Dotsu Yosuke, Yamaguchi Hiroyuki, Fukuda Minoru, Suyama Takayuki, Honda Noritaka, Umeyama Yasuhiro, Taniguchi Hirokazu, Gyotoku Hiroshi, Takemoto Shinnosuke, Tagawa Ryuta, Ogata Ryosuke, Tomono Hiromi, Shimada Midori, Senju Hiroaki, Nakatomi Katsumi, Nagashima Seiji, Soda Hiroshi, Ikeda Hiroaki, Ashizawa Kazuto, Mukae Hiroshi
Department of Respiratory Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki 852-8501, Japan.
Clinical Oncology Center, Nagasaki University Hospital, Nagasaki 852-8501, Japan.
J Clin Med. 2021 Sep 17;10(18):4221. doi: 10.3390/jcm10184221.
Single-agent amrubicin chemotherapy is a key regimen, especially for small cell lung cancer (SCLC); however, it can cause severe myelosuppression.
The purpose of this study was to determine the real-world incidence of febrile neutropenia (FN) among patients treated with single-agent amrubicin chemotherapy for thoracic malignancies.
The medical records of consecutive patients with thoracic malignancies, including SCLC and non-small cell lung cancer (NSCLC), who were treated with single-agent amrubicin chemotherapy in cycle 1 between January 2010 and March 2020, were retrospectively analyzed.
One hundred and fifty-six patients from four institutions were enrolled. Their characteristics were as follows: median age (range): 68 (32-86); male/female: 126/30; performance status (0/1/2): 9/108/39; SCLC/NSCLC/others: 111/30/15; and prior treatment (0/1/2/3-): 1/96/31/28. One hundred and thirty-four (86%) and 97 (62%) patients experienced grade 3/4 and grade 4 neutropenia, respectively. One hundred and twelve patients (72%) required therapeutic G-CSF treatment, and 47 (30%) developed FN. Prophylactic PEG-G-CSF was not used in cycle 1 in any case. The median overall survival of the patients with FN was significantly shorter than that of the patients without FN (7.2 vs. 10.0 months, = 0.025).
The real-world incidence rate of FN among patients with thoracic malignancies that were treated with single-agent amrubicin chemotherapy was 30%. It is suggested that prophylactic G-CSF should be administered during the practical use of single-agent amrubicin chemotherapy for patients who have already received chemotherapy.
单药氨柔比星化疗是一种关键方案,尤其对于小细胞肺癌(SCLC);然而,它可导致严重的骨髓抑制。
本研究的目的是确定接受单药氨柔比星化疗治疗胸部恶性肿瘤患者中发热性中性粒细胞减少症(FN)的真实世界发生率。
回顾性分析2010年1月至2020年3月期间在第1周期接受单药氨柔比星化疗的连续性胸部恶性肿瘤患者的病历,包括SCLC和非小细胞肺癌(NSCLC)。
来自四个机构的156例患者入组。他们的特征如下:中位年龄(范围):68岁(32 - 86岁);男/女:126/30;体能状态(0/1/2):9/108/39;SCLC/NSCLC/其他:111/30/15;既往治疗(0/1/2/3 - ):1/96/31/28。分别有134例(86%)和97例(62%)患者发生3/4级和4级中性粒细胞减少症。112例(72%)患者需要接受治疗性G - CSF治疗,47例(30%)发生FN。在任何情况下,第1周期均未使用预防性聚乙二醇化重组人粒细胞集落刺激因子(PEG - G - CSF)。发生FN的患者的中位总生存期显著短于未发生FN的患者(7.2个月对10.0个月,P = 0.025)。
接受单药氨柔比星化疗治疗的胸部恶性肿瘤患者中FN的真实世界发生率为30%。建议在对已接受化疗的患者实际应用单药氨柔比星化疗期间给予预防性G - CSF。