Addition of chemoradiotherapy to palliative chemotherapy in de novo metastatic nasopharyngeal carcinoma: a real-world study.

Addition of chemoradiotherapy to palliative chemotherapy in de novo metastatic nasopharyngeal carcinoma: a real-world study.
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姑息化疗联合放化疗治疗新发转移性鼻咽癌:一项真实世界研究

DOI:
10.1186/s12935-022-02464-7
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发表时间:
2022-01-24
影响因子:
5.8
通讯作者:
Xia YF
Xia YF
中科院分区:
医学2区
文献类型:
--
作者:
Zheng SH;Wang YT;Liu SR;Huang ZL;Wang GN;Lin JT;Ding SR;Chen C;Xia YF

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确定在NOKO转移性鼻咽癌(MNPC)患者姑息化疗(PCT)后局部放疗(RT)期间是否需要进行化疗。 在我们医院共有746例MNPC患者,在他们的医院中进行了回顾,其中有355例患者接受了PCT,其次是RT。通过Kaplan-Meier方法和对数秩比例的模型,LRPFS)和拆卸无进展生存率(DPF)。分析,可靠性得分匹配和亚组分析用于解决混杂问题。 在我们的研究中包括的患者中,192例PCT(PCT+RT)单独接受了放射疗法,而PCT后163例(PCT+CCRT)同时进行了化学放疗(PCT+CCRT)。 OS,53.0 vs 36.2%; p = 0.004。 (p = 0.034)和中位数为29.4和18.7个月(p = 0.052)。 PCT的4–6个周期或与​​单药铂进行同时进行化学疗法与匹配的队列中的显着生存率有关(5年OS率,分别为60.4或57.4%),在评估生存的1年的患者时,组之间的生存差异仍然很大(P≉= 0.028)。 MNPC的最佳治疗策略是PCT的组合,然后是同时进行的化学疗法。 在线版本包含的补充材料可获得10.1186/s12935-022-02464-7。
To determine whether concurrent chemotherapy is necessary during locoregional radiotherapy (RT) after palliative chemotherapy (PCT) in patients with de novo metastatic nasopharyngeal carcinoma (mNPC). A total of 746 patients with mNPC from 2000 to 2017 at our hospital were retrospectively reviewed. Among them, 355 patients received PCT followed by RT. Overall survival (OS) and progression-free survival (PFS), including locoregional progression-free survival (LRPFS) and distant progression-free survival (DPFS) were estimated with the Kaplan–Meier method and log-rank test. Cox proportional-hazards models, landmark analyses, propensity score matching, and subgroup analyses were used to address confounding. Of the patients included in our study, 192 received radiotherapy alone after PCT (PCT + RT), and 163 received concurrent chemoradiotherapy after PCT (PCT + CCRT). The prognosis of PCT + CCRT was significantly better than that of PCT + RT (5 year OS, 53.0 vs 36.2%; P = 0.004). After matching, the 5 year OS rates of the two groups were 55.7 and 39.0%, respectively (P = 0.034) and the median DPFS were 29.4 and 18.7 months, respectively (P = 0.052). Multivariate Cox regression analysis indicated that PCT + CCRT was an independent favorable prognostic factor (P = 0.009). In addition, conducting concurrent chemoradiotherapy after 4–6 cycles of PCT or conducting concurrent chemotherapy with single-agent platinum was associated with significant survival benefit in the matched cohort (5 year OS rate, 60.4 or 57.4%, respectively). The survival difference between groups remained significant when evaluating patients who survived for ≥ 1 year (P = 0.028). The optimal treatment strategy of mNPC is the combination of PCT followed by concurrent chemoradiotherapy. More specifically, concurrent chemoradiotherapy with single-agent platinum after 4–6 cycles of PCT is suggested. The online version contains supplementary material available at 10.1186/s12935-022-02464-7.
DOI: 10.1016/s0140-6736(01)06103-7
发表时间: 2001-09-22
期刊: LANCET
影响因子: 168.9
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