Ahmed Tamjeed, Lycan Thomas, Dothard Andy, Ehrlichman Paul, Ruiz Jimmy, Farris Michael, Topaloglu Umit, Levine Beverly, Grant Stefan, Klepin Heidi D, Petty W Jeffrey
Section of Hematology/Oncology, Wake Forest School of Medicine, Wiston-Salem, NC; Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC.
Section of Hematology/Oncology, Wake Forest School of Medicine, Wiston-Salem, NC; Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC.
Clin Lung Cancer. 2020 Jul;21(4):e286-e293. doi: 10.1016/j.cllc.2020.01.001. Epub 2020 Jan 23.
Immunotherapy has become a key treatment for patients with advanced non-small-cell lung cancer (NSCLC). While a survival advantage has been proven for patients who are medically fit, it is unknown whether a benefit exists for patients with poor performance status (PS).
We performed a retrospective analysis of NSCLC patients who received immunotherapy in our health system. Age and PS at the time of initial immunotherapy administration were assigned based on physician documentation. Radiographic response and date of progression were assigned according to the treating physician's assessment and confirmed by the study team. Immune-related adverse events were extracted from records.
We identified 285 NSCLC patients who received immunotherapy between January 2014 and April 2018. In this group, 153 patients (53.7%) had PS 0-1, 114 (40.0%) had PS 2, and 18 (6.3%) had PS 3. Response rates were similar across PS groups with 26.6% for PS 1, 25.2% for PS 2, and 23.1% for PS 3 (P = .95). Survival outcomes varied with pretreatment PS. For PS 0-1, PS 2, and PS 3, median overall survival was 14.7, 8.3, and 1.5 months (P < .001), and progression-free survival was 7.4, 5.1, and 1.3 months (P < .001). Patients aged < 70 had a lower rate (7.6%) of immune-related adverse events requiring steroids compared to patients ≥ 70 (15%) (P = .04).
Patients with poor baseline PS demonstrate similar response rate but inferior progression-free survival and overall survival compared to medically fit patients. Prospective trials are needed to optimize treatment for this large population.
免疫疗法已成为晚期非小细胞肺癌(NSCLC)患者的关键治疗方法。虽然已证明身体状况适合的患者有生存优势,但对于体能状态(PS)较差的患者是否有益尚不清楚。
我们对在我们医疗系统中接受免疫疗法的NSCLC患者进行了回顾性分析。初始免疫疗法给药时的年龄和PS根据医生记录确定。影像学反应和疾病进展日期根据主治医生的评估确定,并由研究团队确认。免疫相关不良事件从记录中提取。
我们确定了2014年1月至2018年4月期间接受免疫疗法的285例NSCLC患者。在该组中,153例患者(53.7%)PS为0 - 1,114例(40.0%)PS为2,18例(6.3%)PS为3。各PS组的缓解率相似,PS 1组为26.6%,PS 2组为25.2%,PS 3组为23.1%(P = 0.95)。生存结果因预处理时的PS而异。对于PS 0 - 1、PS 2和PS 3,中位总生存期分别为14.7、8.3和1.5个月(P < 0.001),无进展生存期分别为7.4,、5.1和1.3个月(P < 0.001)。年龄<70岁的患者与≥70岁的患者相比,需要使用类固醇治疗的免疫相关不良事件发生率较低(7.6% 对15%)(P = 0.04)。
基线PS较差的患者与身体状况适合的患者相比,缓解率相似,但无进展生存期和总生存期较差。需要进行前瞻性试验以优化对这一庞大群体的治疗。