TY - JOUR
T1 - Treatment patterns and outcomes in patients with unresectable or metastatic renal cell carcinoma in Japan
AU - Harada, Kenichi
AU - Nozawa, Masahiro
AU - Uemura, Motohide
AU - Tatsugami, Katsunori
AU - Osawa, Takahiro
AU - Yamana, Kazutoshi
AU - Kimura, Go
AU - Fujisawa, Masato
AU - Nonomura, Norio
AU - Eto, Masatoshi
AU - Shinohara, Nobuo
AU - Tomita, Yoshihiko
AU - Kondo, Yukihiro
AU - Ochi, Kenya
AU - Anazawa, Yoshio
AU - Uemura, Hirotsugu
N1 - Funding Information:
and personal fees from Pfizer and Novartis; and personal fees from Bayer and Shionogi outside the submitted work. Dr Shi-nohara has received the grants from Ono Pharmaceutical and Pfizer, and the speaker honoraria from Ono Pharmaceutical, Pfizer, Novartis and GSK. Dr Tomita reports grants from Bristol-Myers Squibb and Ono Pharmaceutical whole the study was being carried out; grants from Astellas, Ono Pharmaceutical and Pfizer; personal fees from Novartis, Ono Pharmaceutical, Taiho, Astellas, from Bristol-Myers Squibb, Novartis and Pfizer outside the submitted work. Mr Ochi is an employee of Ono Pharmaceutical. Mr Anazawa is an employee of Bristol-Myers Squibb. Dr H Uemura reports non-financial support from Sanofi, Janssen, Ono Pharmaceutical and Bristol-Myers Squibb; personal fees from Compensation: Bayer, Novartis, Astellas, Sanofi, AstraZeneca, Ono Pharmaceutical and Bristol-Myers Squibb; and grants from Pfizer, Novartis, AstraZeneca, Janssen, Takeda, Astellas, Sanofi and Taiho outside the submitted work.
Funding Information:
This work was funded by Bristol-Myers Squibb K.K. and Ono Pharmaceutical Co., Ltd. Dr Harada, Dr M Uemura, Dr Osawa, Dr Fujisawa and Dr Yukihiro Kondo have nothing to disclose. Dr Nozawa reports grants and personal fees from Novartis; grants and personal fees from Ono Pharmaceutical; and personal fees from Pfizer, Bayer, Astra Zeneca, Sanofi and Astellas outside the submitted work. Dr Tatsugami reports grants from Novartis Pharma, and other funding from Novartis Pharma, Pfizer Japan and Bayer Yakuhin outside the submitted work. Dr Yamana reports grants from Bristol-Myers Squibb and Ono Pharmaceutical while the study was being carried out. Dr Kimura reports grants and non-financial support from Ono Pharmaceutical and Bristol-Myers Squibb while the study was being carried out; grants and personal fees from Novartis, Pfizer, Chugai, MSD, Bayer, AstraZe-neca, Astellas, Takeda and Fuji Film; personal fees from Nihon Medi-Physics; and grants from Taiho and Eisai outside the submitted work. Dr Nonomura reports grants from Bristol-Myers Squibb and Ono Pharmaceutical while the study was being carried out, and personal fees from Bristol-Myers Squibb and Ono Pharmaceutical outside the submitted work. Dr Eto reports grants from Bristol-Myers Squibb and Ono Pharmaceutical while the study was being carried out; grants
Funding Information:
Professional medical writing assistance was provided by Naoki Okuyama at Mebix Inc., statistical analysis was provided by Koichi Kigawa at Mebix Inc., and the authors were funded by Bristol-Myers Squibb and Ono Pharmaceutical.
Publisher Copyright:
© 2018 The Japanese Urological Association
PY - 2019/2
Y1 - 2019/2
N2 - Objectives: To clarify treatment patterns and outcomes for patients with unresectable or metastatic renal cell carcinoma in the molecular target therapy era in Japan. Methods: A multicenter, retrospective medical chart review study was carried out. Patients diagnosed with unresectable or metastatic renal cell carcinoma between January 2012 and August 2015 were enrolled. Data extracted from medical records included treatment duration, grade ≥3 adverse events, reason for discontinuation for each targeted therapy and survival data until August 2016. Results: Of 277 eligible patients, 266, 170 and 77 received first-, second- and third-line systemic treatment, respectively. Tyrosine kinase inhibitors were the most common first-line therapy (72.2%), followed by mammalian target of rapamycin inhibitors (14.3%) and cytokines (13.5%). Among 170 patients who received second-line treatment, tyrosine kinase inhibitor–tyrosine kinase inhibitor was the most common sequence (58.8%), followed by tyrosine kinase inhibitor–mammalian target of rapamycin inhibitor (14.1%) and cytokine–tyrosine kinase inhibitor (14.1%). With a median follow-up period of 19.8 months, median overall survival was not reached at 48 months. Patients who discontinued first-line tyrosine kinase inhibitors in <6 months showed poorer overall survival compared with patients who received first-line tyrosine kinase inhibitors for ≥6 months. Conclusions: The present analysis illustrates the contemporary treatment patterns and prognosis for patients with unresectable or metastatic renal cancer in a real-world setting in Japan. Tyrosine kinase inhibitor–tyrosine kinase inhibitor represents the most commonly used sequence. Shorter treatment duration of first-line tyrosine kinase inhibitors is associated with poorer prognosis, suggesting the need for better treatment options.
AB - Objectives: To clarify treatment patterns and outcomes for patients with unresectable or metastatic renal cell carcinoma in the molecular target therapy era in Japan. Methods: A multicenter, retrospective medical chart review study was carried out. Patients diagnosed with unresectable or metastatic renal cell carcinoma between January 2012 and August 2015 were enrolled. Data extracted from medical records included treatment duration, grade ≥3 adverse events, reason for discontinuation for each targeted therapy and survival data until August 2016. Results: Of 277 eligible patients, 266, 170 and 77 received first-, second- and third-line systemic treatment, respectively. Tyrosine kinase inhibitors were the most common first-line therapy (72.2%), followed by mammalian target of rapamycin inhibitors (14.3%) and cytokines (13.5%). Among 170 patients who received second-line treatment, tyrosine kinase inhibitor–tyrosine kinase inhibitor was the most common sequence (58.8%), followed by tyrosine kinase inhibitor–mammalian target of rapamycin inhibitor (14.1%) and cytokine–tyrosine kinase inhibitor (14.1%). With a median follow-up period of 19.8 months, median overall survival was not reached at 48 months. Patients who discontinued first-line tyrosine kinase inhibitors in <6 months showed poorer overall survival compared with patients who received first-line tyrosine kinase inhibitors for ≥6 months. Conclusions: The present analysis illustrates the contemporary treatment patterns and prognosis for patients with unresectable or metastatic renal cancer in a real-world setting in Japan. Tyrosine kinase inhibitor–tyrosine kinase inhibitor represents the most commonly used sequence. Shorter treatment duration of first-line tyrosine kinase inhibitors is associated with poorer prognosis, suggesting the need for better treatment options.
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U2 - 10.1111/iju.13830
DO - 10.1111/iju.13830
M3 - Article
C2 - 30345560
AN - SCOPUS:85055260269
VL - 26
SP - 202
EP - 210
JO - International Journal of Urology
JF - International Journal of Urology
SN - 0919-8172
IS - 2
ER -