Johnson Helen M, Song Juhee, Warneke Carla L, Martinez Ashley L, Litton Jennifer K, Oke Oluchi C
Department of Breast Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Department of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Cancer. 2025 Jan 1;131(1):e35619. doi: 10.1002/cncr.35619. Epub 2024 Oct 29.
Prior studies of patients treated for breast cancer during pregnancy (PrBC) report mixed outcomes and are limited by substandard treatment, small cohorts, and short follow-up. This study compared survival outcomes of PrBC patients treated with chemotherapy during pregnancy with nonpregnant patients matched by age, year of diagnosis, stage, and subtype.
PrBC patients treated from 1989 to 2022 on prospective institutional protocols were eligible. Disease-free survival (DFS), overall survival (OS), and progression-free survival (PFS) were estimated using the Kaplan-Meier method and multivariable Cox proportional hazards regression.
Among 143 PrBC and 285 nonpregnant patients, median follow-up was 11.4 years. Survival differences were statistically significant, with median DFS and OS not attained for PrBC patients versus 5.6 years (95% confidence interval [CI], 3.6-15.4; p = .0001) and 19.3 years (95% CI, 14.1-not estimated; p = .0262) for nonpregnant patients, respectively. Median PFS was 24.1 years (95% CI, 15.8-not estimated) for PrBC patients versus 8.4 years (95% CI, 6.4-10.9) for the nonpregnant cohort (p = .0008). Study cohort was associated with DFS, PFS, and OS in multivariable analyses, with the nonpregnant cohort having increased risks of disease recurrence (hazard ratio [HR], 1.91; 95% CI, 1.33-2.76; p = .0005) and disease progression or death (HR, 1.68; 95% CI, 1.19-2.39; p = .0035), and shorter OS (HR, 1.52; 95% CI, 1.01-2.29; p = .0442).
These data suggest that PrBC patients treated with chemotherapy during pregnancy have at least comparable, if not superior, outcomes than nonpregnant patients with similar age, cancer stage, and subtype. Analyses excluding patients with postpartum breast cancer were unable to be performed and are a priority for future confirmatory studies.
既往关于孕期乳腺癌(PrBC)患者治疗的研究报告结果不一,且受治疗不规范、队列规模小和随访时间短的限制。本研究比较了孕期接受化疗的PrBC患者与年龄、诊断年份、分期和亚型相匹配的非孕期患者的生存结局。
符合条件的PrBC患者为1989年至2022年按照前瞻性机构方案接受治疗的患者。采用Kaplan-Meier方法和多变量Cox比例风险回归估计无病生存期(DFS)、总生存期(OS)和无进展生存期(PFS)。
在143例PrBC患者和285例非孕期患者中,中位随访时间为11.4年。生存差异具有统计学意义,PrBC患者未达到中位DFS和OS,而非孕期患者的中位DFS为5.6年(95%置信区间[CI],3.6 - 15.4;p = .0001),中位OS为19.3年(95% CI,14.1 - 未估计;p = .0262)。PrBC患者的中位PFS为24.1年(95% CI,15.8 - 未估计),而非孕期队列的中位PFS为8.4年(95% CI,6.4 - 10.9)(p = .0008)。在多变量分析中,研究队列与DFS、PFS和OS相关,非孕期队列疾病复发风险增加(风险比[HR],1.91;95% CI,1.33 - 2.76;p = .0005),疾病进展或死亡风险增加(HR,1.68;95% CI,1.19 - 2.39;p = .0035),OS更短(HR,1.52;95% CI,1.01 - 2.29;p = .0442)。
这些数据表明,孕期接受化疗的PrBC患者的结局至少与年龄、癌症分期和亚型相似的非孕期患者相当,甚至可能更好。无法进行排除产后乳腺癌患者的分析,这是未来验证性研究的重点。