significant difference in survival between positron emission tomography-primary tumor responders and nonresponders was at a decrease of 60% standardized uptake value, based on every 10% stepwise cutoff analysis (2-year cause-specific survival: 60.2 vs 23.5%; hazard ratio = 2.705; P < .0001). With this cutoff value, the resectability (P = .0307), pathologic response (P = .0004), and pT stage (P < .0001) were associated with positron emission tomography-primary tumor response. Univariate analysis of 2-year cause-specific survival indicated a correlation between cause-specific survival and clinical stages according to TNM classification, esophageal perforation, positron emission tomography-primary tumor response, lymph node status evaluated by positron emission tomography before and after induction treatments, and operative resection. Multivariate analysis further identified positron emission tomography-primary tumor response (hazard ratio = 2.354; P = .0107), lymph node status evaluated by positron emission tomography after induction treatments (hazard ratio = 1.966; P = .0089), and operative resection (hazard ratio = 2.012; P = .0245) as independent prognostic predictors.
CONCLUSION: Positron emission tomography evaluation of the response of primary and metastatic lesions to induction treatments is important to formulate treatment strategies for cT4 esophageal cancer.
Copyright © 2017 Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28711321     DOI: 10.1016/j.surg.2017.06.007

Source DB:  PubMed          Journal:  Surgery        ISSN: 0039-6060            Impact factor:   3.982


  8 in total

1.  Risk factors associated with increased drainage volumes of chest tubes after transthoracic esophagectomy for esophageal cancer.

Authors:  Ryo Kato; Tomoki Makino; Makoto Yamasaki; Koji Tanaka; Yasuhiro Miyazaki; Tsuyoshi Takahashi; Yukinori Kurokawa; Masaaki Motoori; Yutaka Kimura; Kiyokazu Nakajima; Masaki Mori; Yuichiro Doki
Journal:  Surg Today       Date:  2019-07-24       Impact factor: 2.549

Review 2.  Surgical strategies for treatment of clinical T4 esophageal cancer in Japan.

Authors:  Kazuhiko Yamada; Kyoko Nohara; Naoki Enomoto; Hitomi Wake; Syusuke Yagi; Masayoshi Terayama; Daiki Kato; Chizu Yokoi; Yasushi Kojima; Hidetsugu Nakayama; Norihiro Kokudo
Journal:  Glob Health Med       Date:  2021-12-31

3.  The role of 18F-FDG PET/CT in predicting the pathological response to neoadjuvant PD-1 blockade in combination with chemotherapy for resectable esophageal squamous cell carcinoma.

Authors:  Xiaoyan Wang; Weixiong Yang; Qian Zhou; Hui Luo; Wenfang Chen; Sai-Ching Jim Yeung; Shuishen Zhang; Yi Gan; Bo Zeng; Zhenguo Liu; Shiting Feng; Xiangsong Zhang; Chao Cheng
Journal:  Eur J Nucl Med Mol Imaging       Date:  2022-06-23       Impact factor: 10.057

4.  Long-term outcomes of multimodal therapy combining definitive chemoradiotherapy and salvage surgery for T4 esophageal squamous cell carcinoma.

Authors:  Kotaro Sugawara; Koichi Yagi; Yasuhiro Okumura; Masato Nishida; Susumu Aikou; Hiroharu Yamashita; Hideomi Yamashita; Yasuyuki Seto
Journal:  Int J Clin Oncol       Date:  2019-12-11       Impact factor: 3.402

5.  Peritumoral Lymphatic Vessels Associated with Resistance to Neoadjuvant Chemotherapy and Unfavorable Survival in Esophageal Cancer.

Authors:  Takeo Hara; Tomoki Makino; Makoto Yamasaki; Koji Tanaka; Kotaro Yamashita; Yuya Nogi; Takuro Saito; Tsuyoshi Takahashi; Yukinori Kurokawa; Mitsuaki Tatsumi; Kiyokazu Nakajima; Eiichi Morii; Hidetoshi Eguchi; Yuichiro Doki
Journal:  Ann Surg Oncol       Date:  2020-04-23       Impact factor: 5.344

Review 6.  Treatment and clinical outcome of clinical T4 esophageal cancer: A systematic review.

Authors:  Tomoki Makino; Makoto Yamasaki; Koji Tanaka; Yasuhiro Miyazaki; Tsuyoshi Takahashi; Yukinori Kurokawa; Masaaki Motoori; Yutaka Kimura; Kiyokazu Nakajima; Masaki Mori; Yuichiro Doki
Journal:  Ann Gastroenterol Surg       Date:  2018-12-13

7.  Clinicopathological characteristics and survival of primary malignant melanoma of the esophagus.

Authors:  Tadayoshi Hashimoto; Tomoki Makino; Makoto Yamasaki; Koji Tanaka; Yasuhiro Miyazaki; Tsuyoshi Takahashi; Yukinori Kurokawa; Masaaki Motoori; Yutaka Kimura; Kiyokazu Nakajima; Eiichi Morii; Masaki Mori; Yuichiro Doki
Journal:  Oncol Lett       Date:  2019-06-21       Impact factor: 2.967

8.  Prognostic relevance of lymph node regression on survival in esophageal cancer: a systematic review and meta-analysis.

Authors:  Eliza Hagens; Karina Tukanova; Sara Jamel; Mark van Berge Henegouwen; George B Hanna; Suzanne Gisbertz; Sheraz R Markar
Journal:  Dis Esophagus       Date:  2022-01-07       Impact factor: 3.429

  8 in total

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