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Outcomes of colorectal cancer patients with peritoneal carcinomatosis treated with chemotherapy with and without targeted therapy
被引:145
|作者:
Klaver, Y. L. B.
[1
]
Simkens, L. H. J.
[2
]
Lemmens, V. E. P. P.
[3
,4
]
Koopman, M.
[5
]
Teerenstra, S.
[6
]
Bleichrodt, R. P.
[7
]
de Hingh, I. H. J. T.
[1
]
Punt, C. J. A.
[8
]
机构:
[1] Catharina Hosp, Dept Surg, NL-5623 EJ Eindhoven, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, NL-6525 ED Nijmegen, Netherlands
[3] Comprehens Canc Ctr S IKZ, Eindhoven Canc Registry, Eindhoven, Netherlands
[4] Erasmus Univ, Med Ctr, Dept Publ Hlth, Rotterdam, Netherlands
[5] Univ Med Ctr Utrecht, Dept Med Oncol, Utrecht, Netherlands
[6] Radboud Univ Nijmegen, Med Ctr, Dept Epidemiol Biostat & Hlth Technol Assessment, NL-6525 ED Nijmegen, Netherlands
[7] Radboud Univ Nijmegen, Med Ctr, Dept Surg, NL-6525 ED Nijmegen, Netherlands
[8] Univ Amsterdam, Acad Med Ctr, Dept Med Oncol, NL-1105 AZ Amsterdam, Netherlands
来源:
EJSO
|
2012年
/
38卷
/
07期
关键词:
Colorectal cancer;
Metastasis;
Chemotherapy;
Peritoneal carcinomatosis;
PHASE-III;
COMBINATION CHEMOTHERAPY;
SYSTEMIC CHEMOTHERAPY;
RANDOMIZED-TRIAL;
GROUP DCCG;
CAPECITABINE;
OXALIPLATIN;
SURVIVAL;
FLUOROURACIL;
IRINOTECAN;
D O I:
10.1016/j.ejso.2012.03.008
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Background: Although systemic therapies have shown to result in survival benefit in patients with metastatic colorectal cancer (mCRC), outcomes in patients with peritoneal carcinomatosis (PC) are poor. No data are available on outcomes of current chemotherapy schedules plus targeted agents in mCRC patients with PC. Methods: Previously untreated mCRC patients treated with chemotherapy in the CAIRO study and with chemotherapy and targeted therapy in the CAIRO2 study were included and retrospectively analysed according to presence or absence of PC at randomisation. Patient demographics, primary tumour characteristics, progression-free survival (PFS), overall survival (OS), and occurrence of toxicity were evaluated. Results: Thirty-four patients with PC were identified in the CAIRO study and 47 patients in the CAIRO2 study. Median OS was decreased for patients with PC compared with patients without PC (CAIRO: 10.4 versus 17.3 months, respectively (p <= 0.001); CAIRO2: 15.2 versus 20.7 months, respectively (p < 0.001)). Median number of treatment cycles did not differ between patients with or without PC in both studies. Occurrence of major toxicity was more frequent in patients with PC treated with sequential chemotherapy in the CAIRO study as compared to patients without PC. This was not reflected in reasons to discontinue treatment. In the CAIRO2 study, no differences in major toxicity were observed. Conclusion: Our data demonstrate decreased efficacy of current standard chemotherapy with and without targeted agents in mCRC patients with PC. This suggests that the poor outcome cannot be explained by undertreatment or increased susceptibility to toxicity, but rather by relative resistance to treatment. (c) 2012 Elsevier Ltd. All rights reserved.
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页码:617 / 623
页数:7
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