- Open Access
Multi-Institutional Analysis of Early Glottic Cancer from 2000 to 2005
© Hirasawa et al.; licensee BioMed Central Ltd. 2012
- Received: 11 April 2012
- Accepted: 25 July 2012
- Published: 1 August 2012
The purpose of this study is to analyze the outcome of patients with early glottic cancer (GC) treated with radiotherapy (RT) with or without chemotherapy at 10 institutions in the Tokai District, Japan.
Ten institutions combined data from 279 patients with T1-T2 GC treated with RT with or without chemotherapy between 2000 and 2005. The overall survival rate, disease-specific survival rate, and local control rate were evaluated in 270 patients, except for incomplete cases due to issues such as discontinuation, using the method of Kaplan-Meier and compared using the log-rank test. Results were considered statistically significant at the level of p < 0.05.
For 122 patients, the tumors were classified as T1a, while 64 patients had T1b tumors, and 84 patients had T2 tumors. In three cases of T1 tumors, the subtype was unknown. Combined chemoradiotherapy (CRT) was administered during each stage, and various chemotherapy drugs and regimens were used. The median follow-up period was 55.4 months. The 5-year LC rates for T1a, Tb, and T2 tumors in all patients were 87.9%, 82.7%, and 74.1%, respectively. The difference between T1a and T2 was statistically significant (p = 0.016). The 5-year LC rates for T1a, Tb, and T2 with CRT were 92.7%, 78.6%, and 80.7%, respectively, while the rates with radiation alone were 86.5%, 83.8%, and 64.4%, respectively. The difference between CRT and RT alone was not statistically significant in each stage.
In this survey, CRT was performed for early GC at most institutions in clinical practice. Our data showed no statistical difference in the LC rates between CRT and RT alone in each stage. However, there was a tendency for the LCRs of the CRT group to be more favorable than those of the RT group in the T2-stage.
- Glottic cancer
- Multiple institutes
Many clinical studies in the 1990s showed that concurrent chemoradiotherapy (CRT) improved therapeutic efficacy for local advanced head and neck cancers more than radiotherapy (RT) alone did [1–4]. For example, in a phase III study  of patients with locally advanced laryngeal cancer, the rate of laryngeal preservation was 84% among patients receiving RT with concurrent cisplatin. These studies had great impact on the treatment of head and neck cancers in clinical practice. In evidence-based medicine (EBM), CRT is recommended for laryngeal preservation in advanced cases.
On the other hand, in early glottic cancer (GC), RT alone has been reported to be about 80-90% effective [6–15] for local control (LC) of T1 GC and 65-80% [6, 7, 10, 13] effective for T2 GC. Some reports have shown that the LC for bulky T1 is only about 70% [14, 15]. The LC rate with treatment by RT alone for bulky T1 and T2 is insufficient. According to recently published guidelines [16, 17] for the treatment of head and neck cancer, all patients with T1-T2 laryngeal cancer should be treated, at least initially, with the intent of larynx preservation. The recommended strategies for early GC with the intent of larynx preservation are radiation therapy, transoral laser therapy, and partial laryngectomy. CRT is not recommended for early GC. However, most otolaryngologists in Japan believe that LC by RT alone is insufficient in early stage GC [18–20]. Reports recently released by several institutes in Japan [21–26] have indicated that chemoradiation for T2GC is promising and yields LC rates higher than those for RT alone. Therefore, chemoradiation for bulky T1 and T2 GC is used to improve LC in clinical practice in Japan. The details of CRT treatment for early GC, however, are unknown because no multicenter survey as a comprehensive study of the patterns of care in clinical practice has been conducted. The rates of chemoradiotherapy for early GC according to analyses of multiple institutions have been reported elsewhere . In this study, we analyzed the treatment outcomes of patients with early GC treated with RT with or without chemotherapy at 10 institutions in the Tokai District, Japan.
The Tokai Study group for Therapeutic Radiology and Oncology (TOSTRO) administered a questionnaire survey concerning radiotherapy for early GC in 2008. The questionnaire included questions about the stage of cancer (T1a, T1b, or T2 according to the 6th UICC International Union against the Cancer classification system, 2002), age, sex, performance status, histology, radiation dose, fraction size, method, total radiation dose, and combination chemotherapy among patients for whom RT was started between January 2000 and December 2005, at about the time when CRT became popular. The data from 10 institutions were recorded. This study was approved by the ethics committee of each participating hospital.
Performance status (ECOG)
Fractionation method and radiation dose in each stage
( 60–74 Gy )
( 60–70.4 Gy )
( 64–82 Gy )
( 60–82 Gy)
( 67.6-76.8 Gy )
(76.8 Gy )
( − )
( − )
CF + HF
( − )
( 54.4-76 Gy )
CF + AHF
( 68 Gy )
( 67 Gy )
( 56.5-71 Gy )
Combination rates of chemotherapy and these regimens
Combination rate (%)
Low dose CDDP (daily)
Low dose CDDP/5FU (daily)
High dose CDDP/5FU
UFT (oral antidrug)
TS-1 (oral antidrug)
The median follow-up period was 55.4 months (range, 1.7 - 96 months). LC rates were assessed from the beginning of RT until evidence of recurrence or until laryngectomy. The overall survival rate, disease-specific survival rate and local control rate were evaluated in 270 patients, except for incomplete cases due to issues such as discontinuation, using the method of Kaplan-Meier, and compared using the log-rank test. Results were considered statistically significant at the level of p < 0.05.
Local response, local control, and patterns of failure
Of 279 patients, six had finished with discontinuation or insufficient irradiation. Items from the six patients are described as follows. Two patients were interrupted for a simultaneous esophagus cancer. One case with 6 Gy was stopped by aggravation of an advanced esophagus cancer. The other completed the irradiation at 52 Gy, and surgery was performed for esophagus cancer. The 4 remaining patients interrupted for 18 Gy, 36 Gy, 52 Gy, and 53 Gy were changed into an operation, and each of these is controlled by operation. Evaluation of the primary tumor effect and a local control rate were analyzed except in these 6 patients and the 3 patients with T1 of an unknown subtype. For the reasons presented above, 270 of 279 patients were analyzed.
Local control rate and survival rate according to the staging
5-year local control rate
T1a vs. T2 p = 0.016
T1b vs. T2 p = 0.187
5-year overall survival
5-year cause-specific survival
T1a vs. T1b p = 0.013
T1a vs. T2 p = 0.006
5- year local control rate with or without chemotherapy
P = 0.416
P = 0.567
P = 0.149
Overall survival (OS) and cause-specific survival (CSS) rates
At the present time, 237 patients are living, and 33 have died. eight of the 33 died of GC. Twenty-six had intercurrent diseases, including 12 with a second primary cancer. The 5-year OS rates for T1a, Tb, and T2 were 85.9%, 90.3%, and 86.7%, respectively (Table 4). The difference between the sub-stage OS rates was not statistically significant. The 5-year CSS rates for T1a, Tb, and T2 were 100%, 93.6%, and 93.5%, respectively (Table 4).The difference between the CSS rate for T1a or T1b and that for the T2 stage was statistically significant (T1a vs. T2, p = 0.013; T1b vs. T2, p = 0.006).
There were no severe acute complications with Grade 3 or above, and no patient required hospitalization due to late complications.
The survey showed that CRT was performed for early GC at most institutions in clinical practice in Japan. The rates of combination therapy for T1a, T1b, and T2 were 23%, 22%, and 60%, respectively (Table 3, T1a vs. T2, p < 0.001; T1b vs. T2, p < 0.001). The combination rate was higher in T2 in particular. However, CRT for early GC is not reported in well-known textbooks of radiation oncology [6, 7]. Patients in the T2 stage with CRT underwent a high rate of therapy, and the 5-year LC of T2 GC was 80.7%. The outcome was favorable compared with that for radiation alone (64.4%), but there was no statistical difference between the outcomes in cases with chemotherapy and those without chemotherapy.
Recent studies have shown an improvement in LC for patients with T1 and T2 GC when total radiation is delivered following a high-dose fractionation [8, 27] or hyperfractionation schedule [28–31] over a shorter overall treatment time. In the current study, 15% of the 270 patients were treated on hyperfractionation schedules. In the T2 stage, the tendency toward hyperfractionation was stronger than that in the T1a stage (Table 2). This selection of both CRT and hyperfractionation schedules demonstrates that most otolaryngologists and radiation oncologists in Japan are dissatisfied with the results of standard RT alone in early stage GC. As otolaryngologists have to perform salvage surgery for local failure, they tend to choose combined CRT to improve the LC rate . In fact, many of the CRT regimens listed in Table 3 are used for advanced head and neck cancers. In short, we concluded that an improvement of CRT on LC of advanced head and neck cancers [1–5] had significant influence on the treatment of not only advanced cancers but also early GC in clinical practice in Japan. Several recent reports in Japan [21–26] have indicated that CRT for T2GC is promising and yields LC rates higher than those for RT alone. By means of these questionnaire surveys, we have demonstrated that CRT for T1 and T2 GC is used with the intent to improve LC in clinical practice at most institutions.
In recent papers [32, 33], concurrent systemic platinum-based chemotherapy was recommended, preferably weekly cisplatin (30 mg/m2), for patients with T2 tumors with impaired cord mobility. As suggested in these studies, the current recommended strategy for T2 GC is CRT, and CRT for early GC will likely become more common worldwide in the near future.
In this survey, CRT was administered for early GC in clinical practice at most of the participating institutions; however, whether chemotherapy is effective for patients with very early GC, such as T1a or T1b, and whether or not chemoradiation therapy for these very early cancers is an overtreatment remain controversial.
By means of a questionnaire survey regarding RT for early GC, we demonstrated that combined CRT was administered for early GC in clinical practice at most of the participating institutions. It is unknown whether chemotherapy should be combined with definitive radiotherapy for early GC. The results of this study showed no statistically significant difference in LCR between the RT group and the CRT group. However, there was a tendency for the LCRs of the CRT group to be more favorable than those of the RT group in the T2 stage. The results of this study with several limitations suggest that chemoradiation therapy might improve the local control rates of patients with T2-stage cancer.
We declare no actual or potential conflict of interest.
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