Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan; Department of Oncology and Hemato-Oncology, University of Milan, Milan.
Division of Pathology and Laboratory Medicine, European Institute of Oncology, IRCCS, Milan.
ESMO Open. 2024 Aug;9(8):103662. doi: 10.1016/j.esmoop.2024.103662. Epub 2024 Aug 6.
Carcinoma of unknown primary (CUP) with a gastrointestinal profile is categorized by the European Society of Medical Oncology (ESMO) guidelines into favorable and unfavorable subsets. Favorable CUPs benefit from site-specific chemotherapy (CT), while the optimal treatment for unfavorable CUPs is still undefined.
We conducted a single-center retrospective study to describe outcomes of patients with CUP with a gastrointestinal profile referred to our center from January 2000 to August 2023. Favorable CUPs were defined as CK7-/CK20+/CDX2+ by immunohistochemistry, according to the ESMO definition; all other cases were considered unfavorable. The main endpoint was the progression-free survival (PFS) of first-line CT for advanced disease in all patients and in the unfavorable group.
A total of 56 patients were included, of whom 46 (82%) had unfavorable CUPs. After a median follow-up of 43.9 months, the median overall survival (mOS) was 11.8 months [95% confidence interval (CI) 8.3-15.3 months]. At univariate analysis, the presence of peritoneal metastases and residual tumor after primary surgery were associated with a shorter OS. The median PFS (mPFS) was 6.1 months (95% CI 3.6-8.7 months). In the unfavorable CUP subgroup, the mOS was 12.6 months (95% CI 8.7-16.5 months), the mPFS was 6.1 months (95% CI 3.5-8.9 months) and none of the CT regimens used showed to portend better PFS. The most relevant altered genes included: KRAS (9/29; 31%), BRAF (1/26; 4%), NRAS (1/25; 4%), TP53 (9/23; 39%).
CUPs with a gastrointestinal profile are characterized by poor prognosis and the absence of biomarker for treatment personalization. No CT regimen was superior in terms of PFS in patients with unfavorable CUPs.
欧洲肿瘤内科学会(ESMO)指南将具有胃肠道表现的不明原发癌(CUP)分为有利和不利亚组。有利的 CUP 从基于部位的化疗(CT)中获益,而不利的 CUP 的最佳治疗方法仍未确定。
我们进行了一项单中心回顾性研究,描述了 2000 年 1 月至 2023 年 8 月期间被转诊至我们中心的具有胃肠道表现的 CUP 患者的结局。根据 ESMO 定义,有利的 CUP 通过免疫组化被定义为 CK7-/CK20+/CDX2+;所有其他病例均被认为是不利的。主要终点是所有患者和不利组中晚期疾病一线 CT 的无进展生存期(PFS)。
共纳入 56 例患者,其中 46 例(82%)为不利的 CUP。中位随访 43.9 个月后,中位总生存期(mOS)为 11.8 个月[95%置信区间(CI)8.3-15.3 个月]。单因素分析显示,存在腹膜转移和原发手术后残留肿瘤与较短的 OS 相关。中位 PFS(mPFS)为 6.1 个月(95%CI 3.6-8.7 个月)。在不利的 CUP 亚组中,mOS 为 12.6 个月(95%CI 8.7-16.5 个月),mPFS 为 6.1 个月(95%CI 3.5-8.9 个月),且使用的任何 CT 方案均未显示出更好的 PFS。最相关的改变基因包括:KRAS(9/29;31%)、BRAF(1/26;4%)、NRAS(1/25;4%)、TP53(9/23;39%)。
具有胃肠道表现的 CUP 预后较差,且缺乏治疗个体化的生物标志物。在不利的 CUP 患者中,没有任何 CT 方案在 PFS 方面具有优势。