The efficacy of computed tomography imaging-based radiotherapy for external auditory canal squamous cell carcinoma

DOI: https://doi.org/10.21203/rs.3.rs-1764225/v1

Abstract

Background: External auditory canal (EAC) cancer is a rare disease for which there are no adequate evidence-based treatment strategies. Radical radiotherapy is often used as the initial treatment for EAC cancer from the viewpoint of organ preservation. This study aimed to elucidate the efficacy of radiotherapy for squamous cell carcinoma (SCC) of the EAC.

Methods: Fifteen consecutive patients with SCC of the EAC who were treated with radical radiotherapy were retrospectively analyzed. The fractional dose was 2.0 or 3.0, and the total dose ranged from 66 to 70 Gy. Three-dimensional conformal radiation therapy was performed on seven patients. Intensity-modulated radiation therapy was performed on eight patients. Patients with T1 disease were treated with radiotherapy alone. Patients with T2-4 disease were treated with chemoradiotherapy.

Results: The median follow-up period was 30.4 months. The 3 year local control (LC) rate for all patients was 51%, the disease-free survival (DFS) rate was 44%, and the overall survival (OS) rate was 73%. For T1-3 disease, the 3 year LC rate was 74%, DFS was 62%, and OS was 89%. However, for T4 disease, the 3 year LC rate was 17%, DFS was 17%, and OS was 50%. In a univariate analysis, only the T-category was a significant factor for predicting LC and DFS (p = 0.006 and 0.02, respectively). All local recurrences were within the high-dose irradiated area.

Conclusions: The results of this study suggest that chemoradiotherapy is a reasonable first-line treatment for T1-3 SCC of the EAC. However, the efficacy of chemoradiotherapy in T4 cases was inadequate. Further research is warranted to elucidate the efficacy of treatments with more intensive antitumor effects for locally advanced EAC cancers.

Background

External auditory canal (EAC) cancer is a rare disease with an incidence of only one per 1,000,000 in the general population [1]. There are no large-scale studies on the treatment outcomes for EAC cancer, and no adequate evidence-based treatment strategies.

Several previous studies concluded that surgery alone or radiotherapy alone is recommended for early-stage EAC cancer, whereas a combinatorial treatment with surgery and chemoradiotherapy is recommended for advanced EAC cancer [2-6]. However, subtotal or total temporal bone resection is highly invasive. In recent years, radical radiotherapy has often been performed as the initial treatment for advanced EAC cancer, from the viewpoint of organ preservation.

Most of the data on radiotherapy outcomes for EAC cancer are based on conventional two-dimensional conformal radiation therapy, and there is a dearth of data on computed tomography (CT)-based three-dimensional conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) [3, 7, 8]. Some studies also mention the importance of evaluating tumor progression [9, 10]. There is therefore a strong need to review the efficacy of CT-based radiotherapy.

This study aimed to elucidate the efficacy of radiotherapy for squamous cell carcinoma (SCC) of the EAC through a retrospective analysis of the outcomes of 3D-CRT or IMRT for patients with intact SCC of the EAC.

Methods

Patients

Fifteen consecutive patients with SCC of the EAC who were treated using radical radiotherapy at Gunma University Hospital between 2001 and 2021 were retrospectively analyzed. All patients were histologically diagnosed with SCC of the EAC. The Pittsburg staging system was used to determine T-category [11]. Lymph node metastases (N category) and distant metastases (M category) were classified using the 8th UICC TNM staging system for cancers of the head and neck region. The characteristics of the patients and their treatments are summarized in Table 1. The age of the patients ranged from 45 to 90 years (median 70). Their performance status according to the Eastern Cooperative Oncology Group classification was 0-1. Two patients had T1 disease, four had T2 disease, three had T3 disease, and six had T4 disease. Patients with metastatic lymph nodes localized to cervical lymph areas were included. One patient was classified as N1 and two as N2b. All patients were classified as M0. This single-institution retrospective study was approved by the institutional review board of Gunma University Hospital (approval number: HS2021-268), and a waiver for the requirement for informed consent was granted.

Table 1. Characteristics of the patients and their treatment

Total


15

Age



Range

45–90 years

Median

70 years

Sex



Male

9

Female

6

PS



0

9

1

6

T-category


1

2

2

4

3

3

4

6

N-category


0

12

1

1

2b

2

Total dose


66 Gy

8

68 Gy

1

70 Gy

6

RT technique


3D-CRT

7

IMRT

8

Concurent therapy


CDDP

7

Cetuximab

4

CDDP and DTX

2

None

2

CDDP, cysplatin; DTX, docetaxel; IMRT, intensity-modulated radiation therapy; PS, performance status; RT, radiotherapy

3D-CRT; three-dimensional conformal radiotherapy.

Treatment

All patients registered in this study underwent external beam radiotherapy planned on a Xio (Elekta, Stockholm, Sweden), Pinnacle (Pinnacle X-Ray Solutions, Suwanee, GA, USA), or Eclipse (Varian, Palo Alto, CA, USA) treatment planning system according to CT imaging (2 mm slice thickness). The gross tumor in the EAC and any metastatic lymph nodes were delineated as the gross tumor volume (GTV). Contrast-enhanced CT, magnetic resonsance imaging (MRI), or positron emission tomography-computed tomography (PET-CT) was used as the reference imaging to delineate the GTV. The clinical target volume (CTV) had at least a 5 mm margin around the GTV and included the entire lymph area where any metastatic lymph nodes were. The planned target volume (PTV) had a 5 mm margin around the CTV. The leaf margin of the multileaf collimator from the PTV was 5 mm. When the target was close to organs at risk (OAR), the leaf margin was modified to reduce the dose to the OAR. No patients received prophylactic irradiation of lymph node areas that were clinically determined to be free of metastases. Irradiation was performed with four, six, or ten megavolt linear accelerators: Synergy (Elekta), Oncor (Siemens Healthineers, Erlangen, Germany), or Trilogy (Varian). The fractional dose was 2.0 or 3.0, and the total dose was 66–70 Gy in all 15 patients. Three-dimensional CRT was performed on seven patients, and IMRT was performed on eight patients. All patients were immobilized using thermoplastic shells (Karin, Tokyo, Japan).

Two patients with T1 disease were treated with radiotherapy alone. One patient with T4 disease was treated with radiotherapy and concomitant intra-arterial cisplatin (CDDP; 150 mg/m2, four times). Twelve patients with T2–T4 disease were treated with concurrent chemoradiotherapy. Of the 12 patients who received concurrent chemotherapy regimens, six received intravenous administration of CDDP (60–80 mg/m2, weekly, three times), two received intravenous administration of CDDP (6 mg/m2, daily, 20 times) and docetaxel (DTX; 10 mg/m2, weekly, four times), and four received intravenous administration of cetuximab (initial: 400 mg/m2, 2nd–9th: 250 mg/m2, weekly). The treatment and clinical data of each patient are summarized in Supplementary Data 1.

Follow-up

After completion of radical radiotherapy, all patients were examined by radiation oncologists and otolaryngologists. The follow-up intervals and imaging modalities differed across the patients. Recurrence was diagnosed by CT, MRI, PET-CT, or tissue biopsy. Acute and late adverse events were evaluated using the Common Terminology Criteria for Adverse Events, version 4.0 [12].

Statistical analysis

The time data for local control (LC), disease-free survival (DFS), and overall survival (OS) from the start of treatment were analyzed using the Kaplan–Meier method. Univariate analyses of clinical and treatment factors were performed using the log-rank test. Statistical significance was set at ≤ 0.05. All statistical analyses were performed using Prism8 (GraphPad Software, San Diego, CA, USA).

Results

Treatment outcomes

Among the 15 patients, the follow-up period ranged from 7.6 to 120.8 months (median of 30.4 months). Eleven of the 15 patients were alive at the end of the designated observation period (Supplementary Data 1), whereas four patients had died from the primary disease. Eight patients experienced recurrence: seven had local recurrence, one had cervical lymph node recurrence, and one had concurrent local recurrence and cervical lymph node recurrence. Five of seven patients with local recurrence had T4 disease before treatment. All local recurrences were within the high-dose irradiated area, and no patient had distant metastasis. The 3 year LC rate for all patients was 51%, the DFS rate was 44%, and the OS rate was 73% (Figure 1). For patients with T1-3 disease, the 3 year LC rate was 74%, the DFS rate was 62%, and the OS rate was 89% (Figure 2). For patients with T4 disease, the 3 year LC rate was 17%, the DFS rate was 17%, and the OS rate was 50%. Representative images before and after treatment and the dose distribution for a patient with T3 disease are shown in Figure 3.

The results of the univariate analyses are shown in Table 2. T-category was the only factor showing a significant association with LC rate (T1-3: 74% vs T4: 17%, = 0.006) and DFS rate (T1-3: 62% vs T4: 17%, = 0.020). No factors showed a significant association with OS, although T-category and radiotherapy dose approached significance at = 0.071, and larger patient numbers may well have revealed significant associations.

Table 2. Treatment outcome according to the clinical and treatment factors

 

 

 



LC


DFS


OS

Factors

n

3y rate

p

 

3y rate

p

 

3y rate

p

age










≦70

8

56.3

0.59


60.0

0.27


87.5

0.25

≧71

7

42.9


28.6


57.1

Sex










female

9

50.0 

0.86


50

0.86


83.3

0.43

male

6

53.3 


55.3


66.7

T-category










T1-3

9

74.1

0.006


62.2

0.020


88.9

0.071

T4

6

16.7


16.7


50.0

PS










0

9

55.6

0.62


44.4

0.83


77.8

0.53

1

6

50


50


66.7

RT technique










3D-CRT

7

71.4

0.20


57.1

0.47


85.7

0.27

IMRT

8

25


25


62.5

Dose










<70

9

55.6

0.92


44.4

0.90


55.6

0.071

70

6

33.3

 

33.3

 

100

LC; local control rate, DFS; disease free survival rate, OS; overal survival rate, PS; perfomance status.
 RT; radiotherapy.

Toxicity

The adverse events are summarized in Table 3. Acute adverse events included four patients with G2 dermatitis, four with G3 dermatitis, one with G1 mucositis, one with G2 nausea, one with dryness in the mouth, one with a G2 taste disorder, four with G2 leukopenia, and one with G3 neutropenia. All acute adverse events improved with symptomatic treatment. The only late adverse event was a G2 hearing impairment in one patient. No patient had facial or trigeminal nerve paralysis.

Table 3. Numbers of adverse events

 



Grade 1

Grade 2

Grade 3

Grade 4-5

Acute Adverse Event





Dermatitis radiation

6

4

4

0

Alopecia

4

0

-

-

Mucositis oral

1

0

0

0

Cheilitis

1

0

0

0

Nausea

0

1

0

0

Dry mouth

6

1

0

0

Dysgeusia

6

1

0

0

White blood cell decreased

0

4

0

0

Neutrophil count decreased

0

0

1

0






Late Adverse Event





Hearing impaired

0

1

0

0

Adverse event names and grade are in accordance with the Common Terminology Criteria for Adverse Events, version 4.0.

Discussion

In the present study, we retrospectively analyzed the results of radiotherapy in 15 patients with intact SCC of the EAC. The 3 year LC rate for all patients was 51%, the DFS rate was 44%, and the OS rate was 73%. In the univariate analysis, T-category was found to be a significant prognostic factor for LC and DFS. The 3 year LC, DFS, and OS rates in T1−3 cases were 74%, 62%, and 89%, respectively. However, in T4 cases, the 3 year LC, DFS, and OS rates were 17%, 17%, and 50%, suggesting that the efficacy of chemoradiotherapy for T4 cases was inadequate. Direct comparison with previous publications is difficult because of the inclusion of inner ear cancer or differences in stage classification. However, most studies demonstrated that T4 cases showed a poor prognosis after treatment (Supplementary Data 2).

Takenaka et al. performed a meta-analysis of data from 274 patients who were treated with chemoradiotherapy (and surgery) for EAC cancer [13]. They concluded that the treatment outcomes of chemoradiotherapy without surgery in T3−4 cases were comparable with those of surgery with postoperative radiotherapy, and that T4 cases had a significantly poorer prognosis than T3 cases. These findings are consistent with the results of the present study, in which the T4 cases had a poorer prognosis than the T1−3 cases (Fig. 3, Supplementary Data 2). In the present study, the LC rate of T4 cases was low (17%), and all five recurrences in T4 cases occurred in the high-dose area within the irradiation field. This suggests that T4 cases are resistant to X-rays, and that the chemoradiotherapy for T4 cases showed insufficient local efficacy. To address this issue, dose-escalation or more intense modalities are needed. For example, carbon-ion radiotherapy is a promising modality with a strong antitumor effect on X-ray-resistant tumors [14]. Koto et al. reported the treatment outcomes of carbon-ion radiotherapy for T3−4 squamous cell carcinoma of the EAC and middle ear [15]. Of the 13 patients in their study, three had T3 tumors and ten had T4 tumors. The LC rates at 1 and 3 years were 72% and 54%, respectively, and the OS rates were 70% and 40%. Although most of the patients had T4 tumors, the LC rate of carbon-ion radiotherapy appeared to be favorable compared with other studies using X-ray-based treatment, including the present study (Supplementary Data 2).

Several studies on treatment strategies for EAC cancer concluded that a combination treatment of surgery and postoperative radiation was the most curative for T2−3 disease [3, 5, 6, 16, 17]. However, adverse events from surgery are not uncommon [3, 18]. In cases with middle ear cavity invasion, subtotal temporal resection is often performed, and the facial nerve and inner ear are resected together. Generally, facial paralysis or hearing impairment caused by surgery does not recover [19]. In the present study, patients with T2−3 disease were treated with chemoradiotherapy without surgery. Only one patient with T2 disease experienced local recurrence, and no patients developed a grade 3 or worse later adverse event. Although the number of T2−3 cases in our study was too small to compare the two treatment strategies, considering the balance between efficacy and toxicity, chemoradiotherapy as a primary treatment may be a reasonable choice for T2−3 cases.

The optimal regimen for chemotherapy remains unknown. In the present study, patients with T2−4 tumors were treated by radiotherapy combined with concurrent CDDP, CDDP and DTX, or cetuximab. In the group who underwent radiotherapy with CDDP, there were three cases of T2 disease, two cases of T3 disease, and three cases of T4 disease. The CDDP was administered weekly, and the total dose was at least 200 mg/m2. In the T2–3 cases, only one out of five patients experienced local recurrence. A previous study recommended a total CDDP dose of more than 200 mg/m2 for nasopharyngeal cancer [20]. The results of the present study suggest that the total CDDP dose should also be more than 200 mg/m2 for EAC cancer. Of the two patients who underwent radiotherapy with CDDP and DTX, one had T2 disease and one T4 disease, and both achieved CR. It should be noted that among the T4 cases, only the combination of radiotherapy with CDDP and DTX resulted in CR. However, it is important to interpret this result carefully because only two patients underwent this treatment. Radiotherapy with cetuximab was also performed in T3−4 cases. One patient with T3 disease achieved CR, and their follow-up was terminated after 5 years. Two patients with T4 disease experienced local recurrence at a relatively early period (4.4 and 7.7 months), and the treatment effect of radiotherapy with cetuximab appears to be insufficient for T4 disease.

In the present study, acute adverse events improved quickly, while late adverse events did not improve. One patient with T3 disease (patient number 7 in Supplementary Data 1) experienced G2 hearing impairment as a late adverse event (Table 3). Marks et al. showed that the mean dose to the cochlea should be less than 45 Gy to avoid hearing impairment [21]. In our case, the mean dose to the cochlea was 64 Gy because the tumor was very close to the inner ear, and high-dose irradiation to the cochlea was unavoidable, despite using an IMRT technique. Hearing impairment should be avoided as it is directly linked to worse quality of life, but tumor localization can make it difficult to avoid hearing impairment in some cases, especially in T3–4 cases with inner ear invasion. When treating such patients, clinicians need to fully explain the possibility of hearing impairment at the time of informed consent. Brain necrosis, bone necrosis, and soft tissue necrosis, which have all been reported in previous studies, did not occur in the present study [8, 17].

One limitation of the present study is its single-institution retrospective design with a small number of patients. Another limitation is the variation in treatment methods in terms of beam delivery technique, radiation dose, and combined systemic therapy. Further prospective studies using unified radiotherapy and concurrent chemotherapy are warranted.

Conclusions

We retrospectively analyzed the treatment outcomes of CT-based radiotherapy in 15 patients with SCC of the EAC. The results of the present study suggest that chemoradiotherapy is a reasonable first-line treatment for T1−3 SCC of the EAC. However, the efficacy of chemoradiotherapy in T4 cases is inadequate. Further research is warranted to elucidate the efficacy of treatments with more intensive antitumor effects for locally advanced EAC cancers.

Abbreviations

CDDP: cisplatin; CR: complete response; CT: computed tomography; CTV: clinical target volume; DFS: disease-free survival; DTX: docetaxel; EAC: external auditory canal; GTV: gross tumor volume; IMRT: intensity-modulated radiotherapy; MRI: magnetic resonance imaging; OAR: organs at risk; OS: overall survival; PET-CT: positron emission tomography-computed tomography; PTV: planning target volume; SCC: squamous cell carcinoma; 3D-CRT: three-dimensional conformal radiation therapy.

Declarations

Ethics approval and consent to participate

The treatment protocol for the current study was reviewed and approved by the Gunma University Institutional Review Board, and all patients signed an informed consent form before the initiation of therapy.

Consent for publication

Not applicable.

Availability of data and materials

The dataset generated and/or analyzed during the current study is not publicly available because it contains personal information, but anonymized data are available from the corresponding author on reasonable request.

Competing interests

The authors declare no conflicts of interest.

Funding

This research received no external funding.

Authors’ contributions

Conceptualization, Naoto.O., A.M.; investigation, Naoto.O., A.M.; patient treatment, Naoto.O., A.M., H.Y., K.O., N.K., Naoko.O., H.K.; writing—original draft preparation, Naoto.O., A.M.; writing—review and editing, A.M., H.Y., K.O., N.K., Naoko.O., H.K., T.O.; visualization, N.O.; supervision, H.K., T.O.; project administration, T.O.; funding acquisition, T.O.

Acknowledgments

We wish to thank all the patients who participated in this study and our colleagues at the Department of Radiation Oncology, Gunma University Graduate School of Medicine. We would like to thank Bioedit (www.bioedit.com) for providing assistance in English-language editing.

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