Shien Tadahiko, Hara Fumikata, Aogi Kenjiro, Yanagida Yasuhiro, Tsuneizumi Michiko, Yamamoto Naohito, Matsumoto Hiroshi, Suto Akihiko, Watanabe Kenichi, Harao Michiko, Kanbayashi Chizuko, Itoh Mitsuya, Kadoya Takayuki, Anan Keisei, Maeda Shigeto, Sasaki Keita, Ogawa Gakuto, Saji Shigehira, Fukuda Haruhiko, Iwata Hiroji
Okayama University Hospital, Okayama, Japan.
Cancer Institute Hospital, Tokyo, Japan.
Br J Cancer. 2025 Sep;133(5):625-632. doi: 10.1038/s41416-025-03097-z. Epub 2025 Jul 4.
Several prospective studies have evaluated the benefit of primary tumour resection (PTR) in de novo Stage IV breast cancer (BC) patients, but it remains controversial. We aimed to investigate whether PTR improves the survival of de novo stage IV BC patients.
De novo stage IV BC patients were enrolled in the first registration and received systemic therapies according to clinical subtypes. Patients without progression after primary systemic therapy for 3 months were randomly assigned 1:1 to systemic therapy alone (arm A) or PTR plus systemic therapy (arm B). The primary endpoint was overall survival (OS), and the secondary endpoints included local relapse-free survival (LRFS).
Five hundred seventy patients were enrolled between May 5, 2011, and May 31, 2018. Of these, 407 were randomised to arm A (N = 205) or arm B (N = 202). The median follow-up time of all randomised patients was 60 months. The difference in OS was not statistically significant (HR 0.86 90% CI 0.69-1.07, one-sided p = 0.13). Median OS was 69 months (arm A) and 75 months (arm B). In the subgroup analysis, PTR was associated with improved OS in pre-menopausal patients, or those with single-organ metastasis. LRFS in arm B was significantly longer than that in arm A (median LRFS 20 vs. 63 months: HR 0.42, 95% CI 0.33-0.53, p < 0.0001). There were no treatment-related deaths.
PTR did not prolong OS. However, it improved local control and might benefit a subset of patients, such as those with premenopausal status or with single-organ metastasis. It also improved local relapse-free survival (LRFS), which is a clinically meaningful outcome in trials of systemic therapy.
UMIN Clinical Trials Registry (UMIN000005586); Japan Registry of Clinical Trials (jRCTs031180151).
多项前瞻性研究评估了原发性肿瘤切除术(PTR)对初诊IV期乳腺癌(BC)患者的益处,但仍存在争议。我们旨在研究PTR是否能提高初诊IV期BC患者的生存率。
初诊IV期BC患者首次登记入组,并根据临床亚型接受全身治疗。在接受一线全身治疗3个月后无进展的患者被随机1:1分配至单纯全身治疗组(A组)或PTR联合全身治疗组(B组)。主要终点为总生存期(OS),次要终点包括局部无复发生存期(LRFS)。
2011年5月5日至2018年5月31日期间共纳入570例患者。其中,407例被随机分配至A组(N = 205)或B组(N = 202)。所有随机分组患者的中位随访时间为60个月。OS差异无统计学意义(HR 0.86,90%CI 0.69 - 1.07,单侧p = 0.13)。中位OS分别为69个月(A组)和75个月(B组)。亚组分析显示,PTR与绝经前患者或单器官转移患者的OS改善相关。B组的LRFS显著长于A组(中位LRFS 20个月 vs. 63个月:HR 0.42,95%CI 0.33 - 0.53,p < 0.0001)。无治疗相关死亡。
PTR未延长OS。然而,它改善了局部控制,可能使一部分患者受益,如绝经前患者或单器官转移患者。它还改善了局部无复发生存期(LRFS),这在全身治疗试验中是一个具有临床意义的结果。
UMIN临床试验注册中心(UMIN000005586);日本临床试验注册中心(jRCTs031180151)。