腹膜转移性胰腺导管腺癌序贯化疗后的长期持续临床缓解:病例报告

Sen Yang, Yuze Hua, Qiaofei Liu, Quan Liao
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引用次数: 0

摘要

血清碳水化合物抗原(CAs)水平较高的腹膜转移性胰腺导管腺癌(pmPDAC)患者的预后总是非常糟糕,中位生存期仅为几个月。在此,我们报告了一例伴有高血清CAs的pmPDAC患者,化疗后CAs恢复正常,长期临床缓解。2019年11月,一名64岁的男性患者因胰腺体靠近腹腔干处有一个2.8×2.5×2.0cm的实性肿块而入住我中心。正电子发射计算机断层扫描(PET-CT)显示 SUVmax 为 4.2。血清 CA 242 水平超过 150.0 U/ml(正常范围:0-20 U/ml),CA 19-9 升高至 975.2 U/ml(正常范围:0-34 U/ml)。腹腔镜检查发现,肿瘤环绕腹腔主干超过 180 度,小网膜腔内有多个腹膜小结节。病理检查确诊为 pmPDAC。下一代测序显示 RAS G12V、表皮生长因子受体突变(-)、低 TMB(肿瘤突变负荷)和 MSS(微卫星稳定性)。患者接受了6个周期的AG方案(吉西他滨+纳布-紫杉醇)治疗,结果肿瘤明显缩小,CA急剧下降。患者的病情得到了部分缓解。然而,由于无法耐受神经毒性,AG 方案被终止。随后,患者接受了同步口服氟尿嘧啶(S1)和放射治疗。放疗五个月后,所有 CA 均恢复正常。口服 S1 继续了三个月。最终,所有抗癌药物均被停用。计算机断层扫描显示,肿瘤仍然包围着腹腔干和肝总动脉。经过充分讨论后,医生采取了观望策略。值得注意的是,在停用抗癌药物 32 个月后,患者的健康状况依然良好,CA 值持续正常。最后一次随访时,他已经活了 50 个月,CA 正常化持续了 36 个月。虽然他仍然面临疾病进展的风险,但这是一个成功的病例,即用最先进的化疗方法治疗了一名病情恶化的 pmPDAC 患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-term Sustained Clinical Remission of Peritoneal Metastatic Pancreatic Ductal Adenocarcinoma After Sequential Chemoradiation Therapy: A Case Report
Patients with peritoneal metastatic pancreatic ductal adenocarcinoma (pmPDAC) with high-level serum carbohydrate antigens (CAs) always suffer extremely dismal prognosis, with a median survival of several months. Herein, we reported a case of pmPDAC with high serum CAs who had long-term clinical remission with normalization of CAs after chemoradiation. In November 2019, a 64-year-old male patient was admitted to our center with a solid mass measuring 2.8×2.5×2.0cm in the body of the pancreas near the celiac trunk. Positron emission tomography-computed tomography (PET-CT) revealed an SUVmax of 4.2. The serum CA 242 level exceeded 150.0 U/ml (normal range: 0-20 U/ml), and CA 19-9 was elevated at 975.2 U/ml (normal range: 0-34 U/ml). During laparotomy, the tumor was found to encircle the celiac trunk over 180 degrees, with several small peritoneal nodules in the lesser omental cavity. Pathological examination confirmed the diagnosis of pmPDAC. Next-generation sequencing revealed RAS G12V, EGFR mutation (-), low TMB (tumor mutation burden), and MSS (microsatellite stability). The patient underwent six cycles of the AG regimen (gemcitabine plus nab-paclitaxel), resulting in significant tumor shrinkage and a sharp decline in CAs. Partial remission was achieved. However, due to intolerant neurotoxicity, the AG regimen was discontinued. Subsequently, synchronous oral fluorouracil (S1) and radiation therapy were administered. Five months after radiation treatment, all CAs normalized. Oral S1 was continued for an additional three months. Eventually, all anti-cancer drugs were stopped. Computed tomography scans indicated that the tumor still surrounded the celiac trunk and common hepatic artery. After a thorough discussion, a wait-and-see strategy was adopted. Remarkably, 32 months after stopping anti-cancer medication, the patient remains in good health, with sustained normalization of CAs. At the last follow-up, he had lived for 50 months, and the normalization of the CAs was sustained for 36 months. Although he still suffers the risk of disease progression, it is a successful case of state-of-the-art chemoradiation for a dismal pmPDAC patient.
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