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
中科院分区:
文献类型:
--
作者:
Zheng SH;Wang YT;Liu SR;Huang ZL;Wang GN;Lin JT;Ding SR;Chen C;Xia YF
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.
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影响因子:
168.9
作者:
Mickisch, GHJ;Garin, A;Sylvester, R
通讯作者:
Sylvester, R
影响因子:
45.3
作者:
Hsu, Chiun;Lee, Se-Hoon;Hansen, Aaron R.
通讯作者:
Hansen, Aaron R.
影响因子:
45.3
作者:
Ma, Brigette B. Y.;Lim, Wan-Teck;Chan, Anthony T. C.
通讯作者:
Chan, Anthony T. C.
DOI:
10.1016/j.ijrobp.2020.08.045
发表时间:
2021-01-01
影响因子:
7
作者:
Li, Wang-Zhong;Lv, Shu-Hui;Liu, Guo-Ying;Liang, Hu;Guo, Xiang;Lv, Xing;Liu, Kui-Yuan;Qiang, Meng-Yun;Chen, Xi;Gu, Sophie Z.;Xie, Chang-Qing;Xia, Wei-Xiong;Xiang, Yan-Qun
通讯作者:
Xiang, Yan-Qun
影响因子:
--
作者:
Shen LJ;Wang SY;Xie GF;Zeng Q;Chen C;Dong AN;Huang ZM;Pan CC;Xia YF;Wu PH
通讯作者:
Wu PH