The Continuation of Bevacizumab Following Disease Progression in Patients with Metastatic Colorectal Cancer Offers a Survival Benefit

被引:3
|
作者
Samelis, Georgios E. [1 ]
Ekmektzoglou, Konstantinos A. [1 ]
Tsiakou, Andriani [1 ]
Konstadoulakis, Manousos [2 ]
机构
[1] Hippokrat Gen Hosp Athens, Dept Oncol, Athens 11527, Greece
[2] Univ Athens, Sch Med, Dept Propaeudeut Surg 1, Hippokrat Gen Hosp Athens, GR-11527 Athens, Greece
关键词
Bevacizumab; Metastatic colorectal cancer; Survival; Toxicity; RANDOMIZED PHASE-III; HIGH-DOSE LEUCOVORIN; CONTINUOUS-INFUSION; 3RD-LINE THERAPY; FLUOROURACIL FAILURE; PLUS FLUOROURACIL; SUPPORTIVE CARE; LINE TREATMENT; COLON-CANCER; IRINOTECAN;
D O I
10.5754/hge11179
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: There is little information in the literature on the use of bevacizumab (BV) combination chemotherapy in multiple lines with regimens including irinotecan and oxaliplatin, in metastatic colorectal cancer (mCRC) patients with disease progression. The aim of this small retrospective institutional study is to compare the efficacy and safety of the continuation of BV in combination with various chemotherapeutic agents, within the framework of multiple line therapy in progressed mCRC patients. Methodology: Our retrospective study included 21 patients with mCRC that had received at least one course of irinotecan-based or oxaliplatin-based chemotherapy with BV before disease progression. BV treatment was continuously dispensed after disease progression. Sub-group analysis was performed in terms of age, site of metastases, spread and co-morbidity. Results: The median overall survival (OS) was 23+ months (range 4-51 months) with no statistically significant differences between the aforementioned subgroups of patients, except from the subgroup according to spread (p=0.044). Time to progression was 17 months. Anemia (all grades) was reported in 33.3% of the patients, while hemorrhage and thrombosis were reported in 28.6% and 14.3%, respectively. Conclusions: Multiple line treatment in advanced colorectal cancer, including BV combined with standard chemotherapy, may improve OS with an acceptable toxicity profile in patients with mCRC after disease progression.
引用
收藏
页码:1968 / 1971
页数:4
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