Prediction of early progression of metastatic renal cell carcinoma treated with first-line tyrosine kinase inhibitor. 2021

Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
Department of Urology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.

BACKGROUND There are various alternative first-line therapeutic options besides tyrosine kinase inhibitors (TKIs) for metastatic renal cell carcinoma (mRCC). To inform therapeutic decision-making for such patients, this study aimed to identify predictive factors for resistance to TKI. METHODS A total of 239 cases of mRCC patients who received first-line TKI therapy were retrospectively studied. Patients with a radiologic diagnosis of progressive disease within 3 months after initiating therapy were classified as primary refractory cases; the others were classified as non-primary refractory cases. The association between primary refractory cases and age, gender, pathology findings, serum c-reactive protein (CRP) level, metastatic organ status, and 6 parameters defined by the International Metastatic Renal Cell Carcinoma Database Consortium were analyzed. RESULTS Of 239 cases, 32 (13.3%) received a radiologic diagnosis of progressive disease within 3 months after initiating therapy. The rates of sarcomatoid differentiation, hypercalcemia, a serum CRP level of 0.3 mg/dL or higher, presence of liver metastasis, anemia, and time from diagnosis to treatment interval of less than a year were significantly higher in the primary refractory group. Multivariate analysis showed that sarcomatoid differentiation, hypercalcemia, a serum CRP level of 0.3 mg/dL or higher, and liver metastasis were independently associated with primary refractory disease. A risk-stratified model based upon the number of patients with these factors indicated rates of primary refractory disease of 4.0%, 10.1%, and 45.0% for patients with 0, 1, and 2 or more factors, respectively. CONCLUSIONS Sarcomatoid differentiation, hypercalcemia, an elevated serum CRP level, and presence of liver metastasis were associated with primary refractory disease in mRCC patients receiving first-line TKI therapy. These results provide clinicians with useful information when selecting a first-line therapeutic option for mRCC patients.

UI MeSH Term Description Entries

Related Publications

Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
December 2017, Japanese journal of clinical oncology,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
September 2017, Urologic oncology,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
April 2019, Targeted oncology,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
February 2015, Annals of oncology : official journal of the European Society for Medical Oncology,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
March 2019, Future oncology (London, England),
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
May 2024, International journal of urology : official journal of the Japanese Urological Association,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
September 2017, Urologic oncology,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
January 2017, Indian journal of cancer,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
February 2020, Advances in therapy,
Jun Teishima, and Daiki Murata, and Shogo Inoue, and Tetsutaro Hayashi, and Koji Mita, and Yasuhisa Hasegawa, and Masao Kato, and Mitsuru Kajiwara, and Masanobu Shigeta, and Satoshi Maruyama, and Hiroyuki Moriyama, and Seiji Fujiwara, and Akio Matsubara
June 2018, International journal of urology : official journal of the Japanese Urological Association,
Copied contents to your clipboard!