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VIP (etoposide, ifosfamide, and cisplatin) in patients with previously treated soft tissue sarcoma

机译:先前接受过治疗的软组织肉瘤患者的VIP(依托泊苷,异环磷酰胺和顺铂)

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We retrospectively reviewed outcomes of treatment with VIP (combination of etoposide, ifosfamide, and cisplatin) in patients with previously treated soft tissue sarcoma (STS). We analyzed the medical records of patients with advanced or relapsed STS who had undergone VIP treatment as second-line or more chemotherapy between January 2000 and December 2015. The patients were treated with a combination of etoposide (100 mg/m2 for 5 days), ifosfamide (2000 mg/m2 for 2 days), and cisplatin (20 mg/m2 for 5 days) once every 4 weeks. Treatment response, progression-free survival (PFS), and overall survival (OS) were analyzed in all patients and between responder and nonresponder groups (responders showed a tumor response to any prior systemic chemotherapy before VIP). Twenty-four patients with a median age of 50 years (range: 20–68 years) were treated with VIP. Eleven (45.8%) patients were male and 7 (29.2%) received 2 or more chemotherapy regimens before VIP. Median PFS was 3.7 months (95% confidence interval [CI], 1.3–6.1 months) and median OS was 10.0 months (95% CI, 6.6–13.5). The overall response rate was 37.5%, and the disease control rate was 50%. The responder group showed better PFS (7.7 months vs 3.0 months; P = 0.101) and significantly improved OS (11.0 months vs 8.8 months; P = 0.039) compared to those of nonresponders. All patients reported some grade of hematological toxicity. The most frequently encountered hematological toxicity was neutropenia (any grade, 77.7%; grade 3 or 4, 74.0%). VIP might be effective in patients with previously treated STS.
机译:我们回顾性地回顾了先前接受过软组织肉瘤(STS)治疗的患者使用VIP(依托泊苷,异环磷酰胺和顺铂的组合)治疗的结果。我们分析了2000年1月至2015年12月间接受VIP作为第二线或以上化疗的晚期或复发性STS患者的病历。这些患者接受依托泊苷(100 mg / m 2 5天),异环磷酰胺(2000 mg / m 2 2天)和顺铂(20 mg / m 2 5天),每4周一次。分析了所有患者以及有反应者和无反应者组之间的治疗反应,无进展生存期(PFS)和总生存期(OS)(反应者对VIP之前的任何先前全身化疗均显示了肿瘤反应)。 24位中位年龄为50岁(范围:20-68岁)的患者接受了VIP治疗。十一名(45.8%)患者为男性,七名(29.2%)患者在VIP前接受了2种或更多的化疗方案。 PFS中位数为3.7个月(95%置信区间[CI]为1.3–6.1个月),OS中位数为10.0个月(95%CI为6.6-13.5)。总体缓解率为37.5%,疾病控制率为50%。与无反应者相比,有反应者组表现出更好的PFS(7.7个月比3.0个月; P = 0.101)和显着改善的OS(11.0个月比8.8个月; P = 0.039)。所有患者均报告某种程度的血液学毒性。最常见的血液学毒性是中性粒细胞减少症(任何等级,为77.7%; 3级或4级,为74.0%)。 VIP对先前接受过STS治疗的患者可能有效。

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