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Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report

BACKGROUND: Targeted therapy with tyrosine kinase inhibitors has been shown to reduce tumor volumes and prolong the survival of patients with metastatic renal cell carcinoma. Tyrosine kinase inhibitors, particularly sunitinib, have recently been used in neoadjuvant and presurgical settings. Axitinib...

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Autores principales: Koie, Takuya, Ohyama, Chikara, Okamoto, Akiko, Yamamoto, Hayato, Imai, Atsushi, Hatakeyama, Shingo, Yoneyama, Takahiro, Hashimoto, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222084/
https://www.ncbi.nlm.nih.gov/pubmed/24267160
http://dx.doi.org/10.1186/1756-0500-6-484
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author Koie, Takuya
Ohyama, Chikara
Okamoto, Akiko
Yamamoto, Hayato
Imai, Atsushi
Hatakeyama, Shingo
Yoneyama, Takahiro
Hashimoto, Yasuhiro
author_facet Koie, Takuya
Ohyama, Chikara
Okamoto, Akiko
Yamamoto, Hayato
Imai, Atsushi
Hatakeyama, Shingo
Yoneyama, Takahiro
Hashimoto, Yasuhiro
author_sort Koie, Takuya
collection PubMed
description BACKGROUND: Targeted therapy with tyrosine kinase inhibitors has been shown to reduce tumor volumes and prolong the survival of patients with metastatic renal cell carcinoma. Tyrosine kinase inhibitors, particularly sunitinib, have recently been used in neoadjuvant and presurgical settings. Axitinib is a promising second-line therapy option for advanced or metastatic renal cell carcinoma. Herein, we report a patient with advanced renal cell carcinoma who received presurgical treatment with axitinib. CASE PRESENTATION: A 73-year-old man was transported by ambulance to a community hospital with chief complaints of high fever and a gait disorder. Computed tomography screening revealed a hypervascular tumor (size, 9 × 8.5 cm) in the lower pole of the left kidney. Upon admission to our hospital, his general condition was poor and his performance status was judged as 3, based on the Eastern Cooperative Oncology Group performance status criteria. After biopsy for the renal tumor, he received 5 mg of axitinib twice daily for 3 months. No serious adverse events were reported during this treatment. The tumor diameter shrank by 56%. Left radical nephrectomy was performed, and there were no intraoperative or postoperative complications. Pathological examination indicated a pT3aN0M0, Furman grade 3, clear cell renal cell carcinoma with necrosis, hyaline degeneration, and hemosiderosis. The patient was asymptomatic and disease-free at 1 year post-diagnosis. CONCLUSION: This case study demonstrate that presurgical therapy with axitinib is feasible and might have several potential advantages for patients with advanced renal cell carcinoma.
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spelling pubmed-42220842014-11-07 Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report Koie, Takuya Ohyama, Chikara Okamoto, Akiko Yamamoto, Hayato Imai, Atsushi Hatakeyama, Shingo Yoneyama, Takahiro Hashimoto, Yasuhiro BMC Res Notes Case Report BACKGROUND: Targeted therapy with tyrosine kinase inhibitors has been shown to reduce tumor volumes and prolong the survival of patients with metastatic renal cell carcinoma. Tyrosine kinase inhibitors, particularly sunitinib, have recently been used in neoadjuvant and presurgical settings. Axitinib is a promising second-line therapy option for advanced or metastatic renal cell carcinoma. Herein, we report a patient with advanced renal cell carcinoma who received presurgical treatment with axitinib. CASE PRESENTATION: A 73-year-old man was transported by ambulance to a community hospital with chief complaints of high fever and a gait disorder. Computed tomography screening revealed a hypervascular tumor (size, 9 × 8.5 cm) in the lower pole of the left kidney. Upon admission to our hospital, his general condition was poor and his performance status was judged as 3, based on the Eastern Cooperative Oncology Group performance status criteria. After biopsy for the renal tumor, he received 5 mg of axitinib twice daily for 3 months. No serious adverse events were reported during this treatment. The tumor diameter shrank by 56%. Left radical nephrectomy was performed, and there were no intraoperative or postoperative complications. Pathological examination indicated a pT3aN0M0, Furman grade 3, clear cell renal cell carcinoma with necrosis, hyaline degeneration, and hemosiderosis. The patient was asymptomatic and disease-free at 1 year post-diagnosis. CONCLUSION: This case study demonstrate that presurgical therapy with axitinib is feasible and might have several potential advantages for patients with advanced renal cell carcinoma. BioMed Central 2013-11-24 /pmc/articles/PMC4222084/ /pubmed/24267160 http://dx.doi.org/10.1186/1756-0500-6-484 Text en Copyright © 2013 Koie et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Koie, Takuya
Ohyama, Chikara
Okamoto, Akiko
Yamamoto, Hayato
Imai, Atsushi
Hatakeyama, Shingo
Yoneyama, Takahiro
Hashimoto, Yasuhiro
Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
title Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
title_full Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
title_fullStr Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
title_full_unstemmed Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
title_short Presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
title_sort presurgical therapy with axitinib for advanced renal cell carcinoma: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222084/
https://www.ncbi.nlm.nih.gov/pubmed/24267160
http://dx.doi.org/10.1186/1756-0500-6-484
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