J Transl Med. 2012 Jan 3;10:1. doi: 10.1186/1479-5876-10-1.
The outcome prediction in cancer is usually achieved by evaluating tissue samples obtained during surgical removal of the primary tumor focusing on their histopathological characteristics. Tumor staging (AJCC/UICC-TNM classification) summarizes data on tumor burden (T), presence of cancer cells in draining and regional lymph nodes (N), and evidence for metastases (M). However, this classification provides limited prognostic information in estimating the outcome in cancer and does not predict response to therapy. It is recognized that cancer outcomes can vary significantly among patients within the same stage. Recently, many reports suggest that cancer development is controlled by the host's immune system underlying the importance of including immunological biomarkers for the prediction of prognosis and response to therapy. Data collected from large cohorts of human cancers demonstrated that the immune-classification has a prognostic value that may be superior to the AJCC/UICC TNM-classification. Thus, it is imperative to begin incorporating immune scoring as a prognostic factor and to introduce this parameter as a marker to classify cancers, as part of the routine diagnostic and prognostic assessment of tumors. At the same time, the inherent complexity of quantitative immunohistochemistry, in conjunction with variable assay protocols across laboratories, the different immune cell types analyzed, different region selection criteria, and variable ways to quantify immune infiltration underscore the urgent need to reach assay harmonization. In an effort to promote the immunoscore in routine clinical settings worldwide, the Society for Immunotherapy of Cancer (SITC), the European Academy of Tumor Immunology, the Cancer and Inflammation Program, the National Cancer Institute, National Institutes of Health, USA and "La Fondazione Melanoma" will jointly initiate a task force on Immunoscoring as a New Possible Approach for the Classification of Cancer that will take place in Naples, Italy, February 13th, 2012. The expected outcome will include a concept manuscript that will be distributed to all interested participants for their contribution before publication outlining the goal and strategy to achieve this effort; a preliminary summary to be presented during the "Workshop on Tumor Microenvironment" prior to the SITC annual meeting on October 24th - 25th 2012 in Bethesda, Maryland, USA and finally a "Workshop on Immune Scoring" to be held in Naples in December of 2012 leading to the preparation of a summary document providing recommendations for the harmonization and implementation of the Immune Score as a new component for the classification of cancer.
癌症的预后预测通常通过评估手术切除原发性肿瘤时获得的组织样本来实现,重点是其组织病理学特征。肿瘤分期(AJCC/UICC-TNM 分类)总结了肿瘤负荷(T)、引流和区域淋巴结(N)中癌细胞的存在以及转移证据(M)的数据。然而,这种分类在估计癌症的预后方面提供的预后信息有限,并且不能预测对治疗的反应。人们认识到,即使在同一分期的患者中,癌症的结局也可能有很大差异。最近,许多报告表明,癌症的发展受到宿主免疫系统的控制,因此纳入免疫标志物对于预测预后和对治疗的反应非常重要。从大量人类癌症队列中收集的数据表明,免疫分类具有预后价值,可能优于 AJCC/UICC TNM 分类。因此,必须开始将免疫评分作为预后因素纳入,并将该参数作为分类癌症的标志物,作为肿瘤常规诊断和预后评估的一部分。同时,定量免疫组织化学的固有复杂性,结合实验室之间不同的检测方案、分析的不同免疫细胞类型、不同的区域选择标准以及量化免疫浸润的不同方法,突显了迫切需要实现检测协调。为了在全球范围内推动免疫评分在常规临床环境中的应用,癌症免疫治疗学会(SITC)、欧洲肿瘤免疫学会、癌症和炎症计划、美国国立癌症研究所、美国国立卫生研究院和“La Fondazione Melanoma”将联合发起一个免疫评分作为癌症分类新方法的工作组,该工作组将于 2012 年 2 月 13 日在意大利那不勒斯举行。预期的结果将包括一份概念手稿,该手稿将分发给所有感兴趣的参与者,供他们在发表前发表意见,概述实现这一努力的目标和策略;在 2012 年 10 月 24 日至 25 日在美国马里兰州贝塞斯达举行的 SITC 年会上之前,在“肿瘤微环境研讨会”上提交一份初步总结,最后在 2012 年 12 月在那不勒斯举行“免疫评分研讨会”,为准备一份总结文件提供建议,以协调和实施免疫评分作为癌症分类的新组成部分。