Fu Yu, Karanian Marie, Perret Raul, Camara Axel, Le Loarer François, Jean-Denis Myriam, Hostein Isabelle, Michot Audrey, Ducimetiere Françoise, Giraud Antoine, Courreges Jean-Baptiste, Courtet Kevin, Laizet Yech'an, Bendjebbar Etienne, Du Terrail Jean Ogier, Schmauch Benoit, Maussion Charles, Blay Jean-Yves, Italiano Antoine, Coindre Jean-Michel
Owkin, Inc., New York, NY, USA.
Cancer Research Center of Lyon, Centre Léon Bérard, Lyon, France.
NPJ Precis Oncol. 2023 Jul 24;7(1):71. doi: 10.1038/s41698-023-00421-9.
Risk assessment of gastrointestinal stromal tumor (GIST) according to the AFIP/Miettinen classification and mutational profiling are major tools for patient management. However, the AFIP/Miettinen classification depends heavily on mitotic counts, which is laborious and sometimes inconsistent between pathologists. It has also been shown to be imperfect in stratifying patients. Molecular testing is costly and time-consuming, therefore, not systematically performed in all countries. New methods to improve risk and molecular predictions are hence crucial to improve the tailoring of adjuvant therapy. We have built deep learning (DL) models on digitized HES-stained whole slide images (WSI) to predict patients' outcome and mutations. Models were trained with a cohort of 1233 GIST and validated on an independent cohort of 286 GIST. DL models yielded comparable results to the Miettinen classification for relapse-free-survival prediction in localized GIST without adjuvant Imatinib (C-index=0.83 in cross-validation and 0.72 for independent testing). DL splitted Miettinen intermediate risk GIST into high/low-risk groups (p value = 0.002 in the training set and p value = 0.29 in the testing set). DL models achieved an area under the receiver operating characteristic curve (AUC) of 0.81, 0.91, and 0.71 for predicting mutations in KIT, PDGFRA and wild type, respectively, in cross-validation and 0.76, 0.90, and 0.55 in independent testing. Notably, PDGFRA exon18 D842V mutation, which is resistant to Imatinib, was predicted with an AUC of 0.87 and 0.90 in cross-validation and independent testing, respectively. Additionally, novel histological criteria predictive of patients' outcome and mutations were identified by reviewing the tiles selected by the models. As a proof of concept, our study showed the possibility of implementing DL with digitized WSI and may represent a reproducible way to improve tailoring therapy and precision medicine for patients with GIST.
根据美国武装部队病理研究所(AFIP)/米耶蒂宁(Miettinen)分类法和突变分析对胃肠道间质瘤(GIST)进行风险评估是患者管理的主要工具。然而,AFIP/Miettinen分类法严重依赖有丝分裂计数,这既费力,而且病理学家之间有时也不一致。它在对患者进行分层方面也被证明并不完美。分子检测成本高且耗时,因此,并非在所有国家都系统地开展。因此,改进风险和分子预测的新方法对于优化辅助治疗的定制至关重要。我们基于数字化苏木精-伊红(HES)染色的全切片图像(WSI)构建了深度学习(DL)模型,以预测患者的预后和突变情况。模型使用1233例GIST患者队列进行训练,并在286例GIST独立队列中进行验证。对于未接受辅助伊马替尼治疗的局限性GIST患者,DL模型在无复发生存预测方面产生了与Miettinen分类法相当的结果(交叉验证中的C指数=0.83,独立测试中的C指数=0.72)。DL将Miettinen中度风险GIST分为高/低风险组(训练集中p值=0.002,测试集中p值=0.29)。在交叉验证中,DL模型预测KIT、血小板衍生生长因子受体α(PDGFRA)和野生型突变的受试者操作特征曲线(ROC)下面积(AUC)分别为0.81、0.91和0.71,在独立测试中分别为0.76、0.90和0.55。值得注意的是,对伊马替尼耐药的PDGFRA外显子18 D842V突变在交叉验证和独立测试中的预测AUC分别为0.87和0.90。此外,通过回顾模型选择的切片,确定了预测患者预后和突变的新组织学标准。作为概念验证,我们的研究显示了利用数字化WSI实施DL的可能性,并且可能代表了一种可重复的方法,用于改善GIST患者的治疗定制和精准医疗。