Toriyama Kazuhiro, Masago Katsuhiro, Shibata Noriko, Haneda Masataka, Kuwahara Takamichi, Natsume Seiji, Kobayashi Shota, Fujita Yasuko, Sasaki Eiichi, Yamao Kenji, Kawashima Hiroki, Shimizu Yasuhiro, Hara Kazuo, Yatabe Yasushi, Hosoda Waki
Department of Pathology and Molecular Diagnostics, Aichi Cancer Center, Nagoya, Japan.
Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
J Pathol. 2025 Jul;266(3):337-351. doi: 10.1002/path.6432. Epub 2025 May 2.
Pancreatic ductal adenocarcinomas (PDACs) with wild-type KRAS constitute a small fraction of PDACs, and these tumors were recently shown to harbor frequent actionable oncogenic mutations and fusions. However, the clinicopathological features of KRAS wild-type PDAC have not been well studied. Additionally, precancerous lesions occurring in patients with KRAS wild-type PDACs have rarely been characterized. Here, we investigated the clinicopathological characteristics and outcomes of 75 patients with KRAS wild-type PDAC. Molecular analyses were performed in 40 patients using targeted DNA and whole-exome sequencing and targeted RNA sequencing. We demonstrated that patients with metastatic PDAC with wild-type KRAS were younger (median 59.5 years) than those with mutated KRAS (median 67 years, p < 0.000055). The wild-type KRAS status was not a significant prognostic factor for metastatic disease. Molecularly, genes in the RAS pathway are frequently mutated or rearranged (46%, 16/35), including mutations in BRAF, NRAS, HRAS, EGFR, MAP2K1, FGFR1, FGFR3 and ERBB4 and fusions of FGFR2 (FGFR2::CCDC147, FGFR2::CAT, FGFR2::TXLNA), ALK (STRN::ALK, EML4::ALK), and BRAF (TRIP11::BRAF). Mismatch repair deficiency was identified in 10% (4/39) of patients. Potentially actionable alterations were identified frequently in KRAS wild-type PDACs (30%, 12/40), in which nontubular-type carcinomas were significantly enriched with actionable alterations compared with tubular adenocarcinomas [67% (6/9) versus 16% (5/31); p = 0.007]. Finally, we investigated the precursors of PDACs in 13 pancreatectomy specimens from patients with KRAS wild-type PDAC. We identified three pancreatic intraepithelial neoplasias (PanINs) and two intraductal papillary mucinous neoplasms (IPMNs) harboring oncogenic fusions of ALK and BRAF and driver mutations in BRAF and AKT1. This study suggests that in the context of unmutated KRAS, PDAC is driven by alternative oncogenic mutations or fusions of RAS pathway genes, which may be introduced during the early phase of tumorigenesis. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.
KRAS基因野生型的胰腺导管腺癌(PDAC)在PDAC中占比小,且最近研究表明这些肿瘤常存在可靶向治疗的致癌突变和融合。然而,KRAS基因野生型PDAC的临床病理特征尚未得到充分研究。此外,KRAS基因野生型PDAC患者的癌前病变也鲜有特征描述。在此,我们研究了75例KRAS基因野生型PDAC患者的临床病理特征及预后。对40例患者进行了靶向DNA和全外显子测序以及靶向RNA测序的分子分析。我们发现,KRAS基因野生型的转移性PDAC患者(中位年龄59.5岁)比KRAS基因突变型患者(中位年龄67岁,p<0.000055)更年轻。KRAS基因野生型状态并非转移性疾病的显著预后因素。分子层面,RAS通路中的基因常发生突变或重排(46%,16/35),包括BRAF、NRAS、HRAS、EGFR、MAP2K1、FGFR1、FGFR3和ERBB4的突变以及FGFR2(FGFR2::CCDC147、FGFR2::CAT、FGFR2::TXLNA)、ALK(STRN::ALK、EML4::ALK)和BRAF(TRIP11::BRAF)的融合。10%(4/39)的患者存在错配修复缺陷。KRAS基因野生型PDAC中常可发现潜在的可靶向治疗改变(30%,12/40),其中非管状腺癌相较于管状腺癌,可靶向治疗改变显著富集[67%(6/9)对16%(5/31);p=0.007]。最后,我们研究了13例KRAS基因野生型PDAC患者胰腺切除标本中的PDAC前体。我们发现了3例胰腺上皮内瘤变(PanIN)和2例导管内乳头状黏液性肿瘤(IPMN),它们存在ALK和BRAF的致癌融合以及BRAF和AKT1的驱动突变。本研究表明,在KRAS基因未突变的情况下,PDAC由RAS通路基因的其他致癌突变或融合驱动,这些改变可能在肿瘤发生的早期阶段出现。© 2025作者。《病理学杂志》由John Wiley & Sons Ltd代表大不列颠及爱尔兰病理学会出版。