Department of Pathology, Millennium Institute on Immunology and Immunotherapy, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Department of Hepato-pancreato-biliary (HPB) Surgery, Mahatma Gandhi Medical College & Hospital (MGMCH), Jaipur, India.
Nat Rev Dis Primers. 2022 Oct 27;8(1):69. doi: 10.1038/s41572-022-00398-y.
Gallbladder cancer (GBC) is the most common cancer of the biliary tract, characterized by a very poor prognosis when diagnosed at advanced stages owing to its aggressive behaviour and limited therapeutic options. Early detection at a curable stage remains challenging because patients rarely exhibit symptoms; indeed, most GBCs are discovered incidentally following cholecystectomy for symptomatic gallbladder stones. Long-standing chronic inflammation is an important driver of GBC, regardless of the lithiasic or non-lithiasic origin. Advances in omics technologies have provided a deeper understanding of GBC pathogenesis, uncovering mechanisms associated with inflammation-driven tumour initiation and progression. Surgical resection is the only treatment with curative intent for GBC but very few cases are suitable for resection and most adjuvant therapy has a very low response rate. Several unmet clinical needs require to be addressed to improve GBC management, including discovery and validation of reliable biomarkers for screening, therapy selection and prognosis. Standardization of preneoplastic and neoplastic lesion nomenclature, as well as surgical specimen processing and sampling, now provides reproducible and comparable research data that provide a basis for identifying and implementing early detection strategies and improving drug discovery. Advances in the understanding of next-generation sequencing, multidisciplinary care for GBC, neoadjuvant and adjuvant strategies, and novel systemic therapies including chemotherapy and immunotherapies are gradually changing the treatment paradigm and prognosis of this recalcitrant cancer.
胆囊癌(GBC)是胆道系统最常见的癌症,由于其侵袭性行为和有限的治疗选择,在晚期诊断时预后极差。由于患者很少出现症状,因此在可治愈阶段进行早期检测仍然具有挑战性;事实上,大多数 GBC 是在因症状性胆囊结石而行胆囊切除术时偶然发现的。无论结石性还是非结石性起源,长期慢性炎症都是 GBC 的重要驱动因素。组学技术的进步为 GBC 的发病机制提供了更深入的了解,揭示了与炎症驱动的肿瘤起始和进展相关的机制。手术切除是唯一具有治愈意图的 GBC 治疗方法,但只有极少数病例适合切除,大多数辅助治疗的反应率非常低。为了改善 GBC 的管理,需要解决几个未满足的临床需求,包括发现和验证可靠的生物标志物用于筛查、治疗选择和预后。癌前和肿瘤病变命名的标准化,以及手术标本的处理和取样,现在提供了可重复和可比的研究数据,为确定和实施早期检测策略以及改善药物发现提供了基础。对下一代测序、GBC 的多学科治疗、新辅助和辅助策略以及包括化疗和免疫疗法在内的新型全身治疗的理解的进步正在逐渐改变这种难治性癌症的治疗模式和预后。