Cargando…

Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report

BACKGROUND: Regorafenib is an oral multikinase inhibitor that has been demonstrated as clinically effective in patients with metastatic colorectal cancer in phase III studies. Although disease control was achieved in 40% of the pretreated patients with metastatic colorectal cancer in the pivotal stu...

Descripción completa

Detalles Bibliográficos
Autores principales: Yoshino, Kenji, Manaka, Dai, Kudo, Ryo, Kanai, Shunpei, Mitsuoka, Eisei, Kanto, Satoshi, Hamasu, Shinya, Konishi, Sayuri, Nishitai, Ryuta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561601/
https://www.ncbi.nlm.nih.gov/pubmed/28818109
http://dx.doi.org/10.1186/s13256-017-1366-4
_version_ 1783257859957456896
author Yoshino, Kenji
Manaka, Dai
Kudo, Ryo
Kanai, Shunpei
Mitsuoka, Eisei
Kanto, Satoshi
Hamasu, Shinya
Konishi, Sayuri
Nishitai, Ryuta
author_facet Yoshino, Kenji
Manaka, Dai
Kudo, Ryo
Kanai, Shunpei
Mitsuoka, Eisei
Kanto, Satoshi
Hamasu, Shinya
Konishi, Sayuri
Nishitai, Ryuta
author_sort Yoshino, Kenji
collection PubMed
description BACKGROUND: Regorafenib is an oral multikinase inhibitor that has been demonstrated as clinically effective in patients with metastatic colorectal cancer in phase III studies. Although disease control was achieved in 40% of the pretreated patients with metastatic colorectal cancer in the pivotal studies, radiological response has rarely been reported. Severe adverse events associated with regorafenib are known to occur during the first and second courses of treatment. We present a case of a 62-year-old Japanese patient whose metastatic colorectal cancer has been responding to treatment with regorafenib for 2 years. CASE PRESENTATION: A 54-year-old Japanese man visited our institute exhibiting general malaise, and he was diagnosed with ascending colon cancer in April 2006. He underwent right hemicolectomy, and the final staging was T3N0M0, stage II. After 19 months, pulmonary metastasis and anastomotic recurrences were detected, and a series of operations were performed to resect both metastatic lesions. After that, liver metastasis, a duodenal metastasis with right renal invasion, right adrenal metastasis, and para-aortic lymph node metastases were observed during follow-up, and chemotherapy and resection were performed. The patient had metastatic para-aortic lymph nodes after the fifth tumor resection and underwent multiple lines of chemotherapy in April 2014. Regorafenib monotherapy was started at 80 mg/day. Then, regorafenib was increased to 120 mg/day in the second cycle. Regorafenib monotherapy led to 60% tumor shrinkage within the initial 2 months, and the tumor further decreased in size over 4 months until it became unrecognizable on imaging studies. The clinical effects of regorafenib monotherapy have shown a partial response according to Response Evaluation Criteria in Solid Tumors criteria. No severe adverse events were observed, except for mild fatigue and hand-foot syndrome. The patient has received 24 courses of regorafenib over 2 years without exhibiting tumor progression. CONCLUSIONS: To the best of our knowledge, this is the longest treatment with regorafenib without tumor progression ever reported. A reduced dosage of regorafenib at induction may ameliorate the cutaneous and hepatic toxicity associated with its use.
format Online
Article
Text
id pubmed-5561601
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-55616012017-08-18 Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report Yoshino, Kenji Manaka, Dai Kudo, Ryo Kanai, Shunpei Mitsuoka, Eisei Kanto, Satoshi Hamasu, Shinya Konishi, Sayuri Nishitai, Ryuta J Med Case Rep Case Report BACKGROUND: Regorafenib is an oral multikinase inhibitor that has been demonstrated as clinically effective in patients with metastatic colorectal cancer in phase III studies. Although disease control was achieved in 40% of the pretreated patients with metastatic colorectal cancer in the pivotal studies, radiological response has rarely been reported. Severe adverse events associated with regorafenib are known to occur during the first and second courses of treatment. We present a case of a 62-year-old Japanese patient whose metastatic colorectal cancer has been responding to treatment with regorafenib for 2 years. CASE PRESENTATION: A 54-year-old Japanese man visited our institute exhibiting general malaise, and he was diagnosed with ascending colon cancer in April 2006. He underwent right hemicolectomy, and the final staging was T3N0M0, stage II. After 19 months, pulmonary metastasis and anastomotic recurrences were detected, and a series of operations were performed to resect both metastatic lesions. After that, liver metastasis, a duodenal metastasis with right renal invasion, right adrenal metastasis, and para-aortic lymph node metastases were observed during follow-up, and chemotherapy and resection were performed. The patient had metastatic para-aortic lymph nodes after the fifth tumor resection and underwent multiple lines of chemotherapy in April 2014. Regorafenib monotherapy was started at 80 mg/day. Then, regorafenib was increased to 120 mg/day in the second cycle. Regorafenib monotherapy led to 60% tumor shrinkage within the initial 2 months, and the tumor further decreased in size over 4 months until it became unrecognizable on imaging studies. The clinical effects of regorafenib monotherapy have shown a partial response according to Response Evaluation Criteria in Solid Tumors criteria. No severe adverse events were observed, except for mild fatigue and hand-foot syndrome. The patient has received 24 courses of regorafenib over 2 years without exhibiting tumor progression. CONCLUSIONS: To the best of our knowledge, this is the longest treatment with regorafenib without tumor progression ever reported. A reduced dosage of regorafenib at induction may ameliorate the cutaneous and hepatic toxicity associated with its use. BioMed Central 2017-08-18 /pmc/articles/PMC5561601/ /pubmed/28818109 http://dx.doi.org/10.1186/s13256-017-1366-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Yoshino, Kenji
Manaka, Dai
Kudo, Ryo
Kanai, Shunpei
Mitsuoka, Eisei
Kanto, Satoshi
Hamasu, Shinya
Konishi, Sayuri
Nishitai, Ryuta
Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
title Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
title_full Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
title_fullStr Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
title_full_unstemmed Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
title_short Metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
title_sort metastatic colorectal cancer responsive to regorafenib for 2 years: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561601/
https://www.ncbi.nlm.nih.gov/pubmed/28818109
http://dx.doi.org/10.1186/s13256-017-1366-4
work_keys_str_mv AT yoshinokenji metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT manakadai metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT kudoryo metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT kanaishunpei metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT mitsuokaeisei metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT kantosatoshi metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT hamasushinya metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT konishisayuri metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport
AT nishitairyuta metastaticcolorectalcancerresponsivetoregorafenibfor2yearsacasereport