Background
Lung cancer represents a major health problem world-wide. It is the leading cause of cancer-related death in Europe [
1], with a 5-year survival of approximately 15% for all stages [
2]. Non-Small Cell Lung Cancer (NSCLC) represents approximately 80-85% of all lung carcinomas. The vast majority of patients are diagnosed with advanced, unresectable disease (stage IIIB/IV) which remains incurable with a 5-year survival rate of less than 5% [
3].
Front-line chemotherapy for the treatment of patients with inoperable locally advanced or/and metastatic NSCLC has been substantially improved during the last decade with the introduction of new cytotoxic agents such as gemcitabine, vinorelbine, gemcitabine, paclitaxel, docetaxel and pemetrexed; combination of these agents with a platinum compound represents the standard of care for front-line treatment [
4]. Nevertheless, several individual phase III trials have demonstrated that there is no difference between platinum-based and platinum-free doublets in terms of overall response rate (ORR), time to tumor progression (TTP) and overall survival (OS), while platinum-free doublets have a more favorable toxicity profile [
5‐
9]. However, NSCLC patients will inevitably experience tumor progression and at that time some patients will still have a good Performance Status (PS) and will be suitable for second-line treatment.
Two phase III trials have demonstrated that administration of docetaxel in the second-line setting was superior in terms of OS compared to best supportive care [
10] and improved TTP and 1-year survival rate compared to vinorelbine or ifosfamide [
11]. Furthermore, the administration of pemetrexed in the second-line setting was associated with an OS comparable to that of docetaxel with a more favorable toxicity profile [
12].
The epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) erlotinib and gefitinib are also considered as an alternative for second-line treatment since erlotinib was associated with a superior OS compared to placebo [
13] whereas gefitinib was associated with a comparable OS when compared to docetaxel [
14]. However, results of second-line treatment for patients with relapsing or progressing disease are generally poor, with response rate of less than 10% and OS of 7-8 months [
10‐
14]. One logical approach to improve these results is to evaluate combination regimens. Two phase II trials have evaluated the docetaxel/carboplatin combination as second-line treatment in NSCLC demonstrating encouraging results with an ORR of ≥20% and a median OS of 8 months [
15,
16]. However, this combination has not been compared against the standard second line treatment with single agent docetaxel. Furthermore, given that there is no clear evidence that platinum-based doublets offer a survival benefit against third-generation platinum-free regimens [
17] there will be a number of NSCLC patients treated with platinum-free combinations as first line treatment and for whom a platinum-based doublet as second line treatment will be a logical approach. These observations provided the rationale for this phase III trial which was conducted in order to determine whether the combination of docetaxel/carboplatin provides any therapeutic benefit compared to single-agent docetaxel.
Methods
Patients
Eligible patients were aged 18 years or older, with histologically or cytologically confirmed, unresectable locally advanced (stage IIIB with pleural or pericardial effusion) or metastatic (stage IV) NSCLC, that progressed or recurred after one previous platinum-free and docetaxel-free chemotherapy regimen. Patients had to have a life expectancy of more than 3 months and a World Health Organization (WHO) performance status (PS) of ≤ 2, and adequate organ function [serum bilirubin ≤ 1.5 times the upper normal limit (UNL); AST and ALT ≤ 2.5 UNL in the absence of perceptible liver metastases, or ≤ 5 UNL in the presence of liver metastases; serum creatinine ≤ 1.5 times the UNL; neutrophils ≥ 1.5 × 10-9/L, and platelets ≥ 100 × 10-9/L]. Patients with known, symptomatic central nervous system metastases were ineligible. Other eligibility criteria were: absence of active infection, history of significant cardiac disease (unstable angina, congestive heart failure, myocardial infarction within the previous 6 months, ventricular arrhythmias) or malnutrition (loss of ≥ 20% of the original body weight). All patients gave written informed consent to participate in the study and the trial was approved by the Ethics and Scientific Committees of the participating centers. The study was conducted according to the Helsinki Declaration and Good Clinical Practice guidelines.
Treatment
For the docetaxel/carboplatin arm (DC), treatment consisted of docetaxel at a dose of 50 mg/m
2, administered as a 60-min iv infusion on days 1 and 15; carboplatin was administered on days 1 and 15 as a 90-min intravenous infusion, at a dose of AUC 4. Standard pre- and post-medication with 8 mg oral dexamethasone, at 7 h and 1 h before the docetaxel infusion, and 8 mg twice daily for a further 3 days, was used to reduce the risk of allergic reactions and fluid-retention syndrome that can be associated with docetaxel administration. For the docetaxel single-agent arm (D), treatment consisted of docetaxel at a dose of 50 mg/m
2 on days 1 and 15 after appropriate corticosteroid pre- and post-medication. The every two weeks schedule was selected because of its more favorable toxicity profile [
18‐
20]. Treatment was repeated every four weeks, for both arms. Treatment was continued until disease progression, the appearance of unacceptable toxicity, or patient's withdrawal of consent, for a maximum of 6 cycles.
Βaseline and follow-up assessments
Baseline assessment included a complete medical history, evaluation of performance status, physical examination and vital signs, 12-lead ECG, blood tests (complete blood cell count with differential and blood chemistry), chest X-rays and computed tomography scans of the chest, abdomen and brain and a whole-body radionuclide bone scan. Baseline evaluation had to be performed within two weeks prior to therapy initiation. All measurable lesions were identified at baseline and were monitored throughout. A complete medical history and a detailed physical examination with complete blood cell count with differential and blood chemistry, ECG and a chest X-ray were performed before each treatment administration to assess the disease status and treatment toxicity. After completion of study treatment, patients were followed every month until the development of disease progression. Third-line therapy included best supportive care, palliative radiotherapy, or chemotherapy according to the discretion of the responsible physician.
Assessment of antitumor activity and toxicity
Response assessment was evaluated every two chemotherapy cycles, and every one month after treatment completion. Objective tumor responses were evaluated according to RECIST criteria [
21]. All CT scans were reviewed by an independent radiologist. Toxicity was evaluated before each chemotherapy administration and was reported according to National Cancer Institute Common Toxicity Criteria, version 2 [
22].
Statistical analysis
Patients were centrally randomized by computer software to a 1:1 ratio, to receive either DC or D. The randomization to each arm was done by stratification according to PS, stage of disease and response to front-line treatment.
The primary end-point was overall survival (OS); secondary endpoints included overall response rate (ORR), safety profile and progression-free survival (PFS) associated with each regimen. The study was designed to have 90% power (α = 0.05, two-sided log-rank test) to detect an increase in median survival from 4 months for the single agent docetaxel arm [
18] to 8 months for the docetaxel/carboplatin arm [
15,
16] at the statistically significant level of 5%. Sixty-five patients should be enrolled in each arm to achieve the statistical requirements.
Analysis was performed on an intent-to-treat basis. Duration of tumor response is measured from the date the first objective response (complete or partial) was observed to the first date of tumor progression or death from any cause. The PFS was measured from study entry until the day of the first evidence of disease progression whereas OS from the date of study entry to death or last contact. The probability of survival was calculated by the method of Kaplan-Meier [
23] and tested for differences by using the log-rank test. All tests were two-sided and were considered significant when the resulting p-value was ≤ 0.05. This study is registered with ClinicalTrials.gov, number NCT00430651.
Discussion and conclusions
Single agent docetaxel, or pemetrexed or EFGR TKIs (erlotinib and gefitinib) represent the standard of care for second-line treatment for NSCLC patients. However, the results observed with second-line treatment are generally poor with response rate of less than 10% and overall survival of 7-8 months [
10‐
14]. One logical approach to improve these results is to evaluate combination regimens. This is the first phase III trial, at least in our knowledge, comparing docetaxel monotherapy with a docetaxel/carboplatin doublet in patients with recurrent or relapsed NSCLC.
The results of the current study demonstrate that second-line combination treatment with docetaxel/carboplatin offers a statistically significant therapeutic benefit compared to docetaxel monotherapy, in terms of PFS in patients with NSCLC who were not previously treated with docetaxel-based chemotherapy. Indeed, PFS was significantly prolonged in the DC arm as compared to D arm (p = 0.012). However, although there was a difference in terms of PFS this could not be translated to a significant difference in terms of OS (p = 0.550). Additionally, no difference was observed in ORR between the two treatment arms (p = 0.764). Taken together, these observations suggest that the higher percentage of patients with stable disease in the DC arm might have played a role in the differences observed in PFS.
Efficacy results in the current trial were obtained with an acceptable toxicity profile. With the exception of thrombocytopenia, the DC arm was not associated with higher toxicity. Indeed, both chemotherapy regimens were well tolerated, with toxicities being relatively infrequent and mild in the vast majority of cases.
The results observed in the single-agent docetaxel arm of the current study are remarkably similar to those observed in the phase III trials that led to registration of docetaxel as second-line treatment in NSCLC [
10,
11]. Indeed, OS in these trials was 5.7-7.0 months, median PFS 2.12-2.65 months, and ORR 5.8%-6.7%. The current study reported a median OS of 7.70 months, a median PFS of 2.60 months and an ORR of 7.7%. On the other hand, patients in the docetaxel-carboplatin arm had a longer OS (10.27 months) when compared to historical data [
15,
16]. It is noteworthy that the results of the current study are in accordance with the results of a phase III trial [
24] and several randomised phase II trials comparing single-agent versus combination regimens as second-line treatment of NSCLC [
25‐
28]. Although all these trials demonstrated a statistically significant improvement in PFS with chemotherapy combinations, this improvement in PFS was not translated into an OS prolongation. This observation should be attributed to the fact that an important proportion of patients with advanced/metastatic NSCLC have a good performance status and a acceptable expectancy of life making them suitable to receive third-line treatment; in the current study 71 (54%) out of 132 studied patients received third-line chemotherapy or TKIs.
The results of the current study are also in agreement with the results of a recently published meta-analysis based on individual data of 847 patients. Di Maio et al, compared the efficacy of a doublet chemotherapy regimen with single agent treatment as second-line treatment [
29]. The conclusion of this meta-analysis was that although combination treatment was associated with significantly higher ORR and significant prolongation of TTP, this difference was not translated into a significant survival benefit [
29]. Additionally, patients receiving combination treatment experienced significantly more toxicity. So, based on the lack of a survival benefit and the issue of toxicity, someone could argue against the use of combination regimens in the second-line setting. Furthermore, since patients' quality of life is of particular relevance especially for second-line treatment there is a need for a regimen with a favourable toxicity profile. On that basis we selected the bi-weekly mode of docetaxel administration because it has been reported that it is associated with a marked reduction in haematological toxicity [
20].
Another important issue is the timing of administration of second-line treatment. A recently reported phase III study [
30] demonstrated a statistically significant improvement in PFS and a non-statistically significant increase in OS when docetaxel was administered immediately after front-line gemcitabine/carboplatin doublet compared to its administration at the time of clinical disease progression; in addition, this strategy was not associated with increasing toxicity or decreasing QOL. Practically similar results were obtained with pemetrexed; indeed, in a recent phase III study, patients without disease progression after four cycles of platinum-based front-line treatment who received pemetrexed as maintenance treatment experienced a significantly longer median PFS and OS compared to patients who received placebo [
31]. Additionally, erlotinib as maintenance treatment after front-line platinum based chemotherapy resulted in a significant prolongation of PFS [
32].
Another controversial issue is the substitution of carboplatin for cisplatin and it could be argued our decision to use carboplatin instead of cisplatin. It is known that cisplatin-based doublets offer a small survival benefit as front-line treatment, when compared with carboplatin-based doublets [
33]. On the other hand, carboplatin has a more favorable toxicity profile when compared with cisplatin [
33]. Additionally, the administration of cisplatin requires the need for hydration and it is relatively contraindicated in patients with cardiopulmonary co-morbidities and renal insufficiency. Furthermore, given the practical advantage of carboplatin in terms of ease of administration, it could be argued that the small benefit achieved with cisplatin relative to carboplatin does not justify its use in clinical practice.
Another important issue is whether this study is clinically relevant, since many patients receive platinum-based first-line treatment. However, it should be noted that no phase III trial has clearly demonstrated that platinum-based doublets offer a survival benefit over platinum-free regimens. Furthermore, a recently published meta-analysis failed to show any difference in favor of platinum-based doublets when compared with platinum-free third generation combinations [
17]. Thus, a number of NSCLC patients could receive platinum-free regimens as first-line treatment and this trial is relevant for these patients who could receive platinum derivatives as second line.
In conclusion, the combination of docetaxel/carboplatin was well tolerated as second-line treatment for NSCLC patients. Although the primary end-point of the study (prolongation of OS) could not be achieved, the docetaxel/carboplatin combination was associated with a significant clinical benefit in terms of PFS. Based on the results of the current study, docetaxel single-agent should be considered as one of the "standards" options for second-line treatment of advanced/metastatic NSCLC while its combination with carboplatin might be administered in patients with good PS who were not previously treated with a platinum-based doublet or within a well designed clinical trial. Further research is required for the development of more effective chemotherapeutic regimens and for the integration of newer targeted agents into NSCLC treatment.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
AGP, SA and VG have made substantial contribution to conception and design, interpretation of data and been involved in drafting the manuscript. AGP and SA were involved in manuscript writing. AA, IV, KS, NK, GP, AK, and VG enrolled patients to study protocol. EK has made substantial contribution acquisition of data; interpretation of data. All authors read and approved the final manuscript