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一名广泛期小细胞肺癌患者在接受卡铂、依托泊苷和阿替利珠单抗治疗后长期生存且病情稳定

Long-Term Survival and Stable Disease in a Patient with Extensive-Stage Small-Cell Lung Cancer after Treatment with Carboplatin, Etoposide and Atezolizumab.

作者信息

Bernabé Reyes, Liu Stephen V, Sánchez-Gastaldo Amparo, Alonso García Miriam

机构信息

Department of Medical Oncology, Hospital Universitario Virgen del Rocío, Av. Manuel Siurot S/N, 41013, Seville, Spain.

Division of Medical Oncology, Georgetown University, Washington, DC, USA.

出版信息

Oncol Ther. 2024 Mar;12(1):175-182. doi: 10.1007/s40487-023-00257-0. Epub 2024 Jan 27.

Abstract

Survival beyond 2 years is rare in patients with extensive-stage small-cell lung cancer (ES-SCLC) treated with chemotherapy alone. We describe a patient with ES-SCLC who was treated with carboplatin, etoposide and the programmed death-ligand 1 inhibitor atezolizumab in the IMpower133 study (ClinicalTrials.gov registration: NCT02763579) and who achieved exceptionally long-term survival. Treatment-naïve patients with ES-SCLC (n = 403) were included in the IMpower133 study, and the identified patient had been randomised to the investigational treatment arm, where patients received induction therapy with carboplatin and etoposide plus atezolizumab for four 21-day cycles, followed by ongoing maintenance therapy with atezolizumab. The patient had achieved a partial response after induction therapy, and then received seven cycles of atezolizumab maintenance therapy until immune-related toxicities necessitated discontinuation. The patient was alive with an ongoing response and excellent performance status more than 6 years after starting treatment and 5 years after discontinuing atezolizumab maintenance. In conclusion, this patient with ES-SCLC from the IMpower133 study is a rare example of ongoing survival more than 6 years beyond diagnosis and the start of treatment with first-line atezolizumab. This demonstrates the potential durability of response with immunotherapy.

摘要

对于仅接受化疗的广泛期小细胞肺癌(ES-SCLC)患者而言,存活超过2年的情况很罕见。我们描述了一名ES-SCLC患者,在IMpower133研究(ClinicalTrials.gov注册号:NCT02763579)中接受了卡铂、依托泊苷和程序性死亡配体1抑制剂阿特珠单抗治疗,并获得了超长的生存期。IMpower133研究纳入了初治的ES-SCLC患者(n = 403),该患者被随机分配至研究治疗组,患者接受了卡铂和依托泊苷加阿特珠单抗的诱导治疗,共四个21天周期,随后接受阿特珠单抗的持续维持治疗。该患者在诱导治疗后获得了部分缓解,然后接受了七个周期阿特珠单抗维持治疗,直至免疫相关毒性导致停药。在开始治疗6年多以及停用阿特珠单抗维持治疗5年后,该患者仍存活,有持续缓解且身体状况良好。总之,这名来自IMpower133研究的ES-SCLC患者是诊断及开始一线阿特珠单抗治疗后存活超过6年的罕见例子。这证明了免疫疗法疗效的潜在持久性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7f01/10881916/d0db1da9aa7a/40487_2023_257_Fig1_HTML.jpg

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