Oncological outcomes of a multicenter cohort treated with axitinib for metastatic renal cell carcinoma

被引:9
作者
Osawa, Takahiro [1 ]
Kojima, Takahiro [2 ]
Hara, Tomohiko [3 ]
Sugimoto, Mikio [4 ]
Eto, Masatoshi [5 ]
Takeuchi, Ario [5 ]
Minami, Keita [6 ]
Nakai, Yasutomo [7 ]
Ueda, Kosuke [8 ]
Ozawa, Michinobu [9 ]
Uemura, Motohide [10 ]
Miyauchi, Yasuyuki [4 ]
Ohba, Kojiro [11 ]
Suzuki, Toshiro [12 ]
Anai, Satoshi [13 ]
Shindo, Tetsuya [14 ]
Kusakabe, Naohisa [15 ]
Tamura, Keita [16 ]
Komiyama, Motokiyo [17 ]
Goto, Takayuki [18 ]
Yokomizo, Akira [19 ]
Kohei, Naoki [20 ]
Kashiwagi, Akira [21 ]
Murakami, Masaya [22 ]
Sazuka, Tomokazu [23 ]
Yasumoto, Hiroaki [24 ]
Iwamoto, Hideto [25 ]
Mitsuzuka, Koji [26 ]
Morooka, Daichi [27 ]
Shimazui, Toru [28 ]
Yamamoto, Yoshiaki [29 ]
Ikeshiro, Suguru [30 ]
Nakagomi, Hiroshi [31 ]
Morita, Ken [32 ]
Tomida, Ryotaro [33 ]
Mochizuki, Tango [30 ]
Inoue, Takamitsu [34 ]
Kitamura, Hiroshi [35 ]
Yamada, Shuhei [36 ]
Ito, Yoichi M. [37 ]
Murai, Sachiyo [1 ]
Nishiyama, Hiroyuki [2 ]
Shinohara, Nobuo [1 ]
机构
[1] Hokkaido Univ Hosp, Dept Urol, Sapporo, Hokkaido, Japan
[2] Univ Tsukuba Hosp, Dept Urol, Tsukuba, Ibaraki, Japan
[3] Pharmaceut & Med Devices Agcy, Off Pharmacovigilance 2, Tokyo, Japan
[4] Kagawa Univ, Dept Urol, Takamatsu, Kagawa, Japan
[5] Kyushu Univ, Dept Urol, Fukuoka, Japan
[6] Sapporo City Gen Hosp, Dept Urol, Sapporo, Hokkaido, Japan
[7] Osaka Int Canc Inst, Dept Urol, Osaka, Japan
[8] Kurume Univ Hosp, Dept Urol, Kurume, Fukuoka, Japan
[9] Yamagata Univ, Fac Med, Dept Urol, Yamagata, Japan
[10] Osaka Univ Hosp, Dept Urol, Suita, Osaka, Japan
[11] Nagasaki Univ Hosp, Dept Urol, Nagasaki, Japan
[12] Shinshu Univ Hosp, Dept Urol, Matsumoto, Nagano, Japan
[13] Nara Med Univ, Dept Urol, Kashihara, Nara, Japan
[14] Sapporo Med Univ, Dept Urol, Sapporo, Hokkaido, Japan
[15] Obihiro Kosei Hosp, Dept Urol, Obihiro, Hokkaido, Japan
[16] Hamamatsu Univ Sch Med, Dept Urol, Hamamatsu, Shizuoka, Japan
[17] Natl Canc Ctr, Urol Div, Chuo Ku, Tokyo, Japan
[18] Kyoto Univ, Dept Urol, Kyoto, Japan
[19] Harasanshin Hosp, Dept Urol, Fukuoka, Japan
[20] Shizuoka Prefectural Gen Hosp, Dept Urol, Shizuoka, Japan
[21] Teine Keijinkai Hosp, Dept Urol, Sapporo, Hokkaido, Japan
[22] Jikei Univ, Dept Urol, Tokyo, Japan
[23] Chiba Univ, Dept Urol, Chiba, Japan
[24] Shimane Univ, Dept Urol, Izumo, Shimane, Japan
[25] Tottori Univ, Dept Urol, Yonago, Tottori, Japan
[26] Tohoku Univ, Dept Urol, Sendai, Miyagi, Japan
[27] Hakodate Goryoukaku Hosp, Dept Urol, Hakodate, Hokkaido, Japan
[28] Ibaraki Cent Hosp, Ibaraki Canc Ctr, Dept Urol, Kasama, Ibaraki, Japan
[29] Yamaguchi Univ, Dept Urol, Ube, Yamaguchi, Japan
[30] Asahikawa Kosei Hosp, Dept Urol, Asahikawa, Hokkaido, Japan
[31] Univ Yamanashi Hosp, Dept Urol, Chuo, Japan
[32] Kushiro City Gen Hosp, Dept Urol, Kushiro, Japan
[33] Natl Hosp Org Shikoku Canc Ctr, Dept Urol, Matsuyama, Ehime, Japan
[34] Akita Univ, Dept Urol, Akita, Japan
[35] Toyama Univ Hosp, Dept Urol, Toyama, Japan
[36] Otaru Gen Hosp, Dept Urol, Otaru, Hokkaido, Japan
[37] Inst Stat Math, Dept Stat Data Sci, Tokyo, Japan
关键词
axitinib; metastatic; prognostic factor; renal cell carcinoma; risk model; TO-LYMPHOCYTE RATIO; C-REACTIVE PROTEIN; 2ND-LINE TREATMENT; SURVIVAL; PROGNOSIS; EFFICACY; EXPERIENCE; SORAFENIB; PREDICTOR; THERAPY;
D O I
10.1111/cas.14449
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The present study aimed to evaluate the efficacy of the real-world use of axitinib and to develop a prognostic model for stratifying patients who could derive long-term benefit from axitinib. This was a retrospective, descriptive study evaluating the efficacy of axitinib in patients with metastatic renal cell carcinoma that had been treated with 1 or 2 systemic antiangiogenic therapy regimens at 1 of 36 hospitals belonging to the Japan Urologic Oncology Group between January 2012 and February 2019. The primary outcome was overall survival (OS). Using a split-sample method, candidate variables that exhibited significant relationships with OS were chosen to create a model. The new model was validated using the rest of the cohort. In total, 485 patients were enrolled. The median OS was 34 months in the entire study population, whereas it was not reached, 27 months, and 14 months in the favorable, intermediate, and poor risk groups, respectively, according to the new risk classification model. The following 4 variables were included in the final risk model: the disease stage at diagnosis, number of metastatic sites at the start of axitinib therapy, serum albumin level, and neutrophil : lymphocyte ratio. The adjusted area under the curve values of the new model at 12, 36, and 60 months were 0.77, 0.82, and 0.82, respectively. The efficacy of axitinib in routine practice is comparable or even superior to that reported previously. The patients in the new model's favorable risk group might derive a long-term survival benefit from axitinib treatment.
引用
收藏
页码:2460 / 2471
页数:12
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