Miller Kevin C, Chintakuntlawar Ashish V, Hilger Crystal, Bancos Irina, Morris John C, Ryder Mabel, Smith Carin Y, Jenkins Sarah M, Bible Keith C
Mayo Clinic Alix School of Medicine, Rochester, MN, US.
Division of Medical Oncology, Mayo Clinic, Rochester, MN, US.
J Endocr Soc. 2020 Jun 9;4(7):bvaa069. doi: 10.1210/jendso/bvaa069. eCollection 2020 Jul 1.
Median overall survival is 12 to 15 months in patients with metastatic adrenal cortical carcinoma (ACC). Etoposide, doxorubicin, and cisplatin with or without the adrenolytic agent mitotane is considered the best first-line approach in this context, but has limited activity and no curative potential; additional salvage therapeutic options are needed.
Fifteen total patients with recurrent/metastatic ACC were treated with single-agent multikinase inhibitors (MKI) (n = 8), single-agent PD-1 inhibition (n = 8), or cytotoxic chemotherapy plus PD-1 inhibition (n = 4) at our institution as later-line systemic therapies in efforts to palliate disease and attempt to achieve a therapeutic response when not otherwise possible using standard approaches.
Two of 8 patients (25%) treated with single-agent MKI achieved a partial response (PR), including 1 PR lasting 23.5 months. Another 3 patients (38%) had stable disease (SD); median progression-free survival (PFS) with single-agent MKI was 6.4 months (95% confidence interval [CI] 0.8-not reached). On the other hand, 2 of 12 patients (17%) treated with PD-1 inhibitors (either alone or in combination with cytotoxic chemotherapy) attained SD or better, with 1 patient (8%) achieving a PR; median PFS was 1.4 months (95% CI 0.6-2.7).
Our single-institution experience suggests that select ACC patients respond to late-line MKI or checkpoint inhibition despite resistance to cytotoxic agents. These treatments may be attractive to ACC patients with limited other therapeutic options. The use of MKI and immunotherapy in ACC warrants prospective investigation emphasizing parallel correlative studies to identify biomarkers that predict for response.
转移性肾上腺皮质癌(ACC)患者的中位总生存期为12至15个月。依托泊苷、阿霉素和顺铂联合或不联合肾上腺溶解剂米托坦被认为是这种情况下最佳的一线治疗方法,但活性有限且无治愈潜力;需要更多的挽救性治疗选择。
在我们机构,15例复发/转移性ACC患者接受了单药多激酶抑制剂(MKI)(n = 8)、单药PD-1抑制(n = 8)或细胞毒性化疗加PD-1抑制(n = 4)作为后续的全身治疗,以缓解疾病,并在无法使用标准方法时尝试实现治疗反应。
8例接受单药MKI治疗的患者中有2例(25%)获得部分缓解(PR),其中1例PR持续23.5个月。另外3例患者(38%)病情稳定(SD);单药MKI的中位无进展生存期(PFS)为6.4个月(95%置信区间[CI] 0.8 - 未达到)。另一方面,12例接受PD-1抑制剂(单独或与细胞毒性化疗联合)治疗的患者中有2例(17%)病情稳定或更好,1例患者(8%)获得PR;中位PFS为1.4个月(95% CI 0.6 - 2.7)。
我们单机构的经验表明,尽管对细胞毒性药物耐药,但部分ACC患者对后续MKI或检查点抑制有反应。这些治疗方法对于其他治疗选择有限的ACC患者可能具有吸引力。在ACC中使用MKI和免疫疗法值得进行前瞻性研究,重点是平行的相关性研究以识别预测反应的生物标志物。