Cancer immunity and therapy using hyperthermia with immunotherapy, radiotherapy, chemotherapy, and surgery
Topic: Cancer Immunotherapy
Hyperthermia is a type of medical modality for cancer treatment using the biological effect of artificially induced heat. Even though the intrinsic effects of elevated body temperature in cancer tissues are poorly understood, increasing the temperature of the body has been recognized as a popular therapeutic method for tumorous lesions as well as infectious diseases since ancient times. Recently accumulated evidence has shown that hyperthermia amplifies immune responses in the body against cancer while decreasing the immune suppression and immune escape of cancer. It also shows that hyperthermia inhibits the repair of damaged cancer cells after chemotherapy or radiotherapy. These perceptions indicate that hyperthermia has potential for cancer therapy in conjunction with immunotherapy, chemotherapy, radiotherapy, and surgery. Paradoxically, the anticancer effect of hyperthermia alone has not yet been adequately exploited because deep heating techniques and devices to aggregate heat effects only in cancer tissues are difficult in practical terms. This review article focuses on the current understanding concerning cancer immunity and involvement of hyperthermia and the innate and adoptive immune system. The potential for combination therapy with hyperthermia and chemotherapy, radiotherapy, and surgery is also discussed.
Cancer is one of the most fatal diseases in the world, inducing various conditions such as organ disorders from primary lesions or metastatic lesions and cachexia. Three standard therapeutic methods include surgery, chemotherapy, and radiotherapy; however, these are not satisfactory on the whole. Difficulties in treating cancer are due to its distinctive abilities for immune escape, metastasis, and tolerance to cancer therapies. These abilities result from the heterogeneity of cancer cells and the anticancer efficacy of conventional treatment methods has limitations. Recent progress has been made in cancer immunotherapy, a fourth cancer therapeutic method, including activated T-cell therapy and dendritic cell (DC) vaccines; however, their therapeutic efficacy is still limited[2,3]. The more recent discovery of immune check-point inhibitors has demonstrated sensational long-term benefits in patients with advanced cancer and has highlighted the importance of immune responses to cancer, but its efficacy has been recognized only in a minority of patients[4,5]. Hence, current therapeutic methods need to be improved or new therapeutic cancer therapy developed for single or combination use. Recently, many reports have shown that an appropriate heat effect has potential anticancer efficacy and can enhance the efficacy of other cancer therapies. Nonetheless, fever itself is a complex physiological response, with the intrinsic effects of elevated body temperature regarded as an important defense system for the body by increasing the immune reaction not only against infectious disease but also against cancer.
Even though the efficacy of intrinsic effects of elevated body temperature in tissues to cells is still being studied, it has been disclosed that the survival rate of cells is reduced by heating at 39-42 °C, and it is amplified remarkably by heating at ≥ 42.5 °C for ≥ 1 h. There is no variation in tolerance between tissue types[7,8]. Hyperthermia is a type of cancer treatment using this feature to target cancer cells and their surrounding environment. In the early days, hyperthermia alone at 42-44 °C was performed against recurrent tumors derived from head and neck cancer and breast cancer, which appeared on the surface of the body. The objective antitumor response in this set of superficial tumors was around 40%[10-12]. However, most cancers, including primary sites as well as recurrent or metastatic sites, are located deep inside the body. This makes hyperthermia alone less effective because it is quite difficult to heat only cancer tissues to more than 42 °C using currently available heating devices. Recently, the usefulness of mild hyperthermia with 39-42 °C (fever-range hyperthermia) for 1-2 h has been reported for combination use with other cancer therapies. This method takes advantage of the difference in sensitivity to heat stress between normal tissues and cancerous tissues. The logic behind its use is that normal tissues have enough vascular distribution to drain the congestion of fever and avoid tissue damage in these shorter time periods. In contrast, in cancerous tissues, fever and heat stress tend to accumulate. Consequently, an anticancer effect can be obtained within the fever range while normal tissues endure. Nevertheless, irradiation for a long period with a higher temperature than body temperature until cancer is eliminated is still harmful to normal tissues and homeostasis of the body.
In widespread use, the term hyperthermia generally includes regional hyperthermia, whole-body hyperthermia, and hyperthermic intraperitoneal chemotherapy (HIPEC). Ablation therapy, which uses microwave or a laser at 80-100 °C, leading to direct cancer cell death by heat denaturation of proteins or necrosis, may also be categorized as hyperthermia in the broad sense. Regional hyperthermia is a less invasive method of thermal therapy. In this method, heat effects are limited to the range of irradiation and have an expected role as a chemosensitizer or radiosensitizer used to augment the efficacy of chemotherapy or radiotherapy in situ. The currently popular method for hyperthermia in clinical practice is mild hyperthermia applied to the regional cancer area by using an 8 MHz[16,17] or 13.56 MHz radiofrequency capacitive heating device, applied to the surface of the body directly above the cancer. In contrast, whole body hyperthermia heats areas of body and increases the systemic body temperature of patients. This method is suitable for patients with metastases in multiple organs, including carcinomatosis. Increased effects of immune cells such as T cells and DCs located in the peripheral organs or circulation are also expected, in addition to the effect of regional hyperthermia.
T-cell-based immune responses to cancer
T-cells are key immune cells with regard to specific immune responses against cancer. The pivotal events involved in the induction of successful T-cell mediated immune responses and those in the immune effector phase are shown in Figure 1. DCs are the major antigen-presenting cells (APCs), which are capable of initiating T-cell mediated immune response. These cells usually reside in the epidermis of the skin and mucosal tissues to prepare to combat foreign enemies. This includes cancer antigens, which are fragments of tumor cells generated as a consequence of natural death or the interaction of tumors and innate immune cells such like natural killer (NK) cells[22,23]. DCs process and present these fragments on their cell surface along with major histocompatibility complex (MHC) antigens after capturing cancer antigens. The complex of cancer antigens and MHC class I antigens are presented to CD8+ cytotoxic T lymphocytes (CTLs), while the complex of cancer antigens and MHC class II antigens engage to stimulate CD4+ helper T-cells. The CD4+ helper T cells enhance the differentiation of CTLs into effecter T-cells by secreting cytokines such as interferon-γ (IFN-γ) and interleukin-2 (IL-2).
Naïve T-cells receive the presentation of cancer antigens from DCs in the T-cell zones of lymphoid organs to acquire an appropriate immune response. To achieve antigen presentation, these two cells constantly migrate to the lymphoid organs (homing).
Figure 1: T-cell-mediated immune responses against cancer
The homing mechanism is regulated by chemokines and the chemokine receptor axis. CCL21 and CCL19 are homeostatic chemokines that are constantly secreted from secondary lymphoid organs, including lymph nodes and Peyer’s patches, without any exogenous stimulation[25-27]. Meanwhile, C-C chemokine receptor 7 (CCR7) is a concomitant chemokine receptor of CCL21 and CCL19. Cells expressing CCR7 can migrate to organs where CCL21 and CCL19 are secreted depending on the concentration gradient. Most naïve T-cells constantly express CCR7. DCs matured by exogenous stimulation with antigens derived from bacteria or cancers begin to express CCR7, whereas immature DCs do not express CCR7[24,29]. Thus naïve T-cells and antigen-presenting DCs can migrate to secondary lymphoid organs from peripheral organs. As a final step in homing, these immune cells need to carry out transvasation through high endothelial veins to infiltrate into the lymphatic organs from the lymphatic system. To complete homing through the interval between endothelial cells, expression of adhesion molecules such as L-selectin and integrin is up-regulated for rolling and adhesion with intercellular adhesion molecule (ICAM), which is a co-receptor for integrin[30,31]. After antigen presentation, T-cells are induced to proliferate and differentiate into effecter T-cells. The expression of CCR7 on T-cells is then down-regulated to leave the lymphoid tissue for migration to cancer tissues.
Effecter T-cells recognize the complex of cancer antigens and MHC class I antigens expressed on cancer cells through a T-cell receptor (TCR). Then, the lethal effects against cancer cells are triggered along two different pathways: granule exocytosis and death ligand/death receptor system. Granule exocytosis induces the secretion of perforins and granule enzymes (granzymes)[32,33]. Even though the nature and the role of these proteases in response to cancer is still unclear, perforins generally act as a carrier for the delivery of granzymes and build pores in the plasma membrane of target cells to allow granzymes to gain entry to the target cell cytosol. Granzymes are considered to execute the target cells through the cleavage of factors required for replication and defense. Death ligands are proteins including Fas ligand (FasL) that is expressed on effector T-cells. FasL can engage target cells through the Fas receptor, which belongs to the tumor necrosis factor (TNF) superfamily, to induce target cell death by apoptosis. The main role of FasL is to regulate the immune system, but cancer cells may over-express FasL spontaneously or as chemotherapy resistance to make a countercharge by inducing the apoptosis of tumor-infiltrating lymphocytes (TILs) to escape from the immune system.
T-cell based immunotherapy for cancer
As has been mentioned, the human immune system always works in response to antigens expressed on cancer cells, thus distinguishing cancer cells from noncancerous cells. This causes the induction of TILs to be found in the tumor microenvironment. However, anticancer immunity is usually not enough to overcome the tumor’s growing speed owing to the low immunogenicity of cancer cells because these cells are derived from an individual’s own cells. Thus, it was inevitable that immunotherapy would be developed to overcome the low immunity against cancer. With regard to T-cell-based immunotherapy, adoptive transfer of CD3-activated T-cells has been induced traditionally as a compulsory activation stimulus to compensate for the reduction in stimulation frequency due to low antigenicity. Moreover cancer-specific-antigen loaded DC vaccines are also utilized to induce more types of cancer-specific T lymphocytes.
The more recent discovery of immune check-point inhibitors achieved outstanding progress in cancer immunotherapy by showing sensational long-term benefits in patients with advanced cancer[4,5]. The purpose of this medicine is to inhibit immune suppressive signals between cancer cells and T-cells; thus the agent that eliminates a cancer during the final phase is T-cells[36,37]. Immune check-point molecules such as programmed death-1 (PD-1) and T-lymphocyte-associated antigen 4 (CTLA4) are expressed on T cells and play a vital role in limiting the exaggerated immune response in both adaptive immune response and autoimmune response to maintain homeostasis by acting as an inhibitory signal against APCs. Recently, it has been disclosed that cancer cells take advantage of this mechanism to survive. For example, cancer cells express PD-L1, which is a concomitant ligand against PD-1, to attenuate T-cell-based immune reactions in association with cancer progression. With the discovery of this mechanism, immune check-point inhibitors have been shown to carry great promise. However, its efficacy has only been recognized still in a small number of patients, and PD-L1 expression on tumor cells has been regarded as a negative prognostic factor[4,5].
Hyperthermia enhances immune systems in response to cancer
Body temperature elevation has been considered an important phenomenon associated with regulation in both innate and adaptive immune responses. Hyperthermia elicits various effects in several steps of the immune reaction for cancer. It up-regulates the homing of immune cells and the function of adhesion molecules on both immune cells and endothelial cells, activating immune cells including CTLs, DCs, and NK cells, and inhibiting immune suppression. In this section, we discuss how thermal stress up-regulates the immune system.
Hyperthermia, especially whole body hyperthermia, has the potential to increase the homing of immune cells. Continuous secretion of homeostatic chemokines including CCL21 and the expression of adhesion factors including selectin, integrin, and ICAM regulate immune homeostasis by maintaining the homing of these immune cells. Thermal effect can enhance the expression of ICAM-1 and CCL21 in high endothelial venules (HEVs) and can up-regulate L-selectin- and integrin-dependent adhesive interaction to induce the adhesion and migration of DCs and T-cells toward HEVs. Additionally, increases in the migration capacity of DCs ex vivo has been reported.
We reported previously that heat treatment stimulated cytokine production from peripheral T-cells in vitro and in vivo in fresh peripheral venous blood obtained from 5 healthy volunteers. We first incubated peripheral blood mononuclear cells (PBMCs) separated from obtained blood samples at 37 °C or 39 °C for 2 h in a water bath, then PBMCs were co-cultured with anti-CD3/CD28 monoclonal antibodies for 24 h at 37 °C. To evaluate the secretory properties of cytokines in T-cells, IFN-γ and IL-2 levels in the supernatant were measured. Results showed that both cytokine production levels were significantly increased (approximately twofold) when PBMCs were cultured at 39 °C [Figure 2]. Next, the volunteers underwent whole body hyperthermia until the rectal temperature reached 38.5 °C (generally it required 1 h of treatment). After terminating heating, volunteers were covered with a leather tent for 60 min as a heat-retention phase. Blood samples were obtained four times: before the treatment, at the end of the heat-retention phase, and then 24 and 48 h after
37 °C 39 °C 37 °C 39 °C
Figure 2: In vitro hyperthermia stimulates IFN-g and IL-2 production from T-cells stimulated with monoclonal antibodies against CD3 and CD28. Blood samples were collected and incubated at 37 °C and 39 °C for 2 h, then PBMCs were extracted and co-cultured with monoclonal antibodies against CD3 and CD28 to measure IFN-g and IL-2 production levels in each supernatant. Results are shown as twofold over the control (37 °C) for the average of five separate donors, and expressed as mean ± SEM. Statistical differences from the control were evaluated using paired t-test. P < 0.05 was recognized as statistically significant. IFN: interferon; IL: interleukin; PBMCs: peripheral blood mononuclear cells treatment. IFN-γ and IL-2 levels in each supernatant were measured in response to monoclonal antibody against CD3 and CD28. The results showed significant increases in the production of both IFN-γ and IL-2; these were observed not only immediately after but also 24 h after whole body hyperthermia. At 48 h after whole body hyperthermia, the production levels of both cytokines had returned to the pretreatment levels [Figure 3].
The potential mechanisms that stimulate cytokine production after hyperthermia may be explained by an increase in the membrane fluidity of T-cells. It was reported that physiological heat stress enhanced the membrane fluidity of T-cells. It also showed an increase in the cluster formation of the GM1+ CD-microdomain in CD8+ T-cells, clustering TCRβ and the CD8 co-receptor, and enhanced conjugate formation between T-cells and APCs in mice. These results suggest that a heat-stress-induced increase in membrane fluidity is one of the primary events, and it subsequently triggers a cascade of molecular events that eventually make T cells crosstalk more rapidly and efficiently with APCs. These cellular events, including the formation of TCR microclusters, consist of several adhesion and signaling molecules, which accumulate at the immune synapse. This is also known as the central supramolecular activation complex.
Heat-shock proteins (HSPs) have been considered to play an important role in the effects of heat treatment on T-cell function. Indeed, the synthesis of HSPs was shown to increase with elevated body temperature in fever-range whole-body hyperthermia. The essential function of HSPs is known to involve their actions as molecular chaperones. As part of this function, HSPs are involved in antigen presentation and cross-presentation in DCs by delivering chaperoned antigenic peptides to MHC class I molecules, thereby inducing antigen-specific T-cell activation[48-50]. It was reported that the presence of recombinant Hsp60 allows antigen-dependent T-cell activation with antigen-specific IFN-γ secretion in conditions when even stimulation is not sufficient to activate T-cells.
In contrast, Hsp70 is also expressed in cancers and acts as an effective inhibitor of apoptosis caused by heat stress, thereby participating in tumor progression. Hsp70 can prevent aggregation, remodel folding pathways, and regulate activity of cancer cells. However, the effects of HSPs on DCs and T-cells are still contradictory. Thus, the function of HSPs must continue to be investigated in order to clarify whether and how HSPs are involved in antigen presentation between T-cells and DCs during heat stress.
NK cells can behave as a spearhead of the innate immune response toward exogenous antigens and can make an initial attack against targets without prior exposure to the specific antigens. Basically, normal cells express MHC class I molecules, whereas aberrant cells such as cancer cells extinguish the expression of MHC class I molecules on themselves. This phenomenon was especially observed in pancreatic, cervical, breast, prostatic, and penile cancer. Down-regulation of MHC class I molecules on cancer cells is one of the steps for immune escape from cancer-specific immune response by T-cells, because abnormal antigens must be presented with MHC class I molecules when T-cells recognize them. In contrast to T-cells, NK cells target cells that have lost the expression of MHC class I molecules, because NK cells express inhibitory receptors that engage with MHC class I antigens. Hence, the anticancer ability of NK cells is exercised at this time to complement T-cell-based immune reactions owing to attenuated inhibitory signals between NK cells and cancer cells. Activated NK cells have nonspecific anticancer potential by secreting cytotoxic molecules including perforin and granzyme and death receptors such as FasL, TRAIL, and TNF-α[62,63]. Additionally, heat stress can enhance the distinct clustering of NK cell-activating receptors such as NKG2D on the surface of NK cells and the expression of NK cell-activating ligands, including major histocompatibility complex class I-related chain A (MICA)[64,65]. Moreover, an increase in the expression of MICA and increased cytotoxicity of NK cells were also observed in several cancer cell lines. Concerning the contribution of NK cells to cancer-specific immune responses, after an initial attack, fragments including cancer antigens of tumor cells are generated as a result of the interaction of the tumor and NK cells. These cancer antigens are recognized by DCs for T-cell-based cancer-specific immune responses. Additionally, activated NK cells secrete cytokines including IFN-γ and IL-2 to enhance acquired immune responses with immunoglobulin production from B-cells and activation of T-cells[55,61]. This perception leads to the conclusion that increasing the function of NK cells by hyperthermia could be expected to result in the augmentation not only of nonspecific anticancer immune reactions regulated by NK cells but also of specific anticancer immune reactions regulated by T-cells and DCs.
To avoid exaggerated immune responses that cause harmful effects on the body, the immune system is regulated to limit adaptive immune responses and prevent autoimmune responses and auto-inflammatory reactivity in the normal situations. To achieve this, our immune system combines immunological tolerance system. Regulatory T cells (Tregs) are a subpopulation of T-cells, expressing CD4, CD25, and FOXP3, which negatively modulate both innate and adopted immune response by down-regulating or suppressing induction and proliferation of immune cells including T cells, DCs, and NK cells[67-69]. Even though Tregs usually account for about 4% of CD4+ T cells, they can make up as much as 20-30% of the total CD4+ population in the tumor microenvironment and are associated with poor prognosis in many cancers, such as ovarian, breast, renal, and pancreatic cancer. Depletion of Tregs in animal models has been shown to increase the efficacy of immunotherapy. So, achieving the depletion of Tregs is one of the pivotal targets of recent research and therapy associated with cancer immunology. The potential effect of hyperthermia is considered to enhance the cytotoxicity of NK cells against Tregs, and to inhibit the induction of Tregs while the apoptosis of Tregs is induced. A significant decrease in the number of Tregs was observed while NK cell activity and the percentage of NK cells increased in peripheral blood samples of healthy volunteers after irradiation of fever-range hyperthermia to the upper abdominal region. Moreover, combination therapy of intratumoral injection of immature DCs and local hyperthermia for patients with advanced malignant melanoma demonstrated decreased infiltration of Tregs and increased infiltration of activated CTLs, even though there was no statistical difference in overall survival time.
The efficacy of hyperthermia in down-regulating the expression of PD-L1 in some cancer cell lines was reported. In this study, decreased expression of PD-L1 in cancer cell lines was shown when samples were exposed to temperatures between 40 °C and 43 °C. Further accumulation of data associated with this new experimental model is eagerly awaited.
Figure 4: Approach for immunotherapy with whole-body hyperthermia. (A): cell preparation for DC vaccine and activated-T-cell therapy; (B): fever-range hyperthermia using heckle HT-3000 device; (C): representative data of body temperature during whole-body hyperthermia. DC: dendritic cell; PBMCs: peripheral blood mononuclear cells
Combination therapy with immunotherapy
Hyperthermia has been reported to enhance the efficacy of DC vaccines by up-regulating IFN-γ secretion to stimulate naïve T-cells, enhancing DC migration toward lymphatic organs and protecting DC from apoptosis. We introduced a whole body hyperthermia device
(HECKEL HT3000, Heckel medizintechnik GmgH, Esslingen, Germany), and have performed combination therapy with adoptive transfer of CD3-activated T-cells and cancer-antigen loaded DC vaccines. Patients with various solid tumors were vaccinated once a week with DC vaccine prepared from autologous monocyte-derived DCs, which were pretreated with tumor antigens. The DC vaccine was injected intradermally near the inguinal lymph nodes and CD3-activated T-cells were administered intravenously [Figure 4A]. Some patients underwent whole-body hyperthermia at the same time, with the target rectal temperature set at 38.5 °C and heat-retention for another 1 h [Figure 4B and C]. To evaluate the induction of immune responses in patients who received antigen-loaded DC vaccination, we examined the onset of skin reaction at the vaccination site because this reaction indicates antigen-specific T-cell responses against tumor antigens presented by DC vaccine. Then, we examined how much DC vaccination was required in each patient up to the point when delayed hypersensitivity like skin reaction sizes 48 h after DC vaccination became consistently larger than 1.5 cm in diameter. The average number of vaccinations to induce skin reaction was 3.87 and 3.32 in patients without and with whole-body hyperthermia, respectively [Figure 5A]. Moreover, 12 of 19 patients who underwent whole-body hyperthermia successfully elevated their core body temperature above 38.5 °C in every treatment and displayed earlier expression of skin reaction [Figure 5B]. This result indicated that the combined use of hyperthermia with a DC vaccine and activated T-cells had a positive impact on the induction of T-cell based immune responses.
Combination therapy with radiotherapy
The enhancement of anticancer efficacy of combination use of radiotherapy and hyperthermia was clinically recognized in cervical, breast, and head and neck cancer and so on. Even though radiological cytotoxicity induces DNA damage of cancer cells, some cancer cells can come back into existence (termed sublethal damage repair or lethal damage repair)[79,80]. In the analysis of the cell cycling, quiescent tumor cells were more resistant to irradiation because cells in this stage have the potential for lethal damage repair. In contrast, hyperthermia can inhibit the repair of radiation-induced damage in cancer cells, so that combination use of hyperthermia can enhance the anticancer efficacy of radiotherapy[82,83]. Cells in the synthesis (S) phase are also relatively radio-resistant, while they are the most sensitive to hyperthermia. Additionally, hypoxic cells in tumors are also radio-resistant, while hyperthermia improves the anaerobic condition by oxygen delivery due to increased blood flow. These perceptions indicate the synergetic effect of combination use of radiotherapy and hyperthermia. Moreover, additional use of DNA repair inhibitors was reported to further enhance its efficacy.
Combination therapy with chemotherapy
Chemotherapy is the most popular therapeutic method for patients with inoperative cancer and recurrent or metastatic cancer; however, there are serious problems including its uncertain efficacy, drug resistance, and adverse effects. To improve therapeutic results, combination use of hyperthermia was tested, and increased anticancer effect was reported in paclitaxel, docetaxel, gemcitabine, oxaliplatin, and irinotecan. The mechanism of interaction of chemotherapy and hyperthermia was considered as follows: increased drug uptake into cancer cells by causing damage to the membrane of cancer cells and reducing oxygen radical detoxification. Eventually, DNA damage increased while DNA repair decreased. Additionally, hyperthermia was reported to have a potential ability to avoid drug resistance[86,87]. In addition, it is also expected that elevated blood flow could result in a relative increase in anticancer drug concentration within the tumor. Moreover, adverse effects can be decreased because increased drainage of the drugs may accelerate in normal cells due to the up-regulation of metabolism. On the other hand, some anticancer drugs, including 5-fluorouracil, gemcitabine, and oxaliplatin, are considered to enhance cancer immunity by inducing the infiltration of CTLs while reducing Tregs in the tumor. Accordingly, enhancing the efficacy of chemotherapy will result secondarily in up-regulation of cancer immunity.
Combination therapy with surgery
Chemotherapy is usually performed for peritoneal metastases, but its prognosis is nonetheless bad, because blood flow to the peritoneum is poor owing to the presence of the peritoneal-plasma barrier. Hyperthermic effects are considered to impair the peritoneal-plasma barrier and result in increased resorption of anticancer drugs in peritoneal tumors. Hence, the combination of hyperthermia and chemotherapy by intraperitoneal administration resulted in more anticancer drug accumulation in peritoneal tumors than after chemotherapy alone. Using this concept, the effectiveness of cytoreductive surgery with subsequent HIPEC has been reported for peritoneal metastasis from gastric, colorectal[92,93], appendiceal, and adrenal cancer. Generally HIPEC is performed after resection of the cancer lesion with or without systemic peritonectomy by intraperitoneal administration of an anticancer drug containing saline, which is heated in advance to maintain the peritoneal surface at around 43 °C while irrigating the drug solution.
Adjuvant chemotherapy is often given after surgery for certain types of cancer, such as pancreatic, colorectal, and breast cancer, to improve prognosis by reducing the potential for recurrence and metastasis[96-99]. However, in some cancers, including intrahepatic cholangiocarcinoma (ICC), the prognosis of patients is extremely poor because the recurrence rate after curative operation is very high and there is no standard adjuvant setting. We reported previously that postoperative adjuvant immunotherapy with intradermal administration of a DC vaccine and intravenous administration of activated T-cells would be a feasible and effective treatment for preventing recurrence and achieving long-term survival in patients with ICC. In this study, the median 5-year progression-free survival and overall survival were 18.3 and 31.9 months in the patients receiving adjuvant immunotherapy, and 7.7 and 17.4 months in the group with surgery alone (P = 0.005 and 0.022, respectively). Additionally, patients whose skin reactions at the vaccine site were ≥ 3 cm showed dramatically better prognosis in patients receiving adjuvant immunotherapy. As has been explained above, hyperthermia can elicit early skin reactions when used in conjunction with immunotherapy including with DC vaccines and activated T-cell transfer. Hyperthermia can also augment the efficacy of adoptive immunotherapy by up-regulating IFN-γ secretion to stimulate naïve T-cells, and enhancing homing of DCs and T-cells. For the reasons stated above, hyperthermia is considered to be useful for adjuvant settings.
Neoadjuvant chemotherapy and chemoradiotherapy have become well established, especially for esophageal cancer patients. These neoadjuvant therapies improved the long-term survival rate, but the therapeutic benefit was sometimes countered by a significant increase in adverse effects. In addition, postoperative complications, including cardiac diseases and pulmonary diseases, are much more severe after chemoradiotherapy[103,104]. Preoperative radiotherapy increases the risk of postoperative anastomosis leakage, an unfavorable complication. As has been mentioned above, hyperthermia has the potential to augment the effects of chemotherapy or radiotherapy. Combination use of hyperthermia with chemotherapy or radiotherapy may be useful even in the neoadjuvant setting to suppress the possibility and seriousness of adverse effects and complications by reducing the dose of chemotherapy or radiotherapy required while maintaining or increasing its anticancer effects. Indeed, in 1995, the result of a randomized phase III study for patients with resectable squamous cell carcinoma of the thoracic esophagus was disclosed. Patients underwent neoadjuvant chemoradiotherapy with or without radiofrequency wave local hyperthermia, and the 3-year survival rate was 24.2% and 50.4%, respectively. There were no procedural complications. Additionally, in 2010, the results of a randomized phase III trial of patients with high-risk soft-tissue sarcoma were reported. Patients underwent neoadjuvant chemotherapy consisting of etoposide, ifosfamide, and doxorubicin with or without local hyperthermia. The treatment response rate in the group that received regional hyperthermia was 28.8%, compared with 12.7% in the group with chemotherapy alone (P = 0.002).
During the postoperative period, immunity is suppressed by operative invasion and the administration of anesthetic drugs such as opioids, and it results in the encouragement of postoperative cancer metastasis. Concerning the biological effect, preoperative fever-range whole-body hyperthermia was reported to augment postoperative cancer immunity by increasing the blood level of TNFα and HSP60. Thus, hyperthermia increased the benefit of neoadjuvant therapy.
Adverse effects of hyperthermia
Adverse effects of acute or chronic periods of regional hyperthermia do not develop often and are usually minor, owing to a recent development of heating techniques and thermometry, or treatment schedule. Adverse effects of hyperthermia include skin burns and skin pain, but these events usually heal spontaneously. In terms of combination therapies with hyperthermia, radiation toxicity is not increased, but toxicity of chemotherapy might be enhanced depends on the increase in drug efficacy. In rare settings of combination therapy with chemotherapy, the formation of severe subcutaneous fat or muscle necrosis that required surgery to cure was reported. Adverse effects of regional hyperthermia vary with the type of targeted organ or heating device and techniques. Whole body hyperthermia is a slightly more invasive hyperthermal method accompanied by a feeling of heat, tiredness, and loss of sweat due to a rapid elevation of the core body temperature. Dehydration, heat illness, cardiac disease, or thrombosis might appear depending on underlying disease or physical condition. In addition, whole body hyperthermia has a risk for toxicity to the peripheral nervous system. Hence, this method is contraindicated for patients with neurodegenerative diseases, such as multiple sclerosis.
On the other hand, no reports that describe hyperthermia having a positive impact on cancer progression in regard to biological effects are found until now.
Overall, hyperthermia is considered a convenient therapeutic method so long as it is used appropriately. Paradoxically, the safety of hyperthermia is maintained by avoiding excess irradiation with the purpose of deep heating, because it is still difficult to aggregate the heat effect only in cancer tissue. By using hyperthermia in combination with chemotherapy or radiotherapy, the dose of these therapies may be reduced to ease their side-effects without reducing therapeutic effects, because hyperthermia has the potential to augment the effect of chemotherapy or radiotherapy in a less invasive manner.
This report shows that hyperthermia increases the advantage of the following biological features. Heat stress lowers the survival rate of all cells, but normal tissues are better able to tolerate this than cancerous tissues. Heat has a potential to augment immune responses while decreasing immune suppression. Heat inhibits the recovery of cancer cells from DNA damage. Heat enhances the resorption of anticancer drugs into cancer cells. The sensitivity of cancer cells against heat and radiation differs depending on the condition of cancer cells in the cell cycle. The anticancer efficacy of hyperthermia alone with currently available heating devices is not enough to suggest its use as a standalone therapy. However, some studies have shown that combination therapy with conventional methods including immunotherapy, radiotherapy, chemotherapy, and surgery improves its anticancer efficacy in vitro and vivo.
Currently, clinical experience and data of oncological hyperthermia are still limited because both information and devices for hyperthermia have not become common. Therefore, multicenter clinical trials for cancer treatment including hyperthermia should be done to provide convincing data. The combination hyperthermia with immune check-point inhibitors should be involved in these studies to achieve fuller anticancer efficacy with fewer adverse effects. Development of drugs such as DNA repair inhibitors or regulators of HSPs is also expected to augment the efficacy of hyperthermia itself. Additionally, further efforts will be required to solve the mechanism of the involvement of cancer and hyperthermia to optimize cancer therapy. The development of heating devices and thermometry is also needed to achieve more appropriate heat delivery that is limited to the tumor lesion.
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