Next Article in Journal
The Impact of TRAIL on the Immunological Milieu during the Early Stage of Abdominal Sepsis
Previous Article in Journal
Young Adult German Breast Cancer Patients Participating in a Three-Week Inpatient Mother–Child Rehab Program Have High Needs for Supportive Care
Previous Article in Special Issue
Effect of Obesity among Hospitalized Cancer Patients with or without COVID-19 on a National Level
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Perspectives and Challenges of COVID-19 with Obesity-Related Cancers

by
Maria Dalamaga
1,*,
Narjes Nasiri-Ansari
1 and
Nikolaos Spyrou
2
1
Department of Biological Chemistry, School of Medicine, National and Kapodistrian University of Athens, 75 Mikras Asias, 11527 Athens, Greece
2
Tisch Cancer Institute Icahn School of Medicine at Mount Sinai, 1190 One Gustave L. Levy Place, New York, NY 10029, USA
*
Author to whom correspondence should be addressed.
Cancers 2023, 15(6), 1771; https://doi.org/10.3390/cancers15061771
Submission received: 6 March 2023 / Revised: 7 March 2023 / Accepted: 10 March 2023 / Published: 15 March 2023
(This article belongs to the Special Issue The Challenges of COVID-19 with Obesity-Related Cancers)
The emergence of COVID-19 has created an unprecedented threat worldwide, involving overwhelmed health-care systems in the majority of countries [1,2]. Cancer screening and delivering care in oncologic patients has been a challenging task based on the balance between the risk of mortality from untreated malignancy versus the risk of severity of COVID-19 and death in immunocompromised individuals [3].
The COVID-19 pandemic has taken place at a time when the worldwide prevalence rate of overweight and obesity is greater than 39% and 13%, respectively, for adults, and cancer is a leading cause of death globally based on recent WHO data [4,5]. Obesity has become a major global public health concern related to a variety of disorders, including metabolic syndrome, type 2 diabetes mellitus, cardiovascular disease, nonalcoholic fatty liver disease, polycystic ovary syndrome, autoimmune disorders and cancer [6,7,8,9,10,11,12,13].
Interestingly, a growing body of evidence has shown that obesity and increased visceral fat are strongly and independently linked with adverse outcomes and death due to COVID-19 [14,15,16,17,18]. Moreover, there is convincing evidence that excess body weight is associated with an increased risk for cancer of at least 13 anatomic sites, including endometrial, esophageal, renal and pancreatic adenocarcinomas; hepatocellular carcinoma; gastric cardia cancer; meningioma; multiple myeloma; colorectal, postmenopausal breast, ovarian, gallbladder and thyroid cancers [19,20,21].
Two umbrella reviews and meta-analyses on the association between pre-existing health conditions and severe outcomes from COVID-19 have shown that other than diabetes, obesity, heart failure, chronic obstructive pulmonary disease and dementia, active cancer was also linked with a higher risk of death, particularly in Europe and North America [22,23]. Oncologic patients may be more susceptible to SARS-CoV-2 infection. Evidence is mixed regarding COVID-19 severity in cancer patients [24,25,26], while COVID-19 outcomes in these patients are improved with an earlier diagnosis, the availability of effective COVID-19 vaccines, the advent of the omicron outbreak and the timely use of anti-viral therapy [24,27]. Despite all the abovementioned factors, most studies have highlighted an elevated risk of severe COVID-19 in patients with active cancer, particularly in non-vaccinated individuals [22,23,25,28,29]. The risk may vary by type and stage of cancer and treatment. Particularly, older age, hematologic malignancies, lung cancer, advanced or progressive cancer, active chemotherapy, comorbid conditions, including obesity, and smoking are associated with severe COVID-19 [30,31,32,33,34,35,36,37].
COVID-19 had devastating effects on cancer patients, with an immense number of missed diagnoses and delayed treatments attributed mainly to patient’s reluctance to seek medical care and to health systems under pressure [38]. Throughout the pandemic and particularly during the first and second phases, there were significant delays in cancer screening and surveillance that resulted in delayed diagnoses, particularly in obesity-associated cancers, an increased rate of patients diagnosed in an emergency setting, a plethora of diagnoses of advanced stage malignancies with higher tumor burden as well as delays in the treatment of patients with newly diagnosed cancers [39,40,41,42,43,44]. In the initial phase of the pandemic, collective data from 200 sources in 17 European countries have shown that an estimated 100 million screening tests were not performed while up to 50% of all cancer patients were affected by treatment delays [45].
Generally, therapeutic management of oncologic patients with COVID-19 is similar to that used for the general population. In the outpatient setting, available treatment options comprise antiviral agents, such as nirmatrelvir-ritonavir, remdesivir and molnupiravir, as well as monoclonal antibodies active against prevalent variants [46,47]. Persistent SARS-CoV-2 infection may uncommonly occur in immunocompromised patients, particularly those with severe B-cell depletion due to cancer treatment (e.g., rituximab, hematopoietic cell transplantation, etc.) [46,48,49].
Overall, when cancer treatment is indicated according to consensus guidelines, it should be administered without delay [50]. In most hematologic cancers, the efficacy of treatment favors the adoption of curative approaches, despite the infectious risk of COVID-19; however, decisions should be made on a case-by-case basis [51]. In patients who have tested positive for SARS-CoV-2, immune checkpoint inhibitors (ICIs) should be postponed until recovery [50]. Transplantation/cellular therapy should be delayed for 2–3 weeks and until patients are asymptomatic; however, decisions should be made on a case-by-case basis (e.g., prolonged viral shedding should be taken into consideration) [52]. In cases where treatment is not urgent as in indolent lymphomas, treatment can be deferred until nasopharyngeal sampling is negative and symptoms have resolved; less immunosuppressive therapies can also be prioritized [53]. Moreover, in the absence of urgent treatment indication, an individual treatment deferral after anti-SARS-CoV-2 vaccination (at least one injection) may be considered [53]. Therapeutic decisions to proceed with systemic therapies should be preceded by a multidisciplinary discussion, risk/benefit analysis and discussion with the patient.
Up-to-date COVID-19 vaccination is recommended to all patients with active or prior malignancy in order to prevent severe SARS-CoV-2 infection. Data have indicated that vaccine efficacy is relatively diminished in patients with active cancer in comparison to individuals without cancer, especially in patients with hematologic malignancies, and particularly those on anti-CD20 antibody treatment [54,55,56]. Patients with hematologic malignancies present lower seroconversion rates post-vaccination, potentially leading to inferior COVID-19 outcomes despite vaccination, and an elevated risk for breakthrough infections [57,58,59]. Figure 1 depicts the main challenges of COVID-19 associated with cancer.
This Special Issue places emphasis on the challenges surrounding COVID-19 and obesity-related cancers, including, but not limited to: risk factors of severe COVID-19 in cancer patients; complications of COVID-19 in cancer patients; challenges in cancer treatment and surgery; guidelines for cancer care during COVID-19; delayed diagnosis and suboptimal cancer management; impact of COVID-19 on cancer screening, early diagnosis and cancer presentation; immune response after SARS-CoV-2 infection and vaccination in cancer patients; psychological distress among cancer survivors; telehealth in cancer care; role of diet and nutraceuticals in the prevention of severe COVID-19 and cancer as well as effects of COVID-19 pandemic on cancer research.
Although SARS-CoV-2 mainly affects the lower respiratory tract, it can initiate system-wide pathophysiological alterations and dysfunctional immune responses. Habibzadeh et al. reviewed the potential effects of autophagy on cancer development and outcomes [60]. Various SARS-CoV-2 proteins interact with different components of the cellular autophagy pathway and could lead to long-term defects in the cellular autophagy machinery. The authors hypothesize that these defects could mediate alterations in cell proliferation, immunity against cancer cells, cell metabolism and cancer drug efficacy that could eventually impact on carcinogenesis and responsiveness to cancer therapy.
The lack of medications for COVID-19 in the early phases of the pandemic led the public to seek alternative therapies, including nutraceuticals. Bader-Larsen et al. evaluated the safety of “anti-COVID-19” nutraceuticals in patients with cancer [61]. They reported that the use of vitamin C, vitamin D and selenium supplements is likely safe at typically recommended doses. However, they cast caution on the use of omega-3 fatty acids and zinc, as potential risks may outweigh the benefits derived from their use.
Almasri and colleagues reviewed the evidence on the immune response rates and safety profiles of COVID-19 vaccines in patients with hematologic and solid malignancies [62]. In comparison to the general population, lower seropositivity following vaccination was associated with malignancy as well as with hematologic malignancy compared to solid cancers. Patients receiving active chemotherapy, radiotherapy and immunosuppressive therapy generally displayed lower seropositivity rates compared to healthy controls, a phenomenon not observed in patients who received checkpoint inhibitors, endocrine therapies and cyclin-dependent kinase inhibitors. Nevertheless, cancer patients demonstrated the ability to mount safe and effective immune responses to COVID-19 vaccines. Adverse events were comparable to those of the general population; however, inflammatory lymphadenopathy following vaccination was commonly reported and may be mistaken for a lymphadenopathy of malignant etiology. Finally, the authors suggested that vaccination should be promoted, and reluctance to receive it should be addressed in this population.
The SARS-CoV-2 pandemic brought multi-dimensional disruptions in oncology. Ali and Riches reviewed the changes that affected the care of cancer patients as well as clinical trials [63]. The pandemic disrupted routine cancer screenings and decreased the potential for early cancer detection, resulting in many thousands of missed cancer diagnoses. Initially, clinical trials were significantly impacted, resulting in the cessation of trial initiation and recruitment, particularly in oncology clinical trials. Clinical trial practices and protocols underwent significant changes, including a reduction in in-person appointments, use of telemedicine and remote monitoring systems, to minimize the risk of exposure to the virus. Cottenet et al. studied the effect of obesity on the risk of intensive care unit (ICU) admission, severe complications and in-hospital mortality, in 992,899 cancer patients hospitalized with or without COVID-19 from the French national administrative database [64]. The authors found that obese cancer patients had an increased risk of admission to the ICU and severe complications, regardless of the type of obesity. Severe obesity was associated with an increased risk of in-hospital mortality, particularly in patients with hematological cancers. This study showed that among hospitalized cancer patients with or without COVID-19, increased vigilance is needed for obese patients, both in epidemic and non-epidemic periods. Lastly, Sereno et al. conducted a retrospective study in 943 cancer patients, of whom 83 (11.3%) were neutropenic and infected with COVID-19, looking at the effect of G-CSF treatment on outcomes during the first phase of the pandemic [65]. They observed a significant effect of the number of days of G-CSF treatment on severe disease and mortality, suggesting that prolonged treatment could be disadvantageous for these patients.
The management of many diseases was altered after the COVID-19 outbreak. Obesity has a great impact on COVID-19 patients’ outcome while it affects the etiopathogenesis of various types of cancers, including melanoma, thyroid (TC) and hematological cancers. Cariti et al. critically evaluated whether screening, diagnosis and treatment of melanoma have been changed by the COVID-19 pandemic as well as the implications of these changes [66]. The authors found that during the pandemic, there was a delay in the diagnosis of new melanoma cases. After detection, the management of early-stage and advanced melanoma cases was fully guaranteed, whereas the follow-up visits of disease-free patients were delayed or replaced by teleconsultation when possible. The authors reported their valuable experience in the management of patients with melanoma during the COVID-19 pandemic, in a dermatological clinic in Northern Italy.
The interplay between obesity, TC and COVID-19 was extensively evaluated by Deligiorgi et al. [67]. Obesity is associated with an increased risk of differentiated TC (DTC). The authors summarized exciting, published data on the association between COVID-19 and TC into four sections: (i) the interrelationship between obesity, immunity, inflammation and oxidative stress, underlying this association; (ii) the challenging management of (D)TC in the COVID-19 era; (iii) the impact of COVID-19 on (D)TC and vice versa; and (iv) the oncogenic potential of SARS-CoV-2. The researchers highlighted the importance of evidence-based, risk-stratified and consensus-based decision making for providing the safest premium-quality care for (D)TC patients, with or without COVID-19.
Both obesity and hematological cancers are well-known risk factors for severe SARS-CoV-2 infection. Tsilingiris and colleagues comprehensively summarized the evidence linking obesity to the development of hematological cancers as well as their interconnection with severe COVID-19. They analyzed various challenges associated with the management of patients suffering from hematological cancers, including prevention, diagnosis and therapeutic approaches [46]. They thoroughly highlighted the unsolved issues and challenges that need to be overcome in the ongoing COVID-19 pandemic. The co-existence of obesity and hematological malignancies in the frame of SARS-CoV-2 infection may theoretically confer an adverse prognosis. Recent global-scale data have shown that the diagnosis of multiple myeloma has been missed or delayed in the early COVID-19 era compared with the previous year, while a decreased survival among newly diagnosed cases has been noted. The field of hemato-oncology has already overcome the initial blow to a great degree and adjusted to the new reality brought forward by COVID-19. Nonetheless, there is a need for continued appraisal and update of numerous aspects of therapeutic management. Many issues need to be determined, including the optimal timing of hematology–oncology therapy initiation, the post-treatment follow-up and the timely therapeutical planning, including allogeneic hematopoietic stem cell transplantation in the case of infections that emerge during the active medical therapy.
Apart from the abovementioned therapeutic approaches in oncologic patients during the COVID-19 pandemic, special attention must be given to patients who need oncological surgery because of the modification of treatment guidelines, the reduced access of patients to healthcare resources and the postponement of surgery. Prodromidou and colleagues studied how Enhanced Recovery after Surgery (ERAS) protocols may provide optimal management of patients with obesity and malignancy during the COVID-19 pandemic, with a special focus on patients who required surgery for gynecologic malignancy [68]. They highlighted the importance of the establishment of protective measures before surgery in order to reduce the exposure of cancer patients to SARS-CoV-2 while simultaneously improving vaccination access. Finally, the authors emphasized that ERAS protocols may play a crucial role in the management of patients with gynecologic cancer based on their efficiency in many surgical fields, such as general surgery and orthopedics, during the COVID-19 pandemic.
Breast cancer patients and caregivers were also tremendously affected by the healthcare crisis in multiple domains and ways. Petropoulou et al. summarized the challenges in breast cancer management and the subsequent implications in clinical practice [69]. Similar to other obesity-related cancers, screening, diagnosis and surgical intervention were the most affected domains, causing a serious psychological burden to patients. The aftermath of diagnostic and surgical delays is yet to be assessed, while alterations in the treatment plans and the introduction of new therapeutic schemes, such as the extensive use of neoadjuvant hormonal therapy and the significant reduction in the first-line surgical approach, may open a novel era in the management of breast cancer.
Furthermore, the COVID-19 pandemic resulted in changes in surgical practice involving colorectal malignancies. In a systemic review and meta-analysis of ten studies including 26,808 patients, Pararas et al. evaluated the impact of the COVID-19 pandemic on the management of colorectal cancer, the third-most-common cancer worldwide, which is also associated with obesity [70]. The authors found that the number of patients presenting with metastases during the pandemic was significantly increased, with no differences regarding the extent of the primary tumor and the nodal status. In addition, patients with colorectal cancer during the pandemic were more likely to undergo palliative interventions or receive neoadjuvant treatment.
Finally, we expect that these manuscripts contributed by experts in this field will provide useful resources to physicians and scientists interested in the interplay of COVID-19 and obesity-related cancer, as well as the development of relevant preventive and therapeutic strategies.

Author Contributions

M.D., N.N.-A. and N.S. were involved in the preparation and promotion of the Special Issue as well as the writing and review of the Editorial. All authors have read and agreed to the published version of the manuscript.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial or not-for-profit sectors.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Han, X.; Shi, S.K.; Zhao, J.; Nogueira, L.M.; Bandi, P.; Fedewa, S.A.; Jemal, A.; Yabroff, K.R. The first year of the COVID-19 pandemic and health among cancer survivors in the United States. Cancer 2022, 128, 3727–3733. [Google Scholar] [CrossRef] [PubMed]
  2. Syriga, M.; Karampela, I.; Dalamaga, M.; Karampelas, M. The effect of COVID-19 pandemic on the attendance and clinical outcomes of patients with ophthalmic disease: A mini-review. Metab. Open 2021, 12, 100131. [Google Scholar] [CrossRef] [PubMed]
  3. Lewis, M.A. Between Scylla and Charybdis—Oncologic Decision Making in the Time of COVID-19. N. Engl. J. Med. 2020, 382, 2285–2287. [Google Scholar] [CrossRef] [PubMed]
  4. WHO. Cancer. Available online: https://www.who.int/news-room/fact-sheets/detail/cancer (accessed on 20 February 2023).
  5. WHO. Obesity and Overweight. Available online: https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight (accessed on 20 February 2023).
  6. Dalamaga, M.; Papadavid, E.; Basios, G.; Vaggopoulos, V.; Rigopoulos, D.; Kassanos, D.; Trakakis, E. Ovarian SAHA syndrome is associated with a more insulin-resistant profile and represents an independent risk factor for glucose abnormalities in women with polycystic ovary syndrome: A prospective controlled study. J. Am. Acad. Dermatol. 2013, 69, 922–930. [Google Scholar] [CrossRef] [PubMed]
  7. Hroussalas, G.; Kassi, E.; Dalamaga, M.; Delimaris, I.; Zachari, A.; Dionyssiou-Asteriou, A. Leptin, soluble leptin receptor, adiponectin and resistin in relation to OGTT in overweight/obese postmenopausal women. Maturitas 2008, 59, 339–349. [Google Scholar] [CrossRef] [PubMed]
  8. Marouga, A.; Dalamaga, M.; Kastania, A.N.; Antonakos, G.; Thrasyvoulides, A.; Kontelia, G.; Dimas, C.; Vlahakos, D.V. Correlates of serum resistin in elderly, non-diabetic patients with chronic kidney disease. Clin. Lab. 2013, 59, 1121–1128. [Google Scholar] [CrossRef]
  9. Papadavid, E.; Katsimbri, P.; Kapniari, I.; Koumaki, D.; Karamparpa, A.; Dalamaga, M.; Tzannis, K.; Betaoumpas, D.; Rigopoulos, D. Prevalence of psoriatic arthritis and its correlates among patients with psoriasis in Greece: Results from a large retrospective study. J. Eur. Acad. Dermatol. Venereol. 2016, 30, 1749–1752. [Google Scholar] [CrossRef]
  10. Paroutoglou, K.; Papadavid, E.; Christodoulatos, G.S.; Dalamaga, M. Deciphering the Association Between Psoriasis and Obesity: Current Evidence and Treatment Considerations. Curr. Obes. Rep. 2020, 9, 165–178. [Google Scholar] [CrossRef]
  11. Powell-Wiley, T.M.; Poirier, P.; Burke, L.E.; Despres, J.P.; Gordon-Larsen, P.; Lavie, C.J.; Lear, S.A.; Ndumele, C.E.; Neeland, I.J.; Sanders, P.; et al. Obesity and Cardiovascular Disease: A Scientific Statement From the American Heart Association. Circulation 2021, 143, e984–e1010. [Google Scholar] [CrossRef]
  12. Tsigalou, C.; Vallianou, N.; Dalamaga, M. Autoantibody Production in Obesity: Is There Evidence for a Link Between Obesity and Autoimmunity? Curr. Obes. Rep. 2020, 9, 245–254. [Google Scholar] [CrossRef]
  13. Vallianou, N.; Dalamaga, M.; Stratigou, T.; Karampela, I.; Tsigalou, C. Do Antibiotics Cause Obesity Through Long-term Alterations in the Gut Microbiome? A Review of Current Evidence. Curr. Obes. Rep. 2021, 10, 244–262. [Google Scholar] [CrossRef] [PubMed]
  14. Dalamaga, M.; Christodoulatos, G.S.; Karampela, I.; Vallianou, N.; Apovian, C.M. Understanding the Co-Epidemic of Obesity and COVID-19: Current Evidence, Comparison with Previous Epidemics, Mechanisms, and Preventive and Therapeutic Perspectives. Curr. Obes. Rep. 2021, 10, 214–243. [Google Scholar] [CrossRef] [PubMed]
  15. Karampela, I.; Vallianou, N.; Magkos, F.; Apovian, C.M.; Dalamaga, M. Obesity, Hypovitaminosis D, and COVID-19: The Bermuda Triangle in Public Health. Curr. Obes. Rep. 2022, 11, 116–125. [Google Scholar] [CrossRef] [PubMed]
  16. Kritis, P.; Karampela, I.; Kokoris, S.; Dalamaga, M. The combination of bromelain and curcumin as an immune-boosting nutraceutical in the prevention of severe COVID-19. Metab. Open 2020, 8, 100066. [Google Scholar] [CrossRef] [PubMed]
  17. Tsilingiris, D.; Dalamaga, M.; Liu, J. SARS-CoV-2 adipose tissue infection and hyperglycemia: A further step towards the understanding of severe COVID-19. Metab. Open 2022, 13, 100163. [Google Scholar] [CrossRef]
  18. Tsilingiris, D.; Vallianou, N.G.; Karampela, I.; Dalamaga, M. Vaccine induced thrombotic thrombocytopenia: The shady chapter of a success story. Metab. Open 2021, 11, 100101. [Google Scholar] [CrossRef]
  19. Argyrakopoulou, G.; Dalamaga, M.; Spyrou, N.; Kokkinos, A. Gender Differences in Obesity-Related Cancers. Curr. Obes. Rep. 2021, 10, 100–115. [Google Scholar] [CrossRef]
  20. Christodoulatos, G.S.; Antonakos, G.; Karampela, I.; Psallida, S.; Stratigou, T.; Vallianou, N.; Lekka, A.; Marinou, I.; Vogiatzakis, E.; Kokoris, S.; et al. Circulating Omentin-1 as a Biomarker at the Intersection of Postmenopausal Breast Cancer Occurrence and Cardiometabolic Risk: An Observational Cross-Sectional Study. Biomolecules 2021, 11, 1609. [Google Scholar] [CrossRef]
  21. Dalamaga, M.; Karmaniolas, K.; Chamberland, J.; Nikolaidou, A.; Lekka, A.; Dionyssiou-Asteriou, A.; Mantzoros, C.S. Higher fetuin-A, lower adiponectin and free leptin levels mediate effects of excess body weight on insulin resistance and risk for myelodysplastic syndrome. Metabolism 2013, 62, 1830–1839. [Google Scholar] [CrossRef]
  22. Arayici, M.E.; Basbinar, Y.; Ellidokuz, H. The impact of cancer on the severity of disease in patients affected with COVID-19: An umbrella review and meta-meta-analysis of systematic reviews and meta-analyses involving 1,064,476 participants. Clin. Exp. Med. 2022. [Google Scholar] [CrossRef]
  23. Treskova-Schwarzbach, M.; Haas, L.; Reda, S.; Pilic, A.; Borodova, A.; Karimi, K.; Koch, J.; Nygren, T.; Scholz, S.; Schonfeld, V.; et al. Pre-existing health conditions and severe COVID-19 outcomes: An umbrella review approach and meta-analysis of global evidence. BMC Med. 2021, 19, 212. [Google Scholar] [CrossRef] [PubMed]
  24. OnCovid Study, G.; Pinato, D.J.; Patel, M.; Scotti, L.; Colomba, E.; Dolly, S.; Loizidou, A.; Chester, J.; Mukherjee, U.; Zambelli, A.; et al. Time-Dependent COVID-19 Mortality in Patients With Cancer: An Updated Analysis of the OnCovid Registry. JAMA Oncol. 2022, 8, 114–122. [Google Scholar] [CrossRef] [PubMed]
  25. Sengar, M.; Chinnaswamy, G.; Ranganathan, P.; Ashok, A.; Bhosale, S.; Biswas, S.; Chaturvedi, P.; Dhamne, C.; Divatia, J.; D’Sa, K.; et al. Outcomes of COVID-19 and risk factors in patients with cancer. Nat. Cancer 2022, 3, 547–551. [Google Scholar] [CrossRef]
  26. Van Dam, P.A.; Huizing, M.; Mestach, G.; Dierckxsens, S.; Tjalma, W.; Trinh, X.B.; Papadimitriou, K.; Altintas, S.; Vermorken, J.; Vulsteke, C.; et al. SARS-CoV-2 and cancer: Are they really partners in crime? Cancer Treat. Rev. 2020, 89, 102068. [Google Scholar] [CrossRef] [PubMed]
  27. Tagliamento, M.; Gennari, A.; Lambertini, M.; Salazar, R.; Harbeck, N.; Del Mastro, L.; Aguilar-Company, J.; Bower, M.; Sharkey, R.; Dalla Pria, A.; et al. Pandemic Phase-Adjusted Analysis of COVID-19 Outcomes Reveals Reduced Intrinsic Vulnerability and Substantial Vaccine Protection From Severe Acute Respiratory Syndrome Coronavirus 2 in Patients With Breast Cancer. J. Clin. Oncol. 2023, JCO2201667. [Google Scholar] [CrossRef]
  28. Pinato, D.J.; Aguilar-Company, J.; Ferrante, D.; Hanbury, G.; Bower, M.; Salazar, R.; Mirallas, O.; Sureda, A.; Plaja, A.; Cucurull, M.; et al. Outcomes of the SARS-CoV-2 omicron (B.1.1.529) variant outbreak among vaccinated and unvaccinated patients with cancer in Europe: Results from the retrospective, multicentre, OnCovid registry study. Lancet Oncol. 2022, 23, 865–875. [Google Scholar] [CrossRef]
  29. Song, Q.; Bates, B.; Shao, Y.R.; Hsu, F.C.; Liu, F.; Madhira, V.; Mitra, A.K.; Bergquist, T.; Kavuluru, R.; Li, X.; et al. Risk and Outcome of Breakthrough COVID-19 Infections in Vaccinated Patients With Cancer: Real-World Evidence From the National COVID Cohort Collaborative. J. Clin. Oncol. 2022, 40, 1414–1427. [Google Scholar] [CrossRef]
  30. Carrara, E.; Razzaboni, E.; Azzini, A.M.; De Rui, M.E.; Pinho Guedes, M.N.; Gorska, A.; Giannella, M.; Bussini, L.; Bartoletti, M.; Arbizzani, F.; et al. Predictors of clinical evolution of SARS-CoV-2 infection in hematological patients: A systematic review and meta-analysis. Hematol. Oncol. 2023, 41, 16–25. [Google Scholar] [CrossRef]
  31. Chavez-MacGregor, M.; Lei, X.; Zhao, H.; Scheet, P.; Giordano, S.H. Evaluation of COVID-19 Mortality and Adverse Outcomes in US Patients With or Without Cancer. JAMA Oncol. 2022, 8, 69–78. [Google Scholar] [CrossRef]
  32. Kouhpayeh, H. Clinical features predicting COVID-19 mortality risk. Eur. J. Transl. Myol. 2022, 32, 10268. [Google Scholar] [CrossRef]
  33. Lunski, M.J.; Burton, J.; Tawagi, K.; Maslov, D.; Simenson, V.; Barr, D.; Yuan, H.; Johnson, D.; Matrana, M.; Cole, J.; et al. Multivariate mortality analyses in COVID-19: Comparing patients with cancer and patients without cancer in Louisiana. Cancer 2021, 127, 266–274. [Google Scholar] [CrossRef]
  34. Mileham, K.F.; Bruinooge, S.S.; Aggarwal, C.; Patrick, A.L.; Davis, C.; Mesenhowski, D.J.; Spira, A.; Clayton, E.J.; Waterhouse, D.; Moore, S.; et al. Changes Over Time in COVID-19 Severity and Mortality in Patients Undergoing Cancer Treatment in the United States: Initial Report From the ASCO Registry. JCO Oncol. Pract. 2022, 18, e426–e441. [Google Scholar] [CrossRef] [PubMed]
  35. Vallianou, N.G.; Evangelopoulos, A.; Kounatidis, D.; Stratigou, T.; Christodoulatos, G.S.; Karampela, I.; Dalamaga, M. Diabetes Mellitus and SARS-CoV-2 Infection: Pathophysiologic Mechanisms and Implications in Management. Curr. Diabetes Rev. 2021, 17, e123120189797. [Google Scholar] [CrossRef]
  36. Varnai, C.; Palles, C.; Arnold, R.; Curley, H.M.; Purshouse, K.; Cheng, V.W.T.; Booth, S.; Campton, N.A.; Collins, G.P.; Hughes, D.J.; et al. Mortality Among Adults With Cancer Undergoing Chemotherapy or Immunotherapy and Infected With COVID-19. JAMA Netw. Open 2022, 5, e220130. [Google Scholar] [CrossRef] [PubMed]
  37. Wang, Q.; Berger, N.A.; Xu, R. Analyses of Risk, Racial Disparity, and Outcomes Among US Patients With Cancer and COVID-19 Infection. JAMA Oncol. 2021, 7, 220–227. [Google Scholar] [CrossRef] [PubMed]
  38. The Lancet Oncology. COVID-19 and cancer: 1 year on. Lancet Oncol. 2021, 22, 411. [Google Scholar] [CrossRef]
  39. Englum, B.R.; Prasad, N.K.; Lake, R.E.; Mayorga-Carlin, M.; Turner, D.J.; Siddiqui, T.; Sorkin, J.D.; Lal, B.K. Impact of the COVID-19 pandemic on diagnosis of new cancers: A national multicenter study of the Veterans Affairs Healthcare System. Cancer 2022, 128, 1048–1056. [Google Scholar] [CrossRef]
  40. Joung, R.H.; Nelson, H.; Mullett, T.W.; Kurtzman, S.H.; Shafir, S.; Harris, J.B.; Yao, K.A.; Brajcich, B.C.; Bilimoria, K.Y.; Cance, W.G. A national quality improvement study identifying and addressing cancer screening deficits due to the COVID-19 pandemic. Cancer 2022, 128, 2119–2125. [Google Scholar] [CrossRef]
  41. Kuzuu, K.; Misawa, N.; Ashikari, K.; Kessoku, T.; Kato, S.; Hosono, K.; Yoneda, M.; Nonaka, T.; Matsushima, S.; Komatsu, T.; et al. Gastrointestinal Cancer Stage at Diagnosis Before and During the COVID-19 Pandemic in Japan. JAMA Netw. Open 2021, 4, e2126334. [Google Scholar] [CrossRef]
  42. Terashima, T.; Konishi, H.; Sato, Y.; Igarashi, M.; Yanagibashi, T.; Konno, R.; Saya, H.; Doki, Y.; Kakizoe, T. Impact of coronavirus disease 2019 on the number of newly diagnosed cancer patients and examinations and surgeries performed for cancer in Japan: A nationwide study. BMC Cancer 2022, 22, 1303. [Google Scholar] [CrossRef] [PubMed]
  43. Thierry, A.R.; Pastor, B.; Pisareva, E.; Ghiringhelli, F.; Bouche, O.; De La Fouchardiere, C.; Vanbockstael, J.; Smith, D.; Francois, E.; Dos Santos, M.; et al. Association of COVID-19 Lockdown With the Tumor Burden in Patients With Newly Diagnosed Metastatic Colorectal Cancer. JAMA Netw. Open 2021, 4, e2124483. [Google Scholar] [CrossRef] [PubMed]
  44. Toss, A.; Isca, C.; Venturelli, M.; Nasso, C.; Ficarra, G.; Bellelli, V.; Armocida, C.; Barbieri, E.; Cortesi, L.; Moscetti, L.; et al. Two-month stop in mammographic screening significantly impacts on breast cancer stage at diagnosis and upfront treatment in the COVID era. ESMO Open 2021, 6, 100055. [Google Scholar] [CrossRef] [PubMed]
  45. Walsh, D. Available online: https://www.euronews.com/next/2021/12/01/cancer-in-europe-the-devastating-impact-of-covid-on-diagnosis-and-treatment-country-by-cou (accessed on 8 February 2023).
  46. Tsilingiris, D.; Nasiri-Ansari, N.; Spyrou, N.; Magkos, F.; Dalamaga, M. Management of Hematologic Malignancies in the Era of COVID-19 Pandemic: Pathogenetic Mechanisms, Impact of Obesity, Perspectives, and Challenges. Cancers 2022, 14, 2494. [Google Scholar] [CrossRef] [PubMed]
  47. Vallianou, N.G.; Tsilingiris, D.; Christodoulatos, G.S.; Karampela, I.; Dalamaga, M. Anti-viral treatment for SARS-CoV-2 infection: A race against time amidst the ongoing pandemic. Metab. Open 2021, 10, 100096. [Google Scholar] [CrossRef]
  48. DeWolf, S.; Laracy, J.C.; Perales, M.A.; Kamboj, M.; van den Brink, M.R.M.; Vardhana, S. SARS-CoV-2 in immunocompromised individuals. Immunity 2022, 55, 1779–1798. [Google Scholar] [CrossRef]
  49. Hettle, D.; Hutchings, S.; Muir, P.; Moran, E.; COVID-19 Genomics UK (COG-UK) Consortium. Persistent SARS-CoV-2 infection in immunocompromised patients facilitates rapid viral evolution: Retrospective cohort study and literature review. Clin. Infect. Pract. 2022, 16, 100210. [Google Scholar] [CrossRef]
  50. Curigliano, G.; Banerjee, S.; Cervantes, A.; Garassino, M.C.; Garrido, P.; Girard, N.; Haanen, J.; Jordan, K.; Lordick, F.; Machiels, J.P.; et al. Managing cancer patients during the COVID-19 pandemic: An ESMO multidisciplinary expert consensus. Ann. Oncol. 2020, 31, 1320–1335. [Google Scholar] [CrossRef]
  51. El Chaer, F.; Auletta, J.J.; Chemaly, R.F. How I treat and prevent COVID-19 in patients with hematologic malignancies and recipients of cellular therapies. Blood 2022, 140, 673–684. [Google Scholar] [CrossRef]
  52. Waghmare, A.; Abidi, M.Z.; Boeckh, M.; Chemaly, R.F.; Dadwal, S.; El Boghdadly, Z.; Kamboj, M.; Papanicolaou, G.A.; Pergam, S.A.; Shahid, Z. Guidelines for COVID-19 Management in Hematopoietic Cell Transplantation and Cellular Therapy Recipients. Biol. Blood Marrow Transplant. 2020, 26, 1983–1994. [Google Scholar] [CrossRef]
  53. Buske, C.; Dreyling, M.; Alvarez-Larran, A.; Apperley, J.; Arcaini, L.; Besson, C.; Bullinger, L.; Corradini, P.; Giovanni Della Porta, M.; Dimopoulos, M.; et al. Managing hematological cancer patients during the COVID-19 pandemic: An ESMO-EHA Interdisciplinary Expert Consensus. ESMO Open 2022, 7, 100403. [Google Scholar] [CrossRef]
  54. Fendler, A.; Shepherd, S.T.C.; Au, L.; Wilkinson, K.A.; Wu, M.; Schmitt, A.M.; Tippu, Z.; Farag, S.; Rogiers, A.; Harvey, R.; et al. Immune responses following third COVID-19 vaccination are reduced in patients with hematological malignancies compared to patients with solid cancer. Cancer Cell 2022, 40, 438. [Google Scholar] [CrossRef] [PubMed]
  55. Mair, M.J.; Berger, J.M.; Berghoff, A.S.; Starzer, A.M.; Ortmayr, G.; Puhr, H.C.; Steindl, A.; Perkmann, T.; Haslacher, H.; Strassl, R.; et al. Humoral Immune Response in Hematooncological Patients and Health Care Workers Who Received SARS-CoV-2 Vaccinations. JAMA Oncol. 2022, 8, 106–113. [Google Scholar] [CrossRef] [PubMed]
  56. Naranbhai, V.; Pernat, C.A.; Gavralidis, A.; St Denis, K.J.; Lam, E.C.; Spring, L.M.; Isakoff, S.J.; Farmer, J.R.; Zubiri, L.; Hobbs, G.S.; et al. Immunogenicity and Reactogenicity of SARS-CoV-2 Vaccines in Patients With Cancer: The CANVAX Cohort Study. J. Clin. Oncol. 2022, 40, 12–23. [Google Scholar] [CrossRef]
  57. Amanatidou, E.; Gkiouliava, A.; Pella, E.; Serafidi, M.; Tsilingiris, D.; Vallianou, N.G.; Karampela, I.; Dalamaga, M. Breakthrough infections after COVID-19 vaccination: Insights, perspectives and challenges. Metab. Open 2022, 14, 100180. [Google Scholar] [CrossRef]
  58. Chien, K.S.; Peterson, C.; Young, E.; Chihara, D.; Manasanch, E.E.; Ramdial, J.; Thompson, P.A. Outcomes of Breakthrough COVID-19 Infections in Patients with Hematologic Malignancies. Blood Adv. 2023, 8, 827. [Google Scholar] [CrossRef] [PubMed]
  59. Wang, L.; Kaelber, D.C.; Xu, R.; Berger, N.A. COVID-19 breakthrough infections, hospitalizations and mortality in fully vaccinated patients with hematologic malignancies: A clarion call for maintaining mitigation and ramping-up research. Blood Rev. 2022, 54, 100931. [Google Scholar] [CrossRef] [PubMed]
  60. Habibzadeh, P.; Dastsooz, H.; Eshraghi, M.; Los, M.J.; Klionsky, D.J.; Ghavami, S. Autophagy: The Potential Link between SARS-CoV-2 and Cancer. Cancers 2021, 13, 5721. [Google Scholar] [CrossRef] [PubMed]
  61. Bader-Larsen, K.S.; Larson, E.A.; Dalamaga, M.; Magkos, F. A Narrative Review of the Safety of Anti-COVID-19 Nutraceuticals for Patients with Cancer. Cancers 2021, 13, 6094. [Google Scholar] [CrossRef]
  62. Almasri, M.; Bshesh, K.; Khan, W.; Mushannen, M.; Salameh, M.A.; Shafiq, A.; Vattoth, A.L.; Elkassas, N.; Zakaria, D. Cancer Patients and the COVID-19 Vaccines: Considerations and Challenges. Cancers 2022, 14, 5630. [Google Scholar] [CrossRef]
  63. Ali, J.K.; Riches, J.C. The Impact of the COVID-19 Pandemic on Oncology Care and Clinical Trials. Cancers 2021, 13, 5924. [Google Scholar] [CrossRef]
  64. Cottenet, J.; Tapia, S.; Arveux, P.; Bernard, A.; Dabakuyo-Yonli, T.S.; Quantin, C. Effect of Obesity among Hospitalized Cancer Patients with or without COVID-19 on a National Level. Cancers 2022, 14, 5660. [Google Scholar] [CrossRef] [PubMed]
  65. Sereno, M.; Jimenez-Gordo, A.M.; Baena-Espinar, J.; Aguado, C.; Mielgo, X.; Pertejo, A.; Alvarez-Alvarez, R.; Sanchez, A.; Lopez, J.L.; Molina, R.; et al. A Multicenter Analysis of the Outcome of Cancer Patients with Neutropenia and COVID-19 Optionally Treated with Granulocyte-Colony Stimulating Factor (G-CSF): A Comparative Analysis. Cancers 2021, 13, 4205. [Google Scholar] [CrossRef] [PubMed]
  66. Cariti, C.; Merli, M.; Avallone, G.; Rubatto, M.; Marra, E.; Fava, P.; Caliendo, V.; Picciotto, F.; Gualdi, G.; Stanganelli, I.; et al. Melanoma Management during the COVID-19 Pandemic Emergency: A Literature Review and Single-Center Experience. Cancers 2021, 13, 6071. [Google Scholar] [CrossRef]
  67. Deligiorgi, M.V.; Siasos, G.; Vakkas, L.; Trafalis, D.T. Charting the Unknown Association of COVID-19 with Thyroid Cancer, Focusing on Differentiated Thyroid Cancer: A Call for Caution. Cancers 2021, 13, 5785. [Google Scholar] [CrossRef] [PubMed]
  68. Prodromidou, A.; Koulakmanidis, A.M.; Haidopoulos, D.; Nelson, G.; Rodolakis, A.; Thomakos, N. Where Enhanced Recovery after Surgery (ERAS) Protocols Meet the Three Major Current Pandemics: COVID-19, Obesity and Malignancy. Cancers 2022, 14, 1660. [Google Scholar] [CrossRef]
  69. Petropoulou, Z.; Arkadopoulos, N.; Michalopoulos, N.V. Breast Cancer and COVID-19: Challenges in Surgical Management. Cancers 2022, 14, 5360. [Google Scholar] [CrossRef] [PubMed]
  70. Pararas, N.; Pikouli, A.; Papaconstantinou, D.; Bagias, G.; Nastos, C.; Pikoulis, A.; Dellaportas, D.; Lykoudis, P.; Pikoulis, E. Colorectal Surgery in the COVID-19 Era: A Systematic Review and Meta-Analysis. Cancers 2022, 14, 1229. [Google Scholar] [CrossRef]
Figure 1. Main challenges of COVID-19 associated with cancer. This image was derived from the free medical site http://smart.servier.com/ (accessed on 2 March 2023) by Servier, licensed under a Creative Commons Attribution 3.0 Unported License.
Figure 1. Main challenges of COVID-19 associated with cancer. This image was derived from the free medical site http://smart.servier.com/ (accessed on 2 March 2023) by Servier, licensed under a Creative Commons Attribution 3.0 Unported License.
Cancers 15 01771 g001
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Dalamaga, M.; Nasiri-Ansari, N.; Spyrou, N. Perspectives and Challenges of COVID-19 with Obesity-Related Cancers. Cancers 2023, 15, 1771. https://doi.org/10.3390/cancers15061771

AMA Style

Dalamaga M, Nasiri-Ansari N, Spyrou N. Perspectives and Challenges of COVID-19 with Obesity-Related Cancers. Cancers. 2023; 15(6):1771. https://doi.org/10.3390/cancers15061771

Chicago/Turabian Style

Dalamaga, Maria, Narjes Nasiri-Ansari, and Nikolaos Spyrou. 2023. "Perspectives and Challenges of COVID-19 with Obesity-Related Cancers" Cancers 15, no. 6: 1771. https://doi.org/10.3390/cancers15061771

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop