Abstract
Background
N-stage is related to distant metastasis in nasopharyngeal carcinoma (NPC) patients. The purpose of this study was to evaluate the efficacy and toxicity of different nedaplatin-based chemotherapy regimens in advanced N2-3 stage NPC patients treated with intensity modulated radiation therapy (IMRT).
Patients and Methods
Between April 2005 and December 2009, a total of 128 patients with N2-3 advanced NPC were retrospectively analyzed. Patients were treated with IMRT concurrent with 2 cycles of chemotherapy consisting of either nedaplatin plus paclitaxel (NP group, n = 67) or nedaplatin plus fluorouracil and paclitaxel (NFP group, n = 61). Two to four cycles of adjuvant chemotherapy were then administered every 21 days following concurrent chemoradiotherapy.
Results
With a median follow-up of 60 months, the 5-year overall survival (OS), progression-free survival (PFS), local-regional recurrence-free survival (LRRFS), and distant metastasis-free survival (DMFS) for all patients were 81.4%, 71.5%, 87.8% and 82.0%, respectively. No significant difference in PFS (66.6% vs. 76.7%, P = 0.212) and LRRFS rates (89.0% vs. 86.3%, P = 0.664) was observed between the NP and NFP groups. The 5-year OS (75.4% vs. 88.5%, P = 0.046) and DMFS (75.1% vs. 89.0%, P = 0.042) rate were superior in the NFP group compared with the NP group. The NFP group had a higher incidence of grade 3–4 acute toxicities including bone marrow suppression (leukopenia: χ2 = 3.935, P = 0.047; anemia: χ2 = 9.760, P = 0.002; thrombocytopenia: χ2 = 8.821, P = 0.003), and both liver and renal dysfunction (χ2 = 5.206, P = 0.023) compared with the NP group. Late toxicities were moderate and no difference was observed between the two groups.
Conclusion
IMRT concurrent with nedaplatin-based chemotherapy is an advocated regimen for patients with advanced N2-3 stage NPC. Patients with advanced N2-3 stage may be better candidates for the NFP regimen although this regimen was associated with a high acute toxicity rate.
Introduction
Nasopharyngeal carcinoma (NPC) is endemic in south-east Asia, parts of Africa and southern China. Radiotherapy plays a key role in the treatment of all stages of NPC without distant metastasis [1–2]. Approximately 70% of newly diagnosed NPC patients present with stage III or IV disease, and are prone to local-regional recurrence or distant metastases after radiotherapy alone [3]. Intensity-modulated radiotherapy (IMRT) is a major breakthrough in the treatment of NPC. IMRT delivers a higher dose to the tumor, while minimizing the dose to surrounding normal tissues. Previous studies have confirmed that IMRT changed the failure pattern of NPC from local recurrence and distant metastasis to predominantly distant metastasis [4,5].
It is also well known that N-stage is related to distant metastasis in NPC patients. Xu et al. reviewed 181 NPC patients and found that the 3-year distant metastasis-free survival rate (DMFS) was 89.6%, 75.7%, and 76.3% for stageT3-4N0-1, T1-2N2-3, and T3-4 N2-3 patients, respectively. Cox proportional hazards regression analysis showed that advanced N-stage was an independent risk factor for distant metastasis (P = 0.033) [6]. Therefore, it is necessary to explore more effective combined chemoradiotherapy strategies to improve the outcomes of patients with advanced N-stage NPC.
The cisplatin-based Intergroup-0099 regimen resulted in a significantly increased toxicity rate. According to the results of previous research [7–10], nedaplatin-based regimens achieved comparable survival, were well tolerated and had lower toxicity than cisplatin-based regimens in the treatment of head and neck cancer, esophageal cancer, uterine cervix cancer and NPC. Therefore, we retrospectively analyzed the long-term outcomes of advanced N-stage NPC patients treated with concurrent IMRT and nedaplatin-based chemotherapy, followed by adjuvant chemotherapy, and compared the efficacy and toxicity of different nedaplatin-based chemotherapy regimens in these patients.
Patients and Methods
Patients
Between April 2005 and December 2009, 128 pathologically confirmed N2-3 stage NPC patients without distant metastasis in Jiangsu Cancer Hospital were enrolled in this retrospective analysis. All patients had no previous treatment history and underwent definitive IMRT at our hospital. Initial workup included clinical and laboratory examinations, hematologic and biochemistry profiles, fiberoptic endoscope examination of the nasopharynx, magnetic resonance imaging (MRI) and contrast-enhanced computed tomography (CT) of the head and neck to evaluate the extent of the primary tumor and regional lymph nodes. Bone scintigraphy, chest radiography or contrast-CT, and ultrasonography of the abdominal region were performed to exclude distant metastasis. Stages were assigned according to the 6th edition of the American Joint Committee on Cancer (AJCC TNM 2002) staging system [11].
IMRT
Patients received definitive IMRT with 6 MV X-rays as previously reported [6]. Briefly, gross tumor volume (GTV) 1 included the primary tumor and metastatic retropharyngeal lymph nodes found on clinical and imaging examination. Metastatic cervical lymph nodes were defined as GTV2. The high-risk region was defined as clinical target volume (CTV)1 which included the whole nasopharyngeal cavity, GTV1, GTV2 with a margin of 5 to 15 mm, and levels II and III cervical lymphatic drainage region. Low risk area was defined as CTV2 which encompassed CTV1 with a margin of 3 to 5 mm, the lower neck, and the supraclavicular lymphatic drainage region. A total dose of 67.6–78.0 Gy/31–35 F was prescribed to GTV1, 65.0–85.0 Gy/32–39 F to GTV2, 56.0–60 Gy/30 F to CTV1 and 50 Gy/30 F to CTV2, respectively. All patients were irradiated with 1 fraction daily, 5 days per week. An example of the three-dimensional dose distribution described is shown in Fig 1.
Fig 1. Target volume contouring in 3-dimensional intensity-modulated radiotherapy plan of nasopharyngeal carcinoma.
(Red line represents GTV1, pink line represents GTV2, green line represents CTV1 and yellow line represents CTV2; Isodose levels: 50 Gy in blue line, 60 Gy in cyan line, 66 Gy in green line and 70 Gy in yellow line).
Chemotherapy
During the period of concurrent chemoradiotherapy, 61 of 128 patients (47.7%) received the NFP regimen, which consisted of paclitaxel 135–175 mg/m2 per cycle on day 1, fluorouracil 500–600 mg/m2 on days 1 to 5, and nedaplatin with a total dosage of 80–100 mg/m2 per cycle evenly administered on days 1 to 3. The remaining 67 patients (52.3%) were treated with the NP regimen, which consisted of paclitaxel 135–175 mg/m2 per cycle on day 1 and nedaplatin with a total dosage of 80 to 100 mg/m2 per cycle evenly administered on days 2 to 4. Concurrent chemotherapy was limited to two cycles with an interval of 3–4 weeks. Adjuvant chemotherapy with the NP or NFP regimen after approximately 4 weeks’ restoration of combined therapy was given repeatedly every 3 to 4 weeks according to the performance status. The chemotherapy during the whole treatment period was limited to no more than six cycles in total.
Complete blood count, liver and renal function were tested before each chemotherapy cycle. Dose modification was carried out by the attending radiation oncologists according to the toxicity level [10]. Granulocyte colony-stimulating factor (G-CSF) and recombinant erythropoietin (EPO) were not administered unless the white blood cell count dropped to less than 3.5× 109/L and hemoglobin decreased to less than 100 g/L, respectively. Antibiotics were administered to patients with neutropenic fever. Platelet transfusion with or without administration of interleukin 11 or recombinant thrombopoietin was administered when the platelet count was less than 25 ×109/L. Red blood cell transfusions were administered when hemoglobin decreased to less than 70 g/L.
Follow-up and treatment assessment
Toxicity was assessed using the National Cancer Institute Common Terminology Criteria for Adverse Events (CTCAE, version 3.0). Regular follow-up visits were performed at our institution. Patients were evaluated for disease control, survival and toxicity at three-month intervals for the first two years, at 6-month intervals between the third and fifth years, and 1 year intervals thereafter. Each follow-up visit included a clinical physical examination, nasopharyngoscopy, ultrasonography of the abdomen and chest X-ray. A CT scan or MRI of the head and neck region was conducted every 3 to 6 months for the first 2 years and then yearly from year 3. In patients with evidence of local-regional recurrence or distant metastasis, additional examination or imaging modalities were performed to confirm or exclude disease progression at the discretion of the treating physician.
Statistical analysis
Statistical analysis was performed using SPSS 20.0 (International Business Machines Corp, Armonk, NY, USA). Overall survival (OS), progression-free survival (PFS), local-regional recurrence-free survival (LRRFS), and distant metastasis-free survival (DMFS) were defined as follows: OS, survival during the follow-up period; PFS, survival without local-regional failure or distant metastasis; LRRFS, survival without recurrence in the nasopharynx or cervical lymph nodes; and DMFS, survival without distant metastasis. OS, PFS, LRRFS and DMFS rates were determined using the Kaplan-Meier method. Differences between survival curves were compared using log-rank tests. Univariate and multivariate survival analyses were performed using the Cox proportional hazards regression model. Statistical significance was accepted when the P value was <0.05.
Ethical statement
This retrospective study was approved by the Jiangsu Cancer hospital review board and was conducted in accordance with the ethical guidelines of the Declaration of Helsinki.
Results
Patient characteristics
The median duration of follow-up was 60.0 months (range, 11.0–109.0 months). A total of 128 NPC patients with advanced N2-3 stage were enrolled in this retrospective study (67 in the NP group and 61 in the NFP group). The mean age at the time of NPC diagnosis was 49.5 ± 12.9 years. There were 91 males and 37 females. Stage distribution was as follows: stage III, 76; stage IVa, 27; and stage IVb, 25. Patient characteristics and treatment facts of the 2 groups are shown in Table 1.
Table 1. Patient characteristics.
Abbreviations: AJCC, American Joint Committee on Cancer; NP, nedaplatin plus paclitaxel; NFP, nedaplatin, paclitaxel plus fluorouracil
| Characteristic | NP | NFP | ||
|---|---|---|---|---|
| No. of patients | (%) | No. of patients | (%) | |
| Total | 67 | 61 | ||
| Gender | ||||
| Male | 47 | 70.1 | 44 | 72.1 |
| Female | 20 | 29.9 | 17 | 27.9 |
| Age (years) | ||||
| ≤50 | 35 | 52.2 | 34 | 55.7 |
| >50 | 32 | 47.8 | 27 | 44.3 |
| AJCC staging * | ||||
| Ⅲ | 42 | 62.7 | 34 | 55.7 |
| Ⅳa | 12 | 17.9 | 15 | 24.6 |
| Ⅳb | 13 | 19.4 | 12 | 19.7 |
| AJCC T classification * | ||||
| T1 | 5 | 7.5 | 4 | 6.6 |
| T2 | 17 | 25.4 | 9 | 14.8 |
| T3 | 32 | 47.8 | 31 | 50.8 |
| T4 | 13 | 19.4 | 17 | 27.9 |
| AJCC N classification * | ||||
| N2 | 54 | 80.6 | 49 | 80.3 |
| N3 | 13 | 19.4 | 12 | 19.7 |
| Adjuvant chemotherapy | ||||
| No | 3 | 4.5 | 7 | 11.5 |
| 1–2 cycles | 40 | 59.7 | 43 | 70.5 |
| 3–4 cycles | 24 | 35.8 | 11 | 18.0 |
* Defined by the criteria of the AJCC 2002 staging system [11].
Survival
For all patients, the 5-year OS, PFS, LRRFS and DMFS were 81.4%, 71.5%, 87.8% and 82.0%, respectively (Fig 2). There were no significant differences in the 5-year PFS (66.6% vs. 76.7%, P = 0.212) and LRRFS rates (89.0% vs. 86.3%, P = 0.664) between the NP and NFP groups. The 5-year OS (75.4% vs. 88.5%, P = 0.046) and DMFS rate (75.1% vs. 89.0%, P = 0.042) were inferior in the NP group compared with the NFP group (Fig 3A–3D).
Fig 2. Kaplan-Meier curves of overall survival (OS), progression-free survival (PFS), locoregional recurrence-free survival (LRRFS) and distant metastasis-free survival (DMFS) for 128 patients with advanced N2-3 stage NPC.
Fig 3. 5-year OS, PFS, LRRFS and DMFS were 75.4% vs. 88.5%, 66.6% vs. 76.7%, 89.0% vs.86.3%, and 75.1% vs. 89.0% for the NP and NFP groups, respectively.
A and D. Advanced N2-3 stage NPC patients in the concurrent NFP group had a significantly superior OS and DMFS (Log Rank test, OS: χ2 = 3.973, P = 0.046; DMFS: χ2 = 4.130, P = 0.042). B and C. No significant difference in PFS and LRRFS were seen during the observation period. (Log Rank test, PFS: χ2 = 1.560, P = 0.212; LRRFS: χ2 = 0.189, P = 0.664).
Prognostic factors
We performed univariate and multivariate analyses to assess the value of various potential prognostic factors on predicting OS, PFS, LRRFS and DMFS. The following factors were included as covariates: gender, age, AJCC staging (Ⅲ vs. Ⅳ), AJCC T classification (T1–2 vs. T3–4), and AJCC N classification (N2 vs. N3), concurrent chemotherapy regimen (NP vs. NFP), radiation dose to primary lesion and positive lymph nodes (≤70 Gy vs.>70 Gy) and adjuvant chemotherapy cycles. Univariate analysis by log-rank test showed that AJCC staging was significantly associated with OS, PFS, and DMFS (AJCC staging: P = 0.001, P = 0.001, and P = 0.002, respectively). AJCC T classification was associated with LRRFS (P = 0.019) and AJCC N classification was associated with PFS and DMFS (P = 0.034 and P = 0.002). In addition, gender was also significantly associated with PFS and DMFS (P = 0.038 and P = 0.018) (S1 Table).
Multivariate analysis was performed using the Cox progression model to assess the independent risk factors for survival rates and the results are listed in Table 2. Adjusted by age, adjuvant chemotherapy and radiation dose, the results showed that AJCC staging was an independent prognostic predictor of OS, PFS, and DMFS (P = 0.01; P = 0.00; P = 0.02, respectively). Chemotherapy regimen independently influenced OS and DMFS (P = 0.03 and P = 0.01). In addition, gender was an independent prognostic predictor of PFS (P = 0.03) and DMFS (P = 0.02).
Table 2. Multivariate prognostic factor analyses for various clinical endpoints.
Abbreviation: HR: hazard ratio; CI: confidence interval.
| Endpoint | Characteristics | HR (95% CI) | P value |
|---|---|---|---|
| OS | Gender | 0.73(0.30–1.76) | 0.48 |
| AJCC staging | 6.63(1.53–28.70) | 0.01 | |
| T classification | 0.79(0.38–1.62) | 0.51 | |
| N classification | 0.51(0.12–2.18) | 0.36 | |
| Chemotherapy | 0.36(0.15–0.89) | 0.03 | |
| PFS | Gender | 0.37(0.15–0.89) | 0.03 |
| AJCC staging | 5.35(1.76–16.27) | 0.00 | |
| T classification | 0.78(0.46–1.31) | 0.34 | |
| N classification | 0.60(0.19–1.89) | 0.39 | |
| Chemotherapy | 0.58(0.30–1.14) | 0.11 | |
| LRRFS | Gender | 0.74(0.23–2.45) | 0.62 |
| AJCC staging | 4.02 (0.67–24.02) | 0.13 | |
| T classification | 0.92(0.33–2.57) | 0.87 | |
| N classification | 0.27(0.03–2.31) | 0.23 | |
| Chemotherapy | 1.33(0.45–3.94) | 0.61 | |
| DMFS | Gender | 0.18(0.04–0.78) | 0.02 |
| AJCC staging | 5.39(1.26–23.04) | 0.02 | |
| T classification | 0.77(0.41–1.44) | 0.41 | |
| N classification | 0.93(0.22–3.96) | 0.93 | |
| Chemotherapy | 0.32(0.13–0.78) | 0.01 |
Toxic effects
Acute toxicities were assessed in all 128 patients and are summarized in Table 3. The most common acute toxicities were hematological toxicity and mucositis. For patients who received the NP regimen, the incidence of grade 3–4 hematologic toxicities (leukopenia, anemia or thrombocytopenia), oral mucositis, vomiting and both liver and renal function abnormalities (ALT elevation or sCr elevation) was 44.8%, 14.9%, 25.4%, 31.3%, 31.3% and 20.9%, respectively. For patients who received the NFP regimen, these values were 62.3%, 39.3%, 50.8%, 39.3%, 45.9% and 39.3%, respectively. The NFP group had a significantly higher incidence of moderate-to-severe toxicities, including grade 3–4 bone marrow suppression (leukopenia: χ2 = 3.935, P = 0.047; anemia: χ2 = 9.760, P = 0.002; thrombocytopenia: χ2 = 8.821, P = 0.003) and both liver and renal dysfunction (χ2 = 5.206, P = 0.023). For the sake of bone marrow suppression, G-CSF and EPO were used in 44 and 17 patients in the NP group, respectively. The number of patients in the NFP group receiving G-CSF and EPO were 52 and 35, respectively. Vomiting (χ2 = 2.864, P = 0.091) and oral space mucositis (χ2 = 0.897, P = 0.344) were common in the NFP group, however, the differences were not significant.
Table 3. Severe acute toxicities based on the CTCAE3.0 grading system.
Abbreviations: CTCAE, Common Terminology Criteria for Adverse Events.
| Acute toxicities (Grade 3/4 acute toxicities) | No. of the NP group (%) | No. of the NFP group (%) | P value |
|---|---|---|---|
| Leukopenia | 30(44.8) | 38(62.3) | 0.047 |
| Anemia | 10(14.9) | 24(39.3) | 0.002 |
| Thrombocytopenia | 17(25.4) | 31(50.8) | 0.003 |
| Liver/ Renal dysfunction | 14(20.9) | 24(39.3) | 0.023 |
| Oral mucositis | 21(31.3) | 24(39.3) | 0.344 |
| Vomiting | 21(31.3) | 28(45.9) | 0.091 |
The main documented late toxicities in patients treated with IMRT and concurrent NP or NFP chemotherapy who survived for more than 2 years were fibrosis (skin and subcutaneous tissue of the neck), xerostomia, hearing loss and visual impairment. Other late toxicities observed included trismus, radiation-induced brain injury (temporal necrosis, cranial nerve palsy) and subclinical hypothyroidism. No patient had grade 4 or 5 late toxicity. No differences were observed for grade 3 late toxicities (Table 4).
Table 4. Treatment-related late toxicities.
| Late toxicities (Grade 3) | No. of the NP group (%) | No. of the NFP group (%) | P value |
|---|---|---|---|
| Xerostomia | 1(1.5) | 0(0) | 0.338 |
| Fibrosis | 4(6.0) | 4(6.6) | 0.891 |
| Hearing or vision impairment | 7(10.4) | 6(9.8) | 0.909 |
| Hypothyroidism | 1(1.5) | 1(1.6) | 0.991 |
| Trismus | 6(9.0) | 5 (8.2) | 0.878 |
| Radiation-induced brain injury | 2(3.0) | 3(4.9) | 0.573 |
Discussion
Concurrent chemoradiotherapy (CCRT) can achieve significantly better tumor control than radiotherapy alone and it is the standard treatment for locoregionally advanced NPC based on large randomized phase Ⅲ trials and a meta-analysis [12,13]. Although it is generally accepted that platinum monotherapy or platinum-based doublet chemotherapy has been the standard of care for years, the combination of docetaxel, platinum, and fluorouracil has also been evaluated [14–17] and the toxicity is manageable in patients with head and neck squamous cell carcinomas. However, the additive value or the optimal combination schedule of chemotherapy and radiotherapy is largely unknown at present.
With optimized local treatment achieved with IMRT, locoregional control has been markedly improved in NPC [18]. The main cause of failure in NPC is distant metastasis following IMRT [19]. N-stage is a prognostic factor in NPC patients, and irrespective of the radiation technique used, advanced N-stage patients have a high rate of distant metastasis [4,18,20]. Chemotherapy plays an important role in reducing the probability of metastasis. It is reasonable to consider more intensive modifications of chemotherapy in addition to IMRT for advanced N stage disease. To our knowledge, there is no published randomized phase III study confirming the value of chemotherapy in NPC patients treated with IMRT. Our study is the first to compare concurrent chemotherapy regimens in patients with advanced N stage NPC.
Recently, Wu et al. [21] prospectively evaluated the long-term outcome in III–IVb NPC patients treated with IMRT and concurrent cisplatin (80–100 mg/m2). The 5-year OS, LRFS, RRFS, and DMFS were 78.4%, 86.8%, 88.4%, and 78.0%, respectively. In addition, Sun et al. [22] reported that the 5-year OS, RFS, DMFS and PFS in advanced N-stage NPC patients treated with chemoradiotherapy (IMRT) were 73.1%, 91.3%, 68.5% and 63.8%, respectively. The 5-year OS, PFS and DMFS in our series were favorable and comparable, which demonstrated the efficacy of nedaplatin-based chemoradiotherapy in advanced N stage NPC. On the other hand, no significant difference in 5-year PFS and LRRFS rates was observed between the two groups, however, the 5-year OS and DMFS rates were superior in the NFP group compared with the NP group (75.4% vs. 88.5%, 75.1% vs. 89.0%, respectively). The increase in DMFS translate into a substantial improvement in OS. This indicates that aggressive chemotherapy could reduce the risk of metastasis. According to our results, aggressive chemotherapy was more effective in eradicating distant tumors in advanced N-stage NPC patients. TAX324, a randomized phase Ⅲ trial conducted in advanced head and neck cancer patients [23], has shown DMFS advantages due to multi-agent intensive chemotherapy, which also indicated that a more effective regimen of chemotherapy should be considered to overcome the higher incidence of distant metastasis in patients with advanced N stage tumors. Table 5 summarizes the OS and DMFS in advanced N stage NPC patients [4,18,20,22,24–25]. Despite the retrospective nature and limited patient number in our analysis, the outcome of our advanced N stage NPC patients treated with IMRT and concurrent NP or NFP chemotherapy with the addition of adjuvant chemotherapy was comparable to the results published by other groups. In addition, EPO and G-CSF were used when patients had bone marrow suppression. Interestingly, the phase III randomized RTOG trial 9903 showed that administration of EPO in head and neck cancer patients is not helpful and may be harmful[26]. However, in the present study, although more patients in the NFP group than the NF group received EPO treatment, the survival results were still better in the NFP group than the NF group. This discrepancy may be due to different biology behavior and treatment response between NPC and head and neck cancer. Future further exploration in a randomized setting warrants for resolving this issue.
Table 5. OS and DMFS of patients with advanced N stage NPC treated with chemoradiotherapy.
Abbreviations: RT, radiotherapy; 2D-RT, two-dimensional RT; IMRT, intensity-modulated radiotherapy.
| Year | Author | No. | RT | OS (%) | DMFS (%) |
|---|---|---|---|---|---|
| 2001 | Ma et al.[25] | 621 | 2D-RT | - | 5-year |
| N2:62 | |||||
| N3:51 | |||||
| 2005 | Leung et al.[24] | 1070 | 2D-RT | 5-year | 5-year |
| N2:60.3 | N2:71.6 | ||||
| N3:40.2(a) and 48.4 (b) | N3:66.9(a) and 52.1(b) | ||||
| 2010 | Wong et al.[4] | 175 | IMRT | - | 3-year |
| N2:76.6 | |||||
| N3:67.3 | |||||
| 2011 | Lai et al.[18] | 1276 | 2D-RT | - | 5-year |
| N2:75.1 | |||||
| N3:65.4 | |||||
| IMRT | N2:80.5 | ||||
| N3:60.9 | |||||
| 2013 | Sun et al.[22] | 198 | IMRT | 5-year | 5-year |
| N2:71.0 | N2:68.5 | ||||
| N3:55.7 | N3: 50.1 | ||||
| 2014 | Sun et al.[20] | 868 | IMRT | 5-year | 5-year |
| Ⅲ:83.6 | N2:73.7 | ||||
| Ⅳ:70.5 | N3:62.1 |
The dose-limiting toxicity of nedaplatin is bone marrow suppression [27]. However, bone marrow suppression was reversible and no treatment-related deaths were observed in the present study. In addition, the incidence of severe gastrointestinal toxicity (grade ≥3) was 27.3–32.1% in cisplatin-based CCRT [28,29]. The nedaplatin-based CCRT study showed a lower incidence of grade ≥2 vomiting [10]. As fluorouracil has additive gastrointestinal toxicity with cisplatin, concurrent cisplatin plus fluorouracil with radiotherapy produced a relatively high incidence of moderate to severe gastrointestinal toxicity in the treatment of locoregionally advanced NPC [5,28]. Nedaplatin causes less gastrointestinal toxicity and is suitable for combination with other chemotherapy agents. When fluorouracil was added to nedaplatin and paclitaxel, the incidence of vomiting significantly increased in the NFP group. Acute mucositis was common in the present study (31.3% vs. 50.8%). However, this toxicity was also common (61%) in studies on cisplatin regimens [29]. Thus, oncologists should be aware of these common adverse events, and symptomatic treatment should be offered to patients, which may have an impact on patient compliance to therapy and quality of life. Moreover, the nedaplatin regimen took less time to administer as there was no pre- and post-hydration. Furthermore, the most common late toxicity was grade 1–2 neck fibrosis, xerostomia, hearing impairment and vision loss, similar to other reports [22]. No differences were observed in the two groups regarding grade 3 late toxicities.
Our results demonstrated that AJCC staging was significantly associated with OS, PFS, and DMFS. Chemotherapy independently influenced OS and DMFS. These results suggest that aggressive and intensive systemic therapy for advanced N stage NPC should be considered. In addition, gender was also significantly associated with PFS and DMFS in our study, which might have been associated with the disparity of gender in the enrolled patients.
There are several limitations in the current study, including the retrospective nature of the study design, the wide variation in radiation dose and fractionation, which could affect the outcome. Nevertheless, our report is noteworthy because this is the first study to evaluate concurrent nedaplatin-based chemotherapy for advanced N2-3 stage NPC treated by IMRT.
In summary, our data indicate the benefit of concurrent NP or NFP chemotherapy with IMRT in patients with advanced N stage NPC, especially the NFP regimen which resulted in a good 5-year OS and DMFS. This regimen may be considered as an alternative therapeutic regimen for this patient group even though it is associated with a high acute toxicity rate. Further investigation in the prospective setting is warranted to explore the role of concurrent NFP and adjuvant chemotherapy in IMRT treatment of advanced N stage NPC.
Supporting Information
(SAV)
(DOCX)
Acknowledgments
We thank Prof. Mu-Shui Dai in Oregon Health & Science University for his revision of this manuscript and language assistance. We thank the anonymous reviewers for useful comments and suggestions.
Data Availability
All relevant data are within the paper and its Supporting Information files.
Funding Statement
This research was supported by grants from the JiangSu Clinical medicine Science and Technology Special Fund (No:BL2014091, http://www.jstd.gov.cn/), the JiangSu Provincial Commission of Health and Family Planning Young Scholars Award (Q201501, http://www.jswst.gov.cn/jsswshjhsywyh/). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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