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Original Research

Salvage radiotherapy improves survival in patients with locoregionally relapsed stage IE–IIE extranodal natural killer/T-cell lymphoma, nasal type

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Pages 1083-1090 | Published online: 06 Jun 2018

Figures & data

Figure 1 Primary nasal natural killer/T lymphoma.

Notes: PET/CT scan before initial treatment (A), target (line), and dose profile (dose color wash) for radiotherapy (B) after 3 cycles of induction chemotherapy.
Figure 1 Primary nasal natural killer/T lymphoma.

Figure 2 Laryngeal relapsed natural killer/T lymphoma in patient in after 13 months from initial treatment.

Notes: PET/CT scan before salvage treatment (A), target (line), and dose profile (dose color wash) for salvage radiotherapy (B).
Figure 2 Laryngeal relapsed natural killer/T lymphoma in patient in Figure 1 after 13 months from initial treatment.

Table 1 Primary clinical features of 56 patients with LRR ENKTCL who received salvage treatment with or without salvage RT

Figure 3 Overall survival rates after initial treatment (A) or after recurrence (B) in 56 patients with relapsed extranodal natural killer/T-cell lymphoma, nasal type.

Figure 3 Overall survival rates after initial treatment (A) or after recurrence (B) in 56 patients with relapsed extranodal natural killer/T-cell lymphoma, nasal type.

Figure 4 Overall survival rates after initial treatment (A) or after recurrence (B) of 56 patients stratified by salvage radiotherapy (RT) or lack thereof.

Figure 4 Overall survival rates after initial treatment (A) or after recurrence (B) of 56 patients stratified by salvage radiotherapy (RT) or lack thereof.

Figure 5 Overall survival rates after initial treatment (A) or after recurrence (B) of 38 patients stratified by re-irradiation or lack thereof.

Figure 5 Overall survival rates after initial treatment (A) or after recurrence (B) of 38 patients stratified by re-irradiation or lack thereof.

Table 2 Comparison of clinical characteristics in 38 patients with LRR ENKTCL treated with re-irradiation or ChT alone

Table 3 Univariate and multivariate prognostic analyses for OS-ar in overall 56 patients