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阿霉素与奥拉单抗治疗英格兰和北爱尔兰软组织肉瘤的真实世界经验。

Real-world experience with doxorubicin and olaratumab in soft tissue sarcomas in England and Northern Ireland.

作者信息

Gennatas Spyridon, Chamberlain Florence, Carter Thomas, Slater Susanna, Cojocaru Elena, Lambourn Beth, Stansfeld Anna, Todd Radha, Verrill Mark, Ali Nasim, Jones Robin L, Simmonds Peter, Keay Nicola, McCarty Heather, Strauss Sandra, Karavasilis Vassilios, Dileo Palma, Benson Charlotte

机构信息

1Sarcoma Unit, Royal Marsden Hospital, Fulham Road, London, SW3 6JJ UK.

2University College Hospital London, 235 Euston Rd, London, NW1 2BU UK.

出版信息

Clin Sarcoma Res. 2020 May 6;10:9. doi: 10.1186/s13569-020-00131-x. eCollection 2020.

Abstract

BACKGROUND

A randomised phase II trial demonstrated that the addition of olaratumab to doxorubicin significantly increased overall survival (OS) in patients with advanced soft tissue sarcomas (STS) compared to doxorubicin alone. The recently presented phase III study of doxorubicin and olaratumab in advanced soft tissue sarcoma was discordant with this finding.

METHODS

We performed a retrospective analysis of adult patients with advanced-/metastatic STS treated with at least two cycles of doxorubicin and olaratumab at eight sarcoma units across England and Northern Ireland between May 2017 and March 2019.

RESULTS

172 patients were evaluable and 40 patients (23.3%) had died at the time of analysis. Median ECOG performance status (PS) was 1. Median progression free survival (PFS) was 6.8 months (95% CI 5.9-7.7 months). Leiomyosarcoma was the most common histological subtype (75 patients, 43.6%), followed by liposarcomas (19, 11.0%). The mean number of cycles was 5 (doxorubicin range 2-6; olaratumab range 2-23). Two patients (1.2%) had a complete response and 34 (19.8%) had a partial response. 79 (45.9%) had stable and 58 (33.7%) progressive disease. 57 patients (33.1%) experienced grade ≥ 3 neutropenia and 7 patients (4.1%) grade ≥ 3 febrile neutropenia. Grade ≥ 3 anaemia was seen in 21 patients (12.2%). Grade ≥ 3 non-haematological toxicities were seen in 35 patients (20.3%). A clinically significant drop in left ventricular ejection fraction was seen in 6 patients (3.5%). 48 patients (27.9%) required a dose reduction. Overall survival (OS) is pending.

CONCLUSIONS

Our results are in keeping with the phase III study findings: response rate, PFS and OS were similar to those reported in the phase III ANNOUNCE trial.

摘要

背景

一项随机II期试验表明,与单独使用阿霉素相比,在阿霉素基础上加用奥拉单抗可显著提高晚期软组织肉瘤(STS)患者的总生存期(OS)。最近公布的阿霉素和奥拉单抗治疗晚期软组织肉瘤的III期研究结果与此发现不一致。

方法

我们对2017年5月至2019年3月期间在英格兰和北爱尔兰的8个肉瘤治疗中心接受至少两个周期阿霉素和奥拉单抗治疗的成年晚期/转移性STS患者进行了回顾性分析。

结果

172例患者可评估,40例患者(23.3%)在分析时死亡。中位东部肿瘤协作组(ECOG)体能状态(PS)为1。中位无进展生存期(PFS)为6.8个月(95%CI 5.9 - 7.7个月)。平滑肌肉瘤是最常见的组织学亚型(75例,43.6%),其次是脂肪肉瘤(19例,11.0%)。平均周期数为5(阿霉素范围2 - 6;奥拉单抗范围2 - 23)。2例患者(1.2%)完全缓解,34例患者(19.8%)部分缓解。79例患者(45.9%)病情稳定,58例患者(33.7%)病情进展。57例患者(33.1%)出现≥3级中性粒细胞减少,7例患者(4.1%)出现≥3级发热性中性粒细胞减少。21例患者(12.2%)出现≥3级贫血。35例患者(20.3%)出现≥3级非血液学毒性。6例患者(3.5%)出现具有临床意义的左心室射血分数下降。48例患者(27.9%)需要减量。总生存期(OS)有待确定。

结论

我们的结果与III期研究结果一致:缓解率、PFS和OS与III期ANNOUNCE试验报告的结果相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1782/7203838/628e9e092ccd/13569_2020_131_Fig1_HTML.jpg

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