Acquired resistance to immunotherapy in MMR-D pancreatic cancer

被引:25
作者
Hu, Zishuo Ian [1 ]
Hellmann, Matthew D. [1 ,2 ,3 ,4 ]
Wolchok, Jedd D. [1 ,2 ,3 ,4 ]
Vyas, Monika [1 ,5 ]
Shia, Jinru [1 ,5 ,6 ]
Stadler, Zsofia K. [1 ,2 ,4 ]
Diaz, Luis A., Jr. [1 ,2 ]
O'Reilly, Eileen M. [1 ,2 ,4 ,7 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[2] Div Solid Tumor Oncol, New York, NY 10065 USA
[3] Mem Sloan Kettering, Parker Inst Canc Immunotherapy, New York, NY USA
[4] Weill Cornell Med Coll, Dept Med, New York, NY USA
[5] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[6] Weill Cornell Med Coll, Dept Pathol, New York, NY USA
[7] David M Rubenstein Ctr Pancreat Canc Res, New York, NY USA
关键词
Pancreatic cancer; Acquired resistance; Immunotherapy; Mismatch repair deficiency; MISMATCH REPAIR DEFICIENCY; CHECKPOINT BLOCKADE; IFN-GAMMA; CELLS; ADENOCARCINOMA; THERAPY; BETA(2)-MICROGLOBULIN; METASTASES; MUTATIONS;
D O I
10.1186/s40425-018-0448-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: 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. Case presentation: 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 3months, 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. Conclusions: 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.
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页数:6
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