Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction

Backgrounds Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combinat...

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Veröffentlicht in:Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association 2022-09, Vol.25 (5), p.966-972
Hauptverfasser: Saito, Takuro, Kurokawa, Yukinori, Takahashi, Tsuyoshi, Yamamoto, Kazuyoshi, Yamashita, Kotaro, Tanaka, Koji, Makino, Tomoki, Nakajima, Kiyokazu, Eguchi, Hidetoshi, Doki, Yuichiro
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container_title Gastric cancer : official journal of the International Gastric Cancer Association and the Japanese Gastric Cancer Association
container_volume 25
creator Saito, Takuro
Kurokawa, Yukinori
Takahashi, Tsuyoshi
Yamamoto, Kazuyoshi
Yamashita, Kotaro
Tanaka, Koji
Makino, Tomoki
Nakajima, Kiyokazu
Eguchi, Hidetoshi
Doki, Yuichiro
description Backgrounds Since the prognosis of patients with adenocarcinoma of the esophagogastric junction (AEG) remains poor, more intensive treatments, including neoadjuvant chemotherapy (NAC), should be developed. We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG. Methods This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m 2 ) and oxaliplatin (100 mg/m 2 ) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC. Results Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively. Conclusions Neoadjuvant DOS therapy for AEG produced high pathological response rates with an acceptable safety profile, and may be a promising treatment strategy.
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We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG. Methods This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m 2 ) and oxaliplatin (100 mg/m 2 ) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC. Results Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively. 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We retrospectively examined whether neoadjuvant docetaxel, oxaliplatin, and S‑1 (DOS) combination chemotherapy resulted in a favorable clinical response and acceptable toxicity in patients with AEG. Methods This retrospective cohort study included 36 consecutive patients with cStage IIB–IV AEG (Siewert types I–III). Regarding stage IV disease, patients with resectable distant lymph node metastasis (M1-LYM) were eligible. Patients underwent three 3-week cycles of docetaxel (40 mg/m 2 ) and oxaliplatin (100 mg/m 2 ) on day 1 plus oral S-1 (80–120 mg according to body surface area) from day 1 to 14. Surgical resection was performed within 2–4 weeks after completion of NAC. Results Three cycles of neoadjuvant DOS were completed in 28 (78%) patients. Grade 3–4 neutropenia, anorexia, and diarrhea were observed in 26 (72%), 7 (19%), and 4 (11%) patients, respectively. Febrile neutropenia occurred in six (17%) patients. There were no treatment-related deaths. R0 resection was achieved in 35 (97%) patients, and postoperative morbidities of Clavien–Dindo grade III or higher were observed in 6 (17%) patients. Pathological complete response was observed in 11 (31%) of 36 patients. Pathological response rates of grade ≥ 2 and grade ≥ 1b were 47 and 72%, respectively. Two-year progression-free and overall survival rates were 60.1 and 81.2%, respectively. Conclusions Neoadjuvant DOS therapy for AEG produced high pathological response rates with an acceptable safety profile, and may be a promising treatment strategy.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>35488968</pmid><doi>10.1007/s10120-022-01300-1</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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source SpringerLink Journals; EZB-FREE-00999 freely available EZB journals
subjects Abdominal Surgery
Adenocarcinoma
Anorexia
Cancer
Cancer Research
Chemotherapy
Diarrhea
Gastric cancer
Gastroenterology
Lymph nodes
Medical prognosis
Medicine
Medicine & Public Health
Metastases
Neutropenia
Oncology
Original Article
Oxaliplatin
Patients
Response rates
Surgical Oncology
Toxicity
title Neoadjuvant docetaxel, oxaliplatin and S‑1 (DOS) combination chemotherapy for patients with resectable adenocarcinoma of esophagogastric junction
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