2008
DOI: 10.1200/jco.2008.26.15_suppl.4603
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Phase II study of bevacizumab (A) plus capecitabine (X) in patients (pts) with advanced/metastatic hepatocellular carcinoma (HCC): Final report

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Cited by 15 publications
(12 citation statements)
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“…These results should be interpreted with caution because a sorafenib-alone arm was not included and high incidence of adverse events related to doxorubicin was noted. Many small-scale trials of combining MTT with cytotoxic chemotherapy have been reported [385][386][387][388][389]. However, the treatment efficacy in terms of tumor response rate and patient survival were similar to those reported for the cytotoxic regimens alone (Table 3) [372,[375][376][377][378][379][380][381][382].…”
Section: Future Directionsmentioning
confidence: 64%
“…These results should be interpreted with caution because a sorafenib-alone arm was not included and high incidence of adverse events related to doxorubicin was noted. Many small-scale trials of combining MTT with cytotoxic chemotherapy have been reported [385][386][387][388][389]. However, the treatment efficacy in terms of tumor response rate and patient survival were similar to those reported for the cytotoxic regimens alone (Table 3) [372,[375][376][377][378][379][380][381][382].…”
Section: Future Directionsmentioning
confidence: 64%
“…1,7,[73][74][75][76][77][78] The cancer cell has been the only target of anticancer therapy for more than 50 years. However, the cancer cell is genetically unstable, and mutations accumulate.…”
Section: Clinical Trials Of Antiangiogenic Agents In Patients With Hccmentioning
confidence: 99%
“…One, a phase II study, will compare bevacizumab and erlotinib versus sorafenib alone in a similar population as in the SHARP study, and the second, a phase III study, will compare erlotinib and sorafenib versus sorafenib alone. The safety and efficacy of bevacizumab and erlotinib is also being investigated in an ongoing study in Asian patients with advanced HCC (77). A recent interim analysis of safety data from this trial reported that, of the 51 enrolled patients, 2 patients had confirmed partial responses and 1 patient with an unconfirmed partial response remained on treatment.…”
Section: Monotherapy and Combination Therapymentioning
confidence: 99%
“…Brivanib has shown activity in mouse models of human HCC (77). Interim analyses from a study of single-agent brivanib as first-and second-line therapy showed that, in a largely Asian population of 55 patients with advanced HCC, first-line treatment with brivanib was associated with a median time to progression of 2.8 months, with a disease control rate of 60% (47 evaluable patients) and median OS of 10 months (79).…”
Section: Monotherapy and Combination Therapymentioning
confidence: 99%