Division of Medical Oncology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, 270 Rama VI Road, Ratchathewi, Bangkok, 10400, Thailand.
Division of Medical Oncology, Department of Medicine, Faculty of Medicine, Songklanagarind Hospital, Prince of Songkla University, Hat Yai, Thailand.
BMC Cancer. 2020 Jun 3;20(1):518. doi: 10.1186/s12885-020-07024-8.
Chemoradiotherapy (CRT) with high cumulative doses (CDs) of cisplatin has been considered the standard of care for non-metastatic nasopharyngeal carcinoma (NPC). However, given most patients' inability to tolerate high CDs due to cisplatin-related toxicities, the optimal CD of cisplatin during CRT remains undetermined.
Patients with non-metastatic NPC who received CRT with cisplatin between 2007 and 2017 were identified through the Thai head and neck cancer multicenter database and then categorized according to cisplatin CD (mg/m) received. All complications and cisplatin-related toxicities during CRT were recorded.
We identified 779 non-metastatic NPC patients receiving low (≤150; n = 97), intermediate (151-250; n = 411), and high (> 250; n = 271) CDs of cisplatin. Low CD patients had significantly lower mean actual radiation dose (p < 0.001) and more radiotherapy delay (p = 0.010), while intermediate CD patients had the least hospitalization (p < 0.001). Overall, 39.3% of the patients experienced cisplatin-related toxicity, which was associated with poor overall survival (OS) (p = 0.001). Acute kidney injury was observed in 7% in all patients, which was highest among low CD patients (15.5%; p = 0.002). Intermediate CD patients had significantly longer median OS than the low and high groups (64 vs. 49.8 vs. 53.2, respectively; p = 0.015). Univariate, but not multivariate, analysis showed that CD of cisplatin was significantly associated with OS.
CD of cisplatin during CRT was not an independent prognostic factor for OS. An intermediate CD induced minimal toxicity without compromising survival and should be considered the optimal CD. Nonetheless, a randomized phase 3 study evaluating the optimal CD of cisplatin is warranted.
高累积剂量(CD)顺铂的放化疗(CRT)已被认为是治疗局部晚期鼻咽癌(NPC)的标准治疗方法。然而,由于大多数患者无法耐受顺铂相关毒性导致的高 CD,CRT 期间顺铂的最佳 CD 仍未确定。
通过泰国头颈部癌症多中心数据库确定了 2007 年至 2017 年间接受 CRT 联合顺铂治疗的局部晚期 NPC 患者,并根据接受的顺铂 CD(mg/m)进行分类。记录 CRT 期间所有并发症和顺铂相关毒性。
共纳入 779 例局部晚期 NPC 患者,低剂量(≤150;n=97)、中剂量(151-250;n=411)和高剂量(>250;n=271)顺铂组。低剂量组患者的平均实际放射剂量明显较低(p<0.001),放疗延迟更多(p=0.010),而中剂量组患者的住院时间最短(p<0.001)。总体而言,39.3%的患者发生顺铂相关毒性,与总生存(OS)不良相关(p=0.001)。所有患者中急性肾损伤发生率为 7%,其中低剂量组最高(15.5%;p=0.002)。中剂量组患者的中位 OS 明显长于低剂量组和高剂量组(分别为 64、49.8 和 53.2;p=0.015)。单因素而非多因素分析显示,顺铂 CD 与 OS 显著相关。
CRT 期间的顺铂 CD 不是 OS 的独立预后因素。中等 CD 诱导的毒性最小,且不影响生存,应被视为最佳 CD。尽管如此,仍需要开展评估顺铂最佳 CD 的随机 3 期研究。