a Department of Surgical Oncology , Medical School of Crete University Hospital , Heraklion , Greece.
b Department of Surgical Oncology , Catharina Hospital , Eindhoven , The Netherlands.
Acta Oncol. 2018 Jun;57(6):712-722. doi: 10.1080/0284186X.2018.1433321. Epub 2018 Jan 30.
Small bowel adenocarcinoma (SBA) is rare despite the fact that the small bowel represents the longest part and has the largest surface of all alimentary tract sections. Its incidence is 50-fold lower than that of colorectal carcinoma. It is often diagnosed at an advanced stage due to atypical and late symptoms, its low index of suspicion, difficult endoscopic access and poor detection by radiological imaging, resulting in impaired outcome. Due to its rarity and being molecularly a unique intestinal cancer, data regarding its optimal management are relatively sparse.
A PubMed search was performed to identify relevant manuscripts that were recently published. Emerging data regarding the pathogenesis, the diagnosis and the treatment of SBA that resulted from recent research are discussed in this comprehensive review.
Genomic analysis has demonstrated that SBA is a molecularly unique intestinal cancer. Double balloon enteroscopy and capsule endoscopy are novel techniques which may result in earlier diagnosis and consequently in improvement of the generally poor prognosis. For clinically localized disease, the quality of surgery has recently been defined, with removal of at least 8-10 lymph nodes correlating with improved prognosis. Moreover, adjuvant chemotherapy seems to improve outcome of stage III disease. The combination of a fluoropyrimidine and oxaliplatin appears to be the most effective systemic chemotherapy for disseminated disease. Genomic profiling can identify potentially targetable genomic alterations in a significant proportion of SBA patients. The role of administration of targeted agents or immune checkpoint inhibitors is still unknown and subject of ongoing clinical trials. In the common case of peritoneal metastases, recent studies have shown that cytoreductive surgery and intraoperative hyperthermic intraperitoneal chemotherapy may be an attractive treatment option in selected patients.
SBA is a rare and unique malignancy, whose diagnostic approach and treatment are evolving, resulting in improved outcome.
尽管小肠是所有消化道中最长的部分,表面积最大,但小肠腺癌(SBA)仍然较为罕见。其发病率比结直肠癌低 50 倍。由于症状不典型且较晚、怀疑指数低、内镜检查困难以及影像学检查对其的检出率差,导致其常常在晚期才被诊断,预后较差。由于其罕见性以及在分子水平上是一种独特的肠道癌,因此有关其最佳治疗方法的数据相对较少。
对 PubMed 进行了检索,以确定最近发表的相关文献。本文对最近的研究得出的关于 SBA 的发病机制、诊断和治疗的新数据进行了讨论。
基因组分析表明 SBA 在分子水平上是一种独特的肠道癌。双气囊小肠镜和胶囊内镜是两种新的技术,可能会更早地诊断出疾病,从而改善通常较差的预后。对于局部疾病,最近已经确定了手术质量,切除至少 8-10 个淋巴结与改善预后相关。此外,辅助化疗似乎可以改善 III 期疾病的预后。氟嘧啶联合奥沙利铂似乎是治疗转移性疾病最有效的全身化疗方案。基因组分析可以在相当一部分 SBA 患者中识别出潜在的可靶向基因组改变。靶向药物或免疫检查点抑制剂的给药作用仍不清楚,是正在进行的临床试验的主题。对于常见的腹膜转移,最近的研究表明,细胞减灭术和术中腹腔内高温化疗可能是某些患者有吸引力的治疗选择。
SBA 是一种罕见且独特的恶性肿瘤,其诊断方法和治疗方法正在不断发展,从而改善了预后。