Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Division of Solid Tumor Oncology, New York, NY, USA.
J Immunother Cancer. 2018 Nov 20;6(1):127. doi: 10.1186/s40425-018-0448-1.
MMR-D pancreatic cancer have been reported to respond to checkpoint inhibitor therapy. Here, we report the first case of acquired resistance to immunotherapy in MMR-D pancreatic cancer.
A 45-year-old woman with unresectable MMR-D pancreatic cancer was initially treated with FOLFIRINOX, FOLFIRI, and stereotactic body radiation with stable disease burden. After 3 months, imaging showed progression of disease with an increase in CA19-9. She was subsequently enrolled in a clinical trial of an anti-PD-L1 antibody in combination with an IDO1 inhibitor. She demonstrated a partial response to therapy by RECIST 1.1 criteria with declining tumor markers. Twenty-two months after beginning immunotherapy, imaging revealed an increasing left ovarian cystic mass. There were no other sites of progressive disease. The patient underwent a total hysterectomy and bilateral salpingo-oophorectomy, appendectomy, omentectomy and pelvic lymphadenopathy. Pathology was consistent with a metastasis from the pancreas involving the endometrium and left ovary. Thereafter, the patient continued with PD-1 blockade therapy off protocol with no further progressive disease. Immune profiling showed high levels of CD8+ T cells and PD-1 positive immune cells infiltrating the tumor, with a moderate level of PD-L1 expression in both the immune cells and the tumor cells. Next generation sequencing found only the KRAS G12D and RNF43 G659Vfs*41 mutations were retained from the pre-treatment tumor in the treatment-resistant tumor.
This is the first report describing acquired resistance to immunotherapy in MMR-D pancreatic cancer with accompanying genomic and immune profiling. This case of oligoprogression in the setting of immunotherapy demonstrates the feasibility of localized treatment followed by continuation of immunotherapy to sustain ongoing response.
已有报道称 MMR-D 胰腺癌对检查点抑制剂治疗有反应。在此,我们报告首例 MMR-D 胰腺癌对免疫治疗产生获得性耐药的病例。
一名 45 岁女性患有不可切除的 MMR-D 胰腺癌,最初接受 FOLFIRINOX、FOLFIRI 和立体定向体部放疗,疾病负担稳定。3 个月后,影像学显示疾病进展,CA19-9 升高。随后她参加了一项抗 PD-L1 抗体联合 IDO1 抑制剂的临床试验。根据 RECIST 1.1 标准,她对治疗有部分反应,肿瘤标志物下降。免疫治疗开始后 22 个月,影像学显示左侧卵巢囊性肿块增大。无其他部位进展性疾病。患者接受了全子宫切除术、双侧输卵管卵巢切除术、阑尾切除术、网膜切除术和盆腔淋巴结清扫术。病理结果与胰腺转移有关,累及子宫内膜和左侧卵巢。此后,患者继续按方案外进行 PD-1 阻断治疗,无进一步进展性疾病。免疫谱分析显示,肿瘤内浸润的 CD8+T 细胞和 PD-1 阳性免疫细胞水平较高,肿瘤细胞和免疫细胞中 PD-L1 表达水平中等。下一代测序发现,治疗耐药性肿瘤中仅保留了治疗前肿瘤中的 KRAS G12D 和 RNF43 G659Vfs*41 突变。
这是首例描述 MMR-D 胰腺癌对免疫治疗产生获得性耐药的病例,并伴有基因组和免疫谱分析。在免疫治疗中寡进展的情况下,局部治疗后继续进行免疫治疗以维持持续反应是可行的。