GEMOX 方案联合尼莫妥珠单抗成功治疗 KRAS 野生型和 BRCA 突变型胰腺癌:两例病例报告。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL AME Case Reports Pub Date : 2024-09-06 eCollection Date: 2024-01-01 DOI:10.21037/acr-24-68
Puxiongzhi Wang, Li Zhang, Liqin Yu, Chao Huang, Wei Wang
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摘要

背景胰腺癌具有化疗耐药的特点。近年来,更多潜在的胰腺癌治疗分子靶点被开发出来,因此精准化疗以改善晚期胰腺癌患者的预后越来越受到重视:本研究报告了两例罕见的晚期胰腺癌病例。其中一名患者被诊断为胰腺导管腺癌根治性切除术后腹膜后淋巴结转移。另一名患者的诊断结果为胰腺导管腺癌伴肝转移。他们肿瘤组织的全基因组测序均检测到野生型 Kirsten 大鼠肉瘤病毒癌基因同源物(KRAS)和突变型乳腺癌易感基因(BRCA)。免疫组化显示,她们的肿瘤组织表皮生长因子受体呈阴性。我们采用吉西他滨(1,000 mg/m2)+奥沙利铂(135 mg/m2)+尼莫妥珠单抗(400 mg)联合化疗。经过九次化疗后,正电子发射断层扫描-计算机断层扫描等影像学检查显示,两例患者均获得完全缓解。化疗期间也没有出现严重的副作用。随后,患者口服奥拉帕利(600 毫克/天)治疗一年,生存超过 1.5 年,肿瘤无进展:这两例患者均取得了良好的精准化疗效果,为KRAS野生型和BRCA突变型胰腺癌患者的治疗提供了重要参考。
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Successful treatment of GEMOX regimen combined with nimotuzumab in the pancreatic cancer with wild KRAS and mutant BRCA: a report of two cases.

Background: Pancreatic cancer is characterized by chemoresistance. In recent years, more potential therapeutic molecular targets for pancreatic cancer have been developed, and thus increasing attention has been paid to precise chemotherapy to improve the prognosis of patients with advanced pancreatic cancer.

Case description: In this study, we reported two rare cases of advanced pancreatic cancer. One patient was diagnosed with retroperitoneal lymph node metastasis after radical resection of pancreatic ductal adenocarcinoma. The diagnosis of another patient was pancreatic ductal adenocarcinoma with liver metastasis. The whole genome sequencing of their tumor tissues detected both wild-type Kirsten rat sarcoma viral oncogene homolog (KRAS) and mutant breast cancer susceptibility gene (BRCA). And immunohistochemistry showed their tumor tissue was negative for epidermal growth factor receptor. We used the combined chemotherapy of gemcitabine (1,000 mg/m2) + oxaliplatin (135 mg/m2) + nimotuzumab (400 mg). After nine times of chemotherapy, the imaging examinations including positron emission tomography-computed tomography showed that both cases achieved complete remission. And there were no serious side effects during chemotherapy. Then, the patients were treated with oral olaparide (600 mg/day) for one year, and survived without tumor progress for more than 1.5 years.

Conclusions: These two cases achieved excellent effects of precise chemotherapy, which provided an important reference for the treatment of pancreatic cancer patients with wild KRAS and mutant BRCA.

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