2021年12月
Second-line chemotherapy after early disease progression during first-line chemotherapy containing bevacizumab for patients with metastatic colorectal cancer
BMC Cancer
- 巻
- 21
- 号
- 1
- 記述言語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1186/s12885-021-08890-6
- 出版者・発行元
- Springer Science and Business Media LLC
<title>Abstract</title><sec>
<title>Background</title>
The ML18174 study, which showed benefits of bevacizumab (BEV) continuation beyond progression (BBP) for metastatic colorectal cancer (mCRC), excluded patients with first-line progression-free survival (PFS) shorter than 3 months. The present study was conducted to evaluate the efficacy of second-line chemotherapy after early disease progression during first-line chemotherapy containing bevacizumab.
</sec><sec>
<title>Methods</title>
The subjects of this study were mCRC patients who experienced disease progression < 100 days from commencement of first-line chemotherapy containing BEV initiated between Apr 2007 and Dec 2016. Second-line chemotherapy regimens were classified into two groups with and without BEV/other anti-angiogenic agents (BBP and non-BBP) and efficacy and safety were compared using univariate and multivariate analysis.
</sec><sec>
<title>Results</title>
Sixty-one patients were identified as subjects of this study. Baseline characteristics were numerically different between BBP (<italic>n</italic> = 37) and non-BBP (<italic>n</italic> = 25) groups, such as performance status (0–1/<underline>></underline> 2/unknown: 89/8/3 and 56/40/4%), <italic>RAS</italic> status (wild/mutant/unknown: 32/54/16 and 76/16/8%). Response rate was 8.6% in BBP group and 9.1% in non-BBP group (<italic>p</italic> = 1.00). Median PFS was 3.9 months in BBP group and 2.8 months in non-BBP group (HR [95%CI]: 0.79 [0.46–1.34], <italic>p</italic> = 0.373, adjusted HR: 0.87 [0.41–1.82], <italic>p</italic> = 0.707). Median overall survival was 8.5 months in BBP group and 5.4 months in non-BBP group (HR 0.66 [0.38–1.12], <italic>p</italic> = 0.125, adjusted HR 0.53 [0.27–1.07], <italic>p</italic> = 0.078).
</sec><sec>
<title>Conclusion</title>
In mCRC patients who experienced early progression in first-line chemotherapy, second-line chemotherapy showed poor clinical outcomes regardless use of anti-angiogenic agents.
</sec>
<title>Background</title>
The ML18174 study, which showed benefits of bevacizumab (BEV) continuation beyond progression (BBP) for metastatic colorectal cancer (mCRC), excluded patients with first-line progression-free survival (PFS) shorter than 3 months. The present study was conducted to evaluate the efficacy of second-line chemotherapy after early disease progression during first-line chemotherapy containing bevacizumab.
</sec><sec>
<title>Methods</title>
The subjects of this study were mCRC patients who experienced disease progression < 100 days from commencement of first-line chemotherapy containing BEV initiated between Apr 2007 and Dec 2016. Second-line chemotherapy regimens were classified into two groups with and without BEV/other anti-angiogenic agents (BBP and non-BBP) and efficacy and safety were compared using univariate and multivariate analysis.
</sec><sec>
<title>Results</title>
Sixty-one patients were identified as subjects of this study. Baseline characteristics were numerically different between BBP (<italic>n</italic> = 37) and non-BBP (<italic>n</italic> = 25) groups, such as performance status (0–1/<underline>></underline> 2/unknown: 89/8/3 and 56/40/4%), <italic>RAS</italic> status (wild/mutant/unknown: 32/54/16 and 76/16/8%). Response rate was 8.6% in BBP group and 9.1% in non-BBP group (<italic>p</italic> = 1.00). Median PFS was 3.9 months in BBP group and 2.8 months in non-BBP group (HR [95%CI]: 0.79 [0.46–1.34], <italic>p</italic> = 0.373, adjusted HR: 0.87 [0.41–1.82], <italic>p</italic> = 0.707). Median overall survival was 8.5 months in BBP group and 5.4 months in non-BBP group (HR 0.66 [0.38–1.12], <italic>p</italic> = 0.125, adjusted HR 0.53 [0.27–1.07], <italic>p</italic> = 0.078).
</sec><sec>
<title>Conclusion</title>
In mCRC patients who experienced early progression in first-line chemotherapy, second-line chemotherapy showed poor clinical outcomes regardless use of anti-angiogenic agents.
</sec>
- リンク情報
- ID情報
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- DOI : 10.1186/s12885-021-08890-6
- eISSN : 1471-2407