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Significance of boost dose for T4 nasopharyngeal carcinoma with residual primary lesion after intensity-modulated radiotherapy
- Source :
- Journal of cancer research and clinical oncology. 147(7)
- Publication Year :
- 2020
-
Abstract
- Previous studies showed poorer survival in T4 disease with residual lesion. To evaluate the efficacy and toxicity of a boost dose for T4 nasopharyngeal carcinoma (NPC), patients with a residual primary lesion after intensity-modulated radiotherapy (IMRT). 398 T4 NPC patients with residual primary lesions after radical IMRT were retrospectively reviewed. An IMRT boost dose of 4–6.75 Gy was delivered to the residual lesions in 2–3 fractions. Propensity score matching (PSM) was applied to balance potential confounders between groups (ratio, 1:2). The presence of Epstein–Barr virus (EBV) DNA in plasma after IMRT was used for risk stratification. Patients who received boost radiation had significantly improved overall survival (OS) and local recurrence-free survival (LRFS) compared with those who did not (all P
- Subjects :
- 0301 basic medicine
Adult
Male
Cancer Research
medicine.medical_specialty
Epstein-Barr Virus Infections
Herpesvirus 4, Human
Neoplasm, Residual
Adolescent
medicine.medical_treatment
Urology
Subgroup analysis
Lesion
03 medical and health sciences
Young Adult
0302 clinical medicine
Internal medicine
Medicine
Humans
Aged
Retrospective Studies
Hematology
Nasopharyngeal Carcinoma
business.industry
Dose-Response Relationship, Radiation
Nasopharyngeal Neoplasms
General Medicine
Middle Aged
Primary lesion
medicine.disease
Prognosis
Radiation therapy
Survival Rate
030104 developmental biology
Oncology
Nasopharyngeal carcinoma
030220 oncology & carcinogenesis
Propensity score matching
Toxicity
DNA, Viral
Retreatment
Disease Progression
Female
Radiotherapy, Intensity-Modulated
medicine.symptom
business
Follow-Up Studies
Subjects
Details
- ISSN :
- 14321335
- Volume :
- 147
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Journal of cancer research and clinical oncology
- Accession number :
- edsair.doi.dedup.....9326d9f4d6bbc1d60a6493cdb0fa6282