Takahashi Mitsuru, Takahashi Shunji, Araki Nobuhito, Sugiura Hideshi, Ueda Takafumi, Yonemoto Tsukasa, Morioka Hideo, Hiraga Hiroaki, Hiruma Toru, Kunisada Toshiyuki, Matsumine Akihiko, Shimura Masashi, Kawai Akira
Division of Orthopaedic Surgery, Shizuoka Cancer Center Hospital, Shizuoka, Japan
Department of Medical Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo, Japan.
Oncologist. 2017 Aug;22(8):979-988. doi: 10.1634/theoncologist.2016-0064. Epub 2017 May 18.
Trabectedin is reported as effective, especially against translocation-related sarcomas (TRSs) after failure of or intolerance to standard chemotherapy. We conducted two phase II studies of TRS, confirming high efficacy of 1.2 mg/m trabectedin. The updated data of 66 patients in these studies was integrated to evaluate the efficacy of trabectedin against each histological subtype, and analyze final overall survival (OS).
Trabectedin was administered on day one of a 21-day cycle. Efficacy was assessed using progression-free survival (PFS), OS, and best overall response. An analysis of OS and PFS was performed for subgroups divided by baseline lymphocyte count (<1,000/μL, ≥1,000/μL) or number of previous chemotherapy regimens (0, 1, 2, ≥3 regimens), and a Weibull parametric model was used to estimate the numerical relationship between lymphocyte count and PFS and OS.
Median PFS and OS in overall patients were 5.6 (95% confidence interval [CI]: 4.1-7.3) and 17.5 months (95% CI: 12.6-23.6), respectively. PFS in the myxoid and round-cell liposarcoma (MRCL) group (7.4 months [95% CI: 5.6-11.1]) was longer than in the other subtypes. The response rate was also highest in the MRCL group. Median OS was longer in patients with baseline lymphocyte counts ≥1,000/μL than in those with counts of <1,000/μL, but median PFS was not different between the two subgroups.
Our updated and pooled data showed that trabectedin exerted prolonged disease control and antitumor effects in patients with advanced TRS, especially in MRCL. We consider that the subgroup analyses also provide important information for trabectedin treatment in patients with TRS.
The progression-free survival (PFS) for the integrated data of 66 patients with translocation-related sarcomas (TRSs) in two phase II studies of trabectedin 1.2 mg/m was 5.6 months (95% confidence interval: 4.1-7.3). PFS and response rate in myxoid/round-cell liposarcoma was longer than that of other subtypes. The overall survival (OS) in all TRS subtypes was similar to previous data of TRS patients. In subgroup analysis, the patients with baseline lymphocyte count ≥1,000/μL exhibited better OS, although PFS was not different by baseline lymphocyte count. Our data are considered important information for trabectedin treatment in TRS patients.
据报道,曲贝替定具有疗效,尤其对于标准化疗失败或不耐受的与易位相关的肉瘤(TRS)有效。我们开展了两项TRS的II期研究,证实了1.2mg/m²曲贝替定具有高疗效。整合这些研究中66例患者的最新数据,以评估曲贝替定对各组织学亚型的疗效,并分析最终总生存期(OS)。
在21天周期的第1天给予曲贝替定。使用无进展生存期(PFS)、OS和最佳总体缓解来评估疗效。对根据基线淋巴细胞计数(<1000/μL、≥1000/μL)或既往化疗方案数量(0、1、2、≥3个方案)划分的亚组进行OS和PFS分析,并使用威布尔参数模型估计淋巴细胞计数与PFS和OS之间的数值关系。
总体患者的中位PFS和OS分别为5.6个月(95%置信区间[CI]:4.1 - 7.3)和17.5个月(95%CI:12.6 - 23.6)。黏液样和圆形细胞脂肪肉瘤(MRCL)组的PFS(7.4个月[95%CI:5.6 - 11.1])长于其他亚型。MRCL组的缓解率也最高。基线淋巴细胞计数≥1000/μL的患者中位OS长于计数<1000/μL的患者,但两个亚组之间的中位PFS无差异。
我们更新和汇总的数据表明,曲贝替定在晚期TRS患者中发挥了延长疾病控制和抗肿瘤作用,尤其是在MRCL中。我们认为亚组分析也为TRS患者的曲贝替定治疗提供了重要信息。
在两项曲贝替定1.2mg/m²的II期研究中,66例与易位相关的肉瘤(TRS)患者的整合数据的无进展生存期(PFS)为5.6个月(95%置信区间:4.1 - 7.3)。黏液样/圆形细胞脂肪肉瘤的PFS和缓解率长于其他亚型。所有TRS亚型的总生存期(OS)与TRS患者的既往数据相似。在亚组分析中,基线淋巴细胞计数≥1000/μL的患者OS较好,尽管PFS在基线淋巴细胞计数方面无差异。我们的数据被认为是TRS患者曲贝替定治疗的重要信息。