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Efficacy and Safety of Nanosomal Docetaxel Lipid Suspension-Based Chemotherapy in Sarcoma: A Multicenter, Retrospective Study

机译:纳米组织多西紫杉醇脂悬浮液中肉瘤的疗效和安全性:多中心,回顾性研究

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摘要

Objective. To evaluate the efficacy and safety of nanosomal docetaxel lipid suspension (NDLS, DoceAqualip) based chemotherapy in patients with sarcoma. Methods. In this retrospective, multicenter (6 centers), observational study, we analyzed the medical charts of adult patients of either sex, who were treated with NDLS (75 mg/m2 in 3-weekly cycles) based chemotherapy for the treatment of sarcoma. The efficacy outcomes were overall response rate (ORR: complete response (CR) + partial response (PR)) and disease control rate (DCR: CR + PR + stable disease (SD)) in patients who received NDLS-based chemotherapy in neoadjuvant and metastatic settings. Overall survival (OS) and safety were evaluated for all settings. Results. Of 11 patients (neoadjuvant: 1, adjuvant: 3, and metastatic: 7) in this study, majority had leiomyosarcoma (63.6%, 7/11) followed by extraskeletal myxoid chondrosarcoma (EMC), high grade pleomorphic sarcoma of mandible, malignant fibrous histiocytoma of right thigh, and osteosarcoma of femur (9.1% each, 1/11 each). NDLS plus gemcitabine combination was used in 10 patients (90.9%), and NDLS plus cyclophosphamide was used in one patient with EMC (9.1%). Efficacy evaluation was performed for 7 patients (neoadjuvant: 1/1; metastatic: 6/7). Complete response was reported in one patient (soft tissue sarcoma of mandible) treated in neoadjuvant setting. In metastatic setting, ORR was 50% and DCR was 66.7% (CR: 16.7% (1/6), PR: 33.3% (2/6), SD: 16.7% (1/6)). At a median follow-up of 6.5 months (range: 0.06–20.2 months), median OS was not reached in neoadjuvant and adjuvant settings, but it was 15.8 months in metastatic setting. At least 1 AE was reported in 7 (63.6%) patients. Neutropenia, thrombocytopenia, lymphopenia, and anemia were the hematological AEs, whereas nausea, vomiting, and diarrhea were the most common nonhematological AEs. NDLS treatment was well tolerated without any new safety concerns. Conclusion. Nanosomal docetaxel lipid suspension-based chemotherapy was efficacious and well tolerated in the treatment of sarcoma. Further prospective trials are needed to confirm the data.
机译:客观的。评价纳米组织多西紫杉醇脂悬浮液(NDLS,DoceAqualip)化疗的肉瘤患者的疗效和安全性。方法。在这种回顾性,多中心(6个中心),观测研究中,我们分析了任何性别的成人患者的医学图表,他们在基于NDLS(3-每周循环中的75mg / m2)治疗的化学疗法治疗肉瘤。在接受Neoadjuvant的NDLS的化疗的患者中,疗效结果是总体反应率(ORR:完全反应(CR)+部分反应(PR))和疾病控制率(DCR:Cr + PR +稳定疾病(SD))转移设置。对所有设置评估总生存(OS)和安全性。结果。在11名患者(Neoadjuvant:1,佐剂:3和转移:7)在本研究中,大多数有Leiomyosarcoma(63.6%,7/11),其次是外核肌瘤软骨肉瘤(EMC),高级茂物肉瘤的下颌骨,恶性纤维右大腿的组织细胞瘤,股骨的骨肉瘤(每次9.1%,每次1/11)。 NDLS Plus Gemcitabine组合用于10名患者(90.9%),NDLS加环磷酰胺用于患有EMC的一名患者(9.1%)。 7例患者进行疗效评估(Neoadjuvant:1/1;转移性:6/7)。在Neoadjuvant设置中的一个患者(软组织肉瘤)中报告了完全反应。在转移性环境中,ORR为50%,DCR为66.7%(Cr:16.7%(1/6),Pr:33.3%(2/6),SD:16.7%(1/6))。在6.5个月(范围:0.06-20.2个月)的中位随访中,Neoadjuvant和佐剂设置中未达到中位操作系统,但在转移环境中是15.8个月。报告了7名(63.6%)患者中报道了至少1 AE。中性粒细胞减少症,血小板减少症,淋巴结和贫血是血液学AES,而恶心,呕吐和腹泻是最常见的非生物AES。没有任何新的安全问题,NDLS治疗非常耐受。结论。纳米体多西紫杉醇脂质悬浮液化疗是有效且耐受性在肉瘤的治疗中。需要进一步的预期试验来确认数据。

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