Background
Chemotherapy combined with radiotherapy (RT) is crucial for patients with locally advanced squamous cell carcinoma of the head and neck (SCCHN) who are inoperable or who require organ preservation. It includes concurrent chemoradiotherapy (CRT) and induction chemotherapy (ICT) followed by RT or CRT [
1,
2]. The most common ICT regimen included cisplatin plus 5-fluorouracil (PF) [
3]. However, the PF ICT group was inferior to the CRT group in locoregional control and event-free survival [
4]. To improve the efficacy of ICT, a revolutionary treatment strategy in the recent decade has been the addition of docetaxel to PF ICT. Two phase III trials confirmed that TPF ICT provides a significant survival advantage compared with PF ICT [
5,
6]. However, whether TPF ICT plus CRT may also obtain better survival outcomes than the standard CRT is controversial. Two phase III trials showed that TPF ICT plus CRT did not reveal a statistically significant survival benefit compared with CRT alone [
7,
8]. Furthermore, only a phase III trial of TPF ICT reached the OS benefit compared with the no-induction group [
9]. The most significant clinical concern is the more severe adverse events especially of grade 3/4 neutropenia, and TPF-related deaths, which may compromise treatment efficacy [
10].
In the TPF regimen, 75 mg/m
2 of docetaxel every 3 weeks is a widespread prescription based on the TAX 323 study [
5]. However, the toxicities of triweekly docetaxel have attracted a lot of worries especially for the elderly patients and the Asian population [
11,
12]. In a prospective pharmacokinetic study of 75 mg/m2 docetaxel every 3 weeks for patients with solid tumors, 63% of elderly patients experienced grade 4 neutropenia compared to 30% of younger patients [
12]. The analysis from published data of phase II and III clinical trials showed that a higher incidence of docetaxel-induced grade 3/4 neutropenia in Asian clinical studies than the non-Asian studies (odds ratio 19.0, [
13]). In addition, hematologic toxicity still occurs in these patients even with the reduced dose of triweekly TPF [
14,
15].
Therefore, although TPF regimen is an effective regimen for patients with SCCHN, the optimal scheduling remains unclear. One of the promising alternatives is the dose-dense chemotherapy regimen, which can be reached by the same dose intensity administered at a shorter time-interval, for instance at a biweekly interval. Dose-dense chemotherapy does not mean greater toxicity. In fact, the experience from the C9741 trial for patients with breast cancer showed that more dose-dense administration was associated with less neutropenia and less need for hospitalization due to febrile neutropenia [
16].
In terms of SCCHN, to the best of our knowledge, only one retrospective study reported the biweekly modified TPF chemotherapy was safe and was as effective as triweekly TPF [
17]. However, the decreased dose-intensity of cisplatin and docetaxel in this study made the interpretation of the study difficult when compared to the “classical “triweekly TPF regimen. Additionally, the clinical trials in bladder and breast cancers have shown that the benefit of a dose-dense approach in the neoadjuvant setting, but the studies had not been explored in SCCHN [
18]. Therefore, we designed a phase II study to evaluate the efficacy and toxicity of the biweekly dose-dense TPF.
Methods
Patients
This prospective single-arm phase II trial enrolled the patients with newly diagnosed locally advanced SCCHN. The study was conducted in accordance with the World Medical Association Declaration of Helsinki (version 2002) and was approved by the China Medical University Hospital Review Board (CMUH103-REC2–038). Patients provided IRB-approved, protocol-specific written informed consent prior to initiating therapy for study-specific treatment and inclusion in the present study. The study was retrospectively registered in
ClinicalTrials.gov (Identifier: NCT04397341).
The inclusion criteria were as follows: (1) histopathologically confirmed diagnosis of AJCC 7th edition stage 3 or 4 unresectable squamous cell carcinoma of the oral cavity, larynx, oropharynx, or hypopharynx; (2) age > 20 years; (3) ECOG performance status, 0, 1, or 2 at study entry; and (4) adequate organ function. The exclusion criteria were as follows: (1) previous chemotherapy or RT for SCCHN, (2) previous or concurrent malignancy, and (3) peripheral neuropathy > grade 2. Additionally, patients were defined as having an unsuitable condition for radical surgery after the evaluation of a multidisciplinary team. The inoperability criteria included very advanced T stage (T4b) (tumor invasion into the cervical vertebra, carotid artery, or fixed lymph nodes), risk of significant postoperative dysfunction, and low surgical curability (T3–T4, N2–N3).
Treatment
Patients received ICT after enrollment. The chemotherapy regimen was delivered with docetaxel 50 mg/m2 on day 1, cisplatin 50 mg/m2 on day 1 and 5-fluorouracil 2500 mg/m2 by continuous infusion over 46 h on Day 1–2. Moreover, the treatment was administered every 14 days for 6 cycles or until disease progression or intolerant treatment toxicity. In our study, primary G-CSF support was not allowed, but G-CSF administration can be used when the patients had febrile neutropenia or grade 4 neutropenia.
The dose modification was allowed, which was according to the greatest degree of toxicity that was graded by NCI-CTCAE Version 4.03. Also, the dose modification of study treatment could be according to the investigator’s experiences.
Radiotherapy was administered using the sequential Intensity-Modulated Radiotherapy (IMRT) for 1.8–2.0Gy per fraction with five daily fractions per week for 7 weeks. Two clinical target volumes (CTVs) were designed for risk stratification: CTV1, encompassing the gross tumor volume (GTV) of a primary tumor, metastatic lymph nodes, and regions adjacent to the GTV; and CTV2, encompassing the ipsilateral or contralateral N0 regions at risk of microscopic tumor. During the first course, a dose of 50.4–54.0Gy was included in CTV1 and CTV2. During the second course, a boost of 16.2–21.6Gy was included in CTV1. The median cumulative dose of 70.2 and 54.0Gy was achieved in CTV1 and CTV2, respectively. Concurrent chemotherapy with weekly cisplatin 35 mg/m2 was recommended during the period of radiotherapy. However, it is allowed to give radiotherapy alone or substitute cetuximab for cisplatin as the radiosensitizer for the patients not suitable for concurrent chemoradiotherapy by the assessment and discretion of the attending physician. Cetuximab was used at a 250 mg/m2 on a weekly basis (400 mg/m2 as the initial dose) for seven times.
Study design, end point definition, and statistical considerations
This was a phase II, single-center, prospective clinical trial to evaluate the induction chemotherapy (ICT) with a biweekly dose-dense TPF regimen for SCCNHN patients. The primary endpoint of the study was the response rate (RR) of ICT, while the secondary ones included response rate (RR) of the total treatment, progression-free survival (PFS), overall survival (OS), and toxicity and safety of the treatment. “The response assessment of ICT (the primary endpoint) was performed using CT scan at the end of treatment according to the RECIST 1.1 criteria. Positron emission tomography (PET)/CT scan was also performed to evaluate the response according to the European Organization for Research and Treatment of Cancer (EORTC) 1999 criteria.” In addition, only when CT scans failed to reveal an obvious primary, PET/CT scan was used to confirm the complete response. The response assessment of the total treatment was performed at 10–12 weeks since the end of radiotherapy with CT scan, and the response assessment was confirmed by repeat CT scan at an interval of 6–8 weeks. Then, the CT scan was performed every 3–4 months in the first 2 years and every 6–7 months until progression. The PFS was defined as the time from the study registration date to the first day of disease progression at any site or of death by any cause. The OS was defined as the time from the date of study registration to the date of death, or the last confirmed survival date. The toxicity was recorded by the investigators using the National Cancer Institute Common Toxicity Criteria scale version 4.03 (NCI-CTCAE Version 4.03). Toxicities were assessed at each weekly visit during ICT and at the end of treatment.
At the time of study design, the response rate of standard triweekly TPF regimen was reported to be 68 and 72%, respectively [
5,
6]. Therefore, the study was conducted using Simon’s optimal two-stage phase II design based on response rate for sample-size calculation. A sample size of 35 patients was required to accept the hypothesis that the true response rate was greater than 90% with a 90% power and to reject the hypothesis that the response rate was less than 70% with 5% significance. Initially, we planned to enroll 15 patients in the first stage. If 11 or more responses were observed, we planned to continue to the second stage for a total of 35 patients in the analysis. Assuming a dropout rate of 10%, the total number of enrolled patients needed was calculated to be 40. If the endpoints were achieved, we will extend the number of enrolled patients to 60 for translation study. The translational study aims to study the prognostic significance of the metabolic parameters of PET in tumour response to ICT.
Kaplan-Meier survival analysis was used to estimate survival endpoints, and the log-rank test was used to compare the differences between curves. All tests are two-sided, and a p-value < 0.05 was considered to indicate a statistically significant difference. Multivariate analysis was carried out using a Cox proportional hazards regression model. The age was classified into > 50 and ≦50 years old using the receiver operating characteristic (ROC) curve.
Statistical analysis was performed with the SPSS software (version 17.0; SPSS, Chicago, IL) and EZR version 1.32. software [
19].
Discussion
Our study showed that biweekly dose-dense TPF ICT in locally advanced SCCHN had a promising treatment response. The overall response rate and complete response rate were 89.7 and 31%, respectively. The 3-year OS and PFS were 56.3 and 34.3%, respectively. Compared to the data from TAX323 and TAX324 trials, standard triweekly TPF ICT regimen achieved 68 and 72% post-induction RR, respectively [
5,
6]. The 3-year OS and PFS for patients in TAX 323 were 37 and 17%, and those in TAX 324 were 62.0 and 49.0%, respectively [
5,
6]. Particularly, 25.9% of the grade 3–4 neutropenia in our study is markedly lower than previously reported. For example, TAX323 trial reported 76.9% of the grade 3–4 neutropenia, and TAX324 trial reported 83% of the grade 3–4 neutropenia [
5,
6].
Toxicity is a major issue of ICT, with up to 6% toxic deaths and 11% of febrile neutropenia [
4,
20]. Some studies had tried to find fewer toxic regimens by reducing chemotherapy dose [
21,
22]. HM. Wang et al. reduced the dose to 90% of the original TPF dosage (docetaxel 67.5 mg/m2 on Day 1, cisplatin 67.5 mg/m2 on Day 1 and 5FU 675 mg/m2 on Day 1–5) as the induction treatment. The grade 3–4 neutropenia was 35%, and the overall response rate was 73.1% after induction therapy [
21]. A retrospective study from J Fayette et al. in France used the modified TPF regimen of docetaxel and cisplatin at 40 mg/2 on day 1 and a bolus of 5FU at 400 mg/m2, then 1000 mg/m2 on Day 1–2 every 2 weeks. The authors reported 10% of febrile neutropenia, 83% of overall response rate and 19% of complete response [
22]. Notably, the regimen adopted by J Fayette et al. was similar to that our study used, such as biweekly administration, and 48-h infusion of high-dose 5FU. Biweekly administration of docetaxel might be better tolerated due to the reduced peak drug concentrations [
23]. Data from colon cancer and gastric cancer had shown that biweekly 48 h infusion of 5FU can increase the response rate with fewer side effects of myelotoxicity [
24,
25]. However, the inherent bias of the retrospective study, the heterogenous post-ICT treatment (including surgery and radiotherapy) and the reduced dose intensity of cisplatin and docetaxel compared to the standard TPF regimen made the interpretation of the results difficult.
Dose-Dense Chemotherapy aims to achieve maximum tumor kill by shortening the interval of chemotherapy delivery. Several clinical trials and metastasis from breast cancer, bladder cancer, and lymphoma had revealed that dose-dense regimen improved response rate and survival outcomes [
26,
27]. However, the associated studies in head and neck cancer are scarce. Our TPF regimen included 50, 50, 2500, and 250 mg/m
2 of docetaxel, cisplatin, 5-fluorouracil, and leucovorin, respectively. We maintained the average dose intensity of the traditional TPF, with less toxicity than triweekly TPF and similar rates of neutropenia (25.86%) compared with the weekly TPF regimen. Additionally, 94.8% of patients completed 6 cycles of treatment without dose reduction. The high rate of treatment completion may explain the better response rate and survival outcomes in our study.
ICT also was a predictor of survival for locally advanced SCCHN. A recent meta-analysis study showed the ICT responders had better survival than nonresponders [
28]. Moreover, a phase II study demonstrated that responders after one cycle of split-dose TPF ICT were a survival predictor for oral and oropharyngeal squamous cell carcinoma (OPSCC) [
29]. A review article that recruited seven studies displayed that the standardized uptake value (SUV) reduction in interim PET scan may predict ICT response, PFS, and OS [
30]. In our study, biweekly TPF ICT demonstrated around 90% RR and a high CR rate (31.0%). Also, the patients with CR had better OS and PFS than those with non-CR. Accordingly, patients with metabolic non-CR may need an additional treatment after ICT.
Limitations of our study include the lack of a comparator group and the relatively small sample size. Although the primary objective of this study is to investigate the response rate of ICT, the heterogeneous treatment during radiotherapy could have introduced major biases in the analysis of OS. Additionally, 14 of 54 (25.9%) patients could receive radiotherapy only, which raised the concern that the administration of ICT may compromise the completion of subsequent concomitant administration of chemotherapy or biotherapy. To draw definitive conclusions is difficult in this regard because compliance and toxicity data are differently reported. However, according to the Spanish TTCC trial, which used standard triweekly TPF regimen followed by concomitant CRT regimen, 30% of patients would never receive radiotherapy, 41% of patients needed dose reduction, and 17% of patients discontinued CRT treatment [
7]. In our study, 4/58 (6.9%) patients did not receive the following radiotherapy, and 3/54 (5.6%) patient discontinued CRT treatment. The relative tolerability of the dose-dense TPF regimen may be attributed to fewer grade 3–4 adverse effects and shortened treatment duration. Additionally, because radiotherapy would follow the induction chemotherapy within 4 weeks, it is impossible to confirm our treatment response by repeat assessments that should be performed no less than 4 weeks after the RECIST criteria for the response classification was initially met. Finally, our study design is unlikely to answer the question of whether the combination of dose-dense induction therapy plus the following radiotherapy can beat conventional concomitant CRT therapy.
Conclusions
In conclusion, the investigational regimen of biweekly TPF ICT appears to have favourable tolerability with an acceptable response rate compared to published studies. This regimen had fewer grade 3/4 hematologic adverse events including neutropenia, anemia, and thrombocytopenia than the triweekly TPF. Also, the survival figures were not inferior to the reported studies of triweekly TPF ICT. The patients with CR after ICT had superior survival outcomes than those with non-CR. Thus, future studies should focus on whether further treatments are necessary for patients with non-CR after ICT.
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