- Open Access
Cellular immunotherapy as maintenance therapy prolongs the survival of the patients with small cell lung cancer
Journal of Translational Medicine volume 13, Article number: 158 (2015)
Small cell lung cancer (SCLC) relapses rapidly after the initial response to chemotherapy and shows drug-resistance. This study was to investigate the efficacy and safety of cellular immunotherapy (CIT) with autologous natural killer (NK), γδT, and cytokine-induced killer (CIK) cells as maintenance therapy for SCLC patients.
A pilot prospective cohort study was conducted with SCLC patients who had responded to initial chemotherapy. Patients elected to receive either CIT as maintenance therapy (study group), or to be followed-up without further treatment (control group). Progression-free survival (PFS), overall survival (OS), and adverse effects were investigated.
We recruited 58 patients (29 in each group). The patient characteristics of the 2 groups were well balanced. PFS was not significantly different between the groups, but OS was significantly longer in the study group than the control (20 vs. 11.5 months, P = 0.005; hazard ratio [HR], 0.434, 95 % confidence interval [CI], 0.236–0.797, P = 0.007). Among patients with limited-stage disease, there was no difference in PFS between the groups, but OS was longer in the study group compared to the control (26.5 vs. 11.8 months, P = 0.033; HR, 0.405, 95 % CI, 0.169–0.972, P = 0.043). Among patients with extensive-stage disease, both PFS and OS were longer in the study group than the control (5 vs. 2.7 months, P = 0.037; HR, 0.403, 95 % CI, 0.162–1.003, P = 0.051, and 14.5 vs. 9 months, P = 0.038; HR, 0.403, 95 % CI, 0.165–0.987, P = 0.047, respectively). No significant adverse reactions occurred in patients undergoing CIT.
CIT maintenance therapy in SCLC prolonged survival with only minimal side effects. Integrating CIT into current treatment may be a novel strategy for SCLC therapy, although further multi-center randomized studies are needed.
Lung cancer is the most commonly diagnosed cancer and also the leading cause of cancer death globally . Small cell lung cancer (SCLC) is usually reported to comprise about 15 % of all lung cancer cases recorded . Despite a high initial response rate to first-line therapy, most patients die rapidly from recurrent, drug-resistant disease. Even with more advanced chemotherapeutic agents and molecularly targeted drugs, the prognosis of this disease remains poor due to limited treatment efficacy [3–5]. Recently, maintenance therapy in advanced non-small cell lung cancer (NSCLC) has been found to be an acceptable treatment paradigm to improve progression free survival (PFS) . However, a meta-analysis of published randomized clinical trials  showed that both maintenance and consolidation therapy failed to improve the outcomes of SCLC, and in some cases even caused severe side effects or toxic death. Thus, there is no recommendation for maintenance therapy in current SCLC treatment guidelines. Given its high recurrence rate and mortality, new therapeutic strategies are urgently needed to improve the outcome of this disease.
Immune escape plays an important role in cancer recurrence and metastasis [8, 9]. With an improved mechanistic understanding of immune response and immune escape, several immunotherapies were investigated in SCLC. Some of them were failed, such as the dendritic cell-based p53 vaccine , but some of them obtained a certain effect, such as phased ipilimumab (an antibody against cytotoxic T-lymphocyte antigen-4 [CTLA-4]) with paclitaxel/carboplatin exhibited improved immune-related PFS (irPFS) . It indicated that immunotherapy might have the potential to improve the prognosis of SCLC. Besides, it also suggested that different patterns of immunotherapy combined with chemotherapy might have an influence on the prognosis of SCLC. Therefore, increasing attention has been paid to the possibility of immunotherapy for SCLC patients in recent years.
SCLC patients have often been found to have a functional deficiency in a variety of immunocytes [12–14], implying that adoptive transfusion of ex vivo-activated and expanded immunocytes may be a feasible and effective therapy. Cellular immunotherapy (CIT) has been shown to be effective for a variety of cancers [15–17], but its use in SCLC patients has not been reported.
Activated immune cells can reach the lungs within minutes of intravenous injection and selectively enter malignant tissue. Consequently, a substantial number of these cells can accumulate at cancer sites within 24 hr of treatment [18, 19]. We postulated that CIT would provide an anti-caner effect and prolong the survival of SCLC patients. However, it is not yet known which cell types are needed in CIT for performing anti-cancer effects optimally.
Several specific immunotherapies to induce cytotoxic T lymphocyte (CTL) for SCLC have been tried, such as the dendritic cell-based p53 vaccine , few of them have lengthened survival, partly due to the complexity of the immune escape mechanism in this malignancy. Decreased expression of HLA-class I antigen has been reported in SCLC, which may be one of the mechanisms of SCLC cells to escape CTL attack . Natural killer (NK) and γδT cells are effector cells of innate immunity, and both can exert anti-cancer effects in a non-MHC-restricted manner. Cytokine-induced killer (CIK) cells are ex vivo-activated lymphocytes, and represent a heterogeneous cell population, including CD3+CD56+, CD3+CD56− (typical T) and CD3−CD56+ (NK) cells. The anti-cancer activity of CIK cells is mainly due to the CD3+CD56+ cells, which show an NK-like, non-MHC-restricted cytolytic activity against cancer cells. CIT based on any of these cell types has proved to be effective against a variety of cancers [15–17]. SCLC cells were also found to be susceptible to NK or γδT cell-mediated cytotoxicity in preclinical studies [20, 21]. In addition, γδT cells can induce the NK cell-mediated killing of cancers that are usually resistant to NK cytolysis  and cross-present tumor antigens to CD8+ CTLs to mediate adaptive immune responses . These findings suggest that the combined application of NK, γδT and CIK cells may provide significantly synergistic anti-cancer effects via different mechanisms, and could provide effective CIT for SCLC patients. We therefore conducted this pilot prospective cohort study to evaluate the efficacy and safety of combined NK, γδT, and CIK cell based CIT as a maintenance therapy for SCLC patients, with the objective of consolidating remission and prolonging survival in patients who responded to first-line therapy.
Patients and study design
A pilot prospective cohort study was conducted to evaluate the efficacy and safety of combined NK, γδT, and CIK cell based CIT as a maintenance therapy for SCLC patients. All patients with SCLC that met the following criteria at the First Hospital of Jilin University were included in this study after June 1, 2009.
Eligibility: Patients had to (i) have been diagnosed as SCLC and have completed first-line therapy, (ii) have achieved stable disease (SD), partial remission (PR) or complete remission (CR) after the first-line treatment, (iii) be at least 18 years old, (iv) have an Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2, (v) have normal kidney, liver, and bone marrow function and be free of cardiac arrhythmias, congestive heart failure or severe coronary artery disease, and (vi) have a life expectancy ≥ 3 months. Exclusion criteria included (i) autoimmune disease, (ii) a clinically serious infection, (iii) for women, pregnancy or lactation, (iv) a history of organ transplantation, and (v) the administration of another immunotherapy. This study was conducted in accordance with the Declaration of Helsinki and was reviewed and approved by the Ethical Committee of the First Hospital of Jilin University [ID #: 2009–020]. Written informed consent was obtained from all patients before their enrollment into the study.
Treatment plan: The treatment regimens of SCLC patients in this study were based on the Small Cell Lung Cancer NCCN Guidelines – version 2.2009 . The first-line therapy regimen for limited stage SCLC (LS-SCLC) patients was platinum based chemotherapy, e.g.: etoposide/cisplatin (EP) regimen or etoposide/carboplatin (EC) regimen for 4–6 cycles plus concurrent chest radiotherapy (1.8–2 Gy once daily to 60–70 Gy) . The initial chemotherapy for extensive stage SCLC (ES-SCLC) patients was the same as those for LS-SCLC patients.
After first-line therapy, patients either received CIT (at least 1 course) as maintenance treatment (study group), or were followed up without further treatment (control group). The decision whether to undergo CIT or to be entered into the control group was made by the patient. For the study group, autologous peripheral blood mononuclear cells (PBMCs) were collected by apheresis on D0, and were induced into NK, γδT, or CIK cells. The expanded immunocytes were then infused back into the patients 14 days later (D14) as the initial transfusion. There were for 6 consecutive transfusion days (D14–D20) with 2 kinds of immune cells for each infusion, and each CIT course was completed within 3 weeks after apheresis. The second course of PBMCs collection was started 1 to 3 weeks after the end of the first course. The treatment schedule is summarized in Fig. 1. Maintenance treatment was continued unless there was progressive disease (PD) or the patient refused to undergo further CIT. In cases of PD, the patient was given either a best supportive treatment or a second or even a third-line chemotherapy regimen, depending on their general health status and/or preference.
The second-line chemotherapy regimens were selected based on the time of relapse. If patients experienced relapse within 6 months after the first-line therapy, patients would be treated with topotecan or irinotecan; if patients relapsed more than 6 months after the completion of first-line therapy, they would receive the original regimen. The third-line chemotherapy regimens were selected based on the previous chemotherapy. Patients could be given irinotecan, topotecan or paclitaxel that had not been used in the previous chemotherapy.
Follow up: In general, follow-up was required every 3 months. Each follow-up included a complete physical examination, basic serum chemistry, and computed tomography (CT) of the chest and abdomen. Brain magnetic resonance imaging (MRI) and a technetium bone scan were performed as clinically indicated.
Preparation of immune cells
All procedures for preparing the autologous immune cells were carried out under Good Manufacturing Practice (GMP) conditions (Certificate ID: A20090047) which were approved by the Jilin Provincial Center for Sanitation Inspection and Test. The preparation of and quality control for each type of immunocytes was performed in strict accordance with the standard operating procedure (SOP). Immune cells were prepared as described in our previous study , with some modifications based upon previously published procedures [26, 27]. Briefly, about 1.5 × 109 (1.0–2.0 × 109) PBMCs were collected from the patient using a Cobe Spectra Apheresis System (Gambro BCT, Inc. USA). These PBMCs were separated into 2 parts and placed in 50 ml centrifuge tubes that were centrifuged for 10 min at 3000 rpm. The supernatant was then removed, and the cell pellets were re-suspended in 30 ml PBS, and placed on top of a 15 ml Ficoll-Hypaque (Amersham Biosciences, Uppsala, Sweden) in a sterile 50 ml tube. Lymphocytes were isolated from PBMCs using Ficoll-Hypaque density centrifugation (Ficoll separation). Approximately 1.3 × 109 (1.0 − 1.8 × 109) mononuclear cells were obtained after these procedures. The cells were then separated into 3 pools to induce NK, γδT and CIK cells using different cytokines.
For expansion of NK cells, PBMCs were cultured in AIM-V medium (Invitrogen, Carlsbad, CA, USA), 700 U/mL IL-2 (Miltenyi, Cologne, German) and 1 ng/mL OK432 (Shandong Lu Ya Pharmaceutical, Jining, China) for 24 hr at 37 °C, in a mouse anti-human CD16 monoclonal antibody (mAb; Beckman Coulter, Marseille, France) coated flask. The cultured cells were then centrifuged, and the supernatant was discarded. The cells were again cultured in AIM-V medium and 700 U/mL IL-2 at 37 °C for 2–3 weeks. IL-15 (Miltenyi, Cologne, Germany) was added to the culture medium to promote the growth of NK cells [25, 26]. To generate γδT cells, PBMCs were stimulated with 1 μM zoledronate (Zometa®, Novartis, Beijing, China) in AIM-V medium containing 400 U/mL human IL-2. Fresh medium and IL-2 supplement at 400 U/mL were added every 3 days [25, 27]. To prepare CIK cells, PBMCs were cultured in AIM-V medium and 1000 U/mL IFN-γ (Miltenyi, Cologne, German) at 37 °C for 24 hr. Then, 100 ng/mL mouse anti-human CD3 mAb (Peprotech, Rocky Hill, NJ, USA), 1000 U/mL IL-2 and 1000 U/mL IL-1α (Miltenyi, Cologne, German) were added to the media. Fresh complete medium and IL-2 supplement at 1000 U/mL were added every 3 days .
Before transfusion, a fraction of cells was collected so that they could be enumerated, evaluated for viability and phenotype, and checked for possible contamination.
Phenotypic analysis of immunocytes before infusion
The phenotype of immunocytes were determined on the basis of their specific cell surface markers using 4-color flow cytometry performed on a FACSCalibur (BD Biosciences, San Diego, CA, USA) with directly conjugated mAbs against the markers. Briefly, cultured NK cells were collected, washed, and incubated with mouse mAbs against human CD3-PerCP, CD69-PE, and CD56-APC (BD Biosciences) for 15 min. The γδT cells were incubated with Vγ9-FITC and CD3-APC (BD Biosciences), and the CIK cells were incubated with CD3-PerCP, CD4-FITC, CD8-PE and CD56-APC (BD Biosciences). Isotype-matched antibodies were used as controls.
Administration of immune cells
The dye-exclusion test was used to assess the viability of the final cell suspension. Possible contamination of the immune cells was tested using a PCR-based assay for mycoplasma, as well as assays for endotoxins, bacteria, and fungi, 24 hr before and on the day of product release. The immunocytes could not be used for patients if they failed to meet the following release criteria: (i) a viability of more than 95 %, (ii) no contamination by bacteria, fungi, endotoxins, or mycoplasma in either of the 2 assessments, (iii) at least 1.2 − 2.0 × 109 of each type of cell per infusion; and (iv) more than 50 % of the cells had the NK (CD3−CD56+) or γδT (CD3+Vγ9+) phenotype, and more than 20 % of cells had the CD3+CD56+ CIK phenotype in NK, γδT and CIK cell culture system respectively, as detected by flow cytometry. Before reinfusion, immunocytes were washed 3 times with normal saline and re-suspended in 50 mL of normal saline. The cells were then administered to patients via an intravenous drip in 30 min. The number of cells in each transfusion ranged from 2.4 − 4.0 × 109.
Cytotoxic effects of immune cells in vitro
The cytotoxicity of immune cells was examined by measuring lactate dehydrogenase (LDH) levels in the culture medium, according to the manufacturer’s instructions for the CytoTox 96 Non-Radioactive Cytotoxicity Assay Kit (Promega, Madison, WI). The target cells used for this assay were the SCLC-derived cell line NCI-H446, and 5 × 104 cells were used to examine the cytotoxic effects of immune cells in vitro. The tested ratios of effector cells to target cells (E/T) were 25:1, 12:1, 6:1, and 3:1. In order to investigate the synergistic effect of the different kinds of the immune cells, we combined the 3 types of immunocytes at a ratio of 1:1:1 to examine their cytotoxic effect on target cells.
Overall survival (OS) was the primary end point, and the secondary end points included PFS, safety of CIT and clinical benefit rate (CBR) of the second-line chemotherapy. Response was determined based on the National Cancer Institute’s Response Evaluation Criteria in Solid Tumors (RECIST 1.1) guidelines . OS was defined as the period from the day on which first-line treatment was completed to death from any cause. PFS was defined as the period between the completion of first-line treatment and the onset of PD or death from any cause. CBR was defined as the percentage of patients with CR + PR + SD.
Proportion of the immune cells in peripheral blood
In order to detect the alteration of the proportion of the immune cells of the patients, two milliliters of peripheral blood was collected before the apheresis and 1 week after the end of one CIT course. T cells (CD3+CD4+, CD3+CD8+), NK cells (CD3−CD56+), NKT cells (CD3+CD56+), B cells (CD19+), regulatory T (Treg) cells (CD4+CD25+Foxp3+) and monocytes (CD14+) populations were analyzed with FACSCalibur (BD Biosciences). All antibodies were purchased from BD Biosciences.
All calculations were performed using SPSS 17.0 software (SPSS, Chicago, IL). PFS and OS were assessed according to the Kaplan-Meier method and compared between groups using the log-rank test. The multivariate Cox proportional hazard model was applied to analyze factors found to be statistically significant by univariate analysis. The Mann–Whitney test was used to compare medians, and Fisher’s exact test was used to compare binary outcomes. P ≤ 0.05 was considered to be statistically significant.
A total of 58 eligible patients were recruited between June 1, 2009 and November 1, 2012, with 29 patients in each group. Follow-up of all patients was ended on December 30, 2013, with a median follow-up time of 13 months (range, 3–54 months). Of the 29 patients in each group, 17 patients had LS-SCLC and 12 had ES-SCLC. Two ES-SCLC patients in CIT group had one solitary pulmonary lesion highly suspected as lung cancer under the CT scan. Their abdominal CT and brain MRI were normal. They underwent surgery after these examinations, and pathologically confirmed SCLC. Considering the properties of invasion and metastasis of SCLC, technetium bone scan was performed after surgery for clinical stage. Bone scan showed that one patient had lumbar metastasis, and the other patient had pelvic metastasis. Therefore, they were diagnosed as ES-SCLC. The patient demographics were well balanced between the groups, including characteristics such as sex, smoking index, ECOG performance status, chemotherapy courses, chemotherapy responses, radiotherapy and surgery (Table 1). The only exception was age, as ES-SCLC patients in the CIT group were on average older than those in the control group (P < 0.05).
Quality of the cultured immune cells
The viability of each type of immune cell in our culture system was found to exceed 95 %, none of the cultured immune cells were found to be contaminated, and all of the preparations met the release criteria. The percentage of NK (CD3−CD56+), γδT (CD3+Vγ9+) and CIK (CD3+CD56+) cells before and after induction was 8.01 % (range, 4.12–17.35 %) vs. 85.32 % (range, 61.33–99.61 %), 4.22 % (range, 2.79–11.26 %) vs. 82.63 % (range, 63.72–98.21 %) and 4.51 % (range, 1.62–7.96 %) vs. 34.52 % (range, 27.25–57.28 %), respectively (Table 2). Thus, each of these cell types was significantly more prevalent after induction. Induction also resulted in a significant increase in the proportion of activated NK cells (CD56+CD69+). Representative results from a single patient are shown in Fig. 2, and the numbers of the 3 types of immunocytes infused into each patient are shown in Additional file 1: Table S1.
Cytotoxic effect of immune cells on cancer cells
The cytotoxic effect of immune cells was examined by measuring LDH release levels. All 3 types of immune cells exhibited a significant cytotoxic effect on NCI-H446 cells when used alone, but a greater cytotoxic effect was achieved when they were combined, and this cytotoxicity increased further as the E/T cell ratio increased. At an E/T cell ratio of 25:1, the median cytotoxicity level of NK, γδT and CIK cells was 75.5 % (range, 59.1–90.7 %), 70.6 % (range, 48.3–80.0 %), and 49.0 % (range, 27.4–68.9 %), respectively. The combined immune cells showed a synergistic anti-cancer effect with a median cytotoxicity level of 85.5 % (range, 63.4–96.5 %) at an E/T cell ratio of 25:1 (Additional file 2: Figure S1).
PFS and OS
The median PFS did not differ significantly between the groups (hazard ratio [HR], 0.667; 95 % confidence interval [CI], 0.380–1.169; P = 0.157). However, the median OS in the study group was significantly longer than that in the control group (20 vs. 11.5 months, P = 0.005; HR, 0.434, 95 % CI, 0.236–0.797, P = 0.007) (Fig. 3A).
Patients were divided into two subgroups according to disease stage: LS-SCLC and ES-SCLC. Among the former, there was no significant difference in PFS (HR, 0.751; 95 % CI, 0.349–1.618; P = 0.465); however, the OS of the study group was longer than that of the control group (26.5 vs. 11.8 months, P = 0.033; HR, 0.405, 95 % CI, 0.169–0.972, P = 0.043) (Fig. 3B). Among the ES-SCLC patients, both the PFS and OS of the study group were longer than those of the control group (5 vs. 2.7 months, P = 0.037; HR, 0.403, 95 % CI, 0.162–1.003, P = 0.051, and 14.5 vs. 9 months, P = 0.038; HR, 0.403, 95 % CI, 0.165–0.987, P = 0.047, respectively) (Fig. 3C, D).
Potential factors influencing the outcome of CIT
In the multivariate analysis, we found that sex, age, smoking history, ECOG performance status, chemotherapy courses, chemotherapy responses, radiotherapy and surgery had no effect on the prognosis of SCLC patients receiving CIT (P > 0.05). We then investigated the influence of the CIT frequency on the prognosis of patients in the study group, in which the median frequency of CIT was 3 courses (range, 1–8 courses). Patients were divided into two subgroups: CIT ≥ 3 courses and < 3 courses. The characteristics of the patients in these subgroups were well balanced (Table 3). The median PFS in the CIT ≥ 3 courses group (n = 17) was longer than that of the CIT < 3 courses group (n = 12) (9.5 vs. 2 months), but this difference was not significant (P = 0.057) (HR, 0.465; 95 % CI, 0.204–1.063; P = 0.070) (Fig. 4A). However, the median OS of the CIT ≥ 3 courses group was significantly longer than that of the CIT < 3 courses group (23 vs. 9 months, P = 0.020; HR, 0.335, 95 % CI, 0.125–0.893, P = 0.029) (Fig. 4B).
Response to second-line chemotherapy
A total of 18 patients accepted second-line therapy in the study group, and 17 patients received second-line therapy in the control group. The median second-line chemotherapy courses in the study and control group were 3 (range, 1–6) and 2 (range, 1–6), respectively, but there was no significant difference between two groups (P > 0.05). None of the patients in two groups achieved a CR after second-line treatment. Eight patients got a PR or SD with a CBR of 44.4 % in the study group, and 5 patients got a PR or SD with a CBR of 29.4 % in the control group, but there was no significant difference between the groups (P = 0.489).
Side effects of CIT infusion
Two patients reported mild fatigue after CIT infusion. One patient had a transient fever of 37.8 °C after one infusion, but recovered after 1 hr. No other significant side effects were observed.
Proportion of the immune cells in peripheral blood before and after CIT
The proportion of T, NK, NKT, B, Treg cells and monocytes were analyzed before and after CIT. However, there was no significant change in these cells. There were relatively less Treg cells at some time points after CIT, but these differences were not significant (data not shown).
Immune escape in SCLC patients is closely associated with the recurrence of the disease, and may contribute to poor patient survival [8, 9, 12–14]. However, the findings of several studies suggest that maintenance and/or consolidation using cytokines and other biological agents fail to improve SCLC outcomes . The therapeutic effects of CIT in SCLC have rarely been reported in either preclinical or clinical studies. Meanwhile, cancers employ multiple mechanisms to evade an immune response [29–31], and thus CIT with only one type of immune cells is unlikely to achieve an optimal anti-cancer effect. NK and γδT cells were shown to have a synergistic anti-cancer effect in a preclinical study . Besides, chemotherapy could not only alleviate immune suppression by reducing the tumor burden [32, 33], but also up-regulate the expression of the NKG2D ligands on cancer cells, thus sensitizing them to lysis mediated by NKG2D-expressing lymphocytes . In this study, we applied CIT with a combination of NK, γδT and CIK cells as maintenance therapy after systemic chemotherapy, and showed survival advantage for SCLC patients for the first time. At the same time, another study conducted by our group also confirmed the efficacy of the CIT with combination of these immunocytes in improving the outcome of patients with hepatocellular carcinoma after radiofrequency ablation (RFA) . Thus, CIT may be a novel treatment for SCLC patients who respond to first-line therapy, and could provide a novel strategy for the devastating disease.
OS is widely used as a primary end point for immunotherapy in many cancers, such as melanoma [35, 36] and prostate cancer . SCLC is a highly malignant tumor associated with short survival and limited chemotherapy regimens, and hence there are less confounding factors in the observation of OS. In our study, OS was significantly longer after CIT both in LS-SCLC and ES-SCLC patients. There are several possible reasons for the prolonged survival of SCLC patients with CIT. Cancer stem cells (CSCs) have been reported to be responsible for cancer progression, metastasis, and the development of drug resistance [38, 39]. They have also been shown to be susceptible to immunocyte-mediated toxicity, suggesting that CIT may be useful in eliminating minimal residual disease (MRD) and thus reducing cancer recurrence [40–42], which may explain why CIT maintenance therapy prolongs PFS and consequently prolongs survival of SCLC patients. Although PFS has recently been shown to be a good predictor of OS in SCLC , but PFS did not differ significantly between the groups in LS-SCLC patients. It is noteworthy though that another study exploring the relationship between PFS and OS in SCLC found no significant relationship between them , suggesting that OS might be affected by other factors, such as second or third-line therapy.
It has been reported that patients who receive cancer vaccines respond better to subsequent chemotherapy than those who do not, suggesting that immunotherapy might sensitize cancer cells to cytotoxic drugs [45, 46]. The CBR of the relapsed patients to second-line treatment was also detected in our study. Patients with CIT tended to have higher CBR than the control, although there was no significant difference between two groups, indicating that CIT might enhance the sensitivity of recurrent SCLC to second-line chemotherapy. This is a potential mechanism by which OS could be extended by CIT, although the exact mechanistic basis for this needs to be further explored.
The quality of the cultured immunocytes is of primary importance in CIT. Both the purity and viability of the immune cells in our study were acceptable, and indeed they were actually better than those in previously reported expansion methods [47, 48]. The percentage of activated NK cells (CD56+CD69+) was also significantly increased after induction, indicating that the activity of NK cells was remarkably improved. Each kind of immunocytes had strong cytotoxicity when used alone, but the highest cytotoxic effect was achieved when they were combined, reflecting a strong synergy between these cells. Safety is another important factor determining the application of CIT. We did not observe any significant side effects after CIT, and only 2 patients felt mild fatigue and 1 patient had a transient fever during 1 of the infusions. All the symptoms diminished without treatment. Thus, CIT was well tolerated in our study, and it may be a good candidate for maintenance therapy when side effects need to be minimized.
Potential factors influencing the outcome of CIT were also detected in this study. Using a multivariate analysis, we found that sex, age, smoking history, ECOG performance status, chemotherapy courses, chemotherapy responses, radiotherapy and surgery were not related to the efficacy of treatment. However, the OS of patients who received more than 3 courses of CIT was significantly longer than that of patients who received less than 3 courses of CIT. PFS also tended to be longer in patients who received more than 3 CIT courses, although this was not statistically significant. It was previously demonstrated that NSCLC patients who received more than 7 courses of CIK cell treatment had a significantly better prognosis than those who received fewer courses . Taken together, our findings and those of a previous report  suggest that a greater number of CIT courses improves patient outcome. However, the optimal number of treatment courses and the duration of treatment are yet to be determined. Besides, bias might exist in the analysis of the influence of the CIT frequency on the prognosis of patients. Even though the characteristics of the patients in these subgroups were well balanced, some patients stopped CIT treatment in CIT < 3 courses group because of disease progression. Therefore, the shorter PFS and OS might be affected not only by less frequency of CIT treatment, but also by other factors, such as the worse features of the disease status in this subgroup of patients. However, these results could provide an instructive reference for subsequent clinical trials.
There is no consensus on the best indicators for assessing immune response after CIT. In this study, T, NK, NKT, B, Treg cells and monocytes populations in the peripheral blood were analyzed before and after CIT. However, there was no significant change in these cells. There were relatively less Treg cells at some time points after CIT, but these differences were not significant. This might reflect the relatively few CIT courses and the small number of patients involved. However, it may also be that the proportion of immune cells in the peripheral blood does not relate to the response to CIT, and this needs to be addressed in a further study.
CIT could improve the quality of life of cancer patients as reported . However, the patients enrolled in this study had a good performance status (ECOG 0–2) before disease progression, and the status of the patients showed no significant difference between the 2 groups. Therefore, it was difficult to determine whether CIT affected the quality of life in this study.
In our study, ES-SCLC patients who underwent CIT were on average older than those who did not undergo therapy. However, the multivariate analysis showed that age had no effect on the prognosis of these patients. It has also been reported that effector cell function decreases in older people, and might be associated with reduced antitumor immunity in these patients . Additionally, patients in the study group had longer PFS and OS, indicating that CIT may effectively reduce immunosuppression, provide an anti-cancer effect and prolong OS, even in elderly patients.
This study was designed as a prospective cohort study. The patients were enrolled to each group of the study based on their choice of the therapeutic options. Therefore, this design allowed us to collect valuable data on the efficacy of CIT, and better reflects a practical clinical settings. At the same time, although innovative cancer treatments might bring benefits to the cancer patients, cost effectiveness is an important aspect that must be considered in the clinical practice. Nowadays, maintenance therapy for SCLC is very limited. CIT as a maintenance therapy has shown its potential to prevent disease recurrence and prolong the survival of SCLC patients with minimal side effects in our study. Besides, the methods of the preparation of immune cells are very simple compared with the complicated preparation methods of other CIT therapies, such as sipuleucel-T, which is used in prostatic cancer and chimeric antigen receptor T-cell immunotherapy (CAR-T) applied in B cell leukemia. And its price might be no more than those of other available maintenance therapies for NSCLC such as erlotinib, bevacizumab and pemetrexate. Therefore, CIT as maintenance therapy may be a novel cost effective strategy for SCLC therapy, and warrants further investigation.
CIT as a maintenance therapy after first-line treatment is well tolerated, and it might prevent disease recurrence and prolong the survival of SCLC patients. We also found that more frequent CIT administration might improve treatment outcome. The exact mechanism through which CIT extends PFS and OS in SCLC patients remains unclear and a multi-center randomized clinical trial is needed to further verify its efficacy.
Clinical benefit rate
Cancer stem cells
Cytotoxic T lymphocyte
Cytotoxic T-lymphocyte antigen-4
Eastern Cooperative Oncology Group
Extensive stage small cell lung cancer
Good Manufacturing Practice
immune-related progression free survival
Limited stage small cell lung cancer
Minimal residual disease
Magnetic resonance imaging
Non-small cell lung cancer
Peripheral blood mononuclear cells
Progression free survival
Small cell lung cancer
Standard operating procedure
Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: Sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. 2015;136:E359–86.
Riaz SP, Lüchtenborg M, Coupland VH, Spicer J, Peake MD, Møller H. Trends in incidence of small cell lung cancer and all lung cancer. Lung Cancer. 2012;75:280–4.
Spigel DR, Townley PM, Waterhouse DM, Fang L, Adiguzel I, Huang JE, et al. Randomized phase II study of bevacizumab in combination with chemotherapy in previously untreated extensive-stage small-cell lung cancer: results from the SALUTE trial. J Clin Oncol. 2011;29:2215–22.
Jotte R, Conkling P, Reynolds C, Galsky MD, Klein L, Fitzgibbons JF, et al. Randomized phase II trial of single-agent amrubicin or topotecan as second-line treatment in patients with small-cell lung cancer sensitive to first-line platinum-based chemotherapy. J Clin Oncol. 2011;29:287–93.
Schmittel A, Sebastian M, Fischer von Weikersthal L, Martus P, Gauler TC, Kaufmann C, et al. A German multicenter, randomized phase III trial comparing irinotecan-carboplatin with etoposide-carboplatin as first-line therapy for extensive-disease small-cell lung cancer. Ann Oncol. 2011;22:1798–804.
Gerber DE, Schiller JH. Maintenance chemotherapy for advanced non-small-cell lung cancer: new life for an old idea. J Clin Oncol. 2013;31:1009–20.
Rossi A, Garassino MC, Cinquini M, Sburlati P, Di Maio M, Farina G, et al. Maintenance or consolidation therapy in small-cell lung cancer: a systematic review and meta-analysis. Lung Cancer. 2010;70:119–28.
Predina J, Eruslanov E, Judy B, Kapoor V, Cheng G, Wang LC, et al. Changes in the local tumor microenvironment in recurrent cancers may explain the failure of vaccines after surgery. Proc Natl Acad Sci U S A. 2013;110:E415–24.
Shiao SL, Ganesan AP, Rugo HS, Coussens LM. Immune microenvironments in solid tumors: new targets for therapy. Genes Dev. 2011;25:2559–72.
Chiappori AA, Soliman H, Janssen WE, Antonia SJ, Gabrilovich DI. INGN-225: a dendritic cell-based p53 vaccine (Ad.p53-DC) in small cell lung cancer: observed association between immune response and enhanced chemotherapy effect. Expert Opin Biol Ther. 2010;10:983–91.
Reck M, Bondarenko I, Luft A, Serwatowski P, Barlesi F, Chacko R, et al. Ipilimumab in combination with paclitaxel and carboplatin as first-line therapy in extensive-disease-small-cell lung cancer: results from a randomized, double-blind, multicenter phase 2 trial. Ann Oncol. 2013;24:75–83.
Koyama K, Kagamu H, Miura S, Hiura T, Miyabayashi T, Itoh R, et al. Reciprocal CD4+ T-cell balance of effector CD62Llow CD4+ and CD62LhighCD25+ CD4+ regulatory T cells in small cell lung cancer reflects disease stage. Clin Cancer Res. 2008;14:6770–9.
Wang W, Hodkinson P, McLaren F, MacKinnon A, Wallace W, Howie S, et al. Small cell lung cancer tumour cells induce regulatory T lymphocytes, and patient survival correlates negatively with FOXP3+ cells in tumour infiltrate. Int J Cancer. 2012;131:E928–37.
Afifi SS, Helal AM. CD11c + and CD123+ dendritic cell subsets in peripheral blood of lung cancer patients. Egypt J Immunol. 2009;16:9–15.
Ohira M, Nishida S, Tryphonopoulos P, Tekin A, Selvaggi G, Moon J, et al. Clinical-scale isolation of interleukin-2-stimulated liver natural killer cells for treatment of liver transplantation with hepatocellular carcinoma. Cell Transplant. 2012;21:1397–406.
Shi L, Zhou Q, Wu J, Ji M, Li G, Jiang J, et al. Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer. Cancer Immunol Immunother. 2012;61:2251–9.
Yu X, Zhao H, Liu L, Cao S, Ren B, Zhang N, et al. A randomized phase II study of autologous cytokine-induced killer cells in treatment of hepatocelluar carcinoma. J Clin Immunol. 2014;34:194–203.
Albertsson PA, Basse PH, Hokland M, Goldfarb RH, Nagelkerke JF, Nannmark U, et al. NK cells and the tumour microenvironment: implications for NK-cell function and anti-tumour activity. Trends Immunol. 2003;24:603–9.
Brand JM, Meller B, Von Hof K, Luhm J, Bähre M, Kirchner H, et al. Kinetics and organ distribution of allogeneic natural killer lymphocytes transfused into patients suffering from renal cell carcinoma. Stem Cells Dev. 2004;13:307–14.
Tsuchida T, Yamane H, Ochi N, Tabayashi T, Hiraki A, Nogami N, et al. Cytotoxicity of activated natural killer cells and expression of adhesion molecules in small-cell lung cancer. Anticancer Res. 2012;32:887–92.
Sato K, Kimura S, Segawa H, Yokota A, Matsumoto S, Kuroda J, et al. Cytotoxic effects of gammadelta T cells expanded ex vivo by a third generation bisphosphonate for cancer immunotherapy. Int J Cancer. 2005;116:94–9.
Maniar A, Zhang X, Lin W, Gastman BR, Pauza CD, Strome SE, et al. Human gammadelta T lymphocytes induce robust NK cell-mediated antitumor cytotoxicity through CD137 engagement. Blood. 2010;116:1726–33.
Brandes M, Willimann K, Bioley G, Lévy N, Eberl M, Luo M, et al. Cross-presenting human gammadelta T cells induce robust CD8+ alphabeta T cell responses. Proc Natl Acad Sci U S A. 2009;106:2307–12.
NCCN Clinical Practice Guidelines in Oncology: Small Cell Lung Cancer version 2.2009. http://www.nccn.org. Accessed 15 Jan 2009.
Cui J, Wang N, Zhao H, Jin H, Wang G, Niu C, et al. Combination of radiofrequency ablation and sequential cellular immunotherapy improves progression-free survival for patients with hepatocellular carcinoma. Int J Cancer. 2014;134:342–51.
Dewan MZ, Terunuma H, Takada M, Tanaka Y, Abe H, Sata T, et al. Role of natural killer cells in hormone-independent rapid tumor formation and spontaneous metastasis of breast cancer cells in vivo. Breast Cancer Res Treat. 2007;104:267–75.
Kondo M, Sakuta K, Noguchi A, Ariyoshi N, Sato K, Sato S, et al. Zoledronate facilitates large-scale ex vivo expansion of functional gammadelta T cells from cancer patients for use in adoptive immunotherapy. Cytotherapy. 2008;10:842–56.
Eisenhauer EA, Therasse P, Bogaerts J, Schwartz LH, Sargent D, Ford R, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer. 2009;45:228–47.
Kim R, Emi M, Tanabe K. Cancer immunoediting from immune surveillance to immune escape. Immunology. 2007;121:1–14.
Whiteside TL. The tumor microenvironment and its role in promoting tumor growth. Oncogene. 2008;27:5904–12.
Facciabene A, Motz GT, Coukos G. T-regulatory cells: key players in tumor immune escape and angiogenesis. Cancer Res. 2012;72:2162–71.
Salama P, Phillips M, Grieu F, Morris M, Zeps N, Joseph D, et al. Tumor-infiltrating FOXP3+ T regulatory cells show strong prognostic significance in colorectal cancer. J Clin Oncol. 2009;27:186–92.
Li H, Yu JP, Cao S, Wei F, Zhang P, An XM, et al. CD4 + CD25+ regulatory T cells decreased the antitumor activity of cytokine-induced killer (CIK) cells of lung cancer patients. J Clin Immunol. 2007;27:317–26.
Gasser S, Orsulic S, Brown EJ, Raulet DH. The DNA damage pathway regulates innate immune system ligands of the NKG2D receptor. Nature. 2005;436:1186–90.
Robert C, Long GV, Brady B, Dutriaux C, Maio M, Mortier L, et al. Nivolumab in Previously Untreated Melanoma without BRAF Mutation. N Engl J Med. 2015;372:320–30.
Robert C, Thomas L, Bondarenko I, O'Day S, Weber J, Garbe C, et al. Ipilimumab plus dacarbazine for previously untreated metastatic melanoma. N Engl J Med. 2011;364:2517–26.
Kantoff PW, Higano CS, Shore ND, Berger ER, Small EJ, Penson DF, et al. Sipuleucel-T immunotherapy for castration-resistant prostate cancer. N Engl J Med. 2010;363:411–22.
Fabian A, Vereb G, Szollosi J. The hitchhikers guide to cancer stem cell theory: markers, pathways and therapy. Cytometry A. 2013;83:62–71.
Sarvi S, Mackinnon AC, Avlonitis N, Bradley M, Rintoul RC, Rassl DM, et al. CD133+ cancer stem-like cells in small cell lung cancer are highly tumorigenic and chemoresistant but sensitive to a novel neuropeptide antagonist. Cancer Res. 2014;74:1554–65.
Gammaitoni L, Giraudo L, Leuci V, Todorovic M, Mesiano G, Picciotto F, et al. Effective activity of cytokine-induced killer cells against autologous metastatic melanoma including cells with stemness features. Clin Cancer Res. 2013;19:4347–58.
Tallerico R, Todaro M, Di Franco S, Maccalli C, Garofalo C, Sottile R, et al. Human NK cells selective targeting of colon cancer-initiating cells: a role for natural cytotoxicity receptors and MHC class I molecules. J Immunol. 2013;190:2381–90.
Todaro M, D'Asaro M, Caccamo N, Iovino F, Francipane MG, Meraviglia S, et al. Efficient killing of human colon cancer stem cells by gammadelta T lymphocytes. J Immunol. 2009;182:7287–96.
Foster NR, Qi Y, Shi Q, Krook JE, Kugler JW, Jett JR, et al. Tumor response and progression-free survival as potential surrogate endpoints for overall survival in extensive stage small-cell lung cancer: findings on the basis of North Central Cancer Treatment Group trials. Cancer. 2011;117:1262–71.
Foster NR, Renfro LA, Schild SE, Redman MW, Wang XF, Dahlberg SE, et al. Multitrial evaluation of progression-free survival (PFS) as a surrogate endpoint for overall survival (OS) in previously untreated extensive-stage small cell lung cancer (ES-SCLC): an alliance-led analysis. J Clin Oncol 31:2013 (suppl; abstr 7510).
Schlom J, Arlen PM, Gulley JL. Cancer vaccines: moving beyond current paradigms. Clin Cancer Res. 2007;13:3776–82.
Wheeler CJ, Das A, Liu G, Yu JS, Black KL. Clinical responsiveness of glioblastoma multiforme to chemotherapy after vaccination. Clin Cancer Res. 2004;10:5316–26.
Sakamoto M, Nakajima J, Murakawa T, Fukami T, Yoshida Y, Murayama T, et al. Adoptive immunotherapy for advanced non-small cell lung cancer using zoledronate-expanded γδTcells: a phase I clinical study. J Immunother. 2011;34:202–11.
Yang YJ, Park JC, Kim HK, Kang JH, Park SY. A trial of autologous ex vivo-expanded NK cell-enriched lymphocytes with docetaxel in patients with advanced non-small cell lung cancer as second- or third-line treatment: phase IIa study. Anticancer Res. 2013;33:2115–22.
Li R, Wang C, Liu L, Du C, Cao S, Yu J, et al. Autologous cytokine-induced killer cell immunotherapy in lung cancer: a phase II clinical study. Cancer Immunol Immunother. 2012;61:2125–33.
Iwai K, Soejima K, Kudoh S, Umezato Y, Kaneko T, Yoshimori K, et al. Extended survival observed in adoptive activated T lymphocyte immunotherapy for advanced lung cancer: results of a multicenter historical cohort study. Cancer Immunol Immunother. 2012;61:1781–90.
Kozlowska E, Biernacka M, Ciechomska M, Drela N. Age-related changes in the occurrence and characteristics of thymic CD4(+) CD25(+) T cells in mice. Immunology. 2007;122:445–53.
This work was supported by National Major Scientific and Technological Special Project for Significant New Drugs Development during the Twelfth Five-year Plan Period (2013ZX09102032), the Chinese Ministry of Science and Technology (2012CB911100), the Provincial Science Foundation of Jilin Provincial Department of Finance (20140414014GH) and the Ministry of Education Key Project of Science and Technology (311015).
The authors declare that they have no competing interests.
XD participated in the acquisition of data, analysis and interpretation of data and the drafting of the manuscript and/or its critical revision. HC and XC participated in acquisition of data and analysis and interpretation of data. HJ, ZL, GW, LC, DL, CN, HT, LY and YZ participated in the acquisition of data. WL and JC participated in the conception, design and coordination of this study, acquisition of data, analysis and interpretation of data and helped to draft the manuscript or revise it critically. All authors read and approved the final manuscript.
Xiao Ding, He Cao and Xiao Chen contributed equally to this work.
Additional file 1: Table S1.
The number of the 3 types of immunocytes infused into each patient.
Additional file 2: Figure S1:
The cytotoxic effect of immune cells on NCI-H446 cells. All 3 types of immune cells exhibited a significant cytotoxic effect on NCI-H446 cells when used alone, but a greater cytotoxic effect was achieved when they were combined, and this cytotoxicity increased further as the E/T cell ratio increased. At an E/T cell ratio of 25:1, the median cytotoxicity level of NK, γδT and CIK cells was 75.5 % (range, 59.1–90.7 %), 70.6 % (range, 48.3–80.0 %), and 49.0 % (range, 27.4–68.9 %), respectively. The combined immune cells showed a synergistic anti-cancer effect with a median cytotoxicity level of 85.5 % (range, 63.4–96.5 %) at an E/T cell ratio of 25:1.
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Ding, X., Cao, H., Chen, X. et al. Cellular immunotherapy as maintenance therapy prolongs the survival of the patients with small cell lung cancer. J Transl Med 13, 158 (2015). https://doi.org/10.1186/s12967-015-0514-0
- Small cell lung cancer
- Cellular immunotherapy
- Maintenance therapy