Dana-Farber Cancer Institute, Boston, MA, USA.
BJU Int. 2010 May;105(9):1247-54. doi: 10.1111/j.1464-410X.2009.08972.x. Epub 2009 Oct 26.
To assess the effectiveness, safety, and treatment patterns of anti-angiogenic agents in metastatic renal cell carcinoma (mRCC) in tertiary clinical practice settings.
We retrospectively reviewed the medical records in two tertiary oncology centres in the USA for all patients treated while off clinical trials from April 2003 to June 2008 who met the entry criteria and received one or more prescriptions for sunitinib or sorafenib, or one or more intravenous administrations of bevacizumab (off-label) as first-line anti-angiogenic treatment. The objective response rate (ORR) reviewed by independent physicians, adverse events (AEs), and treatment modifications were assessed.
Among 144 patients receiving sunitinib (57), sorafenib (62) and bevacizumab (25), the median treatment duration was 10.5, 8.1 and 7.9 months, and the ORR was 37%, 9% and 13%, respectively. The ORR was lower for patients with metastases to bone, brain, lungs or lymph nodes. Common AEs (all grades) for sunitinib were fatigue (53%), diarrhoea (37%); for sorafenib, diarrhoea (50%), fatigue (40%); for bevacizumab, fatigue (40%), nausea (24%). In all, 34 (60%), 51 (82%) and 20 (80%) patients receiving sunitinib, sorafenib and bevacizumab, respectively, discontinued treatment; 10 (18%), 11 (18%) and four (16%) discontinued due to AEs; 21%, 40% and 12% had a dose interruption, and 30%, 35% and 0% had a dose reduction.
Currently available anti-angiogenic agents had considerable effectiveness in clinical practice. However, the response rates appeared to be low in certain subgroups, but sample sizes were small. Patients had significant rates of AEs, many of which led to treatment modifications. The findings from this retrospective study suggest that there is a need for better-tolerated therapies for mRCC.
评估抗血管生成药物在三级临床实践环境中治疗转移性肾细胞癌(mRCC)的疗效、安全性和治疗模式。
我们回顾性分析了美国两家三级肿瘤中心的病历,纳入了 2003 年 4 月至 2008 年 6 月期间所有接受临床试验以外治疗且符合入组标准、并接受舒尼替尼或索拉非尼单一药物治疗或贝伐珠单抗(非适应证用药)静脉给药一线抗血管生成治疗的患者。由独立医生评估客观缓解率(ORR)、不良反应(AE)和治疗调整情况。
在接受舒尼替尼(57 例)、索拉非尼(62 例)和贝伐珠单抗(25 例)治疗的 144 例患者中,中位治疗时间分别为 10.5、8.1 和 7.9 个月,ORR 分别为 37%、9%和 13%。骨转移、脑转移、肺转移或淋巴结转移患者的 ORR 较低。舒尼替尼的常见(所有级别)AE 为乏力(53%)、腹泻(37%);索拉非尼为腹泻(50%)、乏力(40%);贝伐珠单抗为乏力(40%)、恶心(24%)。分别有 34(60%)、51(82%)和 20(80%)例接受舒尼替尼、索拉非尼和贝伐珠单抗治疗的患者停止治疗;10(18%)、11(18%)和 4(16%)例因 AE 停止治疗;21%、40%和 12%例中断剂量;30%、35%和 0%例减少剂量。
目前可用的抗血管生成药物在临床实践中具有显著疗效。然而,某些亚组的缓解率似乎较低,但样本量较小。患者 AE 发生率较高,许多 AE 需要治疗调整。这项回顾性研究的结果表明,mRCC 需要更好耐受的治疗方法。