Division of Medical Oncology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Division of Radiation Oncology, Department of Radiology, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Cancer Med. 2024 Feb;13(4):e7047. doi: 10.1002/cam4.7047.
R/M-HNSCC patients typically receive 1L platinum-based chemotherapy with pembrolizumab or cetuximab. However, the outcomes for patients with early recurrence (<6 months) remain unclear due to their exclusion from most 1L studies. This study aimed to assess the impact of time-to-recurrence intervals (TTRI) and recurrence patterns on the survival of R/M-HNSCC patients.
We identified non-curable R/M-HNSCC patients at our institution from 1/2008 through 6/2020. We analyzed the outcomes of early recurrent patients who received 1L systemic treatment, with different TTRIs and recurrence patterns.
Our study included 234 eligible patients. The majority (47%) experienced early recurrence (<6 months), while 22%, 20%, and 11% had recurrences at 6-12 months, >12 months, and de novo metastasis, respectively. The platinum-based regimen was the most commonly used chemotherapy (86%), with cetuximab and immunotherapy utilized in 3% and 5% of cases, respectively. Significant differences in PFS and OS were observed among TTRI groups. For patients with early recurrence, both platinum-doublet and monotherapy treatments significantly improved OS. Locoregional recurrence (47%) was the most common, followed by distant metastasis (22%) and both (20%). Recurrence patterns were significantly associated with OS but not with PFS. In multivariate analysis, TTRI ≥12 months significantly correlated with improved PFS (HR 0.51; p = 0.004) and OS (HR 0.58; p = 0.009), whereas recurrent pattern did not.
TTRI significantly influenced the survival, while recurrence patterns did not. In our study, the retrospective design limited our ability to definitively establish whether early recurrent R/M-HNSCC patients would benefit more from platinum-doublet. Despite poor prognosis, early recurrent patients benefited from 1L systemic treatments. Given the variation in prognoses, TTRI should be considered a stratification factor in future clinical trials.
R/M-HNSCC 患者通常接受 1L 铂类化疗联合 pembrolizumab 或 cetuximab 治疗。然而,由于大多数 1L 研究将早期复发(<6 个月)的患者排除在外,因此这些患者的预后仍不清楚。本研究旨在评估复发时间间隔(TTRI)和复发模式对 R/M-HNSCC 患者生存的影响。
我们从 2008 年 1 月至 2020 年 6 月在我们的机构中确定了不可治愈的 R/M-HNSCC 患者。我们分析了接受 1L 系统治疗且具有不同 TTRI 和复发模式的早期复发患者的结局。
我们的研究纳入了 234 名符合条件的患者。大多数(47%)患者在 6 个月内出现早期复发(<6 个月),22%、20%和 11%的患者在 6-12 个月、>12 个月和新发转移时出现复发。最常用的化疗方案是铂类方案(86%),分别有 3%和 5%的患者使用 cetuximab 和免疫疗法。在 TTRI 组之间观察到 PFS 和 OS 存在显著差异。对于早期复发患者,铂类双联和单药治疗均可显著改善 OS。局部区域复发(47%)最为常见,其次是远处转移(22%)和两者兼有(20%)。复发模式与 OS 显著相关,但与 PFS 无关。多变量分析显示,TTRI≥12 个月与 PFS(HR 0.51;p=0.004)和 OS(HR 0.58;p=0.009)的改善显著相关,而复发模式则没有。
TTRI 显著影响生存,而复发模式则没有。在我们的研究中,回顾性设计限制了我们确定早期复发的 R/M-HNSCC 患者是否会从铂类双联治疗中获益更多的能力。尽管预后较差,但早期复发患者从 1L 系统治疗中获益。鉴于预后的差异,TTRI 应被视为未来临床试验的分层因素。