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纳米白蛋白结合型紫杉醇联合吉西他滨治疗复发/难治性小细胞肺癌的II期研究

Phase II study of nab-paclitaxel with gemcitabine for relapsed/refractory small cell lung cancer.

作者信息

Byrne Margaret M, Sutamtewagul Grerk, Zeitler William, Mott Sarah L, Zamba Gideon K D, Kojadinovic Arsenije, Zhang Jun, Abu-Hejleh Taher, Clamon Gerald, Furqan Muhammad

机构信息

Division of Hematology, Oncology, and Blood & Marrow Transplantation, Department of Internal Medicine, University of Iowa, Iowa City, IA, United States.

Holden Comprehensive Cancer Center, University of Iowa, Iowa City, IA, United States.

出版信息

Front Oncol. 2024 Jul 31;14:1303268. doi: 10.3389/fonc.2024.1303268. eCollection 2024.

Abstract

BACKGROUND

Patients with small cell lung cancer (SCLC) often respond to first-line chemoimmunotherapy. However, relapse is inevitable and is associated with a poor prognosis. Treatments for relapsed SCLC, such as lurbinectedin and topotecan, are limited by modest efficacy and significant hematologic adverse events, leaving a need for newer therapeutic agents or regimens. The combination of gemcitabine and nab-paclitaxel is active and safe in other types of malignancies, such as pancreatic cancer.

PATIENTS AND METHODS

We conducted a phase II trial evaluating the efficacy and safety of gemcitabine and nab-paclitaxel in patients with relapsed/refractory SCLC. The primary endpoint was objective response rate (ORR), defined as the proportion of patients with confirmed complete or partial response. Secondary endpoints included time to progression (TTP), progression-free survival (PFS), overall survival (OS), and safety.

RESULTS

Between October 2016 and May 2021, 32 patients were enrolled. Patients were followed for a median of 9.3 months (range 1.8-65.2). Median age was 65 years (range 48-81). Fifty percent of patients were female. Fifty-three percent of patients had platinum-resistant/refractory relapsed SCLC. The ORR was 28.1% (95% confidence interval [CI] 15.5-100%). Median PFS was 2.9 months (95% CI 2.4-3.6), and median OS was 9.3 months (95% CI 5.2-12.4). Seven patients (21.9%) developed grade 3 or 4 neutropenia.

CONCLUSION

Our study showed that the combination of gemcitabine and nab-paclitaxel led to encouraging outcomes in relapsed/refractory SCLC. Further studies are needed to compare this combination with other treatments used for relapsed SCLC, including lurbinectedin, temozolomide, and topotecan.

CLINICAL TRIAL REGISTRATION

https://clinicaltrials.gov/study/NCT02769832?cond=NCT02769832&rank=1, identifier NCT02769832.

摘要

背景

小细胞肺癌(SCLC)患者通常对一线化疗免疫疗法有反应。然而,复发不可避免且预后较差。复发SCLC的治疗方法,如鲁比卡丁和拓扑替康,疗效有限且血液学不良事件严重,因此需要更新的治疗药物或方案。吉西他滨和白蛋白结合型紫杉醇的联合用药在其他类型的恶性肿瘤(如胰腺癌)中具有活性且安全。

患者与方法

我们进行了一项II期试验,评估吉西他滨和白蛋白结合型紫杉醇在复发/难治性SCLC患者中的疗效和安全性。主要终点是客观缓解率(ORR),定义为确认完全缓解或部分缓解的患者比例。次要终点包括疾病进展时间(TTP)、无进展生存期(PFS)、总生存期(OS)和安全性。

结果

2016年10月至2021年5月期间,共纳入32例患者。患者的中位随访时间为9.3个月(范围1.8 - 65.2个月)。中位年龄为65岁(范围48 -

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da70/11322450/f30afea3c318/fonc-14-1303268-g001.jpg

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