一种新的肿瘤萌芽-低分化簇联合分级系统预测I-III期结直肠癌的复发和生存

S. Shivji, D. Cyr, Cherry Pun, K. Duan, A. Sari, Rossi Tomin, D. Ng, A. Brar, S. Zerhouni, E. Kennedy, M. Brar, C. Swallow, J. Conner, R. Kirsch
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引用次数: 1

摘要

肿瘤萌芽(TB)和低分化簇(PDCs)是结直肠癌(CRC)的重要预后因素。尽管结核和PDC在形态和生物学上有重叠,但它们是分开评估的,并通过细胞簇大小的任意截止来区分。这一界限在实际应用中具有挑战性,其生物学意义尚不清楚。我们开发了一种新的评分系统,将TB和PDC合并到一个参数中(“综合评分”;CS),消除了这种截止值的需要,并允许将PDC的预后价值与结核病一起获得。在481例I-III期结直肠癌切除术的队列中,CS与美国癌症联合委员会(AJCC)分期、t期、n期、组织学分级、肿瘤沉积、淋巴血管侵袭和神经周围侵袭显著相关(P<0.0001)。此外,CS与5年无复发生存、总生存和疾病特异性生存显著相关(P<0.0001)。结核病和PDC显示出与肿瘤预后相似的相关性,其风险比始终低于CS。在按AJCC分期、解剖位置(直肠/结肠)和新辅助治疗状态分层的亚组分析中,CS与肿瘤预后之间的关联仍然显著。在多变量分析中,CS分别与无复发生存期、疾病特异性生存期和总生存期的肿瘤预后保持显著相关性(P=0.0002、0.005和0.009)。总之,CS在结直肠癌中提供了强有力的风险分层,至少相当于单独评估TB和PDC的风险分层。如果在其他地方得到验证,CS具有实际优势和生物学原理,可能使其成为单独评估这些特征的有吸引力的替代方案。
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A Novel Combined Tumor Budding-Poorly Differentiated Clusters Grading System Predicts Recurrence and Survival in Stage I-III Colorectal Cancer
Tumor budding (TB) and poorly differentiated clusters (PDCs) are powerful prognostic factors in colorectal cancer (CRC). Despite their morphologic and biological overlap, TB and PDC are assessed separately and are distinguished by an arbitrary cutoff for cell cluster size. This cutoff can be challenging to apply in practice and its biological significance remains unclear. We developed a novel scoring system that incorporates TB and PDC into a single parameter (“Combined Score”; CS), eliminating the need for such cutoffs and allowing the prognostic value of PDC to be captured alongside TB. In a cohort of 481 stage I-III CRC resections, CS was significantly associated with American Joint Committee on Cancer (AJCC) stage, T-stage, N-stage, histologic grade, tumor deposits, lymphovascular invasion, and perineural invasion (P<0.0001). In addition, CS was significantly associated with decreased 5-year recurrence-free survival, overall survival, and disease-specific survival (P<0.0001). TB and PDC showed similar associations with oncologic outcomes, with hazard ratios consistently lower than for CS. The association between CS and oncologic outcomes remained significant in subgroup analyses stratified by AJCC stage, anatomic location (rectum/colon) and neoadjuvant therapy status. On multivariable analysis, CS retained its significant association with oncologic outcomes (P=0.0002, 0.005, and 0.009) for recurrence-free survival, disease-specific survival, and overall survival, respectively. In conclusion, CS provides powerful risk stratification in CRC which is at least equivalent to that of TB and PDC assessed individually. If validated elsewhere, CS has practical advantages and a biological rationale that may make it an attractive alternative to assessing these features separately.
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