Defining patient outcomes in stage IV colorectal cancer: a prospective study with baseline stratification according to disease resectability status
Defining patient outcomes in stage IV colorectal cancer: a prospective study with baseline stratification according to disease resectability status
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定义 IV 期结直肠癌患者的结局:根据疾病可切除性状态进行基线分层的前瞻性研究
DOI:
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发表时间:
2010
影响因子:
8.8
通讯作者:
A. Gillbanks
中科院分区:
文献类型:
--
作者:
D. Watkins;I. Chau;D. Cunningham;S. Mudan;N. Karanjia;G. Brown;S. Ashley;A. Norman;A. Gillbanks
Background:Stage IV colorectal cancer encompasses a broad patient population in which both curative and palliative management strategies may be used. In a phase II study primarily designed to assess the efficacy of capecitabine and oxaliplatin, we were able to prospectively examine the outcomes of patients with stage IV colorectal cancer according to the baseline resectability status.Methods:At enrolment, patients were stratified into three subgroups according to the resectability of liver disease and treatment intent: palliative chemotherapy (subgroup A), conversion therapy (subgroup B) or neoadjuvant therapy (subgroup C). All patients received chemotherapy with capecitabine 2000 mg m–2 on days 1–14 and oxaliplatin 130 mg m–2 on day 1 repeated every 3 weeks. Imaging was repeated every four cycles where feasible liver resection was undertaken after four or eight cycles of chemotherapy.Results:Of 128 enrolled patients, 74, 22 and 32 were stratified into subgroups A, B and C, respectively. Attempt at curative liver resection was undertaken in 10 (45%) patients in subgroup B and 19 (59%) in subgroup C. The median overall survival was 14.6, 24.5 and 52.9 months in subgroups A, B and C, respectively. For patients in subgroups B and C who underwent an attempt at curative resection, 3-year progression-free survival was 10% in subgroup B and 37% for subgroup C.Conclusions:This prospective study shows the wide variation in outcome according to baseline resectability status and highlights the potential clinical value of a modified staging system to distinguish between these patient subgroups.
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影响因子:
9
作者:
Fong, Y;Fortner, J;Blumgart, LH
通讯作者:
Blumgart, LH
影响因子:
45.3
作者:
Goldberg, RM;Sargent, DJ;Alberts, SR
通讯作者:
Alberts, SR
影响因子:
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Iwatsuki, S;Dvorchik, I;Starzl, TE
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影响因子:
158.5
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Hurwitz, H;Fehrenbacher, L;Kabbinavar, F
通讯作者:
Kabbinavar, F
影响因子:
45.3
作者:
Alberts, SR;Horvath, WL;Donohue, JH
通讯作者:
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