Background
Small cell lung cancer (SCLC) comprises 10%–20% of all lung cancers [
1]. However, surgery is not appropriate in most SCLC patients, and only about 5% of SCLCs are considered to be surgically resectable [
2]. In the case of postoperative SCLC with regional lymph node metastasis, European Society for Medical Oncology guidelines [
3] and Japanese consensus treatment guidelines recommend adjuvant chemotherapy, with adjuvant chemoradiotherapy as an alternative option, while National Comprehensive Cancer Network guidelines recommend adjuvant chemoradiotherapy, but also note the lack of any data to support this recommendation [
4]. The rarity of resectable SCLC means that, to the best of our knowledge, no prospective studies have compared postoperative adjuvant chemotherapy and chemoradiotherapy in patients with SCLC, and the optimal treatment thus remains unclear, especially in patients with regional lymph node metastasis.
The aim of this study was to compare the prognosis of patients with SCLC diagnosed with regional lymph node metastasis treated with postoperative adjuvant chemotherapy or chemoradiotherapy, using information from a national inpatient database in Japan.
Methods
Data source
The Diagnosis Procedure Combination (DPC) database [
5] is a national inpatient database in Japan, covering approximately 50% of acute-care inpatients. It includes data on the following: patient age, sex, body height and weight (body mass index), primary diagnosis, TNM classification, Charlson comorbidity index, and Barthel index on admission; operative procedures, chemotherapy drugs, and radiotherapy during hospitalization; and discharge status. This study was approved by the Institutional Review Board of The University of Tokyo. The board waived the requirement for informed patient consent because of the anonymous nature of the data.
Patient selection
We retrospectively collected data for patients with SCLC defined by the International Statistical Classification of Diseases and Related Health Problems-10th revision (ICD-10), who underwent surgery to remove one or more lung lobe(s) because of malignant lung cancer, between July 2010 and March 2015. We excluded patients aged ≤17 years and patients with a history of other cancers at the time of lung surgery. We selected patients who were diagnosed with N1–2 lymph node metastasis at their first adjuvant chemotherapy, which included agents such as cisplatin, carboplatin, etoposide, or irinotecan, within 3 months after surgery. We further selected patients who received radiotherapy for ≥17 consecutive days within 5 months after surgery. Patients who received both chemotherapy and radiotherapy were defined as the adjuvant chemoradiotherapy group, and patients who received chemotherapy alone were defined as the adjuvant chemotherapy group.
Primary outcome
The primary outcome of this study was recurrence-free survival, defined as the time to any first event including relapse or death. Relapse was defined as: gamma-knife therapy starting >3 months after surgery; radiotherapy starting >9 months after surgery; diagnosis of distant metastasis (ICD-10 codes, C40, C41, C71, C72, C77, C787, C793 and C797); chemotherapy with the above-mentioned four drugs after >9 months; and chemotherapy with topotecan or amrubicin.
Statistical analysis
Patient characteristics were compared between the groups using χ2 tests. Survival curves were constructed using the Kaplan–Meier method and compared between the groups using log-rank tests. Recurrence-free survival was compared between the groups by multivariable Cox regression analysis, after adjusting for patient backgrounds. The threshold for significance was P < 0.05. All statistical analyses were performed using SPSS version 22.0 (IBM SPSS Inc., Armonk, NY, USA).
Discussion
This study revealed no significant difference in prognosis between patients with SCLC diagnosed with N1-2 lymph node metastasis treated with postoperative adjuvant chemotherapy or chemoradiotherapy. To the best of our knowledge, this is the first study to provide evidence of treatment outcomes in these patients in a nationwide clinical setting.
An earlier study by the National Cancer Institute using information from the Surveillance, Epidemiology, and End Results database reported a median survival of 25.0 months in patients with stage II SCLC who underwent lung resection [
6]. However, the current study had the advantage of including information not available in the previous study, including information on chemotherapy drugs, TNM classification, body mass index, Charlson comorbidity index, and Barthel index, thus allowing the prognostic effects of adjuvant chemotherapy and chemoradiotherapy to be compared after controlling for patient backgrounds. Patients with end-stage SCLC are often discharged to home care, hospices, nursing homes, or community hospitals. However, the DPC database only contains records of deaths occurring in-hospital, and we were therefore unable to follow-up all deaths outside the participating hospitals or home care. In the survival analyses of recurrence-free survival, discharge to another hospital or home was regarded as censored.
Some studies have suggested that resected patients receiving adjuvant chemotherapy had more favorable outcomes than non-resected patients receiving chemoradiotherapy [
7,
8], possibly because surgery provides more effective local control than radiotherapy. The current study showed that adjuvant chemoradiotherapy had no clinical advantage over chemotherapy. Therefore, we were unable to demonstrate the treatment effect of additional radiotherapy in patients with SCLC who underwent lung resection followed by adjuvant chemotherapy. The lack of a significant difference in terms of recurrence-free survival suggests that chemotherapy alone may be preferable to adjuvant chemoradiotherapy, taking into consideration the potential adverse effects of chemoradiotherapy [
9]. However, the present study was a retrospective, observational study, and further randomized clinical trials are needed to address this issue.
The present study also showed that some patients with SCLC received non-standard primary regimens in clinical practice. Although most patients received at least one cycle of chemotherapy containing cisplatin or carboplatin, some received neither etoposide nor irinotecan. This may have been because of the patient’s choice of chemotherapy drugs, or because of trials of new therapies for SCLC in some hospitals.
There were several limitations of this study associated with a lack of information on the pathological status of the dissected lymph nodes, the intent and detailed method of radiotherapy, and the severity of postoperative symptoms. Furthermore, the selection bias in choosing patients for adjuvant chemotherapy or chemoradiotherapy was unknown and might have affected the outcomes. Although it is generally assumed that surgery to remove one or more lung lobe(s) in patients with malignant lung cancer included complete lung resection and lymph node dissection, if more patients in the adjuvant chemoradiotherapy group had positive surgical margins or incomplete lymph node resection, this could have biased the results of our study against chemoradiotherapy. Furthermore, strong trends toward better outcomes in N2 patients in the adjuvant chemotherapy group may have been associated with the smaller number of patients with multiple N2, compared with the chemoradiotherapy group. Data on radiation field, dose, and intent of radiotherapy were also unavailable in the database. However, adjuvant thoracic irradiation usually comprises ≥15 daily fractions, and prophylactic cranial and other palliative irradiation usually involves no more than 10 daily fractions. We therefore defined adjuvant radiotherapy as radiation therapy lasting ≥17 consecutive days, within 5 months after surgery. This definition of adjuvant chemoradiotherapy was used to try and exclude most other palliative radiotherapies. The first course of chemotherapy or chemoradiotherapy for patients with SCLC is generally administered during hospitalization in Japan. Thus, most postoperative SCLC patients treated with adjuvant chemotherapy or chemoradiotherapy were likely to be included in our study. Patients may be followed up at the same hospital where they underwent lung resection, and may be admitted to the same hospital for examination and treatment of cancer relapse. This study may therefore have captured the initiation of chemotherapy or chemoradiotherapy and cancer relapse adequately, though lack of outpatient data may have biased the results.
Despite these limitations, recurrence-free survival in the adjuvant chemotherapy group in our study was similar to that in a previous prospective study [
7], which also reported a 5-year survival of about 40% in stage II-IIIA SCLC patients with postoperative adjuvant chemotherapy.
Acknowledgements
Not applicable.