Skip to main content
Cancer Research and Treatment : Official Journal of Korean Cancer Association logoLink to Cancer Research and Treatment : Official Journal of Korean Cancer Association
. 2015 Mar 13;48(1):45–53. doi: 10.4143/crt.2014.340

Definitive Chemoradiotherapy Versus Surgery Followed by Adjuvant Radiotherapy in Resectable Stage III/IV Hypopharyngeal Cancer

Jun Won Kim 1, Mi Sun Kim 2, Se-Heon Kim 3, Joo Hang Kim 4, Chang Geol Lee 2, Gwi Eon Kim 2, Ki Chang Keum 2,
PMCID: PMC4720057  PMID: 25779363

Abstract

Purpose

The purpose of this study is to compare the treatment outcomes for locally advanced resectable hypopharyngeal cancer between organ-preserving chemoradiotherapy (CRT) and surgery followed by radiotherapy (SRT).

Materials and Methods

We reviewed 91 patients with stage III/IV hypopharyngeal squamous cell carcinoma treated with radiotherapy (RT). In the CRT group (n=34), 18 patients were treated with concurrent CRT and 16 patients with induction chemotherapy plus concurrent CRT. In the SRT group (n=57), six patients were treated with total laryngopharyngectomy, 34 patients with total laryngectomy (TL) and partial pharyngectomy (PP), and 17 patients with PP, which were followed by adjuvant radiotherapy (n=41) or CRT (n=16). The median RT dose was 70 Gy for CRT and 59.4 Gy for SRT.

Results

Five-year local control (84.1% vs. 90.9%), and disease-free survival (DFS, 51.0% vs. 52.7%) and overall survival (OS, 58.6% vs. 56.6%) showed no significant difference between the CRT and SRT groups. The functional larynx-preservation rate was higher in the CRT group (88.2% vs. 29.8%). Treatment-related toxicity, requiring surgical intervention, occurred more frequently in the SRT group (37% vs. 12%). In the SRT group, TL resulted in a significantly higher DFS than larynx-sparing surgery (63.9% vs. 26.5%, p=0.027). Treatment outcome of the SRT group improved when only patients with TL were considered (n=40); however, 5-year OS (67.1% vs. 58.6%, p=0.830) and DFS (63.9% vs. 51.0%, p=0.490) did not improve significantly when compared to the CRT group.

Conclusion

Organ preserving CRT provided a treatment outcome that is comparable to SRT for locally advanced hypopharyngeal cancer, while offering an opportunity for functional larynx-preservation and reduced treatment-related toxicity.

Keywords: Hypopharyngeal neoplasms, Chemoradiotherapy, Adjuvant radiotherapy, Treatment outcome, Organ preservation

Introduction

Squamous cell carcinoma (SCC) of the hypopharynx is rare, consisting of 3%-5% of all head and neck SCC cases [1]. Hypopharynx is characterized with thin mucosal lining (< 1 cm) providing minimal barrier with propensity to submucosal spread. A rich lymphatic network of hypopharynx results in frequent lymph node metastases: ipsilateral nodal metastasis in 60%-80% and contralateral occult nodal metastasis in up to 40% [2] of patients at the time of diagnosis. Stage III or IV in 70%-85% patients are reported in large series, and 5-year survival is only 15%-45% [3].

The preservation of speech and swallowing function in the treatment of laryngeal and hypopharyngeal cancer is important. In early-stage disease, both surgery and radiotherapy (RT) are treatment options that preserve the organ and function [3,4]. For locally advanced hypopharyngeal cancer, traditional approach was laryngopharyngectomy and pharyngeal reconstruction with or without adjuvant RT, resulting in a loss of natural voice production. Addition of chemotherapy to RT alone in advanced cancer improved the outcome compared to surgery plus RT, while allowing larynx preservation [5]. However, no clear guidelines specific to hypopharyngeal cancer are available. Most evidences on laryngeal preservation are from laryngeal cancer or mixed head and neck cancer studies. A few studies reported treatment results dedicated to hypopharyngeal cancer, albeit of mixed population, including early stage cancers and advanced unresectable cancers [6].

We reviewed the treatment outcome of locally advanced resectable SCC of the hypopharynx, with comparative analysis between organ-preserving chemoradiotherapy (CRT) and radical surgery followed by adjuvant RT.

Materials and Methods

1. Patients

A total of 136 consecutive patients, who received definitive or adjuvant RT for stage III or IV SCC of the hypopharynx between January 2002 and June 2012, were reviewed. All patients underwent pretreatment evaluation, including a complete history and physical examination, head and neck examination with laryngoscopy, and computed tomography (CT) and magnetic resonance imaging of the head and neck region. All patients were staged in accordance to the 2010 American Joint Committee on Cancer (AJCC) TNM staging system (seventh edition). Patients treated with definitive RT were staged clinically, while both clinical and pathologic stages were reported in postoperative cases. Patients having T1N1 disease (n=3), distant metastasis (n=3), double primary tumor (n=11), unresectable disease or compromised speech or swallowing functions at presentation (n=4), treated with RT alone (n=2), incomplete RT (n=3), re-irradiation (n=2), and treated with trans-oral robotic surgery (n=17) were excluded, leaving 91 patients for analysis. The study protocol conforms to the Declaration of Helsinki of 1975 as revised in 1983 and was approved by our Institutional Review Board.

2. Treatment

Among 91 patients, 57 patients were treated with upfront surgery followed by adjuvant RT (SRT group), and 34 patients were treated with definitive chemoradiotherapy (CRT group). Decisions to undergo CRT were based upon age, medical co-morbidities, and patients’ preferences. The SRT group included radical surgery followed by RT (n=41) or concurrent CRT (n=16). Types of surgery included total laryngopharyngectomy (n=6), total laryngectomy (TL) and partial pharyngectomy (PP) (n=34), and partial laryngectomy with PP (n=17). The CRT group included patients treated with concurrent CRT (n=18) and induction chemotherapy, followed by concurrent CRT (n=16). Concurrent chemotherapy regimens included weekly DDP (cisplatin 40 mg/m2), weekly FP (5-fluorouracil [5-FU] 750 mg/m2, cisplatin 20 mg/m2), and TPF (5-FU 750 mg/m2, taxotere 70 mg/m2, cisplatin 75 mg/m2) every 3 weeks. Induction chemotherapy regimen consisted of FP every 3 weeks for 3 cycles, or TPF every 3 weeks for 2 cycles. All patients underwent CT-based RT planning with either 3-dimensional conformal RT or intensity-modulated radiotherapy (IMRT). The median RT dose was 59.4 Gy (range, 50.4 to 70.2 Gy) for the SRT group and 70 Gy (range, 59.4 to 72 Gy) for the CRT group. For the SRT group, neck dissection was performed for both sides of the neck. Radical neck dissection or modified neck dissection was performed for the involved neck and lateral neck dissection (selective neck dissection in 2 patients) for the clinically uninvolved neck. For the CRT group, both sides of the neck were included in the RT field. Grossly involved lymph nodes were treated with 66-70 Gy, involved cervical nodal stations with 60-63 Gy, and uninvolved nodal stations with 50-54 Gy. Treatment-related toxicities were reported in accordance to the Common Terminology Criteria for Adverse Events (CTCAE) ver. 3.0. CTCAE grade 4 voice alterations or dysphagia after treatment was considered loss of laryngeal function.

3. Statistical analysis

The two groups were compared by a chi-square test to detect the differences in proportion. Survival was calculated from the start of treatment until death or to the most recent follow-up date. Survival curves were plotted using a Kaplan-Meier method. Survival curves were compared using a log-rank test for a univariate analysis. The Cox proportional hazards model was used to assess independent predictors for survival. A p-value of less than 0.05 was regarded as statistically significant.

Results

1. Patient characteristics

Table 1 shows patient and tumor characteristics. The median age was 64 years (range, 36 to 80 years), and male were predominant (94.5%). Pyriform sinus (80.2%) was the most common subsite of the hypopharyngeal cancer, followed by pharyngeal wall (14.3%) and post-cricoid area (5.5%). Fifty-seven patients (62.7%) had T3-T4a tumors and 65 patients (71.4%) had N2-3 nodal disease. Early disease not requiring total laryngectomy (T1-2N0, T1N1) and unresectable primary tumor (T4b) were excluded in this study.

Table 1.

Patient characteristics

Characteristic Total (n=91) SRT (n=57) CRT (n=34) p-value
Median age (range, yr) 64 (36-80) 64 (39-81) 65.5 (37-81)
Sex Male 86 (94.5) 56 (98.2) 30 (88.2) 0.043
Female 5 (5.5) 1 (1.8) 4 (11.8)
Subsite PS 73 (80.2) 48 (84.2) 25 (73.5) 0.401
PW 13 (14.3) 6 (10.5) 7 (20.6)
PC 5 (5.5) 3 (5.3) 2 (5.9)
cT stage cT1 8 (8.8) 6 (10.5) 2 (5.9) 0.342
cT2 26 (28.6) 17 (29.8) 9 (26.5)
cT3 27 (29.7) 19 (33.3) 8 (23.5)
cT4a 30 (33.0) 15 (26.3) 15 (44.1)
cN stage cN0 12 (13.2) 6 (10.5) 6 (17.6) 0.618
cN1 14 (15.4) 8 (14.0) 6 (17.6)
cN2 60 (65.9) 39 (68.4) 21 (61.8)
cN3 5 (5.5) 4 (7.0) 1 (2.9)
Stage III 17 (18.7) 11 (19.3) 6 (17.6) 0.629
IV a 68 (74.7) 42 (73.7) 27 (79.4)
IV b 6 (6.6) 4 (7.0) 1 (2.9)
RT 3DCRT 73 (80.2) 51 (89.5) 22 (64.7) 0.004
IMRT 18 (19.8) 6 (10.5) 12 (35.3)

Values are presented as number (%) unless otherwise indicated. SRT, surgery plus radiotherapy; CRT, chemoradiotherapy; PS, pyriform sinus; PW, pharyngeal wall; PC, postcricoid; cT, clinical T stage; 3DCRT, 3D conformal radiotherapy; IMRT, intensity-modulated radiotherapy.

2. Survival and prognostic factors

With the median follow-up of 50 months (range, 5 to 141 months), 5-year estimated local failure-free survival (LFFS), locoregional failure-free survival (LRFFS), distant metastasis-free survival (DMFS), disease-free survival (DFS), and overall survival (OS) of all patients (n=91) were 88.3%, 76.9%, 83.3%, 52.1%, and 57.4%, respectively. In a univariate analysis, age ≤ 60 years (vs. > 60) showed a significant correlation with improved OS (p=0.049) while sex, subsite, stage, treatment group, and RT modality showed no significant correlation. Age ≤ 60 also showed a trend towards improved DFS (p=0.076) (Table 2).

Table 2.

Univariate analysis for DFS and OS

Variable No. of patients (%) DFS
OS
5-Yr DFS (%) 95% CI p-value 5-Yr OS (%) 95% CI p-value
Age (yr)
 ≤ 60 36 (40) 56.9 40.2-73.6 0.076 62.7 46.4-79.0 0.049
 > 60 55 (60) 49.1 35.4-62.8 54.2 40.5-67.9
Sex
 Female 5 (6) 80.0 44.9-115.1 0.396 75.0 32.5-117.5 0.260
 Male 86 (94) 50.3 39.3-61.3 55.0 44.0-66.0
Subsite
 PS 73 (80) 54.5 42.7-66.3 0.606 60.2 48.6-71.8 0.887
 PW/PC 18 (20) 42.9 19.2-66.6 46.2 21.5-70.9
T stage
 T1-2 34 (37) 57.8 40.7-74.9 0.539 60.0 42.9-77.1 0.641
 T3-4 57 (63) 48.8 35.3-62.3 56.2 42.7-69.7
N stage
 N0-1 26 (29) 52.6 33.0-72.2 0.652 59.3 39.5-79.1 0.517
 N2-3 65 (71) 51.9 39.2-64.6 56.6 44.1-69.1
Treatment
 SRT 57 (63) 52.7 39.4-66.0 0.991 56.6 43.5-69.7 0.713
 CRT 34 (37) 51.0 33.4-68.6 58.6 41.0-76.2
RT
 IMRT 18 (20) 35.7 12.2-59.2 0.116 53.6 27.1-80.0 0.873
 3DCRT 73 (80) 56.3 44.5-68.1 57.9 46.3-69.5

DFS, disease-free survival; OS, overall survival; CI, confidence interval; PS, pyriform sinus; PW, pharyngeal wall; PC, postcricoid; SRT, surgery plus radiotherapy; CRT, chemoradiotherapy; RT, radiotherapy; IMRT, intensity modulated radiotherapy; 3DCRT, 3 dimensional conformal radiotherapy.

3. Outcome comparison by treatment groups

Clinical features, including subsite, T stage, N stage, and overall stage, were well balanced between the two treatment groups, except for the proportion of female patients (1.8% vs. 11.8%, p=0.043) and use of IMRT (10.5% vs. 35.3%, p=0.004) (Table 1). Five-year DFS (52.7% vs. 51.0%, p=0.991) and OS (56.6% vs. 58.6%, p=0.713) showed no significant difference between the SRT and CRT groups (Fig. 1A and B). LFFS (90.9% vs. 84.1%, p=0.677), LRFFS (78.8% vs. 73.7%, p=0.893), and DMFS (80.5% vs. 88.0%, p=0.507) also showed no significant differences.

Fig. 1.

Fig. 1.

Comparison of 5-year disease-free survival (A) and 5-year overall survival (B) between the surgery followed by radiotherapy (SRT) and chemoradiotherapy (CRT) groups; comparison of 5-year disease-free survival (C) and 5-year overall survival (D) between total laryngectomy and larynx-sparing surgery in the SRT group.

During the follow-up, treatment failure occurred in 21 patients (36.8%) in the SRT group and 12 patients in the CRT group (35.3%). The first sites of failure were three local, five regional, three locoregional, eight distant, one local and distant, and one regional and distant in the SRT group, and five local, three regional, and four distant in the CRT group. Within the SRT group, one local, two locoregional, four regional, and four distant failures occurred among the 40 patients who received total laryngectomy (27.5% failure), and two local, one locoregional, one regional, one local and distant, one regional and distant, four distant failures occurred among the 17 patients who received larynx-sparing surgery (58.8% failure). Five-year DFS was significantly higher after total laryngectomy than after larynx-sparing surgery (63.9% vs. 26.5%, p=0.027), while total laryngectomy showed a trend towards improved OS compared with larynx-preservation surgery (67.1% vs. 31.8%, p=0.094) (Fig. 1C and D).

For a subgroup analysis, patients who received total laryngectomy were selected from the SRT group (the SRT/TL group, n=40) and their treatment outcome was compared with the outcome of the CRT group (n=34). Survival parameters for the SRT/TL group improved when patients who received larynx-sparing surgery were excluded from the subgroup analysis. However, no significant difference was seen in 5-year DFS (63.9% vs. 51.0%, p=0.490), OS (67.1% vs. 58.6%, p=0.830), LFFS (90.9% vs. 84.1%, p=0.677), LRFFS (83.1% vs. 73.7%, p=0.467), and DMFS (89.7% vs. 88.0%, p=0.732) between the SRT/TL and CRT groups.

4. Outcome of salvage treatment

Table 3 shows the outcome of salvage treatment among patients who had experienced local and/or regional failures. Among the 13 patients in the SRT group, only two patients received surgical resection of the recurrent primary tumor or neck nodes, and eight patients were salvaged with chemotherapy or re-irradiation. All patients died of disease progression (survival after recurrence, 1 to 10 months) except for the two patients who were salvaged successfully through re-irradiation with chemotherapy and neck dissection (survival after recurrence, 7 to 24 months). Among eight failures in the CRT group, seven patients were salvaged with dissection of the primary tumor or recurrent cervical lymph nodes. Among the seven patients treated with surgery, three were alive without disease at the time of analysis (survival after recurrence, 5 to 48 months) and three died of intercurrent death without evidence of recurrence (survival after recurrence, 4 to 23 months).

Table 3.

Failure pattern and outcome of salvage treatment

Patient No. Age (yr)/Sex Subsite Stage Treatment Failure pattern Stage at failure Salvage treatment Salvage response Current status Survival after recurrence (mo)
1 70/M PS pT1N2c P/P+RT R & D N2cM1 CTx PD DOD 1
2 63/M PW pT2N2c P/P+RT R N1 (CA invas) None n/a DOD 9
3 50/M PS pT4aN0 P/P+RT L T4aN0 Excision PD DOD 10
4 65/M PW pT2N2b P/P+RT L & R T3N1 None (conservative) n/a DOD 2
5 73/M PW pT3N1 P/P+RT L & D T4aN0M1 CTx PD DOD 4
6 54/M PW pT2N2b P/P+RT L T3N0 CCRT CR AWOD 24
7 55/M PS pT4aN2c T/L+CCRT R N1 None (refused) n/a DOD 4
8 47/M PS pT4aN2c T/L+RT R N2b CCRT PD DOD 10
9 65/M PS pT4aN3 T/L+CCRT L & R T4aN2b CTx PD DOD 4
10 63/M PS pT4aN2b T/L+RT R N2c CTx PD DOD 7
11 72/M PS pT2N1 T/L+CCRT L & R T4aN2c CCRT PD DOD 4
12 54/M PS pT4aN1 T/L+RT R N2c Neck dissection NED AWOD 7
13 57/M PS pT4aN2b T/L+CCRT L T4aN0 CTx PD DOD 5
14 66/M PS cT3N0 Induction+CCRT L T4a None n/a DOD 0
15 66/M PS cT4aN2b Induction+CCRT R N2b Neck dissection PD DOD 9
16 77/M PS cT4aN2b Induction+CCRT L T4N0 Transoral P/P NED DOOC 4
17 63/M PS cT1N2b Induction+CCRT R N1 (CA invas) Neck dissection NED DOOC 17
18 40/M PC cT4aN0 CCRT L T4a TLP NED DOOC 23
19 68/M PS cT3N1 CCRT L T4aN0 TL/PP NED AWOD 48
20 66/M PS cT4aN0 CCRT L T4aN0 TL/PP NED AWOD 45
21 57/F PC cT2N2c CCRT R N2b Neck dissection NED AWOD 5

PS, pyriform sinus; P/P, partial pharyngectomy; RT, radiotherpy; R, regional; D, distant; CTx, chemotherapy; PD, progression of disease; DOD, died of disease; PW, pharyngeal wall; CA, carotid artery; n/a, not available; L, local; CCRT, concurrent chemoradiotherapy; CR, complete remission; AWOD, alive without disease; T/L, total laryngectomy; NED, no evidence of disease; TLP, total laryngopharyngectomy; DOOC, died of other cause; PC, postcricoid; TL/PP, total laryngectomy & partial pharyngectomy.

5. Toxicity and laryngeal-function preservation rate

Treatment-related toxicities requiring surgical intervention are listed in Table 4. Wound infection and flap failure are immediate surgical complications, while esophagopharyngeal stenosis, mucocutaneous fistula, and stoma stenosis are late complications. Treatment-related toxicities were more common in the SRT group (37% vs. 12%). Table 5 shows toxicities in accordance to CTCAE ver. 3.0 after combined treatment, and grade 4 in voice alteration or dysphagia was considered loss of laryngeal function. Among the 57 patients in the SRT group, 17 retained functional larynx by avoiding total laryngectomy, allowing laryngeal function preservation rate of 29.8%. Among the 34 patients in the CRT group, 30 patients retained a functional larynx (88.2%). Loss of laryngeal function in four patients in the CRT group was due to local recurrence: three patients after total laryngectomy and one patient from wound infection after salvage partial laryngectomy.

Table 4.

Complications requiring surgical intervention

Variable SRT (n=57) CRT (n=34)
Wound infection 4 (7) 1 (3)
Flap failure 4 (7) 0
Esophageal/pharyngeal stenosis 8 (14) 2 (6)
Pharyngocutaneous fistula 1 (2) 0
Stoma stenosis 4 (7) 1 (3)

Values are presented as number (%). SRT, surgery plus radiotherapy; CRT, chemoradiotherapy.

Table 5.

Laryngeal function after treatment

Variable CTCAE grade SRT (n=57) CRT (n=34)
Voice alteration 2 3 1
3 1 1
4 40 (40)a) 3 (3)a)
Dysphagia 2 35 (33)a) 7
3 9 (7) 4
4 0 1 (1)a)

CTCAE, Common Terminology Criteria for Adverse Events; SRT, surgery plus radiotherapy; CRT, chemoradiotherapy.

a)

Numbers in parenthesis are due to total laryngectomy or salvage surgery.

Discussion

Selecting the optimal treatment strategy for locally advanced hypopharyngeal cancer needs to take into account the extent of the tumor, status of laryngeal function, and patients’ desire for voice preservation. Early stage hypopharyngeal cancer amenable to larynx preservation (most T1N0 and selected T2N0 tumors) may be treated by definitive RT alone or partial laryngopharyngectomy [3,4]. Concurrent CRT or induction chemotherapy, followed by CRT, is recommended for T4b or unresectable tumors [7]. It is the spectrum of disease that fall between these early and very advanced disease groups, namely locally advanced resectable hypopharyngeal cancer, that have several treatment options with no clear advantage of one treatment modality over another.

The current study makes a comparison between larynx preserving CRT and radical surgery followed by adjuvant RT, which are both feasible options for locally advanced resectable hypopharyngeal cancer. The 5-year DFS and OS of 52.1% and 57.4% for all patients were higher than or at least comparable to the results from previous studies [1,5,8]. In this study, the two treatment groups showed comparable DFS and OS. All patients in SRT group underwent adjuvant RT of median 60 Gy with or without concurrent chemotherapy. It is a well-known fact that postoperative RT or CRT improves tumor control in head and neck cancer patients with high risk features [9]. However, the cost of using adjuvant RT or CRT to improve disease control and survival may be substantial, namely increased treatment-related toxicities and prolongation of the total treatment time. Both treatment groups in the current study were subjected to RT; however, it is difficult to compare treatment-related complications attributable exclusively to RT, since all of the patients received multi-modality treatment. On the other hand, the SRT group experienced higher incidence of surgery-related complications, including wound infection, flap failure, stenosis, and fistula, while patients in the CRT group experienced such complications only when patients were subjected to salvage surgery after a local/regional failure (Table 4).

Another treatment-related complication, which is often overlooked, is a reduced rate of successful salvage treatment in case of treatment failure. In Fig. 1A and B, DFS curve for SRT is slightly higher than that of CRT, while OS curve for CRT is higher than that of SRT, especially through the later period of follow-up. Such reversal may have been caused by increased number of treatment-related toxicities, higher rate of unsuccessful salvage, or higher incidence of deaths unrelated to disease progression or toxicity during follow-up in the SRT group. Analysis of treatment outcome after local and/or regional failure suggests that CRT allowed more effective salvage treatment in comparison with SRT (Table 3). In the CRT group, six out of eight patients were salvaged through dissection of the primary tumor or recurrent cervical lymph nodes: salvage efforts were successful with three of these patients still alive without disease and three patients died of intercurrent death without evidence of recurrence. Outcome of salvage treatment in the SRT group was less than favorable. Eight of the 13 patients were treated with chemotherapy or re-irradiation, three patients did not receive any treatment, and only two patients received surgical resection of the recurrent tumor. All patients died of disease progression, except for the two patients who were salvaged successfully with re-irradiation and neck dissection. In a clinical setting, most patients who are treated with surgery for stage III/IV hypopharyngeal cancer also receive adjuvant RT or CRT. Options for salvage treatment after such intensive combined treatment are limited. These patients have already received radical resection of the primary tumor and/or ipsilateral or bilateral neck dissection, followed by radiation of 60 Gy or higher, which delivers maximum tolerable dose to the critical organs, such as pharyngeal swallowing muscles, spinal cord, and parotid glands. Salvage surgery or re-irradiation is extremely difficult, and chemotherapy alone, a remaining option, is often ineffective against gross recurrent tumor. On the other hand, definitive chemoradiotherapy showed disease control and survival that are comparable to the outcome of surgery plus adjuvant RT or CRT, and in the case of a treatment failure, salvage surgery often results in sustained disease control [5]. In a retrospective series, salvage surgery for failure after chemoradiotherapy has shown acceptable oncologic outcome with no local recurrence after salvage surgery [10].

There are concerns for increased toxicity from intensive chemoradiotherapy, such as impairment of pharyngeal swallowing muscles. Radiation dose to hypopharynx was associated with severe late toxicity in accordance to Radiation Therapy Oncology Group (RTOG) analysis [11], and functional outcome of CRT for head and neck cancer was not so promising, despite improved locoregional control [12]. In unsuccessful organ preservation attempts, failures in function preservation may result from either toxicity from aggressive CRT, extensive tumor infiltration into the organ at the time of diagnosis, or from progression of disease. Patients with functional impairment due to tumor infiltration should be excluded from organ preservation candidates. In this study, patients who had resectable tumor (< T4b) and intact laryngeal function were included for analysis, and outcome of larynx preserving CRT was compared to the outcome of radical surgery followed by adjuvant RT/CRT. The function preservation rate of 88.2% in the CRT group with loss of laryngeal function only due to local recurrence or complication of salvage surgery may lead to decisions favoring larynx preserving treatment options.

Previous studies on treatment outcome of head and neck cancer fail to take into account recent advances in treatment modalities and discovery of new prognostic factors. The use of IMRT allowed for a reduction of radiation-induced toxicity, improved local and regional control, and potential for improved survival in hypopharyngeal and other head and neck cancer patients [13]. The most important factors that contribute to morbidity in head and neck cancer patients undergoing intensive CRT are increased risk of dysphagia and aspiration. By more accurate delineation of target volumes and sparing of pharyngeal constrictors and supraglottic larynx, patients treated with IMRT experienced fewer swallowing problems than those treated with conventional RT [14]. Treatment deintensification in patients with human papillomavirus (HPV) positive oropharyngeal cancer is gaining interests [15]. A number of studies reported implication of HPV-positive hypopharyngeal cancer in organ preservation therapy [16,17]. Further investigations may allow deintensification in HPV-positive hypopharyngeal cancer and reduction of treatment-related toxicities while maintaining treatment outcome.

Efforts have been made to employ less than radical surgery for hypopharyngeal cancer. Partial pharyngectomy and even trans-oral resection of the tumor have been attempted with the purpose of organ preservation [3,18]. However, these limited surgery options should be explored with caution, especially in locally advanced cancer of the hypopharynx. In this study, the outcome of patients treated with partial laryngectomy and pharyngectomy was poor compared to the outcome of total laryngectomy. Close and positive resection margin was reported in six (35.3%) and five (29.4%) of the 17 patients who received larynx-sparing surgery and 11 (27.5%) and six (15%) of 40 patients who received total laryngectomy. Local failure occurred in three patients among the 40 who received total laryngectomy (7.5%) and in four among the 17 patients who received less than total laryngectomy (23.5%) (Table 3). Larynx preservation through avoidance of total laryngectomy does not seem to be effective due to its high rate of local failure. The incidence of submucosal extension is up to 58% [19], and pathological studies showed that extent of submucosal involvement measured from the edge of the tumor ranged 10-20 mm superiorly and 10-30 mm inferiorly [20,21], requiring resections margins of 3 cm inferiorly and 2 cm both superiorly and laterally. In locally advanced hypopharyngeal cancer, it is difficult to perform laryngeal preservation surgery while achieving adequate resection margins.

One of the limitations in the current study is the inclusion of a heterogeneous group of patients in the CRT group. The CRT group consists of patients treated with concurrent CRT as well as sequential CRT (induction chemotherapy plus RT or CRT). Recent reports on the induction chemotherapy for laryngeal preservation have shown equivalent outcome between sequential CRT and concurrent CRT [22,23]. The number of cases reviewed in the current study is relatively small, albeit only locally advanced resectable hypopharyngeal cancer cases are included for analysis. Disease characteristics of SCC of the hypopharynx are unique, and optimizing combined modality treatment needs to be explored further with a larger cohort of patients. In the current study, patient characteristics were well balanced between the SRT and CRT groups except for the proportion of female patients, and the use of IMRT were higher in the CRT group. In a univariate analysis, female sex and use of IMRT did not result in significant improvement in DFS and OS (Table 1). Although women have been found to achieve somewhat improved outcomes compared to men, this may in part be due to earlier-stage disease at diagnosis [24]. Moreover, the proportion of female patients (5.5%) was too small to cause a significant difference in the treatment outcome in this study. IMRT is superior over conventional RT in reducing radiation induced toxicities; however, its advantage in patient survival is unclear. In a randomized trial comparing IMRT and conventional RT for the treatment of oropharyngeal and hypopharyngeal SCC, IMRT was superior in preventing xerostomia; however, no significant differences were observed in non-xerostomia late toxicities, locoregional control or overall survival between IMRT and conventional RT [25].

Conclusion

Organ preservation is not to be confused with function preservation. For hypopharyngeal cancer, functions include voice and swallowing, as well as quality of life. In hypopharyngeal cancer with impaired laryngeal function at presentation, laryngopharyngectomy with pharyngeal reconstruction is a preferred option permeating aspiration-free deglutition and prosthetic voice instead of leaving intact but functionless larynx. However, definitive CRT may be preferred in locally advanced resectable hypopharyngeal cancer with intact laryngeal function, providing treatment outcome comparable to surgery plus RT or CRT, while shortening total treatment time and proving a salvage chance in the case of local/regional failure.

Acknowledgments

This work was supported by a faculty research grant of Yonsei University College of Medicine for 2013 (Grant No. 6-2013-0057).

Footnotes

Conflict of interest relevant to this article was not reported.

References

  • 1.Hall SF, Groome PA, Irish J, O'Sullivan B. The natural history of patients with squamous cell carcinoma of the hypopharynx. Laryngoscope. 2008;118:1362–71. doi: 10.1097/MLG.0b013e318173dc4a. [DOI] [PubMed] [Google Scholar]
  • 2.Buckley JG, MacLennan K. Cervical node metastases in laryngeal and hypopharyngeal cancer: a prospective analysis of prevalence and distribution. Head Neck. 2000;22:380–5. doi: 10.1002/1097-0347(200007)22:4<380::aid-hed11>3.0.co;2-e. [DOI] [PubMed] [Google Scholar]
  • 3.Takes RP, Strojan P, Silver CE, Bradley PJ, Haigentz M, Jr, Wolf GT, et al. Current trends in initial management of hypopharyngeal cancer: the declining use of open surgery. Head Neck. 2012;34:270–81. doi: 10.1002/hed.21613. [DOI] [PubMed] [Google Scholar]
  • 4.Jones AS. The management of early hypopharyngeal cancer: primary radiotherapy and salvage surgery. Clin Otolaryngol Allied Sci. 1992;17:545–9. doi: 10.1111/j.1365-2273.1992.tb01716.x. [DOI] [PubMed] [Google Scholar]
  • 5.Lefebvre JL, Chevalier D, Luboinski B, Kirkpatrick A, Collette L, Sahmoud T. Larynx preservation in pyriform sinus cancer: preliminary results of a European Organization for Research and Treatment of Cancer phase III trial. EORTC Head and Neck Cancer Cooperative Group. J Natl Cancer Inst. 1996;88:890–9. doi: 10.1093/jnci/88.13.890. [DOI] [PubMed] [Google Scholar]
  • 6.Chen SW, Tsai MH, Yang SN, Liang JA, Shiau AC, Lin FJ. Hypopharyngeal cancer treatment based on definitive radiotherapy: who is suitable for laryngeal preservation? J Laryngol Otol. 2008;122:506–12. doi: 10.1017/S0022215107000692. [DOI] [PubMed] [Google Scholar]
  • 7.D'Cruz A, Lin T, Anand AK, Atmakusuma D, Calaguas MJ, Chitapanarux I, et al. Consensus recommendations for management of head and neck cancer in Asian countries: a review of international guidelines. Oral Oncol. 2013;49:872–7. doi: 10.1016/j.oraloncology.2013.05.010. [DOI] [PubMed] [Google Scholar]
  • 8.Blanchard P, Tao Y, Veresezan O, Lusinchi A, Le Ridant AM, Janot F, et al. Definitive radiotherapy for squamous cell carcinoma of the pyriform sinus. Radiother Oncol. 2012;105:232–7. doi: 10.1016/j.radonc.2012.09.004. [DOI] [PubMed] [Google Scholar]
  • 9.Bernier J, Cooper JS, Pajak TF, van Glabbeke M, Bourhis J, Forastiere A, et al. Defining risk levels in locally advanced head and neck cancers: a comparative analysis of concurrent postoperative radiation plus chemotherapy trials of the EORTC (#22931) and RTOG (# 9501) Head Neck. 2005;27:843–50. doi: 10.1002/hed.20279. [DOI] [PubMed] [Google Scholar]
  • 10.Suzuki K, Hayashi R, Ebihara M, Miyazaki M, Shinozaki T, Daiko H, et al. The effectiveness of chemoradiation therapy and salvage surgery for hypopharyngeal squamous cell carcinoma. Jpn J Clin Oncol. 2013;43:1210–7. doi: 10.1093/jjco/hyt136. [DOI] [PubMed] [Google Scholar]
  • 11.Machtay M, Moughan J, Farach A, Martin-O'Meara E, Galvin J, Garden AS, et al. Hypopharyngeal dose is associated with severe late toxicity in locally advanced head-and-neck cancer: an RTOG analysis. Int J Radiat Oncol Biol Phys. 2012;84:983–9. doi: 10.1016/j.ijrobp.2012.03.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Tulunay-Ugur OE, McClinton C, Young Z, Penagaricano JA, Maddox AM, Vural E. Functional outcomes of chemoradiation in patients with head and neck cancer. Otolaryngol Head Neck Surg. 2013;148:64–8. doi: 10.1177/0194599812459325. [DOI] [PubMed] [Google Scholar]
  • 13.Al-Mamgani A, Mehilal R, van Rooij PH, Tans L, Sewnaik A, Levendag PC. Toxicity, quality of life, and functional outcomes of 176 hypopharyngeal cancer patients treated by (chemo)radiation: the impact of treatment modality and radiation technique. Laryngoscope. 2012;122:1789–95. doi: 10.1002/lary.23387. [DOI] [PubMed] [Google Scholar]
  • 14.Vergeer MR, Doornaert PA, Rietveld DH, Leemans CR, Slotman BJ, Langendijk JA. Intensity-modulated radiotherapy reduces radiation-induced morbidity and improves health-related quality of life: results of a nonrandomized prospective study using a standardized follow-up program. Int J Radiat Oncol Biol Phys. 2009;74:1–8. doi: 10.1016/j.ijrobp.2008.07.059. [DOI] [PubMed] [Google Scholar]
  • 15.O'Sullivan B, Huang SH, Siu LL, Waldron J, Zhao H, Perez-Ordonez B, et al. Deintensification candidate subgroups in human papillomavirus-related oropharyngeal cancer according to minimal risk of distant metastasis. J Clin Oncol. 2013;31:543–50. doi: 10.1200/JCO.2012.44.0164. [DOI] [PubMed] [Google Scholar]
  • 16.Joo YH, Lee YS, Cho KJ, Park JO, Nam IC, Kim CS, et al. Characteristics and prognostic implications of high-risk HPV-associated hypopharyngeal cancers. PLoS One. 2013;8: doi: 10.1371/journal.pone.0078718. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Shaughnessy JN, Farghaly H, Wilson L, Redman R, Potts K, Bumpous J, et al. HPV: a factor in organ preservation for locally advanced larynx and hypopharynx cancer? Am J Otolaryngol. 2014;35:19–24. doi: 10.1016/j.amjoto.2013.08.006. [DOI] [PubMed] [Google Scholar]
  • 18.Kuo YL, Chang CF, Chang SY, Chu PY. Partial laryngopharyngectomy in the treatment of squamous cell carcinoma of hypopharynx: analysis of the oncologic results and laryngeal preservation rate. Acta Otolaryngol. 2012;132:1342–6. doi: 10.3109/00016489.2012.700122. [DOI] [PubMed] [Google Scholar]
  • 19.Ho CM, Ng WF, Lam KH, Wei WJ, Yuen AP. Submucosal tumor extension in hypopharyngeal cancer. Arch Otolaryngol Head Neck Surg. 1997;123:959–65. doi: 10.1001/archotol.1997.01900090073010. [DOI] [PubMed] [Google Scholar]
  • 20.Harrison DF. Pathology of hypopharyngeal cancer in relation to surgical management. J Laryngol Otol. 1970;84:349–67. doi: 10.1017/s0022215100071991. [DOI] [PubMed] [Google Scholar]
  • 21.Davidge-Pitts KJ, Mannel A. Pharyngolaryngectomy with extrathoracic esophagectomy. Head Neck Surg. 1983;6:571–4. doi: 10.1002/hed.2890060105. [DOI] [PubMed] [Google Scholar]
  • 22.Forastiere AA, Zhang Q, Weber RS, Maor MH, Goepfert H, Pajak TF, et al. Long-term results of RTOG 91-11: a comparison of three nonsurgical treatment strategies to preserve the larynx in patients with locally advanced larynx cancer. J Clin Oncol. 2013;31:845–52. doi: 10.1200/JCO.2012.43.6097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Haddad R, O'Neill A, Rabinowits G, Tishler R, Khuri F, Adkins D, et al. Induction chemotherapy followed by concurrent chemoradiotherapy (sequential chemoradiotherapy) versus concurrent chemoradiotherapy alone in locally advanced head and neck cancer (PARADIGM): a randomised phase 3 trial. Lancet Oncol. 2013;14:257–64. doi: 10.1016/S1470-2045(13)70011-1. [DOI] [PubMed] [Google Scholar]
  • 24.Spector JG, Sessions DG, Emami B, Simpson J, Haughey B, Harvey J, et al. Squamous cell carcinoma of the pyriform sinus: a nonrandomized comparison of therapeutic modalities and long-term results. Laryngoscope. 1995;105(4 Pt 1):397–406. doi: 10.1288/00005537-199504000-00012. [DOI] [PubMed] [Google Scholar]
  • 25.Nutting CM, Morden JP, Harrington KJ, Urbano TG, Bhide SA, Clark C, et al. Parotid-sparing intensity modulated versus conventional radiotherapy in head and neck cancer (PARSPORT): a phase 3 multicentre randomised controlled trial. Lancet Oncol. 2011;12:127–36. doi: 10.1016/S1470-2045(10)70290-4. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Cancer Research and Treatment : Official Journal of Korean Cancer Association are provided here courtesy of Korean Cancer Association

RESOURCES