Evidence map›Paper›PMID 40764957›Full record

ArticleBMC cancer2025

Two or three cycles of induction chemotherapy in locoregionally advanced nasopharyngeal carcinoma?

Lin-Feng Guo, Yi-Feng Yu, Zhen-Zhen Lu, Qin Lin, San-Gang Wu

Abstract read
In one paragraph

Article in BMC cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lin-Feng GuoDepartment of Radiation Oncology, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, School of Medicine, the First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361003, People's Republic of China.
Yi-Feng YuDepartment of Radiation Oncology, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, School of Medicine, the First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361003, People's Republic of China.
Zhen-Zhen LuThe School of Clinical Medicine, Fujian Medical University, Fuzhou, People's Republic of China.
Qin LinDepartment of Radiation Oncology, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, School of Medicine, the First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361003, People's Republic of China. linqin05@163.com.
San-Gang WuDepartment of Radiation Oncology, Xiamen Cancer Center, Xiamen Key Laboratory of Radiation Oncology, School of Medicine, the First Affiliated Hospital of Xiamen University, Xiamen University, Xiamen, 361003, People's Republic of China. wusg@xmu.edu.cn.

Funding

Medical and Health Guidance Project of Xiamen City 3502Z20224ZD1005Medical and Health Guidance Project of Xiamen City 3502Z20244ZD1001
6 · The paper itself

Abstract

purposeTo investigate the optimal cycles of induction chemotherapy (IC) in patients with locoregionally advanced nasopharyngeal carcinoma (LANPC).

methodsWe included LANPC patients treated with two or three IC cycles from January 2015 to December 2021. The chi-square test, Kaplan-Meier method, propensity score matching (PSM), and Multivariate Cox regression analyses were used for statistical analysis.

resultsA total of 491 patients were included in this study, of whom 166 (33.8%) received two cycles and 325 (66.2%) received three cycles of IC. Patients with stage IVA disease (P < 0.001), advanced T stage (P = 0.011), and advanced N stage (P < 0.001) were more likely to receive three cycles of IC. Cox proportional hazards regression analyses showed that the number of IC cycles was not associated with better survival outcomes. Patients who received three cycles of IC had comparable LRFS (HR 0.992, 95% CI 0.525-1.875, P = 0.981), DMFS (HR 0.805, 95% CI 0.511-1.092, P = 0.351), PFS (HR 0.917, 95% CI 0.633-1.328, P = 0.645) and OS (HR 0.880, 95% CI 0.552-1.402, P = 0.590) compared to those with two cycles of IC. Similar results were found after PSM. No significant differences were found in the incidence of Grade 3-4 acute toxicities between the two and three-cycle groups. However, three cycles of IC significantly increased the incidence of Grade 1-2 leukopenia (P = 0.001), neutropenia (P = 0.015), anemia (P = 0.017), and vomiting (P = 0.024) compared to two cycles of IC.

conclusionsThe number of IC cycles (two or three) did not seem to affect the survival outcome of LANPC patients in this retrospective analysis. However, three cycles of IC were associated with a higher incidence of mild to moderate acute toxicities. Prospective studies in well-defined patient groups with a more uniform treatment program differing only in the number of IC cycles are warranted.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsInduction ChemotherapyNasopharyngeal CarcinomaNasopharyngeal NeoplasmsAdultAgedFemaleHumansKaplan-Meier EstimateMaleMiddle AgedNeoplasm StagingPropensity ScoreRetrospective StudiesCyclesInduction chemotherapyNasopharyngeal carcinomaSurvival outcomesToxicity

Identifiers

PMID40764957
PMCPMC12323084

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