Long-term Survivals, Toxicities and the Role of Chemotherapy in Early-Stage Nasopharyngeal Carcinoma Patients Treated with Intensity-Modulated Radiation Therapy: A Retrospective Study with 15-Year Follow-up.

PURPOSE: This study was aimed to investigate long-term survivals and toxicities of early-stage nasopharyngeal carcinoma (NPC) in endemic area, evaluating the role of chemotherapy in stage II patients.
MATERIALS AND METHODS: Totally 187 patients with newly diagnosed NPC and restaged American Joint Committee on Cancer/International Union Against Cancer 8th T1-2N0-1M0 were retrospectively recruited. All received intensity-modulated radiotherapy (IMRT)±chemotherapy (CT) from 2001 to 2010.
RESULTS: With 15.7-year median follow-up, 10-year locoregional recurrence-free survival, distant metastasis-free survival (DMFS), disease-specific survival (DSS), and overall survival (OS) were 93.3%, 93.5%, 92.9% and 88.2%, respectively. Multivariable analyses showed cervical lymph nodes positive and pre-treatment prognostic nutritional index ≥ 52.0 could independently predict DMFS (p=0.036 and p=0.011), DSS (p=0.014 and p=0.026), and OS (p=0.002 and p < 0.001); Charlson comorbidity index < 3 points could predict DSS (p=0.011); age > 45 years (p=0.002) and pre-treatment lactate dehydrogenase ≥ 240 U/L (p < 0.001) predicted OS. No grade 4 late toxicity happened; grade 3 late toxicities included subcutaneous fibrosis (4.3%), deafness or otitis (4.8%), skin dystrophy (2.1%), and xerostomia (1.1%). No differences on survivals were shown between IMRT+CT vs. IMRT alone in stage II patients, even in T2N1M0 (p > 0.05). Unsurprising, patients in IMRT+CT had more acute gastrointestinal reaction, myelosuppression, mucositis, late ear toxicity, and cranial nerve injury (all p < 0.05) than IMRT alone group.
CONCLUSION: Superior tumor control and satisfying long-term outcomes could be achieved with IMRT in early-stage NPC with mild late toxicities. As CT would bring more toxicities, it should be carefully performed to stage II patients.

Introduction

Nasopharyngeal carcinoma (NPC) is a prevalent head and neck malignancy in the South-eastern part of Asia, especially in the middle and western regions of Guangdong province [1]. Given its exquisite anatomical location and high radio-sensitivity, radiotherapy is the treatment backbone for NPC. Especially with the advent of intensity-modulated radiotherapy (IMRT), dose intensity could be optimized to the gross tumor and subclinical target volumes by sharp dose fall-offs, which has been translated into improved tumor control [2,3]. The 5-year locoregional recurrence-free survival (LRRFS) rate has improved from 70% during the era of conventional radiotherapy (RT) to more than 90% with IMRT for the early-stage NPC [4-7], but the long-term outcomes and late toxicities in early-stage NPC patients treated by IMRT are still in absence.

According to the latest National Comprehensive Cancer Network clinical practice guideline in oncology (NCCN guidelines) version 1.2020, RT alone is recommended for stage I patients, and uniform chemoradiotherapy strategy is recommended for stage II–IV patients. But there are many differences among stage II–IV NPC patients. Foremost, the range of tumor invasion is quite disparate, no bone invasion in stage II patients indicating a relative limited tumor scope [8]. Second, only N0 and N1 could be classified into stage II, without the existence of bilateral, lower neck, or huge (> 6 cm) lymph nodes metastases [8]. The more advanced tumor invasion the higher occurrence of treatment failures. Therefore, the treatment failures, including locoregional recurrence and distant metastasis, are less likely to occur in stage II NPC patients than that in stage III–IV patients. Considering the above-mentioned characteristics, it seems inappropriate to perform uniform therapeutic schedule to stage II and stage III–IV NPC patients. Besides, the role of chemotherapy in stage II NPC patients has always been under debate. Some of the previous studies thought the T2N1M0 or T1-2N1M0 NPC patients could obtain the benefit from chemotherapy under IMRT while the other stage II patients couldn’t [7,9,10]. Most of these studies were retrospective and only reporting the 3- or 5-year survivals. Only one retrospective study had 93-month median follow-up time, which showed chemotherapy could improve T1-2N1M0 patients’ locoregional control in nonendemic area [10]. And in the latest published multicenter phase II randomized trial for stage II NPC patients, the author recruited 84 patients and found that concurrent chemotherapy plus IMRT did not improve patient’s disease control and 5-year survivals [11].

In this study, we retrospectively collected stage I–II NPC patients who received IMRT and had more than 15-year median follow-up in Sun Yat-sen University Cancer Center (SYSUCC), reporting the 10-year survivals and toxicities of these early-stage NPC patients in endemic area, and investigating the role of chemotherapy for stage II patients.

Materials and Methods

1. Patient selection

This study was approved by the Clinical Research Ethics Review Committee of SYSUCC and performed in accordance with the Declaration of Helsinki and Good Clinical Practice Guidelines. Totally, 187 stage I–II NPC patients who underwent IMRT at SYSUCC were retrospectively recruited from February 2001 to September 2010 (Fig. 1). All patients had histologically confirmed World Health Organization (WHO) type II–III NPC and complete medical records. Patients who were < 18 years, receiving conventional RT, previous or coexisting cancers other than NPC were excluded. All patients had detailed evaluations before treatment, including physical examination, Karnofsky performance status evaluation, hematologic and biochemical analyses, chest X-ray, abdominal ultrasound, contrast-enhanced computed tomography and/or magnetic resonance imaging. And all patients were restaged according to the American Joint Committee on Cancer/International Union Against Cancer (AJCC/UICC) stage classification system, 8th edition [8].

Fig. 1

Trial profile. BMI, body mass index; CCI, Charlson comorbidity index; GTVnx, gross tumor volume of nasopharynx; IMRT, intensity-modulated radiation therapy; KPS, Karnofsky performance status; LDH, lactate dehydrogenase; NLR, neutrophil to lymphocyte ratio; NPC, nasopharyngeal carcinoma; PNI, prognostic nutritional index; SYSUCC, Sun Yat-sen University Cancer Center. a)Restaged according to the American Joint Committee on Cancer, 8th edition.

2. Clinical data collection

Demographic and clinical characteristics, including age, sex, Charlson comorbidity index (CCI), WHO histological type, TNM stage, tumor volume of nasopharynx, cervical lymph nodes (CLNs) and retropharyngeal lymph nodes metastasis, pre-treatment body mass index, pre-treatment prognostic nutritional index (PNI), pre-treatment neutrophil to lymphocyte ratio, pre-treatment lactate dehydrogenase (LDH), treatment methods, acute and late toxicities, outcomes and causes of death, were reviewed from the medical records. The CCI contained both advancing ages and 19 medical conditions with a weighted score based on the relative mortality risk [12], which has proven to be a reliable and valid index of survival in a large sample of patients in various oncological settings [12-14]. And PNI, which is calculated based on the serum albumin concentration and total lymphocyte count in the peripheral blood, is known to be an indicator of both the nutritional and immune status of cancer patients [15]. In recent years, many reports have shown that the PNI could be used as a prognostic marker in patients with various malignancies [15-19]. The acute and late toxicities were graded according to the Radiation Therapy Oncology Group radiation morbidity scoring criteria [20].

3. Treatments

All patients received IMRT, which was delivered with a linear accelerator (Varian, Palo Alto, CA) using 6 MV photons. The prescribed doses were 68–70 Gy/30 fractions (fr) to the gross tumor volume of nasopharynx (GTVnx), 60–66 Gy/30 fr to the gross tumor volume of metastatic lymph nodes (GTVnd), 60 Gy/30 fr to the high-risk clinical target volume (CTV1), and 54 Gy/30 fr to the low-risk clinical target volume (CTV2), respectively. All of the following information has been detailed described in our previous published study: the IMRT technique, delineation method of the target volumes, dose limitation to the target volumes and organs at risk [21].

All stage I patients received IMRT alone, except one receiving concurrent chemotherapy for relatively large tumor volume (GTVnx-volume=30.4 cm3). Fifty patients with stage II disease received chemotherapy, 36 of them undertook concurrent chemotherapy (cisplatin, 80–100 mg/m2/day, intravenous infusion over 2 hours on days 1 and 22), three received cisplatin-based induction chemotherapy (IC), and 11 patients received cisplatin-based IC plus concurrent cisplatin chemotherapy.

4. Follow-up

All patients were followed up every 3 months during the first 3 years, every 6 months during the 4th and 5th year then annually thereafter, with routine physical examination and nasopharyngoscopy. The hematologic and biochemical analyses, chest X-ray, abdominal ultrasound, and contrast-enhanced computed tomography and/or magnetic resonance imaging were performed 3 months, 6 months and yearly after IMRT. Further investigations would be arranged when clinically indicated. All patients were followed up until May 31, 2020, or death from any cause.

5. Statistical analysis

Patients’ demographics and clinical characteristics were summarized as frequency and percentage for categorical variables, and median with interquartile range for continuous variables. Patients’ long-term outcomes, including LRRFS (freedom from documented locoregional recurrence or death from any cause), distant metastasis-free survival (DMFS; freedom from documented distant metastasis or death from any cause), disease-specific survival (DSS; freedom from documented death from NPC-related cause or last follow-up) and overall survival (OS; freedom from documented death from any cause or last follow-up), were estimated using the Kaplan-Meier method and compared with the log-rank test. A two-sided p-value of < 0.05 and a 95% confidence interval that did not include one was considered significant. The Cox proportional hazard model using forward stepwise elimination procedure to remove variables with a p-value of ≥ 0.05 was used in multivariate analysis to determine the prognostic significance of variables. Statistical analyses were performed using the SPSS software program ver. 22.0 (IBM Corp., Armonk, NY) and the figures were drawn by GraphPad Prism 8 (GraphPad Software Inc., San Diego, CA).

Results

1. Patient characteristics and radiotherapy dosimetry

From February 2001 to September 2010, 187 patients were enrolled, with the detailed demographic and clinical characteristics shown in Table 1. After being restaged using the AJCC/UICC 8th edition staging system, 41 patients were stage I and 146 patients were stage II. Among them, 51 (27.3%) patients received IMRT plus chemotherapy (IMRT+CT), the other received IMRT alone. Besides, 107 patients (57.2%) had comorbidity except NPC. The median volumes of GTVnx, GTVnd (left), GTVnd (right), CTV1, and CTV2 were 12.2 cm3, 2.8 cm3, 3.9 cm3, 36.5 cm3, and 198.7 cm3, respectively. The median D95 of GTVnx, GTVnd (left), GTVnd (right), CTV1, and CTV2 were 68.8 Gy, 63.2 Gy, 63.8 Gy, 64.1 Gy, and 56.8 Gy, as shown in S1 Table.

Table 1

Demographic and clinical characteristics in this cohort

Characteristic	No. (%)
Age, median (range, yr)	45 (21–76)
Sex
Male	139 (74.3)
Female	48 (25.7)
KPS score
80 points	12 (6.4)
90 points	173 (92.5)
100 points	2 (1.1)
WHO category
Keratinizing, undifferentiated	20 (10.7)
Non-keratinizing, undifferentiated	167 (89.3)
T category a)
T1	71 (38.0)
T2	116 (62.0)
N category a)
N0	64 (34.2)
N1	123 (65.8)
TNM stage a)
I	41 (21.9)
II	146 (78.1)
GTVnx-volume (cm 3 )
≤ 12.0	92 (49.2)
> 12.0	95 (50.8)
CLNs positive
No	69 (36.9)
Yes	118 (63.1)
RLNs positive
No	102 (54.5)
Yes	85 (45.5)
Treatment methods
IMRT+CT	51 (27.3)
IMRT alone	136 (72.7)
CCI (points)
≤ 3	121 (64.7)
> 3	66 (35.3)
Pre-treatment BMI (kg/m 2 )
< 18.5	12 (6.4)
≥ 18.5	175 (93.6)
Pre-treatment PNI
< 52.0	38 (20.3)
≥ 52.0	149 (79.7)
Pre-treatment NLR
< 1.8	68 (36.4)
≥ 1.8	119 (63.6)
Pre-treatment LDH (U/L)
< 240	177 (94.7)
≥ 240	10 (5.3)

BMI, body mass index; CCI, Charlson comorbidity index; CLNs, cervical lymph nodes; CT, chemotherapy; GTVnx, gross tumor volume of nasopharynx; IMRT, intensity-modulated radiation therapy; KPS, Karnofsky performance status; LDH, lactate dehydrogenase; NLR, neutrophil to lymphocyte ratio; PNI, prognostic nutritional index; RLNs, retropharyngeal lymph nodes; WHO, World Health Organization.

According to the American Joint Committee on Cancer, 8th edition.

2. Long-term clinical outcomes

With a median follow-up time of 15.7 years (range, 0.7 to 19.3 years), four patients had local recurrences (all within 5 years after IMRT), and seven suffered regional recurrences (6 within 5 years after IMRT and one on 7.7 years after IMRT). Twelve patients experienced distant metastases (10 within 5 years after IMRT, one on 5.8, and one on 7.1 years after IMRT), including three lung metastases, three bone metastases, two liver metastases, two mediastinal lymph node metastasis, one lung and mediastinal lymph node metastases, and one with liver and bone metastases. We recorded 29 death events: 14 were NPC-related, and 15 were non-NPC–related (three secondary malignancy-related, seven non-cancer-related, and five unknown). The 10-year LRRFS, DMFS, DSS, and OS in whole cohort were 93.3%, 93.5%, 92.9%, and 88.2%, respectively (Fig. 2). And the long-term outcomes of patients with different TNM stage were shown in S2 Fig.

Fig. 2

Survival curves of the whole cohort: locoregional recurrence-free survival (LRRFS) (A), distant metastasis-free survival (DMFS) (B), disease-specific survival (DSS) (C), and overall survival (OS) (D).

In the multivariable analyses (Table 2), CLNs and pre-treatment PNI were statistically significant in predicting DMFS (CLNs, p=0.036; pre-treatment PNI, p=0.011), DSS (CLNs, p=0.014; pre-treatment PNI, p=0.026), and OS (CLNs, p=0.002; pre-treatment PNI, p < 0.001). Besides, CCI could statistically predicted DSS (p=0.011), age and pre-treatment LDH could also predicted OS significantly (p=0.002 and p < 0.001). Additionally, only T category was marginally significant in predicting LRRFS (p=0.075).

Table 2

Univariable and multivariable analyses in this cohort

Characteristic	LRRFS				DMFS				DSS				OS
	Univariable		Multivariable		Univariable		Multivariable		Univariable		Multivariable		Univariable		Multivariable
	10-Year (%)	p-value	HR (95% CI)	p-value	10-Year (%)	p-value	HR (95% CI)	p-value	10-Year (%)	p-value	HR (95% CI)	p-value	10-Year (%)	p-value	HR (95% CI)	p-value
Sex
Male	94.1				94.9				94.8				89.9
Female	93.5	0.890	-	-	89.4	0.187	-	-	87.1	0.113	-	-	83.2	0.204		-
Age (yr)
≤ 45	91.4				93.6				95.7				94.7		1
> 45	96.6	0.139	-	-	93.4	0.962	-	-	90.0	0.236	-	-	81.7	0.003	6.364 (2.014–20.116)	0.002
T category a)
T1	98.4				95.7				92.9				90.1
T2	91.1	0.040	-	0.075	92.2	0.334	-	-	92.9	0.750	-	-	87.0	0.434		-
GTVnx-volume (cm 3 )
≤ 12.0	93.4				95.6				96.7				92.3
> 12.0	94.5	0.773	-	-	91.5	0.242	-	-	89.1	0.093	-	-	84.2	0.077		-
CLNs positive
No	96.6				96.6		1		95.6		1		94.1		1
Yes	89.2	0.046	-	0.145	88.3	0.024	3.616 (1.088–12.018)	0.036	86.4	0.019	4.084 (1.357–12.291)	0.012	78.1	0.005	4.149 (1.650–10.434)	0.002
RLNs positive
No	96.4				97.6				96.4				91.8
Yes	91.8	0.205	-	-	90.0	0.040	-	0.133	89.8	0.173	-	-	85.2	0.401		-
Treatment methods
IMRT+CT	91.5				90.0				83.8				84.3
IMRT alone	94.8	0.439	-	-	94.8	0.231	-	-	90.4	0.218	-	-	89.7	0.217		-
CCI (points)
≤ 3	93.3				95.8				97.5		1		95.9
> 3	95.2	0.619	-	-	89.1	0.077	-	-	84.0	0.002	4.711 (1.435–15.472)	0.011	74.2	< 0.001		0.128
Pre-treatment BMI (kg/m 2 )
< 18.5	88.9				94.4				90.2				88.4
≥ 18.5	95.0	0.494	-	-	90.0	0.545	-	-	80.0	0.301	-	-	70.0	0.023		0.288
Pre-treatment PNI
< 52.0	93.7				83.5		1		77.8		1		67.6		1
≥ 52.0	93.8	0.951	-	-	95.9	0.005	0.229 (0.074–0.713)	0.011	91.1	0.019	0.278 (0.095–0.813)	0.019	93.2	< 0.001	0.178 (0.076–0.420)	< 0.001
Pre-treatment NLR
< 1.8	94.0				98.4				92.4				94.0
≥ 1.8	93.8	0.970	-	-	90.6	0.038	-	0.148	86.3	0.199	-	-	84.7	0.029		0.685
Pre-treatment LDH (U/L)
< 240	93.5				94.2				88.9				86.0		1
≥ 240	100.0	0.459	-	-	80.0	0.048	-	0.236	80.0	0.276	-	-	70.0	0.015	16.563 (4.721–58.106)	< 0.001

BMI, body mass index; CCI, Charlson comorbidity index; CI, confidence interval; CLNs, cervical lymph nodes; CT, chemotherapy; DMFS, distant metastasis-free survival; DSS, disease-specific survival; GTVnx, gross tumor volumes of nasopharynx; HR, hazard ratio; IMRT, intensity-modulated radiation therapy; LDH, lactate dehydrogenase; LRRFS, locoregional recurrence-free survival; NLR, neutrophil to lymphocyte ratio; OS, overall survival; PNI, prognostic nutritional index; RLNs, retropharyngeal lymph nodes.

According to the American Joint Committee on Cancer, 8th edition.

3. Acute and late toxicities

The most common acute toxicities (grade 1–4) in the whole cohort included mucositis (100.0%), radiodermatitis (99.5%), followed by xerostomia (96.3%). As for the grade 3–4 acute toxicity, the top three toxicities were mucositis (23.5%), gastrointestinal reaction (10.7%), and leukopenia (3.2%). The grade 4 acute toxicities only included one leukopenia, one neutropenia, and one thrombocytopenia, all occurred among patients who received chemotherapy.

As for the late toxicity, the most common adverse events were subcutaneous fibrosis (89.8%), deafness or otitis (72.2%), xerostomia (48.7%), and skin dystrophy (47.1%). We also recorded six grade 1 cranial nerve injury and three grade 1 temporal lobe necrosis. No grade 4 late toxicities were .0 observed; and the grade 3 toxicities only included subcutaneous fibrosis (4.3%), deafness or otitis (4.8%), skin dystrophy (2.1%), and xerostomia (1.1%). The detailed acute and late toxicities were shown in Table 3.

Table 3

Incidence of acute and late toxicities

Any event	All grades	Grade 1	Grade 2	Grade 3	Grade 4
Acute toxicities
Mucositis	187 (100)	39 (20.9)	104 (55.6)	44 (23.5)	0
Radiodermatitis	186 (99.5)	150 (80.2)	36 (19.3)	0	0
Xerostomia	180 (96.3)	75 (40.1)	102 (54.5)	3 (1.6)	0
Gastrointestinal reaction	103 (55.1)	52 (27.8)	31 (16.6)	20 (10.7)	0
Ear	79 (42.2)	77 (41.2)	2 (1.1)	0	0
Leukopenia	64 (34.2)	33 (17.6)	25 (13.4)	5 (2.7)	1 (0.5)
Neutropenia	33 (17.6)	16 (8.6)	12 (6.4)	4 (2.1)	1 (0.5)
Anemia	18 (9.6)	13 (7.0)	4 (2.1)	1 (0.5)	0
Thrombocytopenia	14 (7.5)	7 (3.7)	4 (2.1)	2 (1.1)	1 (0.5)
Hepatotoxicity	4 (2.1)	4 (2.1)	0	0	0
Nephrotoxicity	0	0	0	0	0
Late toxicities
Subcutaneous fibrosis	168 (89.8)	102 (54.5)	58 (31.0)	8 (4.3)	0
Deafness or otitis	135 (72.2)	86 (46.0)	40 (21.4)	9 (4.8)	0
Xerostomia	91 (48.7)	76 (40.6)	13 (7.0)	2 (1.1)	0
Skin dystrophy	88 (47.1)	66 (35.3)	18 (9.6)	4 (2.1)	0
Trismus	9 (4.8)	6 (3.2)	3 (1.6)	0	0
Cranial nerve injury	6 (3.2)	6 (3.2)	0	0	0
Temporal lobe necrosis	3 (1.6)	3 (1.6)	0	0	0
Eye	0	0	0	0	0
Larynx	0	0	0	0	0
Mandible	0	0	0	0	0

Values are presented as number (%).

4. Role of chemotherapy in stage II NPC patients

In order to verify the efficacy of chemotherapy in stage II NPC patients, we divided the stage II patients into two subgroups according to their treatment methods, with basic information shown in S3 Table. Fifty patients had chemotherapy, including 36 receiving concurrent chemoradiation therapy (CCRT), 11 receiving IC+CCRT, and 3 receiving IC+IMRT; 96 patients received IMRT alone. As shown in Fig. 3, the 10-year LRRFS, DMFS, DSS, and OS in stage II patients treated with IMRT+CT vs. IMRT alone were 91.3% vs. 92.5% (hazard ratio [HR], 1.16; p=0.821), 89.8% vs. 92.7% (HR, 1.45; p=0.544), 89.6% vs. 92.6% (HR, 1.45; p=0.542), and 84.0% vs. 87.4% (HR, 1.26; p=0.594), respectively. In order to investigate the role of chemotherapy in T2N1M0 and T1N1M0 patients, we did subgroup analysis by dividing stage II patients with different TNM stage. And no significant differences were found between patients with IMRT+CT vs. IMRT alone in the subgroups of T2N0M0, T1N1M0, and T2N1M0 (all p > 0.05), as shown in Table 4.

Fig. 3

Survival curves of IMRT+CT vs. IMRT alone in the stage II nasopharyngeal carcinoma patients: locoregional recurrence-free survival (LRRFS) (A), distant metastasis-free survival (DMFS) (B), disease-specific survival (DSS) (C), and overall survival (OS) (D). CI, confidence interval; CT, chemotherapy; HR, hazard ratio; IMRT, intensity-modulated radiation therapy.

Table 4

Survival analyses in stage II NPC subgroups

Characteristic	10-Year LRRFS			10-Year DMFS			10-Year DSS			10-Year OS
	IMRT +CT (%)	IMRT alone (%)	p-value	IMRT +CT (%)	IMRT alone (%)	p-value	IMRT +CT (%)	IMRT alone (%)	p-value	IMRT +CT (%)	IMRT alone (%)	p-value
Stage IIa) (50 vs. 96)	91.3	92.5	0.821	89.8	92.7	0.544	89.6	92.6	0.542	84.0	87.4	0.594
T2N0M0 (3 vs. 20)	100.0	100.0	-	100.0	100.0	-	100.0	100.0	-	100.0	100.0	-
T1N1M0 (7 vs. 23)	100.0	94.7	0.574	85.7	91.1	0.638	85.7	87.0	0.882	85.7	82.6	0.908
T2N1M0 (40 vs. 53)	89.1	88.5	0.870	89.6	90.6	0.923	89.4	92.3	0.679	82.5	84.8	0.918

CT, chemotherapy; DMFS, distant metastasis-free survival; DSS, disease-specific survival; IMRT, intensity-modulated radiation therapy; LRRFS, locoregional recurrence-free survival; NPC, nasopharyngeal carcinoma; OS, overall survival.

According to the American Joint Committee on Cancer, 8th edition.

Unsurprising, stage II patients treated with IMRT+CT had relatively higher incidence of gastrointestinal reaction (p=0.007), myelosuppression including leukopenia (p < 0.001), neutropenia (p < 0.001), anemia (p=0.004), and thrombocytopenia (p=0.005), and grade 3–4 mucositis (p=0.001) than the IMRT alone group. As for the late toxicity, patients treated with IMRT+CT had significant higher incidence of deafness or otitis (p=0.002) and cranial nerve injury (p=0.046), as shown in S4 Table.

Discussion

As the solely study with over 15-year follow-up in the era of IMRT in the NPC endemic area, it showed satisfied long-term survivals for early-stage NPC with 10-year LRRFS, DMFS, and DSS over 90% with mild late toxicity, especially for the T1-2N0M0 patients. And chemotherapy didn’t improve stage II patients’ tumor control and survivals in the era of IMRT, even for the T2N1M0 patients, but increased patients’ acute and late toxicities.

In the era of conventional RT, the 5-year LRRFS and OS were only 73%–84% and 67%–85% among early-stage NPC patients [4-6]. With the advent of IMRT, superior radiation dosimetry could be delivered, which not only reduce the dose to surrounding normal tissues but also keep high radical irradiation to tumors, the tumor control has greatly improved with 5-year LRRFS over 90% for early-stage NPC [7]. Compared with primary tumor in nasopharynx, metastatic CLNs have a higher radio-sensitivity, so lower dose was given to GTVnd. In our practical application, 60–62 Gy/30 fr was performed to the equivocal lymph nodes (LNs), 62–64 Gy/30 fr to involved LNs with maximal axial diameter < 3 cm, and 64–66 Gy/30 fr to involved LNs, with maximal axial diameter ≥ 3 cm or central necrosis or extracapsular extension [14,16,21]. In this study, the 5-year LRRFS of whole cohort was 95.1% and 10-year LRRFS still reaching 93.3%, which indicating an excellent long-term tumor control with the use of IMRT. Additionally, the 10-year DMFS and DSS were also over 90%, and the 10-year OS reached 88.2% which was far superior than that in the era of conventional RT with a 10-year OS rate 68%–77% [6]. It is worth noting that some patients could suffer tumor relapse even 5 years after IMRT, one had regional recurrence and two had distant metastases beyond 5 years after IMRT in this cohort, which remind us that continuous follow-up is essential. And for these early-stage NPC patients, the CLNs positive and pre-treatment PNI could independently predict the DMFS and DSS; and CCI could predict patients’ DSS. In our previous study, PNI, which represents patient’s nutritional and immune status, has been proven to be an independent predictor for all stage NPC patients and could guide the treatment strategy for stage II–IV NPC patients [16]. Besides, we also found that CCI < 5 points could significantly predict the LRRFS in elderly NPC patients [14], while in this study, CCI < 3 points could independently predict NPC patients’ DSS.

There were rare studies concerning the late toxicities for early-stage NPC no matter in the era of conventional RT or IMRT. In this study, we summarized patients’ acute and late toxicities in detail, especially the latter. Most of patients’ late toxicities were in grade 1–2, and only 4.8% patients had grade 3 deafness or otitis, 4.3% patients had grade 3 subcutaneous fibrosis, 2.1% had grade 3 skin dystrophy and 1.1% had grade 3 xerostomia. As for the radiation-related nerve tissue damage, there were still few patients experienced grade 1 posterior cranial nerve injury with IMRT, which may be related with the severe subcutaneous fibrosis. Besides, three patients had grade 1 temporal lobe necrosis in our study whose temporal lobe irradiation were under corresponding tolerance dose, whether it is due to individual differences on temporal lobe radio-sensitivity still need further investigate.

For stage II NPC patients, whether adding chemotherapy has always been under debate from the era of conventional RT to IMRT. With the publications of the phase III randomized trial comparing CCRT vs. RT alone in stage II NPC and other retrospective studies [4-6,22], chemoradiotherapy has become the standard treatment strategy for stage II NPC in the era of conventional RT. With the widespread application of IMRT, there were mainly two opinions concerning the use of chemotherapy, some thought all of the stage II NPC didn’t need chemotherapy and it couldn’t improve patient’s survivals but increased toxicities [23-25]; while others thought patients with T1-2N1M0 [10] or at least T2N1M0 [7,9] could get benefit from chemotherapy and other subgroups needn’t. In the latest published phase II trial recruited 84 stage II NPC patients, the 5-year OS, local failure-free survival, regional failure-free survival, and DMFS of the IMRT alone vs. CCRT groups were 100% vs. 94.0%, 93.0% vs. 89.3%, 97.7% vs. 95.1%, and 95.2% vs. 94.5% (all p > 0.05). Though 80% patients (4/5) suffering distant metastasis with or without locoregional recurrence were in T2N1M0, the author didn’t perform subgroup analysis by stratifying stage II patients as T1N1M0, T2N0M0, and T2N1M0 due to the relatively small sample size and few events of distant metastasis [11]. In the subgroup analysis of our study, no significant differences were found in 10-year LRRFS, DMFS, DSS, and OS among T2N1M0 patients, which indicated that chemotherapy may not be able to benefit survival in those patients. Due to the small sample size in each subgroups of clinical stages, and uneven tumor volume and N staging between IMRT alone group and IMRT+CT group in all stage II patients, well-designed prospective clinical studies are still needed to confirm this conclusion.

Similar to previous studies, we also found that adding chemotherapy increased patients’ toxicities [9-11,23-26]. Due to cisplatin and other chemotherapeutic such as fluorouracil or docetaxel, more early-stage NPC patients suffered from gastrointestinal reactions, myelosuppression, and severe mucositis and leukopenia when adding chemotherapy. Even after chemoradiotherapy, the incidence of late ear toxicity, such as the deafness or otitis, was still much higher in patients who received chemotherapy. All of these acute and late adverse events would impair early-stage NPC patient’s quality of life.

Besides, there are some limitations to this study. First, as we aim to investigate the long-term outcomes of the early-stage NPC patients, only 187 stage I–II NPC patients who received treatment before 2010 were recruited. Additionally, all patients were from single institution in endemic area, which should be verified in multicenter hospitals. And more importantly, multicenter randomized clinical trials with enough samples are needed to validate our results.

In summary, we report the 10-year tumor control and survivals for early-stage NPC patients in endemic area, indicating that superior tumor control and satisfying outcomes can be achieved with IMRT with mild toxicities. As chemotherapy would bring more acute and late toxicities for patients, so it should be carefully performed to stage II patients considering their individual factors, even for T2N1M0 patients. Multicenter randomized clinical trials should be launched to validate our conclusions, and collectively, it will motivate an optimal treatment strategy for the early-stage NPC patients.