Literature DB >> 28515352

Intensity-modulated radiotherapy provides better quality of life than two-dimensional conventional radiotherapy for patients with stage II nasopharyngeal carcinoma.

Xin-Bin Pan1, Shi-Ting Huang1, Kai-Hua Chen1, Yan-Ming Jiang1, Jia-Lin Ma1, Song Qu1, Ling Li1, Long Chen1, Xiao-Dong Zhu1.   

Abstract

Two-dimensional conventional radiotherapy (2D-CRT) and intensity-modulated radiotherapy (IMRT) are effective for control of nasopharyngeal carcinoma (NPC). The purpose of this study was to compare the quality of life (QoL) of stage II NPC patients treated with 2D-CRT versus IMRT. We conducted a cross-sectional study of 106 patients with stage II NPC treated with 2D-CRT (n = 47) versus IMRT (n = 59) 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. Patients receiving IMRT with or without concurrent chemotherapy had better outcomes in head and neck related symptoms and general aspects of QoL than those receiving 2D-CRT with or without concurrent chemotherapy. Thus, IMRT improves the QoL of patients with stage II NPC as compared to 2D-CRT.

Entities:  

Keywords:  intensity-modulated radiotherapy; nasopharyngeal carcinoma; quality of life; two-dimensional conventional radiotherapy

Mesh:

Year:  2017        PMID: 28515352      PMCID: PMC5542261          DOI: 10.18632/oncotarget.17582

Source DB:  PubMed          Journal:  Oncotarget        ISSN: 1949-2553


INTRODUCTION

Nasopharyngeal carcinoma (NPC) is highly endemic in southern China [1]. Radiotherapy is the primary treatment modality for NPC. Two-dimensional conventional radiotherapy (2D-CRT) has been effective in controlling NPC, but complications to organs at risk resulting from 2D-CRT are severe and lifelong. In the last decade, intensity-modulated radiotherapy (IMRT) has rapidly replaced 2D-CRT due to its technical and dosimetric superiority, and when resources permit, has become the most commonly used radiation technique for NPC. The incidence of stage II NPC has greatly increased with improvements in diagnosis, and after treatment the 5-year overall survival is assumed to be 95% or higher [2, 3]. The high survival rate makes quality of life (QoL) increasingly important. Previous studies suggested that IMRT improved symptoms and QoL for NPC survivors [4-6]. However, all of these studies were confounded by the interference of chemotherapy [7, 8]. Moreover, while the previous studies treated NPC as a whole group and analyzed QoL, most patients had advanced loco-regional NPC. Only one randomized controlled trial compared QoL of IMRT versus 2D-CRT in early stage NPC [9]. This trial suggested that IMRT was superior with regard to speech problems and swallowing. However, another randomized controlled trial reported that there was no significant difference in patient-reported xerostomia between IMRT and 2D-CRT [10]. Moreover, in both studies the sample size was relatively small, and the follow-up time was only 1 year, and neither provided accurate information regarding the QoL of IMRT versus 2D-CRT in early stage NPC. In developing regions, many patients are treated with 2D-CRT rather than IMRT because they have no access to IMRT or the financial burden of IMRT is too great. Although 2D-CRT provides a similar survival benefit for NPC as IMRT [11, 12], clinicians have begun to pay more attention to QoL. We conducted a cross-sectional study to compare the QoL between IMRT and 2D-CRT in patients with stage II NPC. 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

Patient characteristics

Of 106 stage II NPC patients, 47 received 2D-CRT and 59 received IMRT. Disease-free survival of all subjects was more than 3 years. Table 1 summarizes patients’ characteristics.
Table 1

Patient characteristics

2D-CRT (n=47)IMRT (n=59)
Gender
 Male31(65.96%)39(66.10%)
 Female16(34.04%)20(33.90%)
Age (years)
 Median4442
 Range25-6822-64
Follow-up (months)
 Median6450
 Range44-8938-61
AJCC stage
 T1N1M011(23.40%)10(16.95%)
 T2N0M015(31.91%)9(15.25%)
 T2N1M021(44.69%)40(67.80%)
Chemotherapy
 Yes14(29.79%)37(62.71%)
 No33(70.21%)22(37.29%)

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy.

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy.

QoL of IMRT versus 2D-CRT for the whole group

In the whole group, IMRT (n=59) had higher mean scores in head and neck related symptoms and broad aspects of QoL for patients with stage II NPC than 2D-CRT (n=47) (Table 2). Clinical superiority of IMRT for QoL was significant on all functional scales and most symptom scales upon clinical interpretation (difference in mean scores≥10 points).
Table 2

Mean quality of life scores of 2D-CRT versus IMRT for the whole group

Scales2D-CRT (n=47)IMRT (n=59)tp
MeanSDMeanSD
EORTC QLQ-C30
 Global quality of life65.0716.0881.2115.59−4.9390.000
 Physical functioning75.7419.3392.213.43−4.7920.000
 Role functioning74.4722.2190.4314.64−4.1120.000
 Emotional functioning67.3826.7489.0115.65−4.7860.000
 Cognitive functioning60.9929.3487.5913.22−5.6660.000
 Social functioning61.3524.3591.1313.39−7.3480.000
 Fatigue34.2822.212.5317.895.230.000
 Nausea/emesis4.268.841.064.122.2440.028
 Pain18.0917.328.1611.973.2330.002
 Dyspnea11.3515.974.9616.991.8770.064
 Insomnia38.325.9919.1524.813.6540.000
 Appetite loss15.618.191.429.724.7140.000
 Constipation7.0918.313.5517.350.9640.338
 Diarrhea9.2217.992.849.42.1550.035
 Financial problems44.6827.1721.2824.54.3860.000
EORTC QLQ-H&N35
 Pain11.5212.353.375.44.1470.000
 Swallowing25.7117.625.328.937.0760.000
 Senses25.1817.6811.714.294.0640.000
 Speech10.6411.572.847.133.9340.000
 Social contact28.922.514.7910.956.6030.000
 Social eating12.7712.12.556.65.0780.000
 Sexuality54.9632.0220.9220.76.1210.000
 Teeth44.6829.7113.4819.246.0440.000
 Opening mouth29.0823.697.0913.795.4990.000
 Dry mouth58.1622.4922.725.167.2040.000
 Sticky saliva9.9318.284.2616.471.5810.117
 Coughing13.4817.9412.0617.620.3870.7
 Feeling ill22.720.978.5117.683.5450.001
 Pain killers2.849.42.849.40.0001.000
 Nutritional supplements23.418.2812.0616.193.1860.002
 Feeding tube0.0000.0000.0000.0000.0001.000
 Weight loss5.6712.661.426.82.030.046
 Weight gain2.138.247.814.27−2.3610.021

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy; 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.

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy; 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 IMRT versus 2D-CRT without concurrent chemotherapy

In the radiotherapy alone subgroup, IMRT (n=22) had better QoL outcomes than 2D-CRT (n=33), except on scales of nausea/emesis, diarrhea, sticky saliva, coughing, pain killers, feeding tube, weight loss, and weight gain. Differences of most scales between the two groups were significant (Table 3).
Table 3

Mean quality of life scores of 2D-CRT versus IMRT without concurrent chemotherapy

Scales2D-CRT (n=33)IMRT (n=22)tp
MeanSDMeanSD
EORTC QLQ-C30
 Global quality of life69.9515.3086.7411.69−4.3640.000
 Physical functioning80.6119.1097.588.11−4.5280.000
 Role functioning80.8120.4698.484.90−4.7610.000
 Emotional functioning74.4923.7595.0814.47−3.9900.000
 Cognitive functioning66.6730.3394.709.47−4.9590.000
 Social functioning66.6724.6596.976.58−6.7120.000
 Fatigue26.9419.846.068.215.3910.000
 Nausea/emesis4.049.351.524.901.3060.197
 Pain13.6417.905.307.952.3500.023
 Dyspnea9.0915.081.527.112.5000.016
 Insomnia28.2820.6212.1221.932.7770.008
 Appetite loss14.1418.690.000.004.3460.000
 Constipation8.0820.460.000.002.2680.030
 Diarrhea7.0718.181.527.111.5840.120
 Financial problems39.3928.209.0915.195.1520.000
EORTC QLQ-H&N35
 Pain10.8614.051.524.183.5900.001
 Swallowing22.2218.001.895.106.1290.000
 Senses23.7417.696.068.214.9900.000
 Speech9.4311.821.523.903.5640.001
 Social contact24.2422.57.381.786.0460.000
 Social eating12.1211.72.301.425.7300.000
 Sexuality47.4730.0811.3620.825.2600.000
 Teeth40.4032.019.0918.354.5990.000
 Opening mouth27.2725.621.527.115.4680.000
 Dry mouth54.5523.3016.6719.926.2490.000
 Sticky saliva7.0716.151.527.111.7390.089
 Coughing10.1017.6510.6118.93−0.1010.920
 Feeling ill18.1820.576.0616.702.4000.020
 Pain killers3.039.730.000.001.7890.083
 Nutritional supplements21.2120.106.0613.163.3780.001
 Feeding tube0.000.000.000.000.0001.000
 Weight loss2.028.081.527.110.2380.813
 Weight gain1.015.800.000.000.8140.419

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy; 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.

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy; 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 IMRT versus 2D-CRT with concurrent chemotherapy

In the concurrent chemotherapy subgroup, IMRT (n=37) had better QoL outcomes than 2D-CRT (n=14), except for symptoms of nausea/emesis, dyspnea, constipation, sticky saliva, pain killers, and feeding tube. Differences of most scales between the two groups were significant (Table 4).
Table 4

Mean quality of life scores of 2D-CRT versus IMRT with concurrent chemotherapy

Scales2D-CRT (n=14)IMRT (n=37)tp
MeanSDMeanSD
EORTC QLQ-C30
 Global quality of life53.5711.6573.215.48−4.2940.000
 Physical functioning64.2914.9386.3113.96−4.9330.000
 Role functioning59.5219.383.3315.21−4.6280.000
 Emotional functioning50.626.6579.9518.37−4.480.000
 Cognitive functioning47.6222.5177.4815.82−5.3340.000
 Social functioning48.8119.0282.4316.17−6.3130.000
 Fatigue51.5917.7620.1219.925.1780.000
 Nausea/emesis4.767.811.356.061.4740.157
 Pain28.5710.1910.3613.244.6430.000
 Dyspnea16.6717.36.3118.981.780.081
 Insomnia61.922.124.3223.115.2430.000
 Appetite loss19.0517.122.712.123.2760.004
 Constipation4.7612.14.519.50.0460.964
 Diarrhea14.2917.122.79.222.4030.029
 Financial problems57.1420.3735.1427.162.7470.008
EORTC QLQ-H&N35
 Pain13.17.16.316.923.1060.003
 Swallowing33.9314.0511.2610.256.3490.000
 Senses28.5717.8213.0615.283.090.003
 Speech13.4910.8337.73.3190.004
 Social contact39.8818.8311.9413.265.0960.000
 Social eating14.2913.33.787.462.7940.013
 Sexuality72.6230.3932.4321.145.350.000
 Teeth54.7621.1123.4222.034.5830.000
 Opening mouth33.3318.4915.3221.652.9590.006
 Dry mouth66.6718.4928.8325.055.1350.000
 Sticky saliva16.6721.684.517.851.8720.076
 Coughing21.4316.579.9115.452.330.024
 Feeling ill33.3318.499.0116.944.4640.000
 Pain killers2.388.913.610.49−0.3860.701
 Nutritional supplements28.5712.116.2216.892.8980.007
 Feeding tube0.0000.0000.0000.0000.0001
 Weight loss14.2917.120.95.482.870.012
 Weight gain4.7612.114.4116.74−2.2730.03

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy; 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.

2D-CRT: two-dimensional conventional radiotherapy; IMRT: intensity-modulated radiotherapy; 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

This study suggests that IMRT has better outcomes in both functional and symptom scales of EORTC QLQ-C30 compared to 2D-CRT with or without concurrent chemotherapy. The result indicates that IMRT should be provided to NPC patients, irrespective of a concomitant substantial increase in expenditures if resources permit. We observed that 2D-CRT adversely affected patients with regard to symptom scales, global QoL, and functional scales compared to IMRT for the whole group. Differences of most functional and symptom scales were significant upon clinical interpretation. The result was similar to previous studies [4-6]. However, patients included in the previous studies were mostly T3-4 or N2-3. Radiotherapy combined with chemotherapy is the primary treatment modality for advanced loco-regionally NPC. It was suggested that concurrent chemotherapy adversely affected QoL of NPC patients [7]. None of these studies could totally exclude the interference of chemotherapy on QoL. In order to exclude the interference of chemotherapy, we conducted a subgroup analysis to compare the QoL of IMRT versus 2D-CRT without concurrent chemotherapy. The result revealed that IMRT alone significantly improved the QoL compared to 2D-CRT alone. Moreover, our subgroup result also suggested that IMRT had better QoL than 2D-CRT with concurrent chemotherapy. It has been suggested that IMRT has significantly lower radiation-induced toxicity than 2D-CRT [13], but the change in the patient-reported xerostomia scores or QoL may be not statistically different between the two groups [10]. Possibilities to explain this inconsistency are as follow: (1) QoL assessment may contain questions that are not specific to RT-induced toxicities. (2) The criteria used to differentiate between grade 1 and grade 2 of QoL is rather vague and subjective. (3) Physician and patient bias may exist in an unblinded randomization setting. (4) Previous studies used a small sample size and a relatively shorter follow-up time. However, this study shows that IMRT has better QoL with or without concurrent chemotherapy in a longer follow-up time. The result further confirms that lower radiation-induced toxicities of IMRT may produce better QoL compared to 2D-CRT [9]. IMRT increases the expenses for NPC treatment and eventually increases the financial difficulties of individuals in developing countries such as China. Some studies found that financial difficulties adversely affected QoL [14, 15]. Consequently, IMRT would adversely affect QoL. However, we found that patients receiving 2D-CRT suffered from greater financial difficulties than those receiving IMRT. The potential interpretation was that patients received 2D-CRT because of financial difficulties. Financial burden after treatment gave patients receiving 2D-CRT worse QoL, but the relationship between financial problems and QoL is still unclear. Further controlled studies should be performed to test the interference of financial difficulties on QoL. The result of our study should be interpreted with caution. The EORTC QLQ-H&N35 may have some limitations in assessment of QoL of NPC patients. NPC has different biological characteristics and treatment than other head and neck cancers. Xerostomia, deafness, otitis media, and symptoms from organs at risk injury after radiotherapy are the main symptoms in NPC survivors. Although the EORTC QLQ-H&N35 is a specific questionnaire assessing the QoL of head and neck cancer, it does not deal with adverse radiation effects well enough. Limitations of this study should be considered: (1) The small sample size (106 patients) may lead to statistical error. (2) This study assessed the QoL at only one time point. A more methodologically sound approach would employ a longitudinal design in which the same individuals are assessed repeatedly at various time points. In conclusion, this study suggests that IMRT improves most general aspects of QoL for patients with stage II NPC compared to 2D-RCT. IMRT is a better treatment technique for stage II NPC.

MATERIALS AND METHODS

Patients

We 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 proven NPC, (2) stage II NPC per the 7th Edition of the UICC/AJCC staging system, (3) receiving radical radiotherapy or concurrent chemotherapy, and (4) 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, or (6) an incomplete self-reporting questionnaire. From June 2008 to June 2013, 235 patients with stage II NPC received radical treatment at the Cancer Hospital of Guangxi Medical University. There were 129 total 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. This study finally included 106 patients treated with IMRT (n = 59) or 2D-CRT (n = 47).

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 the 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 determined 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. The 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

Patients’ QoL data were obtained by two clinicians from our department, both of whom received a uniform training. A subset of the patients was instructed to answer the questions during the visit to our clinic. Most patients were assessed by telephone. QoL data of all patients was analyzed by a third investigator. Consent was obtained from all patients included in the study. QoL assessment used the Chinese version of the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30-questions (EORTC QLQ-C30) and the Head and Neck 35-questions (EORTC QLQ-H&N35) [16-19]. 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 [20, 21].

Statistical analysis

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

Ethics statement

This cross-sectional study was approved by the Ethics Committee of Cancer Hospital of Guangxi Medical University.
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