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Sunitinib, a Novel Therapy for Anthracycline- and Cisplatin-refractory Malignant Pheochromocytoma
We report a case of malignant pheochromocytoma recurred after debulking surgery. A 17-year-old male patient visited our hospital for right flank pain. He had not experienced palpitations, headache, sweating or weight loss. Level of urinary catecholamine and its metabolite increased above normal valu...
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Published in: | Japanese Journal of Clinical Oncology 2009, Vol.39 (5), p.327-331 |
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container_end_page | 331 |
container_issue | 5 |
container_start_page | 327 |
container_title | Japanese Journal of Clinical Oncology |
container_volume | 39 |
creator | Park, Kyung-Sun Lee, Jae-Lyun Ahn, Hanjong Koh, Jung-Min Park, Inkeun Choi, Jun-Seok Kim, Yi Rang Park, Tai Sun Ahn, Jin-Hee Lee, Dae Ho Kim, Tae Won Lee, Jung Shin |
description | We report a case of malignant pheochromocytoma recurred after debulking surgery. A 17-year-old male patient visited our hospital for right flank pain. He had not experienced palpitations, headache, sweating or weight loss. Level of urinary catecholamine and its metabolite increased above normal values and abdominal computed tomography showed a huge right adrenal mass. One month after debulking surgery, anterior mediastinal and multiple liver metastases were found. These tumors had no response to two conventional regimens of combination chemotherapy (cyclophosphamide, vincristine, dacarbazine and anthracycline; and etoposide and cisplatin). We treated the patient with sunitinib, a multiple tyrosine kinase inhibitor. The tumor showed very good metabolic response to the therapy. In patient with malignant pheochromocytoma, sunitinib might be one therapeutic strategy for malignant pheochromocytomas. |
doi_str_mv | 10.1093/jjco/hyp005 |
format | report |
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A 17-year-old male patient visited our hospital for right flank pain. He had not experienced palpitations, headache, sweating or weight loss. Level of urinary catecholamine and its metabolite increased above normal values and abdominal computed tomography showed a huge right adrenal mass. One month after debulking surgery, anterior mediastinal and multiple liver metastases were found. These tumors had no response to two conventional regimens of combination chemotherapy (cyclophosphamide, vincristine, dacarbazine and anthracycline; and etoposide and cisplatin). We treated the patient with sunitinib, a multiple tyrosine kinase inhibitor. The tumor showed very good metabolic response to the therapy. In patient with malignant pheochromocytoma, sunitinib might be one therapeutic strategy for malignant pheochromocytomas.</description><identifier>ISSN: 0368-2811</identifier><identifier>EISSN: 1465-3621</identifier><identifier>DOI: 10.1093/jjco/hyp005</identifier><language>eng</language><publisher>Oxford University Press</publisher><subject>combination chemotherapy ; malignant pheochromocytoma ; sunitinib</subject><ispartof>Japanese Journal of Clinical Oncology, 2009, Vol.39 (5), p.327-331</ispartof><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>780,784,4490,27925</link.rule.ids></links><search><creatorcontrib>Park, Kyung-Sun</creatorcontrib><creatorcontrib>Lee, Jae-Lyun</creatorcontrib><creatorcontrib>Ahn, Hanjong</creatorcontrib><creatorcontrib>Koh, Jung-Min</creatorcontrib><creatorcontrib>Park, Inkeun</creatorcontrib><creatorcontrib>Choi, Jun-Seok</creatorcontrib><creatorcontrib>Kim, Yi Rang</creatorcontrib><creatorcontrib>Park, Tai Sun</creatorcontrib><creatorcontrib>Ahn, Jin-Hee</creatorcontrib><creatorcontrib>Lee, Dae Ho</creatorcontrib><creatorcontrib>Kim, Tae Won</creatorcontrib><creatorcontrib>Lee, Jung Shin</creatorcontrib><title>Sunitinib, a Novel Therapy for Anthracycline- and Cisplatin-refractory Malignant Pheochromocytoma</title><title>Japanese Journal of Clinical Oncology</title><description>We report a case of malignant pheochromocytoma recurred after debulking surgery. A 17-year-old male patient visited our hospital for right flank pain. He had not experienced palpitations, headache, sweating or weight loss. Level of urinary catecholamine and its metabolite increased above normal values and abdominal computed tomography showed a huge right adrenal mass. One month after debulking surgery, anterior mediastinal and multiple liver metastases were found. These tumors had no response to two conventional regimens of combination chemotherapy (cyclophosphamide, vincristine, dacarbazine and anthracycline; and etoposide and cisplatin). We treated the patient with sunitinib, a multiple tyrosine kinase inhibitor. The tumor showed very good metabolic response to the therapy. In patient with malignant pheochromocytoma, sunitinib might be one therapeutic strategy for malignant pheochromocytomas.</description><subject>combination chemotherapy</subject><subject>malignant pheochromocytoma</subject><subject>sunitinib</subject><issn>0368-2811</issn><issn>1465-3621</issn><fulltext>true</fulltext><rsrctype>report</rsrctype><creationdate>2009</creationdate><recordtype>report</recordtype><recordid>eNqVi81OxCAYAInRxPpz8gV4AHGhtLQezcbNXjQmNlnjhXwiFSqFBtDI29uDL-BpDjOD0BWjN4ze8s00qbAxZaG0PUIVa0RLuKjZMaooFz2pe8ZO0VlKE12LvukqBM9f3mbr7ds1BvwYvrXDg9ERloLHEPGdzyaCKspZrwkG_463Ni0O1odEPa4uh1jwAzj74cFn_GR0UCaGOaiSwwwX6GQEl_TlH88R2d0P2z2xKesfuUQ7QywS4qcUHe9auX95lbUQfHcYDrLh_-1_AbM4Uu4</recordid><startdate>200905</startdate><enddate>200905</enddate><creator>Park, Kyung-Sun</creator><creator>Lee, Jae-Lyun</creator><creator>Ahn, Hanjong</creator><creator>Koh, Jung-Min</creator><creator>Park, Inkeun</creator><creator>Choi, Jun-Seok</creator><creator>Kim, Yi Rang</creator><creator>Park, Tai Sun</creator><creator>Ahn, Jin-Hee</creator><creator>Lee, Dae Ho</creator><creator>Kim, Tae Won</creator><creator>Lee, Jung Shin</creator><general>Oxford University Press</general><scope>BSCLL</scope></search><sort><creationdate>200905</creationdate><title>Sunitinib, a Novel Therapy for Anthracycline- and Cisplatin-refractory Malignant Pheochromocytoma</title><author>Park, Kyung-Sun ; Lee, Jae-Lyun ; Ahn, Hanjong ; Koh, Jung-Min ; Park, Inkeun ; Choi, Jun-Seok ; Kim, Yi Rang ; Park, Tai Sun ; Ahn, Jin-Hee ; Lee, Dae Ho ; Kim, Tae Won ; Lee, Jung Shin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-istex_primary_ark_67375_HXZ_2663FWTW_43</frbrgroupid><rsrctype>reports</rsrctype><prefilter>reports</prefilter><language>eng</language><creationdate>2009</creationdate><topic>combination chemotherapy</topic><topic>malignant pheochromocytoma</topic><topic>sunitinib</topic><toplevel>online_resources</toplevel><creatorcontrib>Park, Kyung-Sun</creatorcontrib><creatorcontrib>Lee, Jae-Lyun</creatorcontrib><creatorcontrib>Ahn, Hanjong</creatorcontrib><creatorcontrib>Koh, Jung-Min</creatorcontrib><creatorcontrib>Park, Inkeun</creatorcontrib><creatorcontrib>Choi, Jun-Seok</creatorcontrib><creatorcontrib>Kim, Yi Rang</creatorcontrib><creatorcontrib>Park, Tai Sun</creatorcontrib><creatorcontrib>Ahn, Jin-Hee</creatorcontrib><creatorcontrib>Lee, Dae Ho</creatorcontrib><creatorcontrib>Kim, Tae Won</creatorcontrib><creatorcontrib>Lee, Jung Shin</creatorcontrib><collection>Istex</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Kyung-Sun</au><au>Lee, Jae-Lyun</au><au>Ahn, Hanjong</au><au>Koh, Jung-Min</au><au>Park, Inkeun</au><au>Choi, Jun-Seok</au><au>Kim, Yi Rang</au><au>Park, Tai Sun</au><au>Ahn, Jin-Hee</au><au>Lee, Dae Ho</au><au>Kim, Tae Won</au><au>Lee, Jung Shin</au><format>book</format><genre>unknown</genre><ristype>RPRT</ristype><atitle>Sunitinib, a Novel Therapy for Anthracycline- and Cisplatin-refractory Malignant Pheochromocytoma</atitle><jtitle>Japanese Journal of Clinical Oncology</jtitle><date>2009-05</date><risdate>2009</risdate><volume>39</volume><issue>5</issue><spage>327</spage><epage>331</epage><pages>327-331</pages><issn>0368-2811</issn><eissn>1465-3621</eissn><abstract>We report a case of malignant pheochromocytoma recurred after debulking surgery. A 17-year-old male patient visited our hospital for right flank pain. He had not experienced palpitations, headache, sweating or weight loss. Level of urinary catecholamine and its metabolite increased above normal values and abdominal computed tomography showed a huge right adrenal mass. One month after debulking surgery, anterior mediastinal and multiple liver metastases were found. These tumors had no response to two conventional regimens of combination chemotherapy (cyclophosphamide, vincristine, dacarbazine and anthracycline; and etoposide and cisplatin). We treated the patient with sunitinib, a multiple tyrosine kinase inhibitor. The tumor showed very good metabolic response to the therapy. In patient with malignant pheochromocytoma, sunitinib might be one therapeutic strategy for malignant pheochromocytomas.</abstract><pub>Oxford University Press</pub><doi>10.1093/jjco/hyp005</doi></addata></record> |
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identifier | ISSN: 0368-2811 |
ispartof | Japanese Journal of Clinical Oncology, 2009, Vol.39 (5), p.327-331 |
issn | 0368-2811 1465-3621 |
language | eng |
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source | Oxford Journals Online |
subjects | combination chemotherapy malignant pheochromocytoma sunitinib |
title | Sunitinib, a Novel Therapy for Anthracycline- and Cisplatin-refractory Malignant Pheochromocytoma |
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