Real-world outcomes of FOLFOXIRI plus bevacizumab in patients with metastatic colorectal cancer: the JS']JSCCR-TRIPON study

被引:0
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作者
Yamamoto, Yoshiyuki [1 ]
Yukami, Hiroki [2 ,3 ]
Yamaguchi, Tatsuro [4 ]
Ohori, Hisatsugu [5 ]
Nagasu, Sachiko [6 ]
Kagawa, Yoshinori [7 ]
Sugimoto, Naotoshi [8 ]
Sonoda, Hiromichi [9 ]
Yamazaki, Kentaro [10 ]
Takashima, Atsuo [11 ]
Okuyama, Hiroyuki [12 ]
Hasegawa, Hiroko [13 ]
Kondo, Chihiro [14 ]
Baba, Eishi [15 ]
Matsumoto, Toshihiko [16 ]
Kawamoto, Yasuyuki [17 ]
Kataoka, Masato [18 ]
Shindo, Yoshiaki [19 ]
Ishikawa, Toshiaki [20 ]
Esaki, Taito [21 ]
Kito, Yosuke [22 ]
Sato, Takeo [23 ]
Funakoshi, Taro [24 ]
Yamaguchi, Toshifumi [3 ]
Shimada, Yasuhiro [25 ]
Moriwaki, Toshikazu [26 ]
机构
[1] Univ Tsukuba, Fac Med, Dept Gastroenterol, Clin Med, 1-1-1 Tennodai, Tsukuba, Ibaraki 3058575, Japan
[2] Natl Canc Ctr Hosp East, Dept Gastroenterol & Gastrointestinal Oncol, Kashiwa, Japan
[3] Osaka Med & Pharmaceut Univ, Canc Chemotherapy Ctr, Takatsuki, Japan
[4] Komagome Hosp, Tokyo Metropolitan Canc & Infect Dis Ctr, Dept Surg, Bunkyo, Japan
[5] Ishinomaki Red Cross Hosp, Dept Clin Oncol, Ishinomaki, Japan
[6] Kurume Univ, Sch Med, Dept Surg, Fukuoka, Japan
[7] Kansai Rosai Hosp, Dept Surg, Amagasaki, Hyogo, Japan
[8] Osaka Int Canc Inst, Dept Clin Oncol, Osaka, Japan
[9] Shiga Univ Med Sci, Div Gastrointestinal Surg, Otsu, Shiga, Japan
[10] Shizuoka Canc Ctr, Div Gastrointestinal Oncol, Nagaizumi, Japan
[11] Natl Canc Ctr Hosp, Gastrointestinal Med Oncol Div, Chuo, Japan
[12] Kagawa Univ, Fac Med, Dept Clin Oncol, Takamatsu, Japan
[13] Natl Hosp Org, Osaka Natl Hosp, Dept Gastroenterol & Hepatol, Osaka, Japan
[14] Toranomon Gen Hosp, Dept Med Oncol, Minato, Japan
[15] Kyushu Univ, Grad Sch Med Sci, Dept Comprehens Oncol & Social Med, Fukuoka, Japan
[16] Himeji Red Cross Hosp, Dept Med Oncol, Himeji, Japan
[17] Hokkaido Univ Hosp, Div Canc Ctr, Sapporo, Japan
[18] Natl Hosp Org, Nagoya Med Ctr, Dept Surg, Nagoya, Japan
[19] Nakadori Gen Hosp, Gastroenterol Surg, Akita, Japan
[20] Juntendo Univ, Dept Med Oncol, Bunkyo, Japan
[21] NHO Kyushu Canc Ctr, Dept Gastrointestinal & Med Oncol, Fukuoka, Japan
[22] Ishikawa Prefectural Cent Hosp, Dept Med Oncol, Kanazawa, Japan
[23] Kitasato Univ, Sch Med, Dept Lower Gastrointestinal Surg, Sagamihara, Japan
[24] Kyoto Univ, Grad Sch Med, Dept Therapeut Oncol, Kyoto, Japan
[25] Kochi Hlth Sci Ctr, Dept Clin Oncol, Kochi, Japan
[26] Kurashiki Cent Hosp, Dept Hepatol & Gastroenterol, 1-1-1 Miwa, Kurashiki, Okayama 7100052, Japan
关键词
Colorectal cancer; FOLFOXIRI; Triplet; Bevacizumab; Real-world outcome; 1ST-LINE TREATMENT; OPEN-LABEL; PHASE-III; WILD-TYPE; FOLFIRI; CHEMOTHERAPY; MULTICENTER; PANITUMUMAB; SURVIVAL; EFFICACY;
D O I
10.1007/s10147-024-02613-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundFOLFOXIRI plus bevacizumab is a standard first-line chemotherapy for patients with metastatic colorectal cancer (mCRC). However, due to the severe toxicities, this regimen is not widely used. There is limited data on the real-world efficacy and safety.MethodsWe conducted a retrospective analysis of clinical data from mCRC patients who received FOLFOXIRI plus bevacizumab as first-line chemotherapy at 31 institutions. The initial dose was standardized according to the TRIBE regimen. Induction therapy was defined as a combination of oxaliplatin, irinotecan, and fluorouracil.ResultsOut of 104 patients who met the criteria, the median age was 58 years (range, 16-72). 81% of patients had an eastern cooperative oncology group performance status (PS) of 0. An initial dose reduction was observed in 63% of patients. The median number of preplanned induction therapy cycles was 12 (range, 4-12). The completion of scheduled induction therapy cycles was observed in 45% of patients, with treatment-related toxicities being the main reason for discontinuation (63%). The median progression-free survival and overall survival were 12.8 months (95% CI, 10.6-15.0) and 27.9 months (95% CI 21.6-34.2), respectively. The objective response rate and disease control rate were 63.7% and 98.9%, respectively. The R0 resection rate was 21.2%. The main grade 3 or higher toxicities were neutropenia (51%), febrile neutropenia (10%), and nausea/vomiting (5%). No treatment-related deaths were observed.ConclusionIn a real-world clinical setting, FOLFOXIRI plus bevacizumab demonstrated efficacy and safety comparable to previous clinical trials.
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页码:1878 / 1886
页数:9
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