Small-cell Lung Cancer Clinical Trial
Official title:
Neoadjuvant Therapy Combined With Radical Surgery for the Treatment of Small Cell Lung Cancer (SCLC) in II and IIIA Stage
The main purpose of this study is to compare the effects of neoadjuvant with radical surgery
on the prognosis of patients with stage II and IIIA small cell lung cancer (SCLC). The
primary endpoint of this study is to observe 5-year survival, disease-free survival (DFS),
and overall survival (OS) in patients. Secondary efficacy indicators include recurrence rate,
surgical complications, resection rate, quality of life (QoL), and exploration biomarker
(tumor tissue).
This is a two-arm, open, multicentral clinical study designed to assess the disease-free
survival (DFS) and overall survival (OS) of neoadjuvant chemotherapy plus radical surgery for
stage II and IIIA small cell lung cancer (SCLC). About 300 patients will be enrolled in the
study and randomly divided into two groups of 150 individuals. The neoadjuvant with radical
surgery group received 2 to 4 cycles of neoadjuvant treatment with etoposide plus
cisplatin/carboplatin before receiving radical surgery, followed by 2 to 4 cycles of adjuvant
chemotherapy (etoposide with cisplatin/carboplatin) plus radiotherapy. Patients in the
control group are planned to receive 4 to 6 courses of etoposide plus cisplatin/carboplatin
for chemotherapy and radiotherapy.
Before chemotherapy is widely used in clinical work, surgery is the main method for the
treatment of lung cancer. However, the prognosis of patients with small cell lung cancer
(SCLC) is significantly worse than that of other histological types of lung cancer. The only
two prospective studies comparing the surgery with other treatments (surgery vs. radiotherapy
alone; induction chemotherapy + surgery vs. chemotherapy + radiotherapy) found that patients
in surgery group had a poorer prognosis. Thus, small cell lung cancer was determined to be a
non-surgically treated disease. Therefore, for patients with stage II and III A SCLC,
combined radiotherapy and chemotherapy are currently recommended. The first-line chemotherapy
regimens are etoposide plus cisplatin and carboplatin. Surgical treatment is currently only
recommended for very early stage SCLC (T1-2N0M0) with postoperative adjuvant chemotherapy,
but these patients only account for about 5% of all SCLC patients. Despite the sensitivity to
chemotherapy, the long-term survival of small cell lung cancer remains unsatisfactory. For
patients with limited SCLC, even if combined with local radiotherapy, there are still 1/4 to
1/3 of patients progressing due to recurrence of local lesions. So the status of surgical
treatment is expected to be reassessed. In recent years, retrospective analysis results of
some large databases in Europe and the United States have provided a basis for the role of
surgery in the treatment of small cell lung cancer (SCLC). It is believed that surgery should
be used as one of the treatment options for SCLC. Based on the results of prospective studies
and retrospective studies, a well-designed, phased, prospective study is urgently needed to
explore the role of surgery in the treatment of SCLC.
In neoadjuvant therapy combined with radical surgery, neoadjuvant chemotherapy is based on
the combination of etoposide and cisplatin/carboplatin. Doses of the drugs are taken from the
NCCN guideline for the recommended adjuvant chemotherapy for the limited-period SCLC: namely
etoposide 120 mg/m2 through intravenous infusion on Day 1, 2, and 3; cisplatin 60 mg/m2
through intravenous infusion on Day 1 (or carboplatin where area under the curve AUC = 5-6);
4 weeks for a cycle, with a total of 2 cycles of neoadjuvant chemotherapy. Radical surgery is
performed according to the growth of SCLC patients after neoadjuvant chemotherapy, using
lobectomy or pneumonectomy combined with mediastinal lymph node dissection or sampling. 4
weeks after surgery, chemotherapy and concurrent radiotherapy will be performed. The
chemotherapy regimen is the same with that of neoadjuvant chemotherapy, with 4 weeks as a
cycle and a total of 2 to 4 cycles. Radiotherapy and adjuvant chemotherapy are planned to be
started synchronously, the patients whose intraoperative pathology showed no lymph node
metastasis (N0) will receive prophylactic brain irradiation (PCI) treatment and adjuvant
chemotherapy synchronously. Within 10 days, the patients will receive a total dose of 25 Gy
of PCI, once a day, 2.5 Gy of brain irradiation each time. The patients whose intraoperative
pathology show that there is lymph node metastasis (N1-2) are planned to receive PCI combined
with mediastinal radiation therapy: namely the patient receive a total of 45 Gy within 3
weeks at the start of adjuvant chemotherapy, twice a day, 1.5 Gy of chest irradiation each
time, and the PCI treatment is the same with patients whose intraoperative pathology show
there is no lymph node metastasis (N0).
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