Literature DB >> 21206220

Evaluation of response to multikinase inhibitor in metastatic renal cell carcinoma by FDG PET/contrast-enhanced CT.

Ryogo Minamimoto1, Noboru Nakaigawa, Ukihide Tateishi, Akiko Suzuki, Kazuya Shizukuishi, Takeshi Kishida, Takeshi Miura, Kazuhide Makiyama, Masahiro Yao, Yoshinobu Kubota, Tomio Inoue.   

Abstract

PURPOSE: Multikinase inhibitor (MKI) is a promising drug for treatment of metastatic renal cell carcinoma (mRCC). We explained the usefulness of [¹⁸F]-2-fluoro-2-deoxyglucose positron emission tomography/contrast-enhanced computed tomography (FDG PET/CECT) for mRCC in evaluating the early response to MKI and in predicting progression-free survival (PFS).
METHODS: Patients who planned MKI treatment for mRCC were included in this prospective study. FDG PET/CECT was performed before MKI treatment and after one cycle of MKI treatment. Evaluation of the response to MKI was assessed by PET according to the European Organization for Research and Treatment of Cancer, by CT according to the Response Evaluation Criteria in Solid Tumors and appearance of central hypoattenuation (CHA).
RESULTS: Twelve patients were enrolled in the study. Equality of response evaluation between PET and CT was in 8 patients (partial response [PR]: 1, stable disease [SD]: 6, progressive disease [PD]: 1). Among the other 4 patients, PET showed 2 patients with PR and 2 patients with PD, in contrast to the CT finding of SD in all 4 patients. PFS according to PET response showed a statistically significant difference between PR and SD (P < 0.05) and between PR and PD (P < 0.05), but not between PR and SD (P = 0.083). Positive CHA in metastatic lesions after MKI treatment was confirmed in 8 patients. PFS with positive CHA was 233.8 days, while that without CHA was 75.0 days (P < 0.05).
CONCLUSION: FDG PET/CECT shows potential for evaluating early treatment response to MKI in mRCC and for predicting PFS.

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Year:  2010        PMID: 21206220     DOI: 10.1097/RLU.0b013e3181f9ddd9

Source DB:  PubMed          Journal:  Clin Nucl Med        ISSN: 0363-9762            Impact factor:   7.794


  12 in total

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Review 2.  [Renal cell carcinoma: what is new in 2010?].

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5.  Evaluation of cancer treatment in the abdomen: Trends and advances.

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6.  Early assessment by FDG-PET/CT of patients with advanced renal cell carcinoma treated with tyrosine kinase inhibitors is predictive of disease course.

Authors:  Daiki Ueno; Masahiro Yao; Ukihide Tateishi; Ryogo Minamimoto; Kazuhide Makiyama; Narihiko Hayashi; Futoshi Sano; Takayuki Murakami; Takeshi Kishida; Takeshi Miura; Kazuki Kobayashi; Sumio Noguchi; Ichiro Ikeda; Yoshiharu Ohgo; Tomio Inoue; Yoshinobu Kubota; Noboru Nakaigawa
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7.  The early response of renal cell carcinoma to tyrosine kinase inhibitors evaluated by FDG PET/CT was not influenced by metastatic organ.

Authors:  Manabu Kakizoe; Masahiro Yao; Ukihide Tateishi; Ryogo Minamimoto; Daiki Ueno; Kazuhiro Namura; Kazuhide Makiyama; Narihiko Hayashi; Futoshi Sano; Takeshi Kishida; Kazuki Kobayashi; Sumio Noguchi; Ichiro Ikeda; Yoshiharu Ohgo; Masataka Taguri; Satoshi Morita; Tomio Inoue; Yoshinobu Kubota; Noboru Nakaigawa
Journal:  BMC Cancer       Date:  2014-06-02       Impact factor: 4.430

Review 8.  The role of fluorine-18-fluorodeoxyglucose positron emission tomography in evaluating the response to tyrosine-kinase inhibitors in patients with metastatic primary renal cell carcinoma.

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9.  Prognostic Value of Quantitative Metabolic Metrics on Baseline Pre-Sunitinib FDG PET/CT in Advanced Renal Cell Carcinoma.

Authors:  Ryogo Minamimoto; Amir Barkhodari; Lauren Harshman; Sandy Srinivas; Andrew Quon
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Review 10.  Tyrosine-Kinase Inhibitors Therapies with Mainly Anti-Angiogenic Activity in Advanced Renal Cell Carcinoma: Value of PET/CT in Response Evaluation.

Authors:  Girolamo Ranieri; Ilaria Marech; Artor Niccoli Asabella; Alessandra Di Palo; Mariangela Porcelli; Valentina Lavelli; Giuseppe Rubini; Cristina Ferrari; Cosmo Damiano Gadaleta
Journal:  Int J Mol Sci       Date:  2017-09-09       Impact factor: 5.923

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