Phase II study of long-course chemoradiotherapy followed by consolidation chemotherapy as total neoadjuvant therapy in locally advanced rectal cancer in Japan: ENSEMBLE-2

被引:1
|
作者
Kagawa, Yoshinori [1 ,2 ]
Ando, Koji [3 ]
Uemura, Mamoru [4 ]
Watanabe, Jun [5 ,6 ]
Oba, Koji [7 ]
Emi, Yasunori [8 ]
Matsuhashi, Nobuhisa [9 ]
Izawa, Naoki [10 ]
Muto, Osamu [11 ]
Kinjo, Tatsuya [12 ]
Takemasa, Ichiro [13 ]
Oki, Eiji [3 ]
机构
[1] Osaka Gen Med Ctr, Dept Gastroenterol Surg, Osaka, Japan
[2] Osaka Int Canc Inst, Dept Gastroenterol Surg, 3-1-69 Otemae,Chuo Ku, Osaka 5418567, Japan
[3] Kyushu Univ, Dept Surg & Sci, Fukuoka, Japan
[4] Osaka Univ, Dept Gastroenterol Surg, Osaka, Japan
[5] Yokohama City Univ, Med Ctr, Gastroenterol Ctr, Dept Surg, Yokohama, Japan
[6] Kansai Med Univ, Dept Colorectal Surg, Osaka, Japan
[7] Univ Tokyo, Grad Sch Med, Dept Biostat, Tokyo, Japan
[8] Saiseikai Fukuoka Gen Hosp, Dept Surg, Fukuoka, Japan
[9] Gifu Univ, Grad Sch Med, Dept Gastroenterol Surg & Pediat Surg, Gifu, Japan
[10] St Marianna Univ, Sch Med, Dept Clin Oncol, Kawasaki, Japan
[11] Akita Redcross Hosp, Dept Clin Oncol, Akita, Japan
[12] Univ Ryukyus, Fac Med, Div Digest & Gen Surg, Okinawa, Japan
[13] Sapporo Med Univ, Dept Surg Surg Oncol & Sci, Sch Med, Sapporo, Japan
来源
关键词
locally advanced rectal cancer; nonoperative management; pathological complete response; total mesorectal excision; total neoadjuvant therapy; TOTAL MESORECTAL EXCISION; SHORT-COURSE RADIOTHERAPY; PREOPERATIVE CHEMORADIOTHERAPY; OPEN-LABEL; ADJUVANT CHEMOTHERAPY; COURSE CHEMORADIATION; RANDOMIZED-TRIAL; MULTICENTER; RECURRENCE; RADIATION;
D O I
10.1002/ags3.12848
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim To evaluate the feasibility and safety of total neoadjuvant therapy with long-course chemoradiotherapy followed by consolidation chemotherapy in Japanese patients with locally advanced rectal cancer. Methods This prospective, multicenter, single-arm, phase II trial was conducted at 10 centers. The eligibility criteria included age >= 20 y, locally advanced rectal cancer within 12 cm of the anal verge, and cT3-4N0M or TanyN+M0 at diagnosis, enabling curative resection. The protocol treatment was capecitabine (1650 mg/m(2)/day)-based long-course chemoradiotherapy (50.4 Gy/28 fractions) and consolidation chemotherapy (CAPOX, four courses) followed by total mesorectal excision. Nonoperative management was allowed if a clinical complete response was achieved. The primary endpoint was the pathologic complete response rate. Results Among 28 enrolled patients (19 men, 9 women; median age, 69.5 [41-79] y), the long-course chemoradiotherapy and consolidation chemotherapy completion rates were 100% and 96.4%, respectively. The clinical responses included clinical complete response, (35.7%, 10/28), near-complete response (28.6%, 8/28), and incomplete response (32.1%, 9/28). Total mesorectal excision and nonoperative management were performed in 21 and six patients, respectively. The final analysis included 21 patients. Five patients (23.8% [90% confidence interval 11.8%-41.8%]) achieved pathologic complete response, while 10 of 28 patients (35.7%) achieved a pathological complete response or a sustained clinical complete response. No treatment-related deaths occurred. Grade >= 3 adverse events included diarrhea (7.1%) and leukopenia (7.1%). Conclusion ENSEMBLE-2 demonstrated comparable pathologic complete response rates and well-tolerated safety of total neoadjuvant therapy with long-course chemoradiotherapy followed by consolidation chemotherapy in Japanese patients with locally advanced rectal cancer.
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收藏
页码:1067 / 1075
页数:9
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