Chen Xialin, Zhu Xiang, Wang Jianfang, Liu Jianjiang, Ji Rong
Department of Oncology, Shaoxing People's Hospital, Shaoxing, Zhejiang 312000, China.
Department of Oncology, Shaoxing Hospital of Zhejiang University, Shaoxing, Zhejiang 312000, China.
Onco Targets Ther. 2019 Feb 22;12:1553-1562. doi: 10.2147/OTT.S183483. eCollection 2019.
The outcomes and safety profiles of neoadjuvant chemotherapy (NACT) + intensity modulated radiotherapy (IMRT) or NACT + IMRT + concurrent chemoradiotherapy (CCRT) in locoregionally advanced nasopharyngeal carcinoma (NPC) patients were retrospectively analyzed.
Between 2010 and 2014, 125 patients with stage III-IVb NPC, who were treated with IMRT (36, 28.8%) or IMRT + CCRT (89, 71.2%) following NACT, participated in the research. There were grade 3-4 toxicities during NACT or radiotherapy (RT) in NACT + IMRT group and NACT + IMRT + CCRT group.
MRI within 3 months demonstrated that no patient suffered with progressive disease, 116 patients (92.8%) achieved a response rate (RR) with the complete response (CR) rate of 70.4% (88/125) and partial response (PR) rate of 22.4% (28/125), and nine patients (7.2%) showed stable disease (SD) at the primary site and metastatic nodes. Compared with NACT + IMRT group, patients in NACT + IMRT + CCRT group did not show significantly better RR (93.3% vs 91.7%, =1.00), CR rate (71.9% vs 66.7%, =0.67), or PR rate (21.4% vs 25%, =0.81). There was no significant difference in overall survival (OS, =0.114), local relapse-free survival (LRFS, =0.124), distant metastasis-free survival (DMFS, =0.668) or progression-free survival (PFS, =0.475) between NACT + IMRT group and NACT + IMRT + CCRT group. T classification (=0.042) and N classification (=0.021) were independent prognostic factors for DMFS.
To sum up, no significant difference was observed in combined RR, CR rate, LRFS, DMFS, PFS, or OS between the two groups.
回顾性分析新辅助化疗(NACT)联合调强放疗(IMRT)或NACT联合IMRT同步放化疗(CCRT)用于局部晚期鼻咽癌(NPC)患者的疗效及安全性。
2010年至2014年间,125例III-IVb期NPC患者参与本研究,这些患者在接受NACT后接受了IMRT(36例,28.8%)或IMRT+CCRT(89例,71.2%)治疗。NACT+IMRT组和NACT+IMRT+CCRT组在NACT或放疗(RT)期间出现3-4级毒性反应。
3个月内的MRI检查显示,无患者出现疾病进展,116例患者(92.8%)达到缓解率(RR),完全缓解(CR)率为70.4%(88/125),部分缓解(PR)率为22.4%(28/125),9例患者(7.2%)在原发部位和转移淋巴结处疾病稳定(SD)。与NACT+IMRT组相比,NACT+IMRT+CCRT组患者的RR(93.3%对91.7%,P=1.00)、CR率(71.9%对66.7%,P=0.67)或PR率(21.4%对25%,P=0.81)均未显示出显著更好的情况。NACT+IMRT组和NACT+IMRT+CCRT组在总生存期(OS,P=0.114)、无局部复发生存期(LRFS,P=0.124)、无远处转移生存期(DMFS,P=0.668)或无进展生存期(PFS,P=0.475)方面均无显著差异。T分期(P=0.042)和N分期(P=0.021)是DMFS的独立预后因素。
综上所述,两组在联合RR、CR率、LRFS、DMFS、PFS或OS方面未观察到显著差异。