Beetz Oliver, Timrott Angelica, Weigle Clara A, Schroeter Andreas, Cammann Sebastian, Klempnauer Juergen, Vondran Florian W R, Oldhafer Felix
Department of General, Visceral and Transplant Surgery, Hannover Medical School, Carl-Neuberg-Str. 1, 30625 Hannover, Germany.
J Clin Med. 2021 Sep 9;10(18):4073. doi: 10.3390/jcm10184073.
Intrahepatic cholangiocarcinoma (ICC) is a rare disease with poor outcome, despite advances in surgical and non-surgical treatment. Recently, studies have reported a favorable long-term outcome of "very early" ICC (based on tumor size and absence of extrahepatic disease) after hepatic resection and liver transplantation, respectively. However, the prognostic value of tumor size and a reliable definition of early disease remain a matter of debate. Patients undergoing resection of histologically confirmed ICC between February 1996 and January 2021 at our institution were reviewed for postoperative morbidity, mortality, and long-term outcome after being retrospectively assigned to two groups: "very early" (single tumor ≤ 3 cm) and "advanced" ICC (size > 3 cm, multifocality or extrahepatic disease). A total of 297 patients were included, with a median follow-up of 22.8 (0.1-301.7) months. Twenty-one (7.1%) patients underwent resection of "very early" ICC. Despite the small tumor size, major hepatectomies (defined as resection of ≥3 segments) were performed in 14 (66.7%) cases. Histopathological analyses revealed lymph node metastases in 5 (23.8%) patients. Patients displayed excellent postoperative outcome compared to patients with "advanced" disease: intrahospital mortality was not observed, and patients displayed superior long-term survival, with a 5-year survival rate of 58.2% (versus 24.3%) and a median postoperative survival of 62.1 months (versus 25.3 months; = 0.013). In conclusion, although the concept of a "very early" ICC based solely on tumor size is vague as it does not necessarily reflect an aggressive tumor biology, our proposed definition could serve as a basis for further studies evaluating the efficiency of either surgical resection or liver transplantation for this malignant disease.
肝内胆管癌(ICC)是一种预后较差的罕见疾病,尽管手术和非手术治疗取得了进展。最近,有研究分别报道了肝切除和肝移植后“极早期”ICC(基于肿瘤大小和无肝外疾病)的良好长期预后。然而,肿瘤大小的预后价值以及早期疾病的可靠定义仍存在争议。对1996年2月至2021年1月在我们机构接受组织学确诊的ICC切除术的患者进行回顾性分析,根据术后发病率、死亡率和长期预后将其分为两组:“极早期”(单个肿瘤≤3 cm)和“进展期”ICC(肿瘤大小>3 cm、多灶性或肝外疾病)。共纳入297例患者,中位随访时间为22.8(0.1 - 301.7)个月。21例(7.1%)患者接受了“极早期”ICC切除术。尽管肿瘤体积小,但14例(66.7%)患者进行了大范围肝切除术(定义为切除≥3个肝段)。组织病理学分析显示5例(23.8%)患者有淋巴结转移。与“进展期”疾病患者相比,这些患者术后预后良好:未观察到院内死亡,患者长期生存率更高,5年生存率为58.2%(相比之下为24.3%),术后中位生存期为62.1个月(相比之下为25.3个月;P = 0.013)。总之,尽管仅基于肿瘤大小的“极早期”ICC概念尚不明确,因为它不一定反映侵袭性肿瘤生物学特性,但我们提出的定义可为进一步评估手术切除或肝移植治疗这种恶性疾病的疗效的研究提供基础。