P864 Combination of fecal microbiota transplantation from healthy donors with anti-PD1 immunotherapy in treatment-naïve advanced or metastatic melanoma patients

Saman Maleki, J. Lenehan, J. Burton, M. Silverman, S. Parvathy, Mikal El-Hajjar, M. Krishnamoorthy
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引用次数: 7

Abstract

Background Checkpoint inhibitors have changed the outcomes for patients with advanced melanoma. However, many patients still show primary resistance to single-agent therapy. Recently, the role of the gut microbiome in influencing antitumor immunity has been established. Currently, various methods of modifying the gut microbiome of cancer patients are being explored. We report the initial safety results of the first two patients treated on a phase I study combining Fecal Microbiota Transplantation (FMT) with single-agent anti-PD1 in treatment-naïve patients with advanced melanoma. Methods Two healthy donors were selected through our screening process and approximately 100 grams of fresh stool was processed and prepared for FMT as per our standardized protocol. FMT recipients were melanoma patients with unresectable or metastatic disease who were treatment naïve for their advanced disease. Bowel preparation was completed the day prior and FMT was performed using oral administration of approximately 40 capsules. Anti-PD1 was started at least 1 week after FMT to allow for microbiome engraftment. Blood and stool were analyzed at baseline (pre-FMT), before immunotherapy, and three weeks after it. Results Patient 1 was diagnosed with recurrent melanoma of the lower limb with multiple in-transit lesions refractory to control with surgery and a single intralesional injection of IL-2. Patient received stool from Donor 1 and did not experience any adverse effects from FMT. At the time of treatment #4, a solitary large cutaneous lesion stabilized but the patient experienced grade 1 diarrhoea, grade 2 nausea, and grade 2 fatigue, and grade 2 depression (NCI-CTCAE v5.0). Patient 2 was diagnosed with recurrent melanoma of the parotid gland with metastatic lesions in the lungs. Patient 2 received stool from Donor 2 and experienced only grade 1 flatus from FMT. At the time of treatment #3, the patient experienced grade 1 constipation. Both patients had a vigorous immune response to FMT measured by changes in the immune subpopulations in peripheral blood one week after FMT, including an increase in CD28+ CD8+ T cells and a decrease in PDL1+ CD3- cells. Following anti-PD1 therapy, both patients had an increase in CD39+ CD8+ T cell population. The PD1+ CD38+ CD8+ dysfunctional T cell levels decreased in both patients post-FMT and anti-PD1 therapy. Conclusions FMT combined with anti-PD1 therapy in patients with advanced melanoma appears to be safe. A measurable immune response was observed one week after FMT in both patients. One patient experienced several grade 2 toxicities with stabilization of a large cutaneous lesion. Acknowledgements This study is funded by a grant from The Lotte & John Hecht Memorial Foundation and a grant from The Medical Oncology Research Funds (MORF) from Western University. Trial Registration NCT03772899 Ethics Approval The study was approved by Western University Institutution‘s Ethics Board, approval number 113131, date of approval March 15, 2019.
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P864健康供体粪便微生物群移植与抗pd1免疫疗法联合治疗treatment-naïve晚期或转移性黑色素瘤患者
检查点抑制剂已经改变了晚期黑色素瘤患者的预后。然而,许多患者对单药治疗仍表现出原发性耐药性。近年来,肠道微生物群在影响抗肿瘤免疫中的作用已被确立。目前,人们正在探索各种改变癌症患者肠道微生物组的方法。我们报告了在treatment-naïve晚期黑色素瘤患者中联合粪便微生物群移植(FMT)和单药抗pd1治疗的前两名患者的初步安全性结果。方法经筛选,选取两名健康供体,按标准方案处理制备新鲜粪便约100克,用于FMT。FMT接受者是患有不可切除或转移性疾病的黑色素瘤患者,他们的晚期疾病接受naïve治疗。前一天完成肠道准备,并口服约40粒胶囊进行FMT。在FMT后至少1周开始抗pd1,以允许微生物组植入。在基线(fmt前)、免疫治疗前和免疫治疗后三周分析血液和粪便。结果患者1被诊断为下肢复发性黑色素瘤,伴有多处转移性病变,手术和单次病灶内注射IL-2难以控制。患者接受了供体1的粪便,并没有经历FMT的任何不良反应。在第4次治疗时,一个孤立的大皮肤病变稳定下来,但患者出现了1级腹泻、2级恶心、2级疲劳和2级抑郁(NCI-CTCAE v5.0)。患者2被诊断为腮腺复发性黑色素瘤,肺部有转移性病变。患者2接受了供体2的粪便,仅经历了FMT的1级放屁。在第3次治疗时,患者经历了1级便秘。通过FMT后一周外周血免疫亚群的变化,两名患者对FMT都有强烈的免疫反应,包括CD28+ CD8+ T细胞的增加和PDL1+ CD3-细胞的减少。在抗pd1治疗后,两名患者的CD39+ CD8+ T细胞群均增加。fmt和抗PD1治疗后,患者的PD1+ CD38+ CD8+功能失调T细胞水平均下降。结论FMT联合抗pd1治疗晚期黑色素瘤是安全的。两名患者在FMT后一周观察到可测量的免疫应答。1例患者出现2级毒性,大面积皮肤病变稳定。本研究由Lotte & John Hecht纪念基金会和Western University肿瘤医学研究基金(MORF)资助。本研究已获得西部大学伦理委员会批准,批准文号113131,批准日期2019年3月15日。
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