Di Marco Mariacristina, Carloni Riccardo, De Lorenzo Stefania, Mosconi Cristina, Palloni Andrea, Grassi Elisa, Filippini Daria Maria, Ricci Angela Dalia, Rizzo Alessandro, Di Federico Alessandro, Santini Donatella, Turchetti Daniela, Ricci Claudio, Ingaldi Carlo, Alberici Laura, Minni Francesco, Golfieri Rita, Brandi Giovanni, Casadei Riccardo
Department of Experimental, Diagnostic, and Specialty Medicine-DIMES, Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna 40138, Italy.
Division of Oncology, Azienda Ospedaliero-Universitaria di Bologna, Bologna 40138, Italy.
World J Gastrointest Oncol. 2020 Dec 15;12(12):1456-1463. doi: 10.4251/wjgo.v12.i12.1456.
Pancreatic mucinous cystadenocarcinoma (MCAC) is a rare malignancy with a poor prognosis when it presents metastases at diagnosis. Due to its very low incidence, there are no clear recommendations for the treatment of advanced disease. Olaparib (an oral PARP inhibitor) has been approved for the maintenance treatment of patients with metastatic pancreatic adenocarcinoma harbouring germline / mutations. Herein, we report the first case of a germline mutated unresectable MCAC which was effectively treated with olaparib.
A 41-year-old woman, without personal or family history of cancer, was diagnosed with ovarian and peritoneal metastases of MCAC. She underwent 12 cycles of gemcitabine plus oxaliplatin (GEMOX) obtaining a partial response and allowing radical surgery. One year later, local recurrence was documented, and other 12 cycles of GEMOX were administered obtaining a complete response. Seven years later, another local recurrence, not amenable to surgical resection, was diagnosed. She started FOLFIRINOX (oxaliplatin, irinotecan, leucovorin and fluorouracil), obtaining a partial response after 8 cycles. Given the excellent response to platinum-based chemotherapy, testing was performed, and a germline mutation was detected. She was switched to maintenance olaparib due to chemotherapy-related toxicities and achieved an almost complete metabolic response, with a reduction in the diameter of the lesion, after three months of therapy.
The current case suggests the beneficial effect of olaparib in mutated MCAC. However, further studies are required
胰腺黏液性囊腺癌(MCAC)是一种罕见的恶性肿瘤,诊断时出现转移则预后较差。由于其发病率极低,对于晚期疾病的治疗尚无明确的推荐方案。奥拉帕利(一种口服聚腺苷酸核糖聚合酶(PARP)抑制剂)已被批准用于维持治疗携带胚系/突变的转移性胰腺腺癌患者。在此,我们报告首例经奥拉帕利有效治疗的胚系突变不可切除MCAC病例。
一名41岁女性,无个人或家族癌症病史,被诊断为MCAC伴卵巢和腹膜转移。她接受了12个周期的吉西他滨联合奥沙利铂(GEMOX)治疗,获得部分缓解并得以进行根治性手术。一年后,记录到局部复发,遂再次给予12个周期的GEMOX治疗,获得完全缓解。七年后,诊断出另一处局部复发,无法进行手术切除。她开始使用FOLFIRINOX方案(奥沙利铂、伊立替康、亚叶酸钙和氟尿嘧啶),8个周期后获得部分缓解。鉴于对铂类化疗反应良好,进行了检测,检测到胚系突变。由于化疗相关毒性,她改用奥拉帕利维持治疗,治疗三个月后实现了几乎完全的代谢缓解,病灶直径缩小。
目前该病例提示奥拉帕利对突变的MCAC有有益作用。然而,还需要进一步研究。