Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma

Background. Renal cell carcinoma accounts for about 2-3% of all malignant tumors. The prevalence of brain metastases from RCC is less than 20% of cases. Traditionally, whole brain radiotherapy as well as the latest stereotactic radiosurgery improves both survival and local tumor control. These treat...

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Main Authors: Michela Roberto, Maria Bassanelli, Elsa Iannicelli, Silvana Giacinti, Chiara D’Antonio, Anna Maria Aschelter, Paolo Marchetti
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Case Reports in Oncological Medicine
Online Access:http://dx.doi.org/10.1155/2015/629046
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author Michela Roberto
Maria Bassanelli
Elsa Iannicelli
Silvana Giacinti
Chiara D’Antonio
Anna Maria Aschelter
Paolo Marchetti
author_facet Michela Roberto
Maria Bassanelli
Elsa Iannicelli
Silvana Giacinti
Chiara D’Antonio
Anna Maria Aschelter
Paolo Marchetti
author_sort Michela Roberto
collection DOAJ
description Background. Renal cell carcinoma accounts for about 2-3% of all malignant tumors. The prevalence of brain metastases from RCC is less than 20% of cases. Traditionally, whole brain radiotherapy as well as the latest stereotactic radiosurgery improves both survival and local tumor control. These treatments also allow stabilization of clinical symptomatology. However, validated treatment guidelines for RCC patients with brain metastases are not yet available on account of the frequent exclusion of such patients from clinical trials. Moreover, limited data about the sequential use of three therapies, changing the class of agent, have been published up to now. Case Report. We report the case of a patient with metastatic RCC who developed disease progression after sunitinib and everolimus as first-line and second-line therapy, respectively. Thus, he underwent a multimodality treatment with pazopanib, as third-line therapy, to control systemic disease and radiosurgery directed on the new brain metastasis. To date, the patient is still receiving pazopanib, with progression-free survival and overall survival of 43 and 103 months, respectively. Conclusion. In a context characterized by different emerging options, with no general consensus on the optimal treatment strategy, the use of pazopanib in pretreated patients could be a suitable choice.
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spelling doaj-art-82c004c9a2f94422b5ec8f5a13c0468e2025-02-03T05:48:27ZengWileyCase Reports in Oncological Medicine2090-67062090-67142015-01-01201510.1155/2015/629046629046Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell CarcinomaMichela Roberto0Maria Bassanelli1Elsa Iannicelli2Silvana Giacinti3Chiara D’Antonio4Anna Maria Aschelter5Paolo Marchetti6Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyDepartment of Radiology, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyDepartment of Medical and Surgical Sciences and Translational Medicine, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyDepartment of Clinical and Molecular Medicine, Faculty of Medicine and Psychology “Sapienza”, St. Andrea Hospital, Via di Grottarossa 1035-1030, 00189 Rome, ItalyBackground. Renal cell carcinoma accounts for about 2-3% of all malignant tumors. The prevalence of brain metastases from RCC is less than 20% of cases. Traditionally, whole brain radiotherapy as well as the latest stereotactic radiosurgery improves both survival and local tumor control. These treatments also allow stabilization of clinical symptomatology. However, validated treatment guidelines for RCC patients with brain metastases are not yet available on account of the frequent exclusion of such patients from clinical trials. Moreover, limited data about the sequential use of three therapies, changing the class of agent, have been published up to now. Case Report. We report the case of a patient with metastatic RCC who developed disease progression after sunitinib and everolimus as first-line and second-line therapy, respectively. Thus, he underwent a multimodality treatment with pazopanib, as third-line therapy, to control systemic disease and radiosurgery directed on the new brain metastasis. To date, the patient is still receiving pazopanib, with progression-free survival and overall survival of 43 and 103 months, respectively. Conclusion. In a context characterized by different emerging options, with no general consensus on the optimal treatment strategy, the use of pazopanib in pretreated patients could be a suitable choice.http://dx.doi.org/10.1155/2015/629046
spellingShingle Michela Roberto
Maria Bassanelli
Elsa Iannicelli
Silvana Giacinti
Chiara D’Antonio
Anna Maria Aschelter
Paolo Marchetti
Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma
Case Reports in Oncological Medicine
title Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma
title_full Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma
title_fullStr Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma
title_full_unstemmed Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma
title_short Clinical Outcome of Third-Line Pazopanib in a Patient with Metastatic Renal Cell Carcinoma
title_sort clinical outcome of third line pazopanib in a patient with metastatic renal cell carcinoma
url http://dx.doi.org/10.1155/2015/629046
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