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首页> 外文期刊>Annals of oncology: official journal of the European Society for Medical Oncology >A randomized phase III study comparing pegylated liposomal doxorubicin with capecitabine as first-line chemotherapy in elderly patients with metastatic breast cancer: Results of the OMEGA study of the Dutch Breast Cancer Research Group BOOG
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A randomized phase III study comparing pegylated liposomal doxorubicin with capecitabine as first-line chemotherapy in elderly patients with metastatic breast cancer: Results of the OMEGA study of the Dutch Breast Cancer Research Group BOOG

机译:一项III期随机研究比较了聚乙二醇脂质体阿霉素和卡培他滨作为老年转移性乳腺癌患者的一线化疗:荷兰乳腺癌研究小组BOOG的OMEGA研究结果

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摘要

Background: Prospective data on chemotherapy for elderly patients with metastatic breast cancer (MBC) remain scarce. We compared the efficacy and safety of first-line chemotherapy with pegylated liposomal doxorubicin (PLD) versus capecitabine in MBC patients aged ≥65 years in a multicentre, phase III trial. Patients and methods: Patients were randomized to six cycles of PLD (45 mg/m2 every 4 weeks) or eight cycles of capecitabine (1000 mg/m2 twice daily, day 1-14 every 3 weeks). Results: The study enrolled 78 of the planned 154 patients and was closed prematurely due to slow accrual and supply problems of PLD. Many included patients were aged ≥75 years (54%) and vulnerable (≥1 geriatric condition: 71%). The median dose intensity was 85% for PLD and 84% for capecitabine, respectively. In both arms, the majority of patients completed at least 12 weeks of treatment (PLD 73%; capecitabine 74%). After a median follow-up of 39 months, 77 patients had progressed and 62 patients had died of MBC. Median progression-free survival was 5.6 versus 7.7 months (P = 0.11) for PLD and capecitabine, respectively. Median overall survival was 13.8 months for PLD and 16.8 months for capecitabine (P = 0.59). Both treatments were feasible, grade 3 toxicities consisting of fatigue (both arms: 13%), hand-foot syndrome (PLD: 10%; capecitabine: 16%), stomatitis (PLD: 10%; capecitabine: 3%), exanthema (PLD: 5%) and diarrhoea (PLD: 3%; capecitabine: 5%). Only 1 of 10 patients aged ≥80 years completed chemotherapy, while 3 and 6 patients discontinued treatment due to toxicity or progressive disease, respectively. Conclusion: Both PLD and capecitabine demonstrated comparable efficacy and acceptable tolerance as first-line single-agent chemotherapy in elderly patients with MBC, even in vulnerable patients or patients aged ≥75 years. However, patients aged ≥80 years were unlikely to complete chemotherapy successfully.
机译:背景:关于老年转移性乳腺癌(MBC)患者化疗的前瞻性数据仍然很少。在一项多中心III期试验中,我们比较了聚乙二醇脂质体阿霉素(PLD)与卡培他滨一线化疗对≥65岁的MBC患者的疗效和安全性。患者和方法:将患者随机分为6个PLD周期(每4周45 mg / m2)或8个卡培他滨(每天1000 mg / m2两次,每3周第1-14天)。结果:这项研究招募了154名计划中的78名患者,由于PLD的累积和供应缓慢,因此提前关闭。其中许多患者年龄≥75岁(54%)且易感(≥1老年病:71%)。 PLD和卡培他滨的中位剂量强度分别为85%和84%。在两组患者中,大多数患者至少完成了12周的治疗(PLD 73%;卡培他滨74%)。中位随访39个月后,有77例进展,62例死于MBC。 PLD和卡培他滨的中位无进展生存期分别为5.6个月和7.7个月(P = 0.11)。 PLD的中位总生存期为13.8个月,卡培他滨的中位总生存期为16.8个月(P = 0.59)。两种治疗都是可行的,三级毒性包括疲劳(两臂:13%),手足综合征(PLD:10%;卡培他滨:16%),口腔炎(PLD:10%;卡培他滨:3%),皮疹( PLD:5%)和腹泻(PLD:3%;卡培他滨:5%)。年龄≥80岁的10名患者中只有1名完成了化疗,而3名和6名患者分别由于毒性或进行性疾病而中止了治疗。结论:PLD和卡培他滨在老年MBC患者,甚至脆弱患者或75岁以上患者中均表现出与一线单药化疗相当的疗效和可接受的耐受性。但是,年龄≥80岁的患者不太可能成功完成化疗。

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