Mousa Luay, Stephens Julie A, Berger Michael, Ramaswamy Bhuvaneswari, Lustberg Maryam, Sardesai Sagar, Williams Nicole, VanDeusen Jeffrey, Stover Daniel, Cherian Mathew, Morgan Evan, Wesolowski Robert
Division of Hematology, The James Cancer Hospital and Solove Research Institute at The Ohio State University Wexner Medical Center, A 332 C Starling Loving Hall, 320 W 10th Ave, Columbus, OH, 43210, USA.
Center for Biostatistics, The Department of Biomedical Informatics, The Ohio State University, Columbus, OH, USA.
Support Care Cancer. 2020 Nov;28(11):5537-5545. doi: 10.1007/s00520-020-05392-2. Epub 2020 Mar 17.
The goal of chemotherapy for metastatic breast cancer (MBC) is palliation of symptoms while minimizing treatment-related toxicities. It remains unclear whether use of granulocyte colony-stimulating factor (G-CSF) to maintain relative dose intensity of chemotherapy for MBC is associated with improved clinical outcomes.
The medical records of MBC patients treated with chemotherapy in 1st-3rd-line settings between May 2010 and April 2014 were reviewed. Time to progression (TTP), progression-free survival (PFS), and overall survival (OS) were compared between patients who received G-CSF and those who did not. Antibiotic use, total clinic visits, and pre- and post-treatment Eastern Cooperative Oncology Group (ECOG) performance status were also compared between the groups.
Of the 169 patients included, 55 (32.5%) received > 1 G-CSF dose and 114 (67.5%) did not receive any G-CSF. The median TTP was similar between the two groups (5.0 months (95% CI 3.4-7.1) vs. 5.2 months (95% CI 4.8-6.2) respectively; p = 0.998). The median PFS (p = 0.955; 5.0 months (95% CI 3.4-5.9) vs. 5.2 months (95% CI 4.7-6.0), respectively) and OS (14.6 (95% CI 9.0-26.6) vs. 18.5 months (95% CI 15.2-22.0) in G-CSF and non-G-CSF groups, respectively; p = 0.628) were also similar between groups. No significant between-group differences were noted in rate of decline in ECOG performance status, antibiotic use, and number of clinic visits and hospitalizations.
This retrospective analysis did not find any evidence that the use of G-CSF to maintain chemotherapy dose intensity for the treatment of MBC improves TTP, PFS, and OS or results in improved ECOG performance status compared with lack of G-CSF use in patients with MBC treated in 1st to 3rd-line settings.
转移性乳腺癌(MBC)化疗的目标是缓解症状,同时将治疗相关毒性降至最低。目前尚不清楚使用粒细胞集落刺激因子(G-CSF)来维持MBC化疗的相对剂量强度是否与改善临床结局相关。
回顾了2010年5月至2014年4月期间接受一线至三线化疗的MBC患者的病历。比较了接受G-CSF和未接受G-CSF的患者的疾病进展时间(TTP)、无进展生存期(PFS)和总生存期(OS)。还比较了两组患者的抗生素使用情况、总门诊次数以及治疗前和治疗后的东部肿瘤协作组(ECOG)体能状态。
在纳入的169例患者中,55例(32.5%)接受了>1次G-CSF剂量,114例(67.5%)未接受任何G-CSF。两组的中位TTP相似(分别为5.0个月(95%CI 3.4-7.1)和5.2个月(95%CI 4.8-6.2);p=0.998)。两组的中位PFS(p=0.955;分别为5.0个月(95%CI 3.4-5.9)和5.2个月(95%CI 4.7-6.0))和OS(G-CSF组和非G-CSF组分别为14.6(95%CI 9.0-26.6)和18.5个月(95%CI 15.2-22.0);p=0.628)也相似。两组在ECOG体能状态下降率、抗生素使用情况以及门诊次数和住院次数方面未发现显著差异。
这项回顾性分析未发现任何证据表明,与一线至三线治疗的MBC患者不使用G-CSF相比,使用G-CSF维持化疗剂量强度来治疗MBC可改善TTP、PFS和OS或改善ECOG体能状态。