A portion of the increased ASCVD risk seen after cancer diagnosis is driven by shared risk factors that predispose to both ASCVD and cancer, such as diabetes mellitus, obesity, and metabolic syndrome (21). However, the cytotoxic therapies involved in cancer treatment can also be a risk factor for ASCVD. In a longitudinal study of 1,413 breast cancer patients with ASCVD, those receiving chemotherapy had 1.7 times higher risk of death due to ASCVD than those not receiving chemotherapy (22). Notably, the difference in morality was not seen until 7 years post-breast cancer diagnosis, likely reflective of the relatively slow progression of ASCVD. Beyond breast cancer, a population cohort study in the United Kingdom found higher risk of coronary artery disease in patients treated with chemotherapy alone for non-Hodgkins lymphoma and a trend toward higher risk in those treated with chemotherapy for lung and breast cancer (23). Immunotherapy and radiation therapy have also been linked to acceleration of atherosclerosis (24, 25). A fundamental issue in this area is the degree to which increased ASCVD risk is attributable to the underlying cancer, cytotoxic therapies, or both. A recent study assessing incident ASCVD among cancer patients found that those with cancer had nearly double the risk of developing ASCVD compared to the population of patients without ASCVD (23.1 vs. 12.0% age-adjusted incidence over 13 years of follow-up). The risk of developing ASCVD was highest among survivors of breast, lung, colorectal, and hematologic cancers, which was independent of traditional cardiovascular risk factors (26). Given the treatability of most cancers, it is unlikely that future studies will evaluate participants with untreated cancer. However, further study of ASCVD risk among cancer patients receiving cytotoxic therapy paired with basic science investigations of these therapies may better elucidate the impact of cytotoxic therapy on ASCVD risk.
As survival among cancer patients improves, the increased risk of death from ASCVD is magnified (27). For example, in breast cancer patients, upwards of 80% of patients are living 5 years after diagnosis (28). Additionally, cytotoxic treatment is becoming a “chronic therapy:” evidence shows duration of chemotherapy and immunotherapy correlates with survival for many cancers (29–31). As cancer survivors live longer and receive more cumulative cytotoxic therapy, they become more likely to die from ASCVD, emphasizing the importance of ASCVD prevention and treatment in this population. Table 1 summarizes the known effects of cancer therapies on cholesterol homeostasis.
Effects of chemotherapeutic agents by class on cholesterol homeostasis
Anthracyclines
Anthracyclines are among the most widely used chemotherapy agents (32). Their main mechanism of action is via topoisomerase II inhibition, mitochondrial impairment, and generation of reactive oxygen species that result in inhibition of DNA and RNA synthesis (33). The most prominent cardiotoxic effect of these drugs is development of cardiomyopathy, however, additional studies have shown a dyslipidemia-inducing effect of anthracycline therapy which may predispose to ASCVD (34–36).
Anthracyclines have been shown to impact ABCA1 and cholesterol efflux perhaps by interfering with the activity of the upstream regulators LXR-alpha and PPAR-gamma (37). The mechanism of anthracycline-induced atherosclerosis pathways was investigated by Sharma et al. in their study of the in vivo effects of doxorubicin, epirubicin, and other agents on human hepatocytes, isolating the effect of each chemotherapy agent on genes involved in lipid metabolism (38). Their study showed that doxorubicin was associated with decreased mRNA transcription of ABCA1. Overall impairment by doxorubicin resulted in a dose-dependent 20–30% cholesterol efflux in their cell model. A similar effect was seen with epirubicin (38). In a study of doxorubicin-treated myocytes and a mouse model, doxorubicin-treated cells exhibited higher cholesterol and cholesterol precursor levels (39). Sharma et al. also showed that anthracyclines reduced HMGCR activity, which in theory should reduce LDL levels (38). Others have shown a significant increase in apolipoprotein B, a known risk factor for ASCVD, with anthracycline use (37).
Clinical studies by Lu et al. (34) and He et al. (36) showed a consistent association of increased total cholesterol (TC), LDL, and triglycerides (TG) measured at the conclusion of anthracycline-predominant combination chemotherapy in a combined sample of over 1,100 patients. Anthracycline effect on HDL was less consistent and was associated with decreased levels in the former study, in line with the decrease in ABCA1 reported in the above mechanistic studies. Limited long-term studies have evaluated lipid levels after anthracycline therapy in isolation, so the duration of this effect is less clear. However, in a group of 433 patients with early breast cancer, Arpino et al. (40) showed anthracycline therapy, in combination with cyclophosphamide followed by taxane therapy, was associated with elevations in TC, LDL, and TG at 24 months of follow up. This provides some evidence that the duration of anthracycline effect on lipid metabolism is durable. Overall, multiple lines of evidence across basic science and clinical studies suggest that anthracyclines may play a role in promoting dyslipidemia, but further study is required.
Taxanes
Taxanes act primarily by stabilizing GDP-bound tubulin in microtubules, preventing effective function of microtubules for cell division (41). They are versatile drugs used to treat various solid tumors, and are a core component of breast cancer therapy (41). In a study of 80 women with breast cancer, a single infusion of paclitaxel was shown to effect expression of at least 188 proteins (42). Proteomic analysis showed that many of these proteins were crucial in lipid metabolism, especially those that involve lipoproteins. Sharma et al. (38) demonstrated increased HMGCR activity in human hepatocytes induced by paclitaxel. Additionally, reduced apolipoprotein-B activity and LDL receptor expression (important for clearance of LDL from the blood stream) were noted with paclitaxel.
Because taxanes are used almost exclusively as combination therapy (often with anthracyclines), it is difficult to assess their unique impact on in vivo lipid metabolism. In a sub-group analysis of patients who received regimens with and without taxane therapy, He et al. (36) showed that taxane-containing regimens resulted in higher magnitude of dyslipidemia than non-taxane containing regimens. Other studies similarly suggest that taxane-inclusive regimens are associated with dyslipidemia especially when used in combination with anthracyclines (34, 35, 40).
Tyrosine kinase inhibitors
Tyrosine kinase inhibitors (TKIs) are a mainstay of therapy for gastrointestinal, genitourinary, hematologic, and lung cancers. They are a diverse class of agents targeting various kinases involved in pathways related to tumor angiogenesis. The off-target effects of TKIs can impact lipid metabolism or promote cardiotoxic side effects. Imatinib, a first-generation TKI targeting BCR-ABL1, reduces cytoplasmic phosphorylation of LDL receptor related protein, a key component of LDL signaling that is involved in activating lysosomal enzymes, glucose-induced insulin secretion, and cholesterol metabolism. For example, in a study of rabbits fed a high cholesterol diet, imatinib therapy reduced cholesterol levels and the toxic effects produced by hyperlipidemia in the aorta and liver. These effects were mediated via significant decreases in lipid levels, C-reactive protein, and hepatic and other enzymes, suggesting that multiple pathways are involved in the atherosclerotic and vasculo-toxic effects of imatinib (43). Other TKIs that act on PDGF-R may have a similar effect (44), while TKIs that act via different target receptors may have opposing or synergistic effects.
Hematologic cancers
TKIs are a key therapeutic agent in chronic myelogenous leukemia (CML) (45). Since imatinib revolutionized CML therapy, multiple other TKIs targeting various receptor pathways have entered the market (45). Second generation agents include nilotinib, dasatinib, and bosutinib. Ponatinib is a third-generation agent used in cases of treatment failure (45). Though the mechanisms through which TKI therapies alter cardiovascular physiology are poorly understood, clinical data suggests numerous cardiotoxic side effects.
As a class, BCR-ABL1 TKIs have been found to have varying toxic effects, including adverse events that may be lipid-independent, such as vascular toxicity, cardiotoxicity, and pulmonary hypertension (45). Among vascular toxicities, peripheral arterial disease, cerebral vascular accidents, ischemic heart disease, hypertension, and hyperglycemia are a few of the better-known adverse effects (46, 47). The first-generation agent imatinib likely has a protective effect on lipid metabolism. In a case series of 9 patients with hyperlipidemia and CML, 8 of 9 patients experienced normalization of lipid levels within 30 days of starting imatinib without the use of cholesterol-lowering agents (44). In a study of 40 patients with CML, of whom 19 were on statin therapy concurrently, after 3 months of imatinib treatment TC, TG, LDL, and non-HDL cholesterol decreased while HDL increased. The lipid-lowering effect of imatinib was similar between the statin and non-statin groups (48). Further research is needed to identify the intermediaries through which this effect occurs, as well as its clinical implications considering long-term use of lipid-lowering agents.
Studies to date on TKI therapy suggest that imatinib may have an atheroprotective effect, while other TKIs may have a more deleterious effect. Ponatinib targets a gatekeeper mutation in the BCR-ABL protein, T3151, that confers resistance to other TKIs among CML patients, but after approval was noted to be linked to myocardial infarction or stroke in 24–48% of patients (49). One study using mouse models suggests that imatinib and ponatinib decrease plasma cholesterol levels and that imatinib can increase plaque stability. The same study found that ponatinib and nilotinib may increase mRNA expression of coagulation factors that activate the clotting cascade, thus inducing a prothrombotic state that may be the driver of increased vascular adverse events (50).
Compared to imatinib, nilotinib, and dasatinib have shown greater affinity for the BCR-ABL1 tyrosine kinase protein and thus more effective BCR-ABL1 inhibition, largely replacing imatinib as first line therapy for CML (51). In small studies available to date, nilotinib as first or second line therapy for CML was associated with increased TC, LDL, and HDL, higher risk of peripheral arterial disease, and worsened glycemic profile, suggesting lipid-dependent and lipid-independent toxicity (52–54). In another study of 57 patients with CML treated with either imatinib or nilotinib, imatinib was associated with a significant increase in HDL and decrease in TG and a non-significant decrease in TC and LDL from baseline compared to 6 month follow up. Nilotinib was associated with a significant increase in TC, LDL, and HDL and a decrease in TG, similar to prior studies (55). Overall, among agents active against BCR-ABL, it appears nilotinib increases risk of dyslipidemia, imatinib may decrease risk, and risk with other agents requires further study. The mechanism for these disparate effects among similar agents is not yet understood.
Solid tumors
Lipid-modulating effects of the more novel TKIs used in gastrointestinal, genitourinary, and lung malignancies are still being elucidated. In a study of 299 patients with lung cancer, patients treated with gefitinib (an EGFR TKI) had lower TC levels after 30 days of treatment (56). Lorlatinib, a third generation TKI used in ALK-positive non-small cell lung cancer, was found to induce hypercholesterolemia in 82.4% of patients and hypertriglyceridemia in 60.7% of patients. The mechanism of this effect is not known; however, one hypothesis is that lorlatinib has off-target effects on tropomyosin receptor kinase B (TrK-B), which is involved in cholesterol recognition (57, 58). Sunitinib, a novel TKI that acts on FGF, VEGF, and PDGF-R, was found to increase TC, LDL, HDL, non-HDL cholesterol, and TG in a study of 127 patients with metastatic renal cell carcinoma, of which 79 were receiving the drug. Paradoxically, higher increase in serum lipids, particularly in all 5 parameters, was associated with better progression-free survival and overall survival in this study (59). Additional studies to confirm this paradoxical relationship between increased lipid levels and better overall survival are warranted, and at the very least suggest that lipid metabolism is an important factor but not the only one in determining mortality risk in TKI recipients.
Mechanistic target of rapamycin inhibitors
The mechanistic Target of Rapamycin (mTOR) signaling pathway is involved in regulation of gene transcription and protein synthesis related to cell proliferation and immune cell differentiation (60). Primarily used as anti-rejection agents, mTOR inhibitors such as everolimus and temsirolimus are sometimes used as targeted anti-neoplastic therapy. mTOR inhibitors increase TG and LDL levels by reduced expression of lipogenic enzymes and LDL receptors, respectively (61). Kasiske et al. reviewed 17 randomized control trials of mTOR inhibitors and found 14 trials with an increase in TC and/or TG compared to the non-mTOR comparator groups (62). Additionally, use of lipid lowering therapy was more common in the mTOR groups. However, all trials evaluated mTOR inhibitor use in kidney transplant recipients, in which the doses of mTOR inhibitors were lower than that for anti-neoplastic treatment. In a phase I clinical trial of the mTOR inhibitor deforolimus for treatment of advanced malignancies, TC exhibited a dose response relationship of 7.4 mg/dL per 10 mg increase in dose (maximum dose 75 mg) (63). In a phase III trial of temsiromilus for treatment of metastatic renal-cell carcinoma, hypercholesterolemia was seen in 24% of patients compared to 4% in the interferon alfa comparator group (64). However, the clinical significance of mTOR inhibitor induced dyslipidemia remains unclear given that mTOR inhibition may actually inhibit pathways involved in the formation of atherosclerosis (65). The long-term impact of mTOR inhibition on cardiovascular risk is unclear, as findings of reduced cardiovascular risk in patients on mTOR inhibitors are confounded by more frequent use of lipid lowering therapy in response to dyslipidemia (65, 66). Further study is needed evaluate the effect mTOR inhibitors on atherosclerotic disease.
Alkylating agents
Alkylating agents cross-link strands of DNA and RNA to prevent cell division (67). Fulminant cardiotoxicity is a rare side effect of high-dose cyclophosphamide, the most common alkylating agent (68). However, the association between alkylating agents and dyslipidemia is unclear. Sharma et al. showed in vitro exposure of human hepatocytes to cyclophosphamide did not affect metabolic pathways involved in lipogenesis (38). In animal models, cyclophosphamide was shown to induce dyslipidemia in rats at toxic doses (69). In contrast, treatment with low dose cyclophosphamide was associated with reduced progression of atherosclerotic disease in mice (70). Clinical studies in humans show cyclophosphamide regimens that do not include anthracyclines do not affect lipid profiles and may even be associated with improved LDL (38). Data on dyslipidemia associated with other alkylating agents is lacking, likely due to limited usage.
Platinums
Platinum complexes are positively charged platinum ions surrounded by negatively charged anions that cross-link DNA to inhibit transcription, resulting in failed mRNA translation and ultimately promoting cell death (71). While cholesterol metabolism appears to affect the efficacy of platinum agents (72, 73), there are minimal human studies linking platinum agents to long-term changes in cholesterol levels (74). Najam et al. investigated the effect of the platinum drugs cisplatin and oxaliplatin on rats. They noted increased levels of LDL and TG 30 days after cessation of therapy compared to controls injected with normal saline (75). Histologic review of sacrificed rats showed evidence of myofibrillar loss and vessel wall thickening in those treated with cisplatin but not oxaliplatin, but these results have not been replicated in human studies. In clinical studies in humans, an adjuvant combination regimen primarily composed of cisplatin, carboplatin, and nedaplatin was found to be associated with increased levels of TC, LDL, HDL, and TG at the end of the treatment period (76). However, in two other studies in human subjects, no changes in plasma cholesterol were seen shortly after cisplatin therapy (77) nor after >5 year follow up (74). Overall, there is limited evidence to suggest treatment with platinum agents leads to dyslipidemia.
Anti-metabolites
Anti-metabolites are purine and pyrimidine analogs that get incorporated into DNA to interfere with cell proliferation (78). They are a very diverse group of medications used to treat various malignancies (79). 5-Fluorouracil (5-FU) was associated with cholesterol lowering in a study in rabbits, but this link has not yet been established in humans (80). Methotrexate may cause decreases in cholesterol levels through alterations in expression of ABCA1 and 27-hydroxylase enzymes (81), an effect seen in a study of rheumatoid arthritis patients taking the drug (82). However, in the Cardiovascular Inflammation Reduction Trial, low dose methotrexate compared to placebo minimally reduced LDL, TG, and HDL but no cardiovascular benefit was observed (83). In patients with colorectal cancer treated with a predominantly anti-metabolite regimen of 5-FU and capecitabine, TC, HDL, and TG increased while LDL decreased at the end of the treatment period (84). Capecitabine alone has been rarely associated with extremely elevated TG levels (85). Other anti-metabolites have no known association with dyslipidemia in the literature and the overall impact of the drug class on ASCVD risk is still unclear.
Hormone therapy
Estrogen and testosterone affect several regulators of cholesterol expression and transport (86, 87). For example, liver HMGCR is inhibited by estrogen, thereby resulting in decreased cholesterol synthesis (88). Additionally, testosterone deficiency has been shown to result in decreased expression of the nuclear receptors LXR and PPAR-gamma which are crucial in controlling the level of serum cholesterol (89). The inhibition of sex hormones, mainly estrogen and testosterone, are a mainstay of breast and prostate cancer therapy (90). Hormone therapy agents act agonistically or antagonistically in different tissues, thus their effects on cholesterol homeostasis are variable. Given that sex-specific hormones are closely involved in cholesterol metabolism, deficiencies in estrogen (91, 92) and testosterone (93–95) are associated with worsening lipid profiles.
In patients with breast cancer, treatment with selective estrogen receptor modulators (SERMs) such as tamoxifen have a protective effect against ASCVD and dyslipidemia (96). SERMs act as estrogen antagonists at treatment target tissues such as the breast or uterus, however, in most other tissues they mimic the effect of estrogen (97). Thus, they can provide a protective effect against chemotherapy-induced dyslipidemia (98). In a study of 55 breast cancer patients in India, participants received 20 mg daily of adjuvant tamoxifen after breast cancer surgery and had significant reductions in TC and LDL (99). However, a separate study of 141 breast cancer patients receiving 3 years of SERM therapy showed that alterations in the lipid profile normalized within 6 months of drug discontinuation (100). Elevations in TG after SERM treatment have occurred in some studies (101, 102) but not others (99, 103).
In a metanalysis of RCTs with variable follow up intervals, tamoxifen reduced cardiovascular events by 25–35% compared to placebo (104). In large scale study of 3,449 breast cancer patients who completed 2 or 5 years of tamoxifen therapy, women 50–59 years of age in the 5-year therapy arm experienced 35% reduction in cardiovascular events and 59% reduction in cardiovascular mortality at 10-year follow up vs. placebo. However, this effect was not found in other age groups (105). In addition, when prophylactic tamoxifen was studied in patients with and without cardiovascular disease at risk of developing breast cancer, there was no change in cardiovascular event rates associated with tamoxifen use (106). Finally, tamoxifen is associated with increased risk of venous thromboembolism and pulmonary embolism, though these end points may have been excluded in studies evaluating cardioembolic events (107).
Aromatase inhibitors (AI) reduce circulating estrogen by reducing production of the hormone (108). Compared to SERMs they are associated with increased cardiovascular risk (104). In a study of over 17,000 patients in the United Kingdom newly diagnosed with breast cancer and initiated on either an AI or tamoxifen, initial treatment with an AI was associated with a risk factor adjusted hazard ratio of 1.5 compared to those initiated on tamoxifen. In one systematic review and meta-analysis, extended treatment (>5 years after initial diagnosis) with AIs was associated with 1.18 higher odds of cardiovascular events compared to placebo (109). Additional data on cardiovascular outcomes comparing AI vs. placebo is lacking and thus comparison of cardiovascular outcomes against protective SERMs may make AIs appear more harmful. However, AIs do appear to increase dyslipidemia at least 3 months after cessation of therapy, though the full duration of effect is unknown (110). Sequential therapy with SERMs prior to AIs may mitigate this effect (111).
Androgen deprivation therapy (ADT) using hormonal treatment such as gonadotropin-releasing hormone antagonism, or less commonly, bilateral orchiectomy, is a standard component of treatment of advanced prostate cancer (112). The typical lipid profile change has been found to be an increase in TC, TG, LDL, and HDL (113). Additionally, increased arterial stiffness at 6 months has been reported following ADT and correlates with increasing cholesterol levels post-therapy (114). Increases in insulin resistance and incidence of type II diabetes have also been reported after ADT. Risk for cardiovascular disease has been shown to increase 20% after at least 1 year of ADT (115) and long-term risk may be increased with chemical ADT vs. orchiectomy (116). However, data translating this risk to higher cardiovascular mortality is mixed (113).
Chemotherapy induced ovarian failure
Due to high cell growth rates, ovarian follicles are exquisitely sensitive to chemotherapy (117). Incidences of chemotherapy-induced ovarian failure (CIOF) as high as nearly 80% have been reported in pre-menopausal cancer patients (118). A review article by Roeters van Lennep et al. summarizes these effects. Chemotherapy can induce apoptosis of ovarian follicles, damage to follicular blood supply, and accelerated maturation of follicles that ultimately lead to premature ovarian failure. Due to the subsequent lack of estrogen production, premature ovarian failure is an established risk factor for ASCVD that may be independent of lipid homeostasis (119). Studies among women with premature ovarian failure suggest this risk may be due to increased abdominal fat, elevated inflammatory markers, or increased TG without a clear link to total cholesterol or LDL levels (120, 121). However, in a study of patients on cyclophosphamide, methotrexate and 5-FU with premature ovarian failure, risk of dyslipidemia was significantly increased (122). Chemotherapy regimens with a high risk for ovarian failure include those with cyclophosphamide, methotrexate, anthracyclines, and 5-FU for 6 or more cycles, especially in patients age > 40 years (123). SERMs may offer protection against the dyslipidemia seen in CIOF. In a study of breast cancer patients treated with a majority cyclophosphamide, methotrexate, and 5-FU regimen in addition to tamoxifen vs. control, 53% of patients had ovarian failure (124). Those treated with tamoxifen after chemotherapy had improved lipid profiles at 12 months after tamoxifen initiation, while those that received placebo after chemotherapy had no change in their dyslipidemia (124). The most effective methods for prevention and treatment of CIOF are the subject of ongoing research (125).
Non-chemotherapy cancer treatments
Cancer treatment in the recent era is most often multimodality, and non-chemotherapy treatment agents affect dyslipidemia and ASCVD risk. Radiation therapy, often used in conjunction with chemotherapy therapy regimens, is an independent risk factor in the development of ASCVD (126). Explosive growth in the use of immunotherapy and stem cell transplant has changed the typical treatment regimens for many common cancer types. These modalities have been associated with increased ASCVD risk but association with dyslipidemia is less clear.
Immunotherapy
Studies of the effects of immunotherapy on lipid metabolism are limited. Chimeric antigen receptor-T cells and Bispecific T cell Engager therapy are growing areas of immunotherapy, particularly for hematologic malignancies, but their effects on lipid metabolism are unknown. Immune checkpoint inhibitors (ICIs) are an increasingly common therapy for a variety of cancers and known to have multiple cardiometabolic toxicities (127, 128). ICIs are monoclonal antibody antagonists to CTLA-4, PD-1, and PD-L1 (129). Abnormal PD-1 and PD1-L expression, as occurs with ICI use, can lead to progression of atherosclerosis (129). Alterations in T-cell mediated intraplaque immune responses are thought to make atherosclerotic disease more vulnerable to rupture. ICI inhibition of key regulatory pathways in cardiomyocytes is thought to promote myocarditis, vasculitis, atherosclerosis, arrhythmias, and pericardial disease. A recent study of 2,842 patients with a variety of cancers undergoing ICI therapy found that those who received ICIs had 3-fold higher risk of experiencing atherosclerosis-mediated cardiac events (130). In a case-control analysis of the same population, the observed rate of cardiovascular events in the 2 years after ICI therapy was 6.55 per 100 person-years compared to 1.37 in the 2 years prior to therapy. In an imaging subgroup analysis of 40 patients, atherosclerotic plaque volume was 3 times higher with ICI therapy (130). A key question remains whether clinicians should be more aggressive with treating CVD risk factors given this population's higher propensity for adverse cardiac events. Moreover, there seems to be evidence that ICIs can enhance ASCVD risk, but their specific effects on lipid metabolism remain to be elucidated.
Stem cell transplant
Hematopoetic stem cell transplant (SCT) patients are at elevated risk of hypertension and diabetes, and further evidence suggests that SCT is an established accelerator of atherosclerosis (131). A retrospective analysis of 194 patients who underwent allogeneic SCT and survived more than 100 days found that 42.8% of patients developed hypercholesterolemia and 50.8% of patients developed hypertriglyceridemia. The development of chronic graft-vs. host disease (GVHD) and use of steroids were associated with development of hypercholesterolemia, while use of calcineurin inhibitors was not (132). Another retrospective analysis of 761 patients who underwent allogeneic SCT and survived more than 100 days found an incidence of hypercholesterolemia and hypertriglyceridemia of 73.4% and 72.5%, respectively, at 2 years post-transplant (133). This study also found an association between acute GVHD and hypercholesterolemia and hypertriglyceridemia, and the authors proposed a role for GVHD-related liver dysfunction in the role of lipid dysregulation. Of note, statin use in this population effectively lowered TC, TG, and LDL levels (133). Thus, as SCT patients continue to experience better long-term survival, SCT must be recognized as a risk factor for accelerated atherosclerotic disease to guide appropriate prophylaxis and treatment (134).
Radiation therapy
Localized radiation therapy (RT) has been shown to promote the development of atherosclerosis in affected tissues (25). Radiation therapy causes local endothelial damage which prompts an inflammatory cascade resulting in atherosclerosis (25). Inflammation and subsequent host immune and healing response lead to fibrosis, stenosis, and development of early atherosclerotic disease. Dyslipidemia has not been identified as a major contributor to early ASCVD in patients treated with RT and there is little mechanistic data in basic science studies to suggest it may play a significant role. In an in vitro study, human bronchial epithelial cells were exposed to radiation doses known to cause cell dysfunction in humans (135). Increases in cholesterol pathway enzymes and a 10–30% increase in intracellular cholesterol were detected 7 days after RT. However, whether this outcome would translate to in vivo studies in a meaningful way is unknown. Small studies in breast (136) and prostate (137) cancer patients showed an association of RT with reduced dyslipidemia. Large-scale clinical trials regarding dyslipidemia after RT—along with treatment strategies—are needed.