Radiotherapy for small cell carcinoma of the esophagus: outcomes and prognostic factors from a retrospective study
Small cell carcinoma of the esophagus (SCCE) is characterized by its progressive feature and poor prognosis. There is no consensus on a standard therapeutic modality for SCCE. In this study, we aimed to characterize the outcomes of primary SCCE patients treated by radiation therapy as part of treatment and investigate prognostic factors.
We retrospectively analyzed the data of 42 SCCE patients who were treated by RT as part of treatment at the Sun Yat-sen University Cancer Center from 2001 to 2014. The Kaplan-Meier and log-rank method were used to analyze survival. Cox’s hazard regression model was applied to determine prognostic factors.
Of the 42 enrolled patients, 25 had limited disease (LD) and 17 with extensive disease (ED). The overall response rate (CR + PR) was 60.0% (21/35). The median overall survival time (OS) for whole and LD group were 12.9 and 36.8 months. The 1-, 3- and 5-year OS rates of the whole cohort were 64.9, 31.3, and 13.9%, respectively. OS was significantly longer in patients with ECOG performance score (ECOG PS) < 2 (p = 0.001), lesion length ≤ 5 cm (p = 0.001), and LD (p = 0.049). In the patients with LD, multivariate analysis indicated that combined with chemotherapy (P = 0.046) and higher radiation dose (P = 0.027) predicted better prognosis in OS. The overall rate of grade 3–4 toxicities in the whole cohort was 37.5%. In total, 65% (17/26) patients with recurrent disease died with the metastasis with or without the primary recurrence.
RT was one of the effective and safe treatments for locoregional control of SCCE. Lower ECOG PS score, shorter lesion length, treated with chemotherapy, and a higher dose of RT were identified as favorable independent prognostic factors.
KeywordsSmall cell carcinoma of esophagus Radiation therapy Chemotherapy IMRT Prognosis
3-Dimensional Conformal Radiotherapy
Clinical target volume
- ECOG PS
The Eastern Cooperative Oncology Group Performance Status Scale
Gross tumor volume
Intensity Modulation Radiated Therapy
Planning target volume
- RECIST 1.1
Response Evaluation Criteria in Solid Tumors 1.1
Squamous cell carcinoma
Small cell carcinoma of the esophagus
Small-cell carcinoma is one kind of highly malignant neoplasm that usually originates from the lung. The first case of primary small cell carcinoma of the esophagus (SCCE) was reported by Mckeown in 1952 . SCCE is characterized by its aggressive feature with poor prognosis and is distinct from the squamous cell carcinoma or adenocarcinoma of the esophagus, but similar to small cell carcinoma arising from lungs or other organs. A consensus on the standard therapeutic modality for SCCE has not been established, but based on retrospective studies, a multimodal therapeutic approach combining surgery, radiotherapy (RT), and chemotherapy is recommended [2, 3]. When combined with chemotherapy, RT is considered a major local therapy approach for treating patients with localized or locoregional disease. Though RT is common in clinical practice in western countries, esophagectomy is more widely used compared to RT as the treatment for localized SCCE in China [2, 4]. A previous retrospective study of all the SCCE cases in our center from September 1990 to June 2011 showed that of 64 SCCE patients, only 15 (26.7%) patients received RT . Due to increasing evidence showing its non-inferiority to esophagectomy, RT technology was developed over the years in China for treating SCCE. In this retrospective study, we focused on SCCE cases who had received RT and explored their outcomes and prognostic factors.
Patients and methods
We retrospectively reviewed 9547 cases of esophagus carcinoma at Sun Yat-sen University Cancer Center from June 2001 to December 2014. Among these cases, 110 (1.15%) patients were pathologically diagnosed as SCCE. Of these 110 patients, 45 (40.9%) had received RT as part of treatment. The inclusion criteria were as follows: 1) age between 18 and 75 years; 2) Eastern Cooperative Oncology Group (ECOG) performance status (PS) score ≤ 3; 3) received RT as part of the treatment; and 4) absence of previous thoracic RT. Finally, 42 patients with complete medical records were enrolled for analysis in this retrospective study.
Medical records retrieved were examined for medical history and physical examination; complete blood count and serum chemistry profile; electrocardiogram; barium-swallow examination; contrast-enhanced computed tomography (CT) scan of the neck, chest and upper abdomen, endoscopic ultrasound, ultrasound of the cervical lymph node, PET-CT, radioactive isotope bone scans, if available. The disease stage was presented as either a limited-stage disease (LD) or an extensive-stage disease (ED) according to the Veteran’s Administration Lung Group’s 2-stage classification scheme (VALSG) for primary pulmonary small cell lung cancer (SCLC) . LD is defined as a tumor confined within a localized anatomical region, which can be safely encompassed within a radiation field and ED is defined as a tumor outside of the local regional region. Tumor location is defined based on the UICC 1987 standard.
The Ethics Committee of Sun Yat-sen University Cancer Center reviewed and approved this study, which was performed according to the principles of the Helsinki Declaration. Informed consent was obtained from each patient for the collection of clinical information at the first visit.
For RT administration, a vacuum cradle for immobilization was made with the patient in a supine position. Patients were scanned from the first cervical vertebra (C1) to the third lumbar vertebra (L3) level. CT scan was performed with 5 mm thick slices. The gross tumor volume (GTV) consisted of tumor shown by CT scans or PET/CT or endoscopy. Lymph nodes were defined as positive nodes if it exhibited any of the following features on CT: short axis ≥ 10 mm, distribution in a cluster of lymph nodes, infiltrative margin, or central necrosis. Lymph nodes that demonstrated high uptake on the PET/CT scan were also included in the GTV, regardless of size. The clinical target volume (CTV) comprised the original tumor or anastomosis site, supraclavicular, and station 1–5 and 7 lymph nodes. The plan target volume (PTV) 1 was defined as the GTV plus a margin of 5 mm and PTV2 was defined as the CTV plus a margin of 5 mm in all directions, respectively. Three-Dimensional Conformal Radiation Therapy (3D-CRT) treatment plans were calculated by Pinnacle planning system and Intensity Modulation Radiated Therapy (IMRT) treatment plans were calculated by the Monacle planning system. All patients were treated with a 6-MV linear accelerator. The prescribed dose was generally 50–66 Gy for PTV1 and 42–50 Gy for PTV2. Dose constraints for critical organs were spinal cord < 45 Gy; mean lung dose< 17 Gy and lung dose V20 < 30%.
Tumor response was assessed using Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1). The Overall Survival (OS) time of patients was calculated from the start of initial treatment to the date of death or last follow-up and calculated and compared using the Kaplan–Meier method and the log-rank p test. Multivariate analysis was performed using Cox regression to analyze the prognostic factors. P value< 0.05 was considered significant. All statistical analysis was performed using SPSS 22.0 software.
Patient demographic and baseline characteristics
Patient information and tumor characteristics
Age (55; range: 42–72 years)
< 60 years
≥ 60 years
Coexisting with SCC
Coexisting with Adenocarcinoma
Radiation Dose(58; Range: 42-66Gy)
Treatment regimen of 42 SCCE patients
R + C
S + R ± C
Tumor response rate and survival
Tumor response was assessed at two to 3 months after the completion of treatment. Among those 35 patients who are eligible for response evaluation (seven patients with adjuvant therapy after surgery were excluded), five patients achieved complete remission (CR) and 16 achieved partial remission (PR). The overall response rate (CR + PR) was 60.0% (21/35). Eight patients achieved stable disease (SD), and six achieved progressive disease (PD). The overall disease control rate is 83%(29/35). There was no evidence of relapse in seven patients who received adjuvant RT after esophagectomy.
At the time of last observation, 16 patients survived with or without the primary disease, while 26 patients died of tumor recurrence or metastases. In patients with LD, four patients died of local recurrence disease, and eight patients died of metastases disease. Similarly, in patients with ED, five patients died of local recurrence disease and nine patients died of metastases disease. In total, 65% (17/26) patients died with the metastasis with or without the primary recurrence.
Univariate analysis and multivariate Cox regression for prognosis of 42 SCCE patients
All cohort(n = 42)
LD(n = 25)
HR (95% CI)
HR (95% CI)
Age (< 60 years vs. ≥60 years)
Sex (Male vs. Female)
ECOG PS (≥2 vs. < 2)
Lesion length (> 5 cm vs. ≤5 cm)
Smoking history (Yes vs. No)
Risky diet (Yes vs. No)
Stage (ED vs. LD)
Treatment (R + C vs. R Only)
Technology (3DCRT vs. IMRT)
RT dose (<56Gy vs. ≥56Gy)
Most treatment-related toxicities were tolerable and reversible and of grade 1 to 2. Of the 24 patients who received radiation combined with chemotherapy, grade 3–4 leukocytopenia occurred in five (20.8%) patients (four with LD and one patient with ED). Other grade 3–4 toxicity included thrombocytopenia (n = 1), esophagitis (n = 1), and nausea and vomiting (n = 2). The overall rate of grade 3–4 toxicities was 37.5%. Toxicity was lower in 15 patients who received only radiation, of which four (25%) experienced grade 3–4 toxicity including leukocytopenia (n = 1), esophagitis (n = 2), and nausea or vomiting (n = 1). There was no radiation-induced lung injury or treatment-related death.
Several studies have shown that SCCE only accounts for 0.4–2.8% of primary esophageal carcinoma [6, 7]. Reports of increasing incidence of SCCE have come in from East Asian countries, including China and Japan, reaching global trends [8, 9]. Indeed, a comparison with our previous findings in 2012, the incidence rate of SCCE in our center rose slightly from 0.94 to 1.15%, perhaps due to the improvement in diagnostic pathology . One study described discrepancies in tumor characteristics and therapeutic modalities in different ethnic groups . For instance, the most common primary location of SCCE was the lower thoracic esophagus in the U. S population, while the Chinese population tends to have middle thoracic SCCE. Localized treatment modalities also differ between these two countries. Esophagectomy was the most popularized local therapy in China, which was performed in ~ 52 to 85% of patients [10, 11], whereas approximately half of the U.S. patients were reported to receive RT as the principal local therapy, regardless of chemotherapy . Nevertheless, more Asian patients were diagnosed with earlier localized disease and the lack of feasibility of RT during the last few decades might explain this difference. We previously reported that 26.7% of patients in our center received RT as one part of the treatment, which increased to 40.9% in the current study, suggesting that RT combined with or without chemotherapy gained more popularity among treating physicians for SCCE recently .
The role of RT on the local control of SCCE is not well-illustrated because of the lacking of the information about the response rate in previous reports. In our study, the overall response (CR + PR) rate of 60% was obtained, suggested that RT alone or combined with chemotherapy was an effective option for locoregional disease control. Also, most published studies focus only on OS, but not PFS or DFS, leading to difficulty in evaluating the efficiency of RT in long-term local control. Our result indicated that the high response rate achieved by RT contributes to the survival benefit through long-duration remission. The median OS was 12.9 months in this study which was similar to previous reports (8–16 months) [2, 4]. The reported OS rates at 1-, 3- and 5-years in SCCE patients who received multiple therapeutics varied from 30 to 74.8%, 13.2–38.8%, and 7.8–18% respectively, and the survival data obtained in our study are almost equivalent to the best outcome [10, 11, 12, 13).
As the two main local therapeutic modalities, surgery and definitive RT, especially for LD SCCE, show vast discrepancies when conducted in individuals with different demographics and clinical characteristics. While Sun et al., retrospectively reported 1-, 3- and 5-year OS rates of 50.7, 13.7 and 8.2% in 73 SCCE patients treated by surgery, these rates are lower than findings we reported previously and here . However, in an analysis of the National Cancer Data Base, esophagectomy was associated with the best OS for patients with localized or local-advanced SCCE comparing to chemoradiation or chemotherapy alone. The 1-, 3- and 5-year OS rates reported in another study were higher than those obtained in our study, but the median overall OS of LD-SCCE patients who received surgery was only 18.0 months, which was consistent with other report but shorter than current analysis [15, 16]. Interestingly, another study comparing the RT and chemotherapy (RT + CT) with surgery and chemotherapy (S + CT) in the management of LD SCCE indirectly favored RT, in which a significantly longer OS with RT + CT compared to S + CT (33.0 vs. 17.5 months, p = 0.02) was observed . To sum up, there is a lack of consensus on whether surgery or RT should be the localized treatment modality for SCCE, especially for LD-SCCE, which must be further investigated in prospective controlled studies.
Here we also have shown that RT is also beneficial for the survival of patients with ED SCCE. Similar to the result of the current study, one accumulative analysis of the SEER data demonstrated that the addition of RT leads to a reduction of 30% risks of death in distant stage ESCC. Despite these promising results, the survival benefit of SCCE from RT was much poorer than that from squamous carcinoma or adenocarcinoma of the esophagus, suggesting the need for novel treatment modalities strategy for SCCE [17, 18]. Chemotherapy is one of the most important modalities for SCCE, it was well-acknowledged as the fundamental part of the multimodalities therapy and improved the survival both in LD and ED patients [13, 19]. In our study, the survival of RT + CT group prone to be longer compared to RT alone but without statistically significant difference (p = 0.088) of the whole cohort. In patients with LD, RT + CT is correlated with better survival (p = 0.046). By summary, the combination of RT and chemotherapy will further improve the survival of SCCE patients. Distant metastasis is the major failure pattern of SCCE despite stages. In accordance with this, over half (65%) of patients were failed in the distant control of our study, which further suggested that systemic chemotherapy is essential for the long-term control of SCCE.
The principles of chemotherapy for SCCE is poorly illustrated. According to a study focusing on the SCCE in locoregional disease treated with RT ± chemotherapy, more cycles of chemotherapy improved the survival, while the regiment and sequence of RT and chemotherapy had no impact on the disease control . Unfortunately, due to a relatively small size of patients received chemotherapy in our study, we could not yield a reliable analysis to answer these questions. There is no consensus on the practice of RT neither, especially the technology and dose in SCCE, which are based on routine RT for SCLC. The dose used in this study is similar to the common RT doses ranging from 40-70Gy based on previous case reports and retrospective studies [20, 21, 22]. We found that a higher dose of RT (≥56Gy) is correlated with better survival. However, Jeene et al. reported that no effect of radiotherapy dose on overall survival in the multivariable analysis, while as it was mentioned, the results should have to be interpreted with caution, as only 5 patients received a higher dose of RT in that study. Despite knowing that IMRT is better at target positioning and avoiding errors for esophageal cancer compared to conventional RT [23, 24]. There are no comparative studies of these two RT technologies for SCCE treatment. We did not find significant differences between the OS of patients treated with 3DCRT or IMRT, which might be related to the small sample size of this study.
The main shortcomings of the current study are the small sample size and its retrospective nature. Nevertheless, compared to other studies, we only enrolled the patients who received RT as one part of the treatments and addressed on the local-control role of RT in SCCE by using consistent detailed individual patient data from a single institution. However, the confounding effect caused by enrolling patients with other treatment strategies cannot be overlooked.
Due to its low incidence, prospective and randomized studies on exploring the novel treatments for SCCE is limited. A phase II study (NCT03811379) in our center was initiated in 2018 and is currently recruiting patients to explore the efficacy of toripalimab (PD-1 antibody) as a monotherapy for patients with SCCE, which provides a hint for the novel exploration of a combination of immunotherapy and radiation therapy for SCCE.
In summary, RT was one of the effective and safe treatment options for locoregional control of SCCE. Lower ECOG PS score, shorter lesion length, treated with chemotherapy, and a higher dose of RT were identified as favorable independent prognostic factors.
All authors should have made substantial contributions to all of the following: (1) BQC, HY, HLM, BQ, YJZ, and YHH contributed to the conception and design of the study. (2) BQC, YH, QQL, and HLM contributed to acquisition of data. (3) BQC, HY, YJZ, and QQL analyzed and interpreted data. (4) BQC and YJZ drafted the article and submitted. All authors revised and approved the final manuscript.
This work was supported by Guangdong Esophageal Cancer Institute Science and Technology Program (No.Q201807).
Ethics approval and consent to participate
This study was approved by the Ethics Committee of Sun Yat-sen University Cancer Center. Written informed con- sent was obtained from the patient for the publication of this report.
Consent for publication
The authors declare that they have no competing financial interests.
- 19.Zhang WN, Chen YP, Chen L, Guo R, Zhou GQ, Tang LL, et al. The Clinical Utility of Plasma Epstein-Barr Virus DNA Assays in Nasopharyngeal Carcinoma: The Dawn of a New Era? Medicine (Baltimore). 2015;94(20).Google Scholar
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