Therapeutic strategies and prognostic challenges in linitis plastica.

Grigorios Christodoulidis, Sara Eirini Agko, Konstantinos Eleftherios Koumarelas, Marina Nektaria Kouliou
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Abstract

Gastric cancer ranks fifth as the most common cancer and third as the leading cause of death worldwide. Risk factors include advancing age, low-fiber diets, high salt intake and Helicobacter pylori infection. Diagnosis relies on histological examination following endoscopic biopsy with staging accomplished through various imaging modalities. Early gastric cancer is primarily managed via endoscopic resection, while non-early operable cases typically undergo surgery. Advanced cases are addressed through sequential chemotherapy lines, with initial treatment usually comprising a platinum and fluoropyrimidine combination. Linitis plastica (LP) is a rare, aggressive form of gastric cancer characterized by diffuse infiltration of the gastric wall, resulting in poor outcomes even after curative resection. The absence of a standardized definition contributes to uncertainty regarding the precise incidence of these tumors. LP is often diagnosed at advanced stages, with a reported median survival rate of approximately 4%-29%, despite "curative resection". Its distinctive biological behavior includes perineural invasion, nodal metastasis, and peritoneal dissemination. The bleak prognosis for LP patients partly stems from delayed diagnosis and its aggressive biological nature, posing significant challenges for clinical management. Currently, no specialized treatment strategy exists for LP, and clinical approaches typically align with those used for general gastric cancer treatment. Surgical resection is the primary treatment, but the optimal surgical approach remains contentious. Recent studies have investigated the efficacy of neoadjuvant chemotherapy and radiotherapy in improving survival outcomes for LP patients. However, controversies persist regarding the role of adjuvant chemotherapy and postoperative radiotherapy. LP requires a multidisciplinary approach and personalized treatment strategies tailored to each patient's condition. Further research is needed to elucidate optimal therapeutic interventions and improve outcomes for LP patients.

可塑性局限性炎的治疗策略和预后挑战。
胃癌在全球最常见的癌症中排名第五,在导致死亡的主要原因中排名第三。风险因素包括年龄增长、低纤维饮食、高盐摄入和幽门螺杆菌感染。诊断依赖于内镜活检后的组织学检查,并通过各种成像方式完成分期。早期胃癌主要通过内镜切除治疗,而非早期可手术的病例通常进行手术治疗。晚期病例通过序贯化疗治疗,初始治疗通常包括铂和氟嘧啶组合。可塑性局限性炎(LP)是一种罕见的侵袭性胃癌,其特征是胃壁弥漫性浸润,即使在根治性切除后,预后也很差。由于缺乏标准化的定义,这些肿瘤的确切发病率存在不确定性。LP通常在晚期被诊断出来,尽管“治愈性切除”,但据报道中位生存率约为4%-29%。其独特的生物学行为包括神经周围侵袭、淋巴结转移和腹膜传播。LP患者预后不佳的部分原因在于其诊断迟缓和具有侵袭性的生物学特性,这给临床治疗带来了重大挑战。目前,LP没有专门的治疗策略,临床方法通常与一般胃癌治疗方法一致。手术切除是主要治疗方法,但最佳手术方法仍有争议。最近的研究调查了新辅助化疗和放疗在改善LP患者生存结果方面的疗效。然而,关于辅助化疗和术后放疗的作用仍存在争议。LP需要多学科的方法和个性化的治疗策略,为每个病人量身定制的条件。需要进一步的研究来阐明最佳的治疗干预措施并改善LP患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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