We conducted a phase III randomized controlled trial (RCT) to investigate the efficacy of postsurgical adjuvant immunotherapy combined with chemotherapy. The immunotherapy targets were residual micrometastases and clones resistant to chemotherapy.
Patients and methods
Between April 2007 and July 2012, 103 postsurgical non-small cell lung cancer patients were randomly assigned to receive either chemo-immunotherapy (group A) or chemotherapy (group B). The immunotherapy consisted of the adoptive transfer of autologous activated killer T cells and dendritic cells obtained from the lung cancer patients’ own regional lymph nodes.
The 2-year overall survival rates in groups A and B were 93.4 and 66.0 %, and the 5-year rates were 81.4 and 48.3 %, respectively. The differences were statistically significantly better in group A. The hazard ratio (HR) was 0.229 (p = 0.0013). The 2- and 5-year recurrence-free survival rates were 68.5, 41.4 and 56.8, 26.2 % in groups A and B, respectively. Those differences were also statistically significant (log-rank test p = 0.0020). The HR was 0.423 (p = 0.0027) in favor of group A. As for adverse reactions to immunotherapy, of a total of 762 courses, 52 (6.8 %) were accompanied with chills and shivering, and 47 (6.2 %), with fever (>38 °C).
Immunotherapy has the potential to improve the postsurgical prognosis of lung cancer patients, but a large-scale multi-institutional RCT is awaited for further confirmation of this study.
Lung cancer is the leading cause of cancer deaths in many advanced countries. Although molecular targeted therapy and new anticancer drugs have improved the prognosis, the overall survival rate is still only 20–30 %. Early diagnosis and surgery are the best ways to cure lung cancer, but most cases are detected at an advanced stage. Only one-third of patients are in stages I–II and become candidates for surgery. Another third receive chemotherapy and/or radiotherapy, while the rest are in far advanced stages and receive only the best supportive care. Furthermore, more than half of the patients, who are supposed to have undergone complete resection, subsequently undergo relapse in distant organs. One of the reasons for this poor prognosis may be the biological nature of lung cancer acquired during the course of cancer onset and progression. Intra-tumor heterogeneity within the primary tumors [1, 2] of lung cancer gives rise to clones resistant to chemotherapy and/or radiation therapy even if the initial response to those treatments is effective. Furthermore, a propensity for early dissemination and metastasis [3, 4] causes relapse after surgery or radiotherapy. Platinum-based doublet chemotherapy has been reported to improve the prognosis of postsurgical patients, but the impact on survival is modest and seems to have reached an efficacy plateau in the past decade [5–7].
We conducted a phase III randomized controlled study to investigate the efficacy of postsurgical adjuvant chemo-immunotherapy  using autologous activated killer T cells and dendritic cells (AKT-DC) . Since most recurrences after surgery with adjuvant chemotherapy derive from chemotherapy-resistant micrometastases, we targeted residual micrometastases resistant to chemotherapy.
Patients and methods
Study design and inclusion criteria
Patients with postsurgical non-small cell lung cancer were randomly assigned to receive either adjuvant chemo-immunotherapy (immunotherapy arm: group A) or adjuvant chemotherapy (control arm: group B) (Fig. 1). Immunotherapy consisted of the adoptive transfer of AKT-DC derived from the regional lymph nodes of lung cancer patients (Fig. 2). Study inclusion criteria were as follows: postsurgical patients aged <76; Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0–1; adequate bone marrow function, liver function, and renal function; histology: primary NSCLC (including combined-type small cell carcinoma); and pathological stage: IB with tumor sizes larger than 5 cm or with severe vessel invasion and stages II–IV (TNM staging system version 6). Although the indications for thoracotomy are limited to clinical stages I–II and stage IIIA after induction chemotherapy, stage IIIB and IV cases with malignant pleural effusion, micrometastasis to mediastinal lymph nodes or intrapulmonary metastasis identified after thoracotomy were also included. Non-curative resection cases were included, but exploratory thoracotomies or cases with macroscopic residual tumors were excluded. The protocol was reviewed and approved by the Ethics Committee of Chiba Cancer Center and the University Hospital Medical Information Network in Japan (UMIN: 000007525). All patients provided written informed consent. This study was conducted in accordance with the ethical principles of the Declaration of Helsinki and the International Conference on Harmonization of Good Clinical Practice guidelines.
Other inclusion criteria
In addition to the criteria cited above, the results of in vitro examination of lymph node activity were also required for inclusion in the study. The autologous AKT-DC from the regional lymph nodes of patients had to grow enough to provide more than 7 × 109 cells for each course of the therapy. Exclusion criteria for the study were as follows: a positive response to HIV, hepatitis C virus, or human T cell lymphotropic virus antibodies; a positive response to hepatitis B surface antigen; and evidence of another active malignant neoplasm.
Before enrolling for randomization after surgery, patients were stratified according to their stage, curability, and whether or not they received induction chemotherapy. Those who had received surgery at first were stratified by pathological stage: group I, stage IB; group II, stage II; group III, stage IIIA; and group IV, stages IIIB and IV. Those who had received induction chemotherapy were stratified to group V, stage IIIA and group VI, stages IIIB and IV. Those patients whose surgery was expiratory thoracotomy or in whom macroscopic residual tumors remained after surgery were excluded from the study. Patients with microscopic residual tumors detected after pathological examinations were included in the study, but were assigned to a more advanced stage. For example, stage IIIA patients with a positive margin of lymph nodes, a bronchial stump, or an arterial stump were stratified to group IV as stages IIIB and IV.
After all criteria had been met and written informed consent for enrollment in the study had been obtained, randomization was performed by the Internet Data and Information Center for Medical Research (INDICE) of the University Hospital Medical Information Network (UMIN) of Japan (file name: CCCI).
Those who were allocated to group A (immunotherapy arm) received 4 monthly courses of postsurgical chemotherapy. Adoptive immunotherapy using AKT-DC was added 1 week after each course of chemotherapy and was then continued once a month for the first 6 months after resection and then every 2 months until 2 years after surgery. This amounted to a total of 12–15 courses in 2 years (Fig. 2). Group B (control arm) received four courses of postsurgical chemotherapy. Stage IIIA patients received two courses of induction chemotherapy before surgery. Those patients underwent thoracotomy with extended lymph node dissection (ND3α) via median sternotomy , followed by two courses of chemotherapy.
Since no standard regimen had been established in the adjuvant setting at the time when this study was designed [11–13], we decided to use platinum doublet regimens belonging to the third-generation drugs described in Data Supplement 1.
Preparation of activated killer T cells and dendritic cells from regional lymph nodes
The procedure for the preparation of AKT-DC has been described elsewhere  (Fig. 2). Tumor-draining lymph nodes include those from the intra-pulmonary to the mediastinal lymph nodes. We used 1–2 g of regional lymph nodes located as near to the primary tumors as possible with no metastasis. If there was no metastasis, we used intra-pulmonary or hilar lymph nodes, and if metastasis had already taken place as far as the mediastinal lymph nodes, we chose mediastinal lymph nodes without metastasis.
Halves of the two or three tumor-draining regional lymph nodes (TDLN) with no tumor metastasis were rinsed with 50 ml of RPMI-1640 medium (Life Technologies Co., Japan) containing antibiotics, while their other halves were submitted for pathological examination for the presence of metastasis. Those in which no metastasis was found were transferred to a sterile Petri dish and minced aseptically into 1-mm3 tissue fragments. Each one showing evidence of metastasis was discarded. The tissue preparation was then suspended in 50 ml KBM-400 (Kojin Bio Co., Tokyo, Japan) or Alyse (ALyS505N: Cell Science and Technology Institute, Inc., Sendai, Japan) serum-free lymphocyte medium containing 400 IU/ml human recombinant interleukin 2 (Proleukin; Chiron B.V., Amsterdam, Netherlands), transferred to a 75-cm2 culture flask, and incubated at 37 °C in air containing 5 % CO2. When the TDLN started to release AKT-DC—usually 2–3 weeks after the initiation of the culture—the tissue and cells were transferred to a culture bag (lot 130129: NIPRO Osaka, Japan) specifically designed for lymph node tissue cultures. Half the volume of fresh medium was added every 2–3 days as long as the cells continued to proliferate exponentially. The AKT-DC generated were separated from the TDLN tissue by filtering through a nylon mesh and were then transferred to another bag. The TDLN tissue culture was continued until the propagation of the cells stopped. The AKT-DC suspension was split 2–3 times every 3–4 days into new bags each containing 800 ml of fresh medium. Then, cells containing AKT-DC were harvested, washed twice using 200 ml of saline suspended in the cryoprotective agent CP-1 (Kyokuto Pharm. Co., Tokyo, Japan) with 4 % human albumin, and stored, 5–10 × 109 cells/bag (freeze bag F-100A: NIPRO Osaka, Japan) at −80 °C until used. Usually, the TDLN cultures continued to release AKT-DC for 2–3 months. When the TDLN stopped releasing cells, 1–2 × 109 peripheral blood lymphocytes (PBL) obtained by lymphocyte apheresis with a COBE Spectra System (COBE BCT, Inc., Colorado, USA) were added. TDLN together with a PBL culture were carried out until we obtained a sufficient number of AKT-DC (1–3 × 1011 cells) for 12–14 courses of immunotherapy.
Certification of cells before transfer to patients
As stated elsewhere, since the cells were cultured in a sealed bag using a serum-free medium, contamination with bacteria or viruses was prevented, but all the cells underwent security tests before transfer to the patients. Cell viability was tested by Trypan blue dye exclusion methods, and cells with <90 % viability were discarded. Bacterial contamination was tested by skilled examiners with light microscopes. Endotoxin tests conducted with an endotoxin single test kit (Wako Co., Osaka, Japan) and a toxinometer (MT-353: Wako Co.), as well as culture tests, were performed whenever bacterial contamination was suspected. The cell surface markers were analyzed before initiation of the culture and just before freezing at −80 °C using two-color methods by FACS analysis with CD3, 4, 8, 25, 80, 83, B7H1, and HLA-DR monoclonal antibodies (Becton–Dickinson Biosciences, CA, USA). Cultures consisting of more than 30 % CD25+CD4+ regulatory T cells were discarded before freezing. Tumor cell contamination was tested by cytological examination with Papanicolaou stain and by immunohistochemical analysis with cytokeratin (Dako Japan Inc., Tokyo Japan) or thyroid transcription factor-1 (TTF-1 Dako) antibodies.
Transfer to patients
Cells qualified by safety examination, and stored at −80 °C, were thawed in a 37 °C water bath and transferred to the patients intravenously with 50 ml saline.
The primary end point of this study was overall survival. Secondary end points were recurrence-free survival, toxicity, and adverse effects of immunotherapy. All eligible patients were included in the analysis of overall survival and progression-free survival.
Patients received regular checkups with tumor markers (CEA, CA-199, SCC, etc.) and chest X-rays every month for the first 6 months, every 2–3 months until 2 years had passed, and every 4–6 months thereafter until 5 years after the thoracotomy. Chest CTs were performed 3, 6, and 12 months after surgery and every 4–6 months thereafter until the 5-year point. One, two, and five years after surgery and whenever recurrence was suspected, PET-CT or a bone scan and/or a brain MRI was performed.
Diagnosis and treatment after recurrence
Recurrence was diagnosed by the Cancer Board of Thoracic Diseases in our center following the preset requirements: (1) histological or cytological evidence of recurrence discovered by biopsy and (2) tumor marker elevation or growth of new lesions accompanied by positive PET findings. Temporary elevation of tumor markers or new lesions with no apparent growth was not considered to show recurrence.
Chemotherapy was used after recurrence, and brain metastasis was treated with a gamma knife or by whole-brain irradiation. Bone or lymph node metastasis was treated by radiation. Immunotherapy was continued or resumed with the patient’s consent in combination with the chemotherapy. EGFR-mutation-positive patients received EGFR-TKI and ALK fusion gene-positive patients received ALK-TKI.
Pretrial assumption of sample size was made according to the following formula :
where S1 is the rate of survival of group A at 5 years after surgery, and S0 is the rate of survival of group B at 5 years. ω represents the rate of dropout and Zα/2 + Zβ = 2.8018 (from the table of normal distribution). We have set the two-sided significance level at 5 % with the power of the test at 80 %.
From the phase II study conducted between 1998 and 2004, it was estimated that 45 patients would be required per arm of the study. Taking into account the possibility of more dropout and death cases, we planned to enroll 60 cases per arm for 5 years.
Statistical analysis was performed on all randomly assigned eligible patients. Overall survival was defined as the time from random assignment to the date of death from any cause. Recurrence-free survival was defined as the time from randomization until the confirmation of recurrence by our Cancer Board. Survival curves were estimated by the Kaplan–Meier technique. Duration of survival was compared between the treatment arms using a two-sided log-rank test. All data analyses were performed using Statistical Analysis Software version 9.3 (Statcom Co., Ltd., Tokyo, Japan) by the Translational Research Informatics Center (TRI) of the Ministry of Education, Culture, Sports, Science and Technology of Japan, and by the Foundation for Biomedical Research and Innovation in Kobe City. Interim analysis was scheduled for 5 years after the initiation of the study, regardless of the time of enrollment.
The study opened on April 1, 2007 and closed on July 30, 2012. Of a total of 556 patients who underwent surgery for lung cancer in our center, 103 cases were enrolled in the study, and 453 cases were ineligible and excluded from it: 110 patients were over 76 years old, 226 cases were stage IA, 46 cases were stage IB with tumor sizes of <5 cm, 35 were stage IIIB, IV with macroscopic residual tumors remaining after surgery and failed to provide enough T cells, 29 had a PS of ≧2, and 7 patients refused randomization (Fig. 1). The demographic characteristics of the patients were evenly distributed between the two groups (Table 1). Projected accrual was 120 cases, but enrollment was stopped at 103 cases in July 2012 on the basis of interim analyses conducted after 5 years. Significant survival benefit was observed in group A, and we felt that further continuation of the study with the group B control arm would be unethical. The median follow-up time was 32.2 months. Among the patients enrolled for the study, two were found to be ineligible after randomization and were finally excluded from the study.
Surgery and chemotherapy
Induction chemotherapy was administered in 12 and 15 clinical stage IIIA cases in groups A and B, respectively. The types of agents administered in this chemotherapy, as well as the surgical procedures, were well balanced in the two arms, and there was no statistical difference between the groups in the numbers of courses of chemotherapy. The chemotherapy regimens of both groups are stated in DS1. The mean total numbers of courses of chemotherapy including those after recurrences in groups A and B were 5.80 ± 3.83 (SD) and 6.41 ± 6.65 (SD), respectively. EGFR-TKI was given to five patients in group A and to seven in group B after recurrences. Eight cases in group A and 11 in group B received bevacizumab in combination with or without chemotherapy. One patient in group A received an ALK fusion gene inhibitor.
A total of 762 courses were administered to group A patients from April 2007 to February 2013. The mean number of effector cells in each course was 10.2 ± 3.1 (standard deviation; SD) × 109 cells, the mean number of courses for a patient was 15.3 ± 6.92 (SD) courses, and the mean total of effector cells delivered was 1.51 ± 0.68 (SD) × 1011 cells. There was no correlation between the number of courses delivered to a patient and either recurrence or survival. The courses and the numbers of cells delivered to each patient are detailed in DS2.
Adverse reactions to immunotherapy
Out of a total of 762 courses, 52 (6.8 %) were accompanied with chills and shivering, and 47 courses (6.2 %) were followed by fever (>38). Of 50 patients treated with immunotherapy, 28 had no adverse reactions and 22 had at least one adverse reaction of chills, shivering and/or fever. Chills and shivering started about 30 min after the start of each cell transfer, continued for 10–20 min, and were followed by fever up to 38–40 °C. These fevers lasted for 2–3 h, and the body temperature then gradually declined to a normal level within the same day. In no case did fever persist until the next day. No adverse reaction other than chills or fever was observed. Adverse reactions are listed in DS2 (Data Supplement 2).
There were 19 cases of recurrence in group A (lungs, 6; lymph nodes, 5; bones, 3; and others, 5) and 33 in group B (lungs, 9; lymph nodes, 8; bones, 8; brain, 5; and others, 3). Seven patients in group A became tumor free after recurrence following treatments combined with immunotherapy: two cases of EGFR-TKI, three cases of resection of lung metastasis, one case of ALK fusion gene inhibitor, and 1 of radiation; and continued to be tumor free until the time of the final analysis. In one case in group B, CR was attained after chemotherapy. Therefore, 38 patients in group A and 19 patients in group B were tumor free at the time of analysis. Recurrence was seen in 14 and 21 cases of adenocarcinoma and in 3 and 7 squamous cell carcinoma cases in groups A and B, respectively. There was no correlation between recurrence and histological types.
Figure 3 shows the Kaplan–Meier estimates of overall survival. The 2- and 5-year overall survival rates were 93.4 % [95 % confidence interval (CI) 80.8–97.8] and 81.4 % (60.1–92.1) in group A, and 66.0 % (50.4–77.7) and 48.3 % (31.4–63.3) in group B, respectively. The difference was statistically significant (log-rank test p = 0.0005, generalized Wilcoxon test p = 0.0005) in group A. The HR was 0.229 (95 % CI 0.093–0.564, p = 0.0013). The median survival time of group B was 47.5 (from 26.3 to not reached) months and was never reached in group A. The 2- and 5-year recurrence-free survival rates (Fig. 4) were 68.5 % (53.2–79.7) and 56.8 % (40.3–70.3) in group A, 41.4 % (27.5–54.7) and 26.2 % (13.1–41.5) in group B, respectively. The difference was statistically significant (log-rank test p = 0.0020). HR was 0.423 (95 % CI 0.241–0.743, p = 0.0027) in group A. The median recurrence-free survival was 16.56 (9.00–32.01) months in group B, but was not reached in group A.
We have reported the results of a phase III randomized controlled study of postsurgical adjuvant immunotherapy with lymphokine-activated killer (LAK) cells conducted between 1986 and 1992 . The in vitro study using regional lymph nodes as a source of killer and dendritic cells indicated a much higher activity against autologous tumor cells than that using LAK cells . A phase II study was conducted between 1998 and 2004 using AKT-DC obtained from the regional lymph nodes of primary lung cancer patients . The results of the phase II study predicted a promising outcome for a phase III study using this modality. Furthermore, this modality yielded a more marked effect in early stage than in advanced-stage cases. Patients with macroscopic residual tumors, such as those with pleural dissemination, or bulky N2–N3 metastases, failed to respond to this treatment. Therefore, we added stage II cases and IB cases with tumor sizes larger than 5 cm to, and excluded cases with macroscopic residual tumors from, the present phase III study.
This phase III study, conducted between 2007 and 2012, is the concluding portion of a series of studies of adjuvant immunotherapy for postsurgical lung cancer patients that lasted from 1986 to 2012. In a clinical study conducted to verify the effects of chemotherapy, placebo groups are included. But in adjuvant settings, control arms do not usually use placebo or blinded procedures, but observation only. The reasons for this originate from the fact that there has been no standard chemotherapy recommended to improve survival in adjuvant settings. In this adjuvant immunotherapy, we thought that blind control with no cell infusion would be deceptive and unethical. Furthermore, there are no cells which have no effect at all—whether favorable or unfavorable—on the immune response.
The successful outcome of this study depended largely on the improvements of the in vitro system, which enabled us to obtain a large quantity of high-quality effector cells for use in each course of treatment. Long-term tissue cultures of lymph nodes in specifically designed culture bags enabled us to transfer 1–2 × 1010 cells for a course of treatment in a contamination-free environment. The most effective dose for immunotherapy remains a matter of conjecture, but the number of lymphocytes and dendritic cells transferred to the patients, and their activity against cancer cells appear to be the key issues that determine whether the immunotherapy will work or not. We obtained sufficient numbers of lymphocytes from N0, N1 patients, but it was difficult to do so from some of the N2, N3 patients. In half of the N2, N3 patients, usually those with tumors that were macroscopically residual, it was difficult to obtain sufficient lymphocytes. Among our 62 stage IIIB and IV cases, 35 (56.5 %) were excluded from the study because macroscopic residual tumors remained after surgery, and we could not obtain enough T cells. The cell surface markers of AKT-DC were CD3 (94.7 %), CD4 (57.9 %), CD8 (55.1 %) and CD83 (21.5 %) . Although we have not evaluated precisely the correlation between cell surface markers and the effects of immunotherapy, we could not detect any relationship between cell surface markers and the results of immunotherapy so far observed.
It has been suggested that immunocompetent cells eliminate or suppress the proliferation of nascent transforming cells in the initiation of tumor growth (known as the immunoediting: elimination phase) [17–19]. However, immune selective pressure favors the growth of tumor cell clones with a low-immunogenic phenotype, and this leads to the equilibrium phase of immunoediting. In this phase, tumor cell generation and apoptosis are equivalent and keep the tumor size unchanged in an equilibrium in which tumors remain occult and asymptomatic for a prolonged period of time [20–22]. In the escape phase, when tumors start proliferating, expanding in size, and forming clinically detectable masses, the immune system, in turn, becomes inefficient or tolerates tumor growth. Numerous mechanisms have been proposed to explain how tumors escape immune control and find a way from dormancy to progression [23–26]. Immunosuppression within the tumor microenvironment has been cited as one of the causes of the ineffectiveness of immunotherapy against cancers [27–30].
The target of the immunotherapy described here is not the primary lesion, but the undetectable tumor cells remaining after the resection of a primary carcinoma [3, 4]. A major cause of tumor recurrence is metastasis that is considered to be derived from circulating and disseminating tumor cells (CDTC). Primary cancers start releasing tumor cells at relatively early stages of tumor development. CDTC released from the primary lesion remain dormant and in a quiescent state for a prolonged period of time as solitary tumor cells or dormant micrometastases [20–22]. A controversial discussion of the main reasons for immune escape mechanisms concerns whether tumor growth depends on the poor immunogenicity of tumor cells, which helps them to escape immune recognition, or on the immunosuppressive mechanisms working within the tumor microenvironment. In other words, either (1) since the tumor cells have already undergone immune surveillance, they are not recognized by the immune system and only the non-immunogenic tumor cells survive after tumor progression, or (2) tumor cells are recognized, but immune suppression in the tumor microenvironment blocks immune attack by killer cells. The results of this study suggest the importance of the latter mechanisms of the tumor microenvironment in immune escape. Immunotherapy using this modality therefore has a role in recurrence control by inhibiting the growth of disseminated micrometastases before an immunosuppressive microenvironment has been achieved.
The majority of the causes of cancer recurrence derive from CDTC, which are clinically undetectable at the time of surgery. The phenotypic diversity of disseminated cells resulting from intra-tumor heterogeneity [1, 2] gives rise to clones resistant to chemotherapy and prevents tumor cell eradication by chemotherapy. The heterogeneity of tumor cells enables them to escape even from molecular targeted therapy . The regional lymph nodes of lung cancer patients are the sites where the first adoptive immune response against cancer develops [32, 33]. Dendritic cells at the tumor site take up antigens, migrate to lymph nodes, and educate antigen-specific naïve T lymphocytes to become cytotoxic T lymphocytes . Using these lymph nodes as a source of dendritic cells and killer cells, we can eradicate the heterogeneous tumor cells disseminating throughout the body carrying a wide variety of antigens.
Our long experience of in vitro cultures of regional lymph nodes [35–37] shows that, although in vitro culture of non- or micrometastatic regional lymph nodes induces AKT-DC in the presence of low-dose IL2, macroscopic metastatic lymph nodes do not propagate those cells in vitro. In other words, tumor cells and lymphocytes are mutually exclusive and never coexist in vitro when cultured in the presence of IL2 for more than 2–3 weeks. Therefore, contamination of tumor cells in AKT-DC is prohibited when lymphocyte growth is dominant. This in vitro phenomenon does not seem to depend on the patient or the tumor cell types, but on the reciprocal quantitative balance between tumor cells and lymphocytes. This phenomenon indirectly provides evidence that tumor cells are recognized even after tumor progression, but the tumor microenvironment blocks the effect of immune responses.
The outcome of the present study was successful, and this may be attributable to the mechanism whereby the target of immunotherapy is the dormant CDTC remaining after surgery before an immunosuppressive microenvironment is developed. Although the results of this study have great significance, this single-institutional small-sample study needs further confirmation with a large-scale multi-institutional RCT before the clinical importance of this modality is fully recognized.
Activated killer T cells and dendritic cells
Anaplastic lymphoma kinase
Circulating and disseminating tumor cells
Epidermal growth factor receptor
Lymphokine-activated killer T cells
Non-small cell lung cancer
Tumor-draining regional lymph nodes
Tyrosine kinase inhibitor
Gerlinger M, Rowan AJ, Horswell S et al (2012) Intratumor heterogeneity and branched evolution revealed by multiregion sequencing. N Engl J Med 366:883–892
Marusyk A, Almendro V, Polyak K (2012) Intra-tumour heterogeneity: a looking glass for cancer? Nat Rev Cancer 12:323–334
O’Flaherty JD, Gray S, Richard D et al (2012) Circulating tumour cells, their role in metastasis and their clinical utility in lung cancer. Lung Cancer 76:19–25
Gorges TM, Pantel K (2013) Circulating tumor cells as therapy-related biomarkers in cancer patients. Cancer Immunol Immunother 62:931–939. doi:10.1007/s00262-012-1387-1
Berghmans T, Paesmans M, Meert AP et al (2005) Survival improvement in resectable non-small cell lung cancer with (neo)adjuvant chemotherapy: results of a meta-analysis of the literature. Lung Cancer 49:13–23
Bennouna J, Senellart H, Hiret S et al (2011) Impact of histology on survival of resected non-small cell lung cancer (NSCLC) receiving adjuvant chemotherapy: subgroup analysis of the adjuvant vinorelbine (NVB) cisplatin (CDDP) versus observation in the ANITA trial. Lung Cancer 74:30–34
Felip E, Martinez-Marti A, Martinez P et al (2013) Adjuvant treatment of resected non-small cell lung cancer: state of the art and new potential developments. Curr Opin Oncol 25:115–120
Chen G, Emens LA (2013) Chemoimmunotherapy: reengineering tumor immunity. Cancer Immunol Immunother 62:203–216. doi:10.1007/s00262-012-1388-0
Kimura H, Dobrenkov K, Iida T et al (2005) Tumor-draining lymph nodes of primary lung cancer patients: a potent source of tumor-specific killer cells and dendritic cells. Anticancer Res 25:85–94
Kimura H, Yasufuku K, Ando S et al (2007) Indications for mediastinoscopy and comparison of lymph node dissections in candidates for lung cancer surgery. Lung Cancer 56:349–355
Burdett S, Stewart LA, Rydzewska L (2006) A systematic review and meta-analysis of the literature: chemotherapy and surgery versus surgery alone in non-small cell lung cancer. J Thorac Oncol 1:611–621
Strauss GM, Herndon JE, Maddaus MA et al (2008) Adjuvant paclitaxel plus carboplatin compared with observation in stage IB non-small-cell lung cancer: CALGB 9633 with the Cancer and Leukemia Group B, Radiation Therapy Oncology Group, and North Central Cancer Treatment Group Study Groups. J Clin Oncol 26:5043–5051
Arriagada R, Bergman B, Dunant A et al (2004) International Adjuvant Lung Cancer Trial Collaborative Group. Cisplatin-based adjuvant chemotherapy in patients with completely resected non-small-cell lung cancer. N Engl J Med 350:351–360
Tango T (2003) Medical Statistics Series 5, Randomized studies: Design and Statistical Analyses. Asakura Shoten, Tokyo, pp 59–62
Kimura H, Yamaguchi Y (1997) A phase III randomized study of interleukin-2 lymphokine-activated killer cell immunotherapy combined with chemotherapy or radiotherapy after curative or noncurative resection of primary lung carcinoma. Cancer 80:42–49
Kimura H, Iizasa T, Ishikawa A et al (2008) Prospective phase II study of post-surgical adjuvant chemo-immunotherapy using autologous dendritic cells and activated killer cells from tissue culture of tumor-draining lymph nodes in primary lung cancer patients. Anticancer Res 28:1229–1238
Dunn GP, Bruce AT, Ikeda H et al (2002) Cancer immunoediting: from immunosurveilance to tumor escape. Nat Immunol 3:991–998
Kim R, Emi M, Tanabe K et al (2007) Cancer immunoediting from immune surveillance to immune escape. Immunology 121:1–14
Schreiber RD, Old LJ, Smyth MJ et al (2011) Cancer immunoediting: integrating immunity’s roles in cancer suppression and promotion. Science 331:1565–1570
Aguirre-Ghiso JA (2007) Models, mechanisms and clinical evidence for cancer dormancy. Nat Rev Cancer 7:834–846
Almog N (2010) Molecular mechanisms underlying tumor dormancy. Cancer Lett 294:139–146
Enderling H, Hahnfeldt P, Hlatky L et al (2012) Systems biology of tumor dormancy: linking biology and mathematics on multiple scales to improve cancer therapy. Cancer Res 72:2172–2175
Gutkin DW, Shurin MR (2014) Clinical evaluation of systemic and local immune responses in cancer: time for integration. Cancer Immunol Immunother 63:45–57. doi:10.1007/s00262-013-1480-0
Pardoll D (2003) Does the immune system see tumors as foreign or self? Annu Rev Immunol 21:807–839
Gajewski TF, Meng Y, Blank C et al (2006) Immune resistance orchestrated by the tumor microenvironment. Immunol Rev 213:131–145
Rabinovich GA, Gabrilovich D, Sotomayor EM et al (2007) Immunosuppressive strategies that are mediated by tumor cells. Annu Rev Immunol 25:267–296
Becker JC, Andersen MH, Schrama D et al (2013) Immune-suppressive properties of the tumor microenvironment. Cancer Immunol Immunother 62:1137–1148. doi:10.1007/s00262-013-1434-6
Rosenberg SA, Yang JC, Restifo NP et al (2004) Cancer immunotherapy: moving beyond current vaccines. Nat Med 10:909–915
Dudley ME, Wunderlich JR, Yang JC et al (2005) Adoptive cell transfer therapy following non-myeloablative but lymphodepleting chemotherapy for the treatment of patients with refractory metastatic melanoma. J Clin Oncol 23:2346–2357
Gattinoni L, Powell DJ Jr, Rosenberg SA et al (2006) Adoptive immunotherapy for cancer: building on success. Nat Rev Immunol 6:383–393
Kuwai T, Nakamura T, Kim SJ et al (2008) Intratumoral heterogeneity for expression of tyrosine kinase growth factor receptors in human colon cancer surgical specimens and orthotopic tumors. Am J Pathol 172:358–366
Maass G, Schmidt W, Berger M et al (1995) Priming of tumor-specific T cells in the draining lymph nodes after immunization with interleukin 2-secreting tumor cells: three consecutive stages may be required for successful tumor vaccination. Proc Natl Acad Sci USA 92:5540–5544
Schweighoffer T, Schmidt W, Buschle M et al (1996) Depletion of naive T cells of the peripheral lymph nodes abrogates systemic antitumor protection conferred by IL-2 secreting cancer vaccines. Gene Ther 3:819–824
Adema GJ, Hartgers F, Verstraten R et al (1997) A dendritic-cell-derived C-C chemokine that preferentially attracts naive T cells. Nature 387:713–717
Kimura H, Yamaguchi Y, Kadoyama C (1983) Cytotoxicity tests against cultured human lung cancer cells with autologous lymphocytes activated in vitro by mitomycin C-treated tumor monolayers in the presence of T-cell growth factor. Jpn J Clin Oncol 13:3–13
Kadoyama C, Kimura H, Yamaguchi Y (1987) Inhibition of cytotoxicity to autologous tumor cells by the regional lymph node cells of patients with primary lung cancer. Jpn J Clin Oncol 17:29–39
Kimura H, Yamaguchi Y (1989) Cytotoxic activity of various LAK cells against autologous lung cancer, K-562 and Daudi cells. Jpn J Clin Oncol 19:222–228
We would like to express our sincere thanks to those who have agreed to participate in this phase III study. Were it not for their participation, the study would not have been possible. The authors are indebted to Ms. Yurie Taguchi, and Professor Emeritus J. Patrick Barron of Tokyo Medical University (TMC) and Mr. CWP Reynolds, associated with TMC, for their editing of this English language manuscript.
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Kimura, H., Matsui, Y., Ishikawa, A. et al. Randomized controlled phase III trial of adjuvant chemo-immunotherapy with activated killer T cells and dendritic cells in patients with resected primary lung cancer. Cancer Immunol Immunother 64, 51–59 (2015). https://doi.org/10.1007/s00262-014-1613-0
- Phase III study
- Lung cancer
- Adjuvant therapy
- Lymph node
- Dendritic cell