Skip to main content
Oncotarget logoLink to Oncotarget
. 2017 Feb 1;8(8):14029–14038. doi: 10.18632/oncotarget.14932

Concurrent chemoradiotherapy degrades the quality of life of patients with stage II nasopharyngeal carcinoma as compared to radiotherapy

Xin-Bin Pan 1, Shi-Ting Huang 1, Kai-Hua Chen 1, Yan-Ming Jiang 1, Jia-Lin Ma 1, Song Qu 1, Ling Li 1, Long Chen 1, Xiao-Dong Zhu 1
PMCID: PMC5355159  PMID: 28152511

Abstract

The purpose of this study was to compare the quality of life (QoL) of stage II nasopharyngeal carcinoma (NPC) patients treated with radiotherapy (RT) versus concurrent chemoradiotherapy (CCRT). In a cross-sectional study, these patients were treated with RT (n = 55) or CCRT (n = 51) between June 2008 and June 2013. For all subjects, disease-free survival was more than 3 years. QoL was assessed using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) questions and the Head and Neck 35 (EORTC QLQ-H&N35) questions. RT had better outcomes than CCRT for global QoL, functional scales, symptom scales of fatigue and insomnia, financial problems, and weight gain. Survivors receiving 1 cycle of concurrent chemotherapy had worse QoL outcomes than survivors receiving 2 cycles of concurrent chemotherapy. Patients receiving 3 cycles of concurrent chemotherapy had the best QoL outcomes. Thus, CCRT adversely affects the QoL of patients with stage II NPC as compared to radiotherapy.

Keywords: nasopharyngeal carcinoma, quality of life, radiotherapy, concurrent chemoradiotherapy

INTRODUCTION

Nasopharyngeal carcinoma (NPC) is an endemic disease in southern China. The incidence of stage II NPC has greatly increased with improvements in diagnosis. Radiotherapy (RT) or concurrent chemoradiotherapy (CCRT) are the primary treatment modalities for stage II NPC. CCRT is recommended by the National Comprehensive Cancer Network, but the evidence is weak [14]. However, RT is recommended by the Chinese Anti-Cancer Association because CCRT does not improve survival, but increases toxic reactions [59]. The best treatment modality is still controversial.

After treatment, the 5-year disease-specific survival rate is as high as 97.3% for stage II NPC [7]. The high survival rate makes QoL increasingly important. Clinicians should pay more attention to QoL because long-term survivors may have problems with swallowing, hearing, and speech, as well as psychological and functional problems. However, previous studies mainly focused on endpoints of overall survival, disease-free survival, or local control rate [19]. These endpoints lack information on patients’ experience with treatment-related toxicities or QoL.

We conducted a cross-sectional study to compare the QoL of patients with stage II NPC treated with RT versus CCRT. The result of this study might help clinicians make treatment decisions and provide information to health workers on which health services are most beneficial.

RESULTS

Patients

From June 2008 to June 2013, 235 patients with stage II NPC received radical treatment in the Cancer Hospital of Guangxi Medical University. This study excluded 129 patients. Among the excluded patients, 8 were lost to follow-up, 4 received induced chemotherapy, 40 received adjuvant chemotherapy, 5 died, 9 were loco-regional failures, 7 were distant failures, 51 were non-compliant, and 5 did not complete the questionnaire. We included 106 patients treated with RT (n = 55) or CCRT (n = 51). Disease-free survival of all subjects was more than 3 years. Table 1 summarizes patient characteristics.

Table 1. Patient characteristics.

RT (n = 55) CCRT (n = 51) P
Gender
 Male 38 (69.10%) 32 (62.75%) 0.473
 Female 17 (30.90%) 19 (37.25%) 0.739
Age (years)
 Median 43 42 0.915
 Range 27-68 22-64
Follow-up (months)
 Median 62 48 0.000
 Range 42-89 38-62
AJCC stage
 T1N1M0 10 (18.18%) 11 (21.57%) 0.827
 T2N0M0 19 (34.55%) 5 (9.80%) 0.004
 T2N1M0 26 (47.27%) 35 (68.63) 0.249
Chemotherapy
 1 cycle / 6 (11.76%)
 2 cycles / 18 (35.29%)
 3 cycles / 27 (52.95%)
Radiotherapy
 2D-CRT 33 (60.00%) 14 (27.45%) 0.006
 IMRT 22 (40.00%) 37 (72.55%) 0.051

RT: radiotherapy.

CCRT: concurrent chemoradiotherapy.

2D-CRT: two-dimensional conventional radiotherapy.

IMRT: intensity-modulated radiotherapy.

QoL of RT versus CCRT for the whole group

RT had higher mean scores in global QoL, physical functioning, role functioning, and emotional functioning but lower mean scores in fatigue, insomnia, financial problems and weight gain compared with CCRT (Table 2). Clinically relevant QoL was significant on the scales of role functioning, emotional functioning, fatigue, insomnia, financial problems, and weight gain based on clinical interpretation (difference in mean scores ≥10 points). The result indicates that CCRT adversely affects the QoL of patients with stage II NPC versus RT.

Table 2. Mean quality of life scores of RT versus CCRT for the whole group.

Scales RT (n = 55) CCRT (n = 51) T-test P
Mean SD Mean SD
EORTC QLQ-C30
 Global quality of life 76.67 16.15 67.81 16.92 9.082 0.000
 Physical functioning 87.39 17.67 80.26 17.23 2.102 0.038
 Role functioning 87.88 18.27 76.80 19.46 3.024 0.003
 Emotional functioning 82.73 22.79 71.90 24.55 2.356 0.020
 Cognitive functioning 77.88 27.79 69.28 22.20 1.751 0.083
 Social functioning 78.79 24.52 73.20 22.63 1.216 0.227
 Fatigue 18.59 19.13 28.76 23.85 −2.431 0.017
 Nausea/emesis 3.03 7.92 2.29 6.68 0.520 0.604
 Pain 10.30 15.21 15.36 14.85 −1.730 0.087
 Dyspnea 6.06 12.97 9.15 18.95 −0.986 0.327
 Insomnia 21.82 22.42 34.64 28.25 −2.597 0.011
 Appetite loss 8.48 16.00 7.19 15.37 0.424 0.672
 Constipation 4.85 16.25 4.58 17.66 0.083 0.934
 Diarrhea 4.85 14.93 5.88 12.83 −0.381 0.704
 Financial problems 27.27 28.03 41.18 27.15 −2.590 0.011
EORTC QLQ-H&N35
 Pain 7.12 12.05 8.17 7.54 −0.532 0.596
 Swallowing 14.09 17.41 17.48 15.21 −1.065 0.289
 Senses 16.67 16.97 17.32 17.31 −0.196 0.845
 Speech 6.26 10.20 5.88 9.78 0.196 0.845
 Social contact 14.70 21.03 19.61 19.42 −1.246 0.216
 Social eating 7.39 10.79 6.67 10.41 0.353 0.725
 Sexuality 33.03 31.99 43.46 29.83 −1.733 0.086
 Teeth 27.88 31.27 32.03 25.79 −0.747 0.457
 Opening mouth 16.97 23.89 20.26 22.19 −0.733 0.465
 Dry mouth 39.39 28.75 39.22 28.83 0.032 0.975
 Sticky saliva 4.85 13.48 7.84 19.54 −0.924 0.358
 Coughing 10.30 18.00 13.07 16.44 −0.825 0.411
 Feeling ill 13.33 19.88 15.69 20.39 −0.601 0.549
 Pain killers 5.45 22.92 9.80 30.03 −0.842 0.402
 Nutritional supplements 45.45 57.15 58.82 49.71 −1.281 0.203
 Feeding tube 0.00 0.00 0.00 0.00 0.000 1.000
 Weight loss 5.45 22.92 13.73 34.75 −1.435 0.155
 Weight gain 1.82 13.48 35.29 48.26 −4.783 0.000

RT: radiotherapy.

CCRT: concurrent chemoradiotherapy.

SD: standard deviation.

EORTC QOL-C30: European Organization for Research and Treatment of Cancer

Quality of Life Questionnaire-Core 30.

EORTC QOL-H&N35: The EOTRC Quality of Life Questionnaire-Head and Neck 35.

QoL of RT versus CCRT by different radiotherapy techniques

In the two-dimensional conventional radiotherapy (2D-CRT) subgroup, RT (n = 33) had better QoL than CCRT (n = 14). Differences between the two groups were clinically relevant (Table 3). Moreover, the intensity modulated radiotherapy (IMRT) subgroup had similar results between RT (n = 22) and CCRT (n = 37) (Table 4). Despite the radiation technique used (2D-CRT or IMRT), RT resulted in better QoL versus CCRT.

Table 3. Mean values for all scales of RT versus CCRT with 2D-CRT technique.

Scales RT (n = 33) CCRT (n = 14) T-test P
Mean SD Mean SD
EORTC QLQ-C30
 Global quality of life 69.95 15.30 53.57 11.65 −3.580 0.001
 Physical functioning 80.61 19.10 64.29 14.93 −2.843 0.007
 Role functioning 80.81 20.46 59.52 19.30 −3.314 0.002
 Emotional functioning 74.49 23.75 50.60 26.65 −3.043 0.004
 Cognitive functioning 66.67 30.33 47.62 22.51 −2.110 0.040
 Social functioning 66.67 24.65 48.81 19.02 −2.417 0.020
 Fatigue 26.94 19.84 51.59 17.76 4.012 0.000
 Nausea/emesis 4.04 9.35 4.76 7.81 0.253 0.801
 Pain 13.64 17.90 28.57 10.19 2.916 0.006
 Dyspnea 9.09 15.08 16.67 17.30 1.508 0.139
 Insomnia 28.28 20.62 61.90 22.10 5.006 0.000
 Appetite loss 14.14 18.69 19.05 17.12 0.843 0.404
 Constipation 8.08 20.46 4.76 12.10 −0.564 0.575
 Diarrhea 7.07 18.18 14.29 17.12 1.265 0.212
 Financial problems 39.39 28.20 57.14 20.37 2.125 0.039
EORTC QLQ-H&N35
 Pain 10.86 14.05 13.10 7.10 0.563 0.576
 Swallowing 22.22 18.00 33.93 14.05 2.165 0.036
 Senses 23.74 17.69 28.57 17.82 0.855 0.397
 Speech 9.43 11.82 13.49 10.83 1.104 0.276
 Social contact 24.24 22.57 39.88 18.83 2.275 0.028
 Social eating 12.12 11.72 14.29 13.30 0.556 0.581
 Sexuality 47.47 30.08 72.62 30.39 2.613 0.012
 Teeth 40.40 32.01 54.76 21.11 1.537 0.131
 Opening mouth 27.27 25.62 33.33 18.49 0.799 0.429
 Dry mouth 54.55 23.30 66.67 18.49 1.896 0.067
 Sticky saliva 7.07 16.15 16.67 21.68 1.490 0.152
 Coughing 10.10 17.65 21.43 16.57 2.048 0.046
 Feeling ill 18.18 20.57 33.33 18.49 2.483 0.019
 Pain killers 3.03 9.73 2.38 8.91 −0.214 0.831
 Nutritional supplements 21.21 20.10 28.57 12.10 1.544 0.131
 Feeding tube 0.00 0.00 0.00 0.00 0.000 1.000
 Weight loss 2.02 8.08 14.29 17.12 3.359 0.002
 Weight gain 1.01 5.80 4.76 12.10 1.107 0.285

2D-CRT: two-dimensional conventional radiotherapy.

RT: radiotherapy.

CCRT: concurrent chemoradiotherapy.

SD: standard deviation.

EORTC QOL-C30: European Organization for Research and Treatment of Cancer

Quality of Life Questionnaire-Core 30.

EORTC QOL-H&N35: The EOTRC Quality of Life Questionnaire-Head and Neck 35.

Table 4. Mean values for all scales of RT versus CCRT with IMRT technique.

Scales RT (n = 22) CCRT (n = 37) T-test P
Mean SD Mean SD
EORTC QLQ-C30
 Global quality of life 86.31 12.49 79.04 16.42 1.481 0.146
 Physical functioning 97.62 8.91 89.90 14.45 2.229 0.032
 Role functioning 98.81 4.45 86.87 16.01 3.941 0.000
 Emotional functioning 92.26 17.74 87.63 14.75 0.927 0.359
 Cognitive functioning 95.24 10.19 84.34 13.14 2.764 0.008
 Social functioning 98.81 4.45 87.88 14.60 3.895 0.000
 Fatigue 4.76 7.18 15.82 20.04 −2.779 0.008
 Nausea/emesis 2.38 6.05 0.51 2.90 1.107 0.285
 Pain 5.95 8.29 9.09 13.24 −0.982 0.332
 Dyspnea 2.38 8.91 6.06 19.46 −0.675 0.503
 Insomnia 11.90 24.83 22.22 24.53 −1.314 0.196
 Appetite loss 0.00 0.00 2.02 11.61 −0.647 0.521
 Constipation 0.00 0.00 5.05 20.62 −0.911 0.367
 Diarrhea 2.38 8.91 3.03 9.73 −0.214 0.831
 Financial problems 7.14 14.19 27.27 25.62 −3.438 0.001
EORTC QLQ-H&N35
 Pain 2.38 5.09 3.79 5.55 −0.814 0.420
 Swallowing 2.98 6.21 6.31 9.78 −1.404 0.169
 Senses 8.33 8.65 13.13 16.01 −1.054 0.298
 Speech 1.59 4.03 3.37 8.09 −0.779 0.440
 Social contact 0.00 0.00 6.82 12.58 −3.114 0.004
 Social eating 0.48 1.78 3.43 7.66 −2.089 0.043
 Sexuality 4.76 10.19 27.78 20.27 −5.164 0.000
 Teeth 7.14 14.19 16.16 20.62 −1.727 0.093
 Opening mouth 2.38 8.91 9.09 15.08 −1.894 0.066
 Dry mouth 19.05 21.54 24.24 26.71 −0.643 0.523
 Sticky saliva 2.38 8.91 5.05 18.86 −0.504 0.617
 Coughing 14.29 21.54 11.11 15.96 0.561 0.578
 Feeling ill 2.38 8.91 11.11 19.84 −2.081 0.043
 Pain killers 0.00 0.00 4.04 11.05 −2.101 0.044
 Nutritional supplements 0.00 0.00 17.17 16.92 −5.831 0.000
 Feeding tube 0.00 0.00 0.00 0.00 0.000 1.000
 Weight loss 2.38 8.91 1.01 5.80 0.628 0.533
 Weight gain 0.00 0.00 11.11 15.96 −4.000 0.000

IMRT: intensity-modulated radiotherapy.

RT: radiotherapy.

CCRT: concurrent chemoradiotherapy.

SD: standard deviation.

EORTC QOL-C30: European Organization for Research and Treatment of Cancer

Quality of Life Questionnaire-Core 30.

EORTC QOL-H&N35: The EOTRC Quality of Life Questionnaire-Head and Neck 35.

Comparisons of QoL scales by different chemotherapy cycles

In the CCRT subgroup, 6 patients received 1 cycle of concurrent chemotherapy, 18 patients received 2 cycles of concurrent chemotherapy, and 27 patients received 3 cycles of concurrent chemotherapy. Survivors who received 1 cycle of concurrent chemotherapy had worse QoL outcomes than survivors who received 2 cycles of concurrent chemotherapy. Patients who received 3 cycles of concurrent chemotherapy had the best QoL outcomes (Table 5). Differences among most scales were clinically relevant. The unexpected results may indicate that survivors who are not tolerant of concurrent chemotherapy will have a worse QoL.

Table 5. Comparisons of mean values for all scales by different chemotherapy cycles.

Scales 1 cycle CT (n = 6) 2 cycles CT (n = 18) 3 cycles CT (n = 27) F-test P
Mean SD Mean SD Mean SD
EORTC QLQ-C30
 Global quality of life 54.17 10.21 66.67 13.71 72.12 18.85 3.023 0.058
 Physical functioning 57.78 15.01 80.00 14.99 86.41 14.79 9.048 0.000
 Role functioning 58.33 20.41 75.00 17.39 83.97 15.97 5.884 0.005
 Emotional functioning 47.22 22.77 67.13 27.19 81.73 17.80 6.687 0.003
 Cognitive functioning 36.11 16.39 69.44 22.32 78.21 13.96 13.836 0.000
 Social functioning 47.22 16.39 65.74 23.20 85.26 15.15 12.769 0.000
 Fatigue 50.00 15.32 33.95 24.84 19.66 21.15 5.493 0.007
 Nausea/emesis 2.78 6.80 4.63 9.58 0.00 0.00 3.047 0.057
 Pain 27.78 13.61 16.67 15.12 10.90 13.29 3.737 0.031
 Dyspnea 16.67 18.26 5.56 12.78 8.97 22.23 0.785 0.462
 Insomnia 55.56 17.21 40.74 24.40 24.36 29.15 4.309 0.019
 Appetite loss 16.67 18.26 7.41 14.26 3.85 14.38 1.864 0.166
 Constipation 0.00 0.00 1.85 7.86 7.69 23.68 0.798 0.456
 Diarrhea 11.11 17.21 5.56 12.78 5.13 12.26 0.528 0.593
 Financial problems 55.56 17.21 37.04 25.28 39.74 29.84 1.079 0.348
EORTC QLQ-H&N35
 Pain 13.89 6.80 7.87 6.69 7.05 8.06 2.070 0.138
 Swallowing 36.11 13.61 20.37 14.64 10.26 10.62 11.381 0.000
 Senses 30.56 19.48 19.44 16.42 12.82 16.54 2.927 0.063
 Speech 14.81 9.07 4.32 9.44 5.13 9.55 2.998 0.059
 Social contact 47.22 17.21 21.30 17.44 11.22 14.52 12.709 0.000
 Social eating 21.11 14.25 4.07 7.97 4.87 8.55 8.724 0.001
 Sexuality 91.67 20.41 48.15 28.52 28.21 17.49 20.327 0.000
 Teeth 55.56 17.21 37.04 22.55 21.79 24.84 5.952 0.005
 Opening mouth 44.44 17.21 20.37 16.72 14.10 23.42 5.291 0.008
 Dry mouth 61.11 25.09 38.89 23.57 33.33 31.27 2.388 0.103
 Sticky saliva 11.11 17.21 9.26 19.15 6.41 21.12 0.190 0.828
 Coughing 27.78 13.61 11.11 16.17 11.54 16.17 2.811 0.070
 Feeling ill 27.78 13.61 20.37 23.26 8.97 17.78 3.177 0.051
 Pain killers 0.00 0.00 3.70 10.78 3.85 10.86 0.363 0.698
 Nutritional supplements 22.22 17.21 18.52 17.04 19.23 16.79 0.109 0.897
 Feeding tube 0.00 0.00 0.00 0.00 0.00 0.00 0.000 1.000
 Weight loss 16.67 18.26 5.56 12.78 1.28 6.54 5.013 0.011
 Weight gain 0.00 0.00 11.11 16.17 15.38 16.95 2.378 0.104

CT: chemotherapy.

SD: standard deviation.

EORTC QOL-C30: European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30.

EORTC QOL-H&N35: The EOTRC Quality of Life Questionnaire-Head and Neck 35.

DISCUSSION

The study suggests that RT has better outcomes in global QoL and functional scales of EORTC QLQ-C30 compared with CCRT. The result might help clinicians make better treatment decisions and provide information to health workers on which health services are most beneficial.

Different questionnaires were used for QoL assessment in NPC patients. A few studies used the EORTC QLQ-C30 questionnaire and the EORTC QLQ-H&N35 questionnaire [1013]. Some studies used the Functional Assessment of Cancer Therapy-General (FACT-G) scale, the Functional Assessment of Cancer Therapy-Head and Neck (FACT-H&N) module [14, 15], and the Functional Assessment of Cancer Therapy-Nasopharyngeal (FACT-NP) subscale [16]. Other studies used the MOS 36-item short-form health survey (SF-36) [17, 18] and the University of Washington Quality of Life Questionnaire [19]. Recently, an NPC-specific scale (QoL-NPC) was developed to assess the physical functioning and health status of Chinese NPC patients [20]. However, FACT-NP has not been updated. SF-36 and the University of Washington Quality of Life Questionnaire are not specific questionnaires for QoL assessment in head-and-neck cancer patients, and QoL-NPC should be further evaluated by a large sample from different centers.

In this study, we used EORTC QLQ-C30 and the EORTC QLQ-H&N35 for QoL assessment because the two questionnaires are comprehensive. The EORTC QLQ-C30 contains a range of QoL issues related to different cancer patients, including head-and-neck cancer. The EORTC QLQ-C30 has been translated into many languages and is a widely used questionnaire. The QLQ-H&N35 is used to assess the QoL of patients with head-and-neck cancer specifically. The EORTC QLQ-C30 and the EORTC QLQ-H&N35 questionnaires are valid, internally consistency, and reliable in patients from different nations and were tested in large patient groups [21]. The Chinese version of the EORTC QLQ-C30 and the EORTC QLQ-H&N35 were previously tested, confirmed, and validated by some studies [1113].

Our study showed no significant difference between RT and CCRT groups, except for weight gain reported in the EORTC QLQ-H&N35 questionnaire. The potential reasons are the following: (1) The EORTC QLQ-H&N35 might have some limitations in assessing QoL of NPC patients, although the EORTC QLQ-H&N35 is a specific questionnaire for assessing the QoL of head-and-neck cancer patients. NPC is different from other head-and-neck cancers because of its location, biological characteristics, and treatment. NPC survivors might experience deafness, otitis media, symptoms from temporal lobe injury, and hypopituitarism after radiotherapy. The EORTC QLQ-H&N35 does not deal with these adverse effects well enough. (2) CCRT was suggested to cause statistically significantly more acute toxic effects but similar late toxic effects compared with RT [4]. This outcome might be interpreted as the result of the few differences between RT and CCRT observed in the symptom scales of the EORTC QLQ-H&N35.

Previous studies mainly analyzed the effect of different radiotherapy techniques (IMRT vs. 2D-CRT) on QoL [1113]. Only one study mentioned the effect of chemotherapy on QoL [10]. The above study found that concurrent chemotherapy adversely affected five symptom scales, but did not affect global QoL and functional scales. However, our study observed that concurrent chemotherapy adversely affected not only symptom scales but also global QoL and functional scales. Our results showed that CCRT had higher scores for fatigue and insomnia than did RT. Fatigue and insomnia might be caused by chemotherapy and contribute to loss of physical functioning, role functioning, and emotional functioning. The results of 2D-CRT and IMRT subgroup analysis further confirmed the above conclusion.

Some studies discussed the impact of financial problems on QoL [14, 22]. These studies found that financial difficulties adversely affect QoL. CCRT will increase the expenses of NPC treatment and eventually increase the financial difficulties of individuals in developing countries such as China. Consequently, CCRT adversely affects QoL. But, the relation between financial problems and QoL is still unclear. Further controlled studies should be performed to test the impact of financial difficulties on QoL.

Our result shows that CCRT adversely affects QoL. Thus, we hypothesize that patients who receive more cycles of chemotherapy will experience worse QoL. However, subgroup analyses of the effect of different chemotherapy cycles on QoL show an opposite result. Survivors who received 1 cycle of concurrent chemotherapy had worse QoL outcomes than survivors who received 2 cycles of concurrent chemotherapy. Patients who received 3 cycles of concurrent chemotherapy had the best QoL outcomes.

The potential interpretations are the following: (1) The 6 patients who received 1 cycle of concurrent chemotherapy received only 1 cycle because of serious toxicity during treatment. Serious toxicity made the 6 patients’ recovery worse. However, survivors who received 2 or 3 cycles of concurrent chemotherapy better tolerated chemotherapy and recovered better. (2) The 6 patients were all irradiated by 2D-CRT, the 18 patients who received 2 cycles of concurrent chemotherapy were treated with 2D-CRT or IMRT, and the 27 patients who received 3 cycles of concurrent chemotherapy were irradiated mostly by IMRT. Use of IMRT is associated with the reduction of physician-assessed late toxicities and improved patient-reported QoL in NPC survivors [1113]. (3) Only 6 patients received 1 cycle of concurrent chemotherapy; thus the sample size of the CCRT group was insufficient. The result should therefore be treated with caution, and a large sample of patients should be investigated to verify the result.

The limitations of our study must be considered: (1) Only 106 patients were enrolled in our study, and the sample size of the CCRT group was insufficient for comparisons of QoL scales by different chemotherapy cycles. (2) The QoL measurement of our study was conducted at only one time point. A more methodologically sound approach is to use a longitudinal design in which the same individuals are assessed repeatedly at various time points.

MATERIALS AND METHODS

Study population

This cross-sectional study analyzed QoL data of patients with stage II NPC in the Cancer Hospital of Guangxi Medical University from June 2008 to June 2013. Inclusion criteria were (1) pathologically proved NPC, (2) stage II NPC per the 7th Edition of the UICC/AJCC staging system, (3) Karnofsky performance status >70, (4) receiving radical RT or CCRT, and (5) disease-free survival >3 years. Exclusion criteria were (1) age >70 or <18 years, (2) recurrent or metastatic NPC, (3) receiving induced or adjuvant chemotherapy, (4) a second malignancy, except for cured skin basal cell carcinoma or early stage cervical cancer, (5) severe cerebral, cardiac, hematologic, renal, hepatic, or mental disease, and (6) incompletion of the self-reporting questionnaire.

Radiotherapy

Patients received 2D-CRT in two phases. In the first phase, patients were irradiated by 6-megavolt bilateral and opposing photon beams. The dose for faciocervical field and lower anterior cervical field was 36 Gy. In the second phase, the dose for primary tumor was boosted from 66 Gy to 70 Gy. The prescribed irradiation dose was 2 Gy per fraction with 5 daily fractions per week.

Patients received IMRT per the International Commission on Radiation Units and Measurements Report 62 guidelines. Gross tumor volume (GTVnx) and cervical lymph node tumor volume (GTVnd) were defined as gross shown by CT/MRI. Clinical target volume (CTV) included the GTV with a 1-cm to 1.5-cm margin, the entire nasopharyngeal space, and the positive lymph node regions. The prescribed radiation dose was 66 Gy to 70.06 Gy in 30 to 31 fractions for GTV, and 54 Gy to 60 Gy in 30 fractions for CTV with 5 daily fractions per week.

Chemotherapy

Patients received concurrent chemotherapy on days 1, 22, and 43 during radiotherapy. Chemotherapy regimen was cisplatin 100 mg/m2/d by intravenous infusion. Chemotherapy was postponed or discontinued for patients who experienced serious toxicity and could not recover before the next schedule.

QoL measurement

QoL assessment used the Chinese version of the EORTC QLQ-C30 questions and the EORTC QLQ-H&N35 questions [21, 2325]. The EORTC QLQ-C30 is a cancer-specific questionnaire containing a global QoL score, five functional scales, three symptom scales, and six single items. The QLQ-H&N35 is a site-specific questionnaire assessing QoL of head-and-neck cancer patients. The QLQ-H&N35 contains seven multiple-item and six single-item scales. The standard score of all scales ranges from 0 to 100. A high score for a global QoL or functional scale represents a high/healthy level of global QoL or functioning, whereas a high score for a symptom scale represents a symptom problem. QoL changes of ≥10 points were considered clinically relevant [26, 27].

Statistical analysis

Statistical analysis was performed using SPSS for Windows version 16.0 (SPSS Inc., Chicago, IL). The χ2 test was used for the comparisons of categorical data. The T-test was used to compare the mean scores of QoL between two groups. The F-test was used for the comparisons among groups. All significant tests were two-sided and P value <0.05 was considered statistically significant.

CONCLUSIONS

This study suggests that CCRT degrades broad aspects of QoL for patients with stage II NPC. RT may be a better treatment choice for stage II NPC compared with CCRT. However, undetected factors still might be related to QoL. The data in this study must be tested, preferably in a prospective, randomized trial.

Footnotes

CONFLICTS OF INTEREST

The authors declare no conflicts of interest.

ROLE OF THE FUNDING SOURCE

This study was supported by the Basic Ability Improvement Project for Young and Middle-aged Teachers of Guangxi Zhuang Autonomous Region 2016: KY2016LX029.

REFERENCES

  • 1.Cheng SH, Tsai SY, Yen KL, Jian JJ, Chu NM, Chan KY, Tan TD, Cheng JC, Hsieh CY, Huang AT. Concomitant radiotherapy and chemotherapy for early-stage nasopharyngeal carcinoma. J Clin Oncol. 2000;18:2040–5. doi: 10.1200/JCO.2000.18.10.2040. [DOI] [PubMed] [Google Scholar]
  • 2.Cheng SH, Tsai SY, Yen KL, Jian JJ, Feng AC, Chan KY, Hong CF, Chu NM, Lin YC, Lin CY, Tan TD, Hsieh CY, Chong V, et al. Prognostic significance of parapharyngeal space venous plexus and marrow involvement: potential landmarks of dissemination for stage I-III nasopharyngeal carcinoma. Int J Radiat Oncol Biol Phys. 2005;61:456–65. doi: 10.1016/j.ijrobp.2004.05.047. [DOI] [PubMed] [Google Scholar]
  • 3.Kang MK, Oh D, Cho KH, Moon SH, Wu HG, Heo DS, Ahn YC, Park K, Park HJ, Park JS, Keum KC, Cha J, Kim JW, et al. Role of Chemotherapy in Stage II Nasopharyngeal Carcinoma Treated with Curative Radiotherapy. Cancer Res Treat. 2015;47:871–8. doi: 10.4143/crt.2014.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Chen QY, Wen YF, Guo L, Liu H, Huang PY, Mo HY, Li NW, Xiang YQ, Luo DH, Qiu F, Sun R, Deng MQ, Chen MY, et al. Concurrent chemoradiotherapy vs radiotherapy alone in stage II nasopharyngeal carcinoma: phase III randomized trial. J Natl Cancer Inst. 2011;103:1761–70. doi: 10.1093/jnci/djr432. [DOI] [PubMed] [Google Scholar]
  • 5.Xu T, Shen C, Zhu G, Hu C. Omission of Chemotherapy in Early Stage Nasopharyngeal Carcinoma Treated with IMRT: A Paired Cohort Study. Medicine (Baltimore) 2015;94:e1457. doi: 10.1097/MD.0000000000001457. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Tham IW, Lin S, Pan J, Han L, Lu JJ, Wee J. Intensity-modulated radiation therapy without concurrent chemotherapy for stage IIb nasopharyngeal cancer. Am J Clin Oncol. 2010;33:294–9. doi: 10.1097/COC.0b013e3181d2edab. [DOI] [PubMed] [Google Scholar]
  • 7.Su SF, Han F, Zhao C, Chen CY, Xiao WW, Li JX, Lu TX. Long-term outcomes of early-stage nasopharyngeal carcinoma patients treated with intensity-modulated radiotherapy alone. Int J Radiat Oncol Biol Phys. 2012;82:327–33. doi: 10.1016/j.ijrobp.2010.09.011. [DOI] [PubMed] [Google Scholar]
  • 8.Guo Q, Lu T, Lin S, Zong J, Chen Z, Cui X, Zhang Y, Pan J. Long-term survival of nasopharyngeal carcinoma patients with Stage II in intensity-modulated radiation therapy era. Jpn J Clin Oncol. 2016;46:241–7. doi: 10.1093/jjco/hyv192. [DOI] [PubMed] [Google Scholar]
  • 9.Zhang LN, Gao YH, Lan XW, Tang J, Su Z, Ma J, Deng W, OuYang PY, Xie FY. Propensity score matching analysis of cisplatin-based concurrent chemotherapy in low risk nasopharyngeal carcinoma in the intensity-modulated radiotherapy era. Oncotarget. 2015;6:44019–29. doi: 10.18632/oncotarget.5806. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Cengiz M, Ozyar E, Esassolak M, Altun M, Akmansu M, Sen M, Uzel O, Yavuz A, Dalmaz G, Uzal C, Hicsonmez A, Sarihan S, Kaplan B, et al. Assessment of quality of life of nasopharyngeal carcinoma patients with EORTC QLQ-C30 and H&N-35 modules. Int J Radiat Oncol Biol Phys. 2005;63:1347–53. doi: 10.1016/j.ijrobp.2005.05.057. [DOI] [PubMed] [Google Scholar]
  • 11.Huang TL, Chien CY, Tsai WL, Liao KC, Chou SY, Lin HC, S Dean Luo, Lee TF, Lee CH, Fang FM. Long-term late toxicities and quality of life for survivors of nasopharyngeal carcinoma treated with intensity-modulated radiotherapy versus non-intensity-modulated radiotherapy. Head Neck. 2016;38(Suppl 1):E1026–32. doi: 10.1002/hed.24150. [DOI] [PubMed] [Google Scholar]
  • 12.Song T, Fang M, Zhang XB, Zhang P, Xie RF, Wu SX. Sustained improvement of quality of life for nasopharyngeal carcinoma treated by intensity modulated radiation therapy in long-term survivors. Int J Clin Exp Med. 2015;8:5658–66. [PMC free article] [PubMed] [Google Scholar]
  • 13.Fang FM, Tsai WL, Chen HC, Hsu HC, Hsiung CY, Chien CY, Ko SF. Intensity-modulated or conformal radiotherapy improves the quality of life of patients with nasopharyngeal carcinoma: comparisons of four radiotherapy techniques. Cancer. 2007;109:313–21. doi: 10.1002/cncr.22396. [DOI] [PubMed] [Google Scholar]
  • 14.Yu CL, Fielding R, Chan CL, Sham JS. Chinese nasopharyngeal carcinoma patients treated with radiotherapy: association between satisfaction with information provided and quality of life. Cancer. 2001;92:2126–35. doi: 10.1002/cncr.1554. [DOI] [PubMed] [Google Scholar]
  • 15.Teckle P, McTaggart-Cowan H, Van der Hoek K, Chia S, Melosky B, Gelmon K, Peacock S. Mapping the FACT-G cancer-specific quality of life instrument to the EQ-5D and SF-6D. Health Qual Life Outcomes. 2013;11:203. doi: 10.1186/1477-7525-11-203. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Tong MC, Lo PS, Wong KH, Yeung RM, van Hasselt CA, Eremenco S, Cella D. Development and validation of the functional assessment of cancer therapy nasopharyngeal cancer subscale. Head Neck. 2009;31:738–47. doi: 10.1002/hed.21023. [DOI] [PubMed] [Google Scholar]
  • 17.Gu MF, Su Y, Chen XL, He WL, He ZY, Li JJ, Chen MQ, Mo CW, Xu Q, Diao YM. Quality of life and radiotherapy complications of Chinese nasopharyngeal carcinoma patients at different 3DCRT. Asian Pac J Cancer Prev. 2012;13:75–9. doi: 10.7314/apjcp.2012.13.1.075. [DOI] [PubMed] [Google Scholar]
  • 18.Wu Y, Hu WH, Xia YF, Ma J, Liu MZ, Cui NJ. Quality of life of nasopharyngeal carcinoma survivors in Mainland China. Qual Life Res. 2007;16:65–74. doi: 10.1007/s11136-006-9113-0. [DOI] [PubMed] [Google Scholar]
  • 19.Chen AM, Farwell DG, Luu Q, Vazquez EG, Lau DH, Purdy JA. Intensity-modulated radiotherapy is associated with improved global quality of life among long-term survivors of head-and-neck cancer. Int J Radiat Oncol Biol Phys. 2012;84:170–5. doi: 10.1016/j.ijrobp.2011.11.026. [DOI] [PubMed] [Google Scholar]
  • 20.Su Y, Mo CW, Cheng WQ, Wang L, Xu Q, Wu ZC, Wu ZL, Liu LZ, Chen XL. Development and validation of quality of life scale of nasopharyngeal carcinoma patients: the QOL-NPC (version 2) Health Qual Life Outcomes. 2016;14:76. doi: 10.1186/s12955-016-0480-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Bjordal K, de Graeff A, Fayers PM, Hammerlid E, van Pottelsberghe C, Curran D, Ahlner-Elmqvist M, Maher EJ, Meyza JW, Bredart A, Soderholm AL, Arraras JJ, Feine JS, et al. A 12 country field study of the EORTC QLQ-C30 (version 3.0) and the head and neck cancer specific module (EORTC QLQ-H&N35) in head and neck patients. EORTC Quality of Life Group. Eur J Cancer. 2000;36:1796–807. doi: 10.1016/s0959-8049(00)00186-6. [DOI] [PubMed] [Google Scholar]
  • 22.Fang FM, Chiu HC, Kuo WR, Wang CJ, Leung SW, Chen HC, Sun LM, Hsu HC. Health-related quality of life for nasopharyngeal carcinoma patients with cancer-free survival after treatment. Int J Radiat Oncol Biol Phys. 2002;53:959–68. doi: 10.1016/s0360-3016(02)02838-9. [DOI] [PubMed] [Google Scholar]
  • 23.Zhao H, Kanda K. Testing psychometric properties of the standard Chinese version of the European Organization for Research and Treatment of Cancer Quality of Life Core Questionnaire 30 (EORTC QLQ-C30) J Epidemiol. 2004;14:193–203. doi: 10.2188/jea.14.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Bjordal K, Hammerlid E, Ahlner-Elmqvist M, de Graeff A, Boysen M, Evensen JF, Biorklund A, de Leeuw JR, Fayers PM, Jannert M, Westin T, Kaasa S. Quality of life in head and neck cancer patients: validation of the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-H&N35. J Clin Oncol. 1999;17:1008–19. doi: 10.1200/JCO.1999.17.3.1008. [DOI] [PubMed] [Google Scholar]
  • 25.Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, Filiberti A, Flechtner H, Fleishman SB, de Haes JC, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85:365–76. doi: 10.1093/jnci/85.5.365. [DOI] [PubMed] [Google Scholar]
  • 26.King MT. The interpretation of scores from the EORTC quality of life questionnaire QLQ-C30. Qual Life Res. 1996;5:555–67. doi: 10.1007/BF00439229. [DOI] [PubMed] [Google Scholar]
  • 27.Osoba D, Rodrigues G, Myles J, Zee B, Pater J. Interpreting the significance of changes in health-related quality-of-life scores. J Clin Oncol. 1998;16:139–44. doi: 10.1200/JCO.1998.16.1.139. [DOI] [PubMed] [Google Scholar]

Articles from Oncotarget are provided here courtesy of Impact Journals, LLC

RESOURCES