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Oudard. Retrospective Evaluation of Tyrosine Kinase Inhibitor (TKI) - Everolimus (Eve) and - or TKI-eve-TKI Sequences in Metastatic Renal Cell Carcinoma (MRCC) - A French Survey-The Sector Study
Oudard. Retrospective Evaluation of Tyrosine Kinase Inhibitor (TKI) - Everolimus (Eve) and - or TKI-eve-TKI Sequences in Metastatic Renal Cell Carcinoma (MRCC) - A French Survey-The Sector Study
Oudard. Retrospective Evaluation of Tyrosine Kinase Inhibitor (TKI) - Everolimus (Eve) and - or TKI-eve-TKI Sequences in Metastatic Renal Cell Carcinoma (MRCC) - A French Survey-The Sector Study
Retrospective evaluation of tyrosine kinase inhibitor (TKI)-everolimus (eve) and/or TKI-eve-TKI sequences in metastatic renal cell carcinoma (mRCC): A Fr
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17/11/2015
Retrospective evaluation of tyrosine kinase inhibitor (TKI)-everolimus (eve) and/or TKI-eve-TKI sequences in metastatic renal cell carcinoma (mRCC): A Fr
who progressed on initial TKI and received eve as 2nd line were recorded. In these pts, 3rd line TKI was recorded. Primary
endpoint was Duration of Treatment (DT) of each sequence. Secondary endpoints were best radiological response for eve
evaluated by 2 independent radiologists, tolerability, dose reduction, overall survival from the start of first TKI (OS). Patients
characteristics: Amongst 164 pts, 144 pts with follow-up > 4 months since initiation of eve were evaluated, 59/144 pts received
TKI-eve-TKI. Before eve initiation: median age was 65 yrs, most pts were male (70.3%), had clear cell histology (92.3%), had
received sunitinib as first TKI (94.4%). Main comorbidities were: hypertension (43.8%), diabetes (15.3%), and
hypercholesterolemia (19.4%). At the time of eve initiation, MSKCC classification was good (24.4%), intermediate (61.5%) or
poor (14.1%). Results: median DT of eve was 4 months and 21% pts were treated >9 months with 2.9% PR and 67.6% SD by
central review. Correlation between response to first TKI and eve was observed. Dose reduction of eve for toxicity was 23.2%.
The most common toxicities (all grades) were: stomatitis (25.3%), PNI (13%), fatigue (40.7%), hyperglycemia (9.3%),
hypercholesterolemia (17.3%) and hypertriglyceridemia (22.8%). Median duration of TKI-eve sequence was 18 months
(IC95%: 15-20), and OS was 36 months (IC95%: 27-56). For TKI-eve-TKI sequence (59 pts), sorafenib was mostly used
(76.3%) with dose reduction and clinical benefit rate of 26.7% and 42.2% respectively. Median DT and OS were 24 and 41
months (IC95%: 19-29; 25-57) respectively. Conclusions: In real world experience, for mRCC pts receiving TKI-eve
sequence, median DT of eve is 4 months with OS of 36 months which compares favorably with RECORD1 and RECORD 3
trials respectively.
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http://meetinglibrary.asco.org/content/123918-142
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17/11/2015
Retrospective evaluation of tyrosine kinase inhibitor (TKI)-everolimus (eve) and/or TKI-eve-TKI sequences in metastatic renal cell carcinoma (mRCC): A Fr
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http://meetinglibrary.asco.org/content/123918-142
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17/11/2015
Retrospective evaluation of tyrosine kinase inhibitor (TKI)-everolimus (eve) and/or TKI-eve-TKI sequences in metastatic renal cell carcinoma (mRCC): A Fr
http://meetinglibrary.asco.org/content/123918-142
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