Skip to main content

Emerging issues related to COVID-19 vaccination in patients with cancer

Abstract

Coronavirus disease 2019 (COVID-19) has resulted in millions of deaths globally. The pandemic has had a severe impact on oncology care and research. Patients with underlying cancer are more vulnerable to contracting COVID-19, and also have a more severe clinical course following the infection. The rollout of COVID-19 vaccines in many parts of the world has raised hopes of controlling the pandemic. In this editorial, the authors outline key characteristics of the currently approved COVID-19 vaccines, provide a brief overview of key emerging issues such as vaccine-induced immune thrombotic thrombocytopenia and SARS-CoV-2 variants of concern, and review the available data related to the efficacy and side effects of vaccinating patients with cancer.

FormalPara Key Summary Points
Patients with underlying cancer who develop infection with SARS-CoV-2 have a high rate of mortality. They constitute a highly vulnerable population and must receive COVID-19 vaccination on priority.
Multiple vaccines have been approved by regulatory agencies around the world.
Patients with cancer were largely excluded from late-stage vaccine trials, leading to a paucity of data related to this population.
Based on the limited data available so far, there is no specific safety concern related to COVID-19 vaccination in patients with cancer.
A rare syndrome of thrombosis associated with thrombocytopenia, known variously as thrombosis with thrombocytopenia syndrome (TTS), vaccine-induced immune thrombotic thrombocytopenia (VITT), or vaccine-induced prothrombotic immune thrombocytopenia (VIPIT), has been reported in people, especially younger women, receiving AstraZeneca’s ChAdOx1 nCoV-19 or Janssen’s Ad.26.COV2.S vaccines. Currently, it is believed that the benefits of these vaccines outweigh the risks in the majority of people.
Patients with cancer may show a weaker immune response to COVID-19 vaccines, compared to the general population.
Results from the UK SOAP-02 study show that a prolonged prime-boost interval may leave patients with cancer vulnerable to COVID-19.
Current SARS-CoV-2 variants of concern (VoC) include B.1.1.7 (alpha), B.1.351 (beta), P.1 (gamma), and B.1.617.2 (delta), which were first identified in the UK, South Africa, Brazil, and India, respectively. These VOCs may differ with respect to transmissibility, lethality, and response to vaccine.
“Mix-and-match” studies with heterologous prime-boost combinations and studies with three-dose schedules are ongoing, and results eagerly awaited.

Digital Features

This article is published with digital features, including a summary slide, to facilitate understanding of the article. To view digital features for this article go to https://doi.org/10.6084/m9.figshare.14687430.

Introduction

Coronavirus disease 2019 (COVID-19) [1], caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has resulted in about 3.5 million deaths globally as of 26 May 2021, including about 721,000 in the European Union, 590,000 in the USA, and 128,000 in the UK.

The pandemic has had a severe impact on oncology care and research [2,3,4,5,6,7]. While the majority of patients with COVID-19 remain pauci- or asymptomatic, about 10–15% have a more severe disease, with some developing a clinical syndrome that shares certain similarities with malignancy, including hyper-inflammation, immune dysfunction, and of most concern, widespread thrombosis [8], with microangiopathy being of particular concern [9].

Patients with underlying cancer who develop COVID-19 constitute a vulnerable population [10]. A meta-analysis of 33,879 patients with both COVID-19 and cancer showed that their probability of death was 25.4% (95% CI 22.9–28.2) [11]. Patients with lung cancer and hematological malignancies are at highest risk, as are recipients of stem cell transplants and adoptive cellular therapies [12,13,14]. Effective measures should be taken to protect patients with cancer from contracting COVID-19, including prioritization of vaccination against SARS-CoV-2 [15].

SARS-CoV-2 has a characteristic spike (S) protein which induces humoral and cellular immune responses against SARS-CoV-2, making it a potent target for vaccine development [16].

Types of COVID-19 vaccines

According to the World Health Organization (WHO), there were 101 COVID-19 vaccines in clinical development and 184 vaccine candidates in preclinical development as of 26 May 2021. Most of them aim to elicit an immune response against the S protein [17], and employ various COVID-19 vaccine platforms, such as nucleic acid, viral vector, protein subunit, inactivated or attenuated whole virus, and virus-like particle [16].

As of 26 May 2021, the US Food and Drug Administration (FDA) has authorized the emergency use of three vaccines (Pfizer-BioNTech’s BNT162b2/tozinameran/Comirnaty, Moderna’s mRNA-1273, and Johnson & Johnson/Janssen’s Ad.26.COV2.S), while the European Medicines Agency (EMA) has approved the conditional use of AstraZeneca-University of Oxford’s ChAdOx1 nCoV-19/Vaxzevria, in addition to the above three. Four other COVID-19 vaccines are currently under rolling review by EMA: Novavax’s NVX-CoV2373, CureVac’s CVnCoV, Gamaleya National Centre of Epidemiology and Microbiology’s Sputnik V, and Sinovac Life Sciences’ COVID-19 Vaccine (Vero Cell) Inactivated.

The BNT162b2 and mRNA-1273 mRNA nucleic acid vaccines contain the prefusion-stabilized S protein encapsulated within a lipid-nanoparticle complex [18]; Ad.26.COV2.S is a recombinant human adenovirus type 26 vector encoding the S protein; and ChAdOx1 nCoV-19 is a recombinant chimpanzee adenoviral vector encoding the S protein. The Ad.26.COV2.S is given as a single dose, but for the other approved vaccines the first (prime) dose is followed by a second (boost) dose a few weeks later.

Several other COVID-19 vaccines have been approved by regulatory agencies of specific countries, including Sputnik V, Sinovac’s CoronaVac, and AstraZeneca-University of Oxford-Serum Institute of India’s Covishield [19].

Safety of COVID-19 vaccines in patients with cancer

Most COVID-19 vaccine phase 3 studies have excluded the participation of patients with cancer. Hence, there are insufficient data regarding the safety or efficacy of these vaccines in this patient population. However, given the high mortality risk from SARS-CoV-2 infection among patients with cancer, the high efficacy of COVID-19 vaccines in preventing serious infection in the general population, and the low incidence of serious adverse effects, several professional oncology societies and other health organizations and agencies have advocated that the risk–benefit ratio is likely to be strongly in favor of vaccinating people with cancer [7, 20, 21]. A majority of patients with cancer, too, are supportive of getting vaccinated [22]. However, the global scenario is heterogeneous, with many low-income countries yet to prioritize vaccination of patients with cancer [23].

Immune checkpoint inhibitors (ICIs) have been approved for the treatment of a wide variety of malignancies [24, 25]. There is a theoretical concern that COVID-19 vaccines that induce a primarily TH1-type response, or contain vaccine adjuvants such as Matrix-M1 [26], or toll-like receptor (TLR) 7/8 agonist molecule adsorbed to alum [27], could have an impact on the toxicity or efficacy of ICIs. However, the safety data available so far are reassuring, with no evidence of increased immune-related adverse events. In a study from Israel, 134 patients with cancer with ongoing ICI therapy were administered two doses of the BNT162b2 vaccine [28]. The commonest local side effects were injection site pain (63%) and local swelling (9%), whereas the most frequent systemic side effects were muscle pain (34%), fatigue (34%), headache (16%), and fever, chills, and gastrointestinal complications (10% each). This toxicity profile was broadly similar between the cohort of ICI-treated patients with cancer and a matched cohort of healthy controls (HCs); no vaccine-related or ICI-related severe adverse events were observed.

In the UK SOAP-02 study, 95 patients with solid cancer, 56 patients with hematological cancer, and 54 healthy controls (HC) were enrolled [29]. Of these, 31 patients with cancer and 16 HCs were vaccinated with two doses of the BNT162b2 vaccine 21 days apart, while the others received only the prime dose of the vaccine at the time of reporting, and were scheduled to receive the boost dose 12 weeks later. In the overall cancer cohort, no toxicities were observed in 54% of the patients following the first dose, and in 71% of the patients following the second dose. In the HC cohort, no toxicities were reported in 38% after the first dose and in 31% after the second dose. Injection-site pain was the most common adverse event, and was recorded in 35% of the patients with cancer. No vaccine-related deaths were reported.

COVID-19 vaccines, thrombosis, and low platelets

Rare events of venous or arterial thrombosis associated with thrombocytopenia (clinically resembling heparin-induced thrombocytopenia [HIT]) have been reported in people receiving AstraZeneca’s ChAdOx1 nCoV-19 or Janssen’s Ad.26.COV2.S [30, 31]. This syndrome has recently been termed by the US Centers for Disease Control and Prevention (CDC) as thrombosis with thrombocytopenia syndrome (TTS) [32], and is also known as vaccine-induced immune thrombotic thrombocytopenia (VITT) [33] or vaccine-induced prothrombotic immune thrombocytopenia (VIPIT) [34]. The thrombosis is often cerebral or abdominal in location and associated with platelet-activating antibodies against platelet factor 4 [33, 35], and younger women seem to be at higher risk [36]. Per current guidance, administration of the anticoagulant heparin should be avoided in patients with potential TTS, unless testing for HIT is negative [37].

As of 12 May 2021, 23.9 million first doses and 9.0 million doses of the of the ChAdOx1 nCoV-19 have been administered in the UK, following which the Medicines and Healthcare products Regulatory Agency (MHRA) received 309 reports (169 in females, 138 in males, 2 of unknown gender) of major thromboembolic events with low platelets, including 116 cases (mean age 46 years) of cerebral venous sinus thrombosis with thrombocytopenia [38]. With 56 reported deaths among these 309 cases to date, the overall case fatality rate is 18%.

In a large population-based study from Denmark and Norway involving 281,264 people who received the ChAdOx1 nCoV-19 vaccine, 59 cases of venous thromboembolic events were observed among the vaccine recipients, compared with 30 expected based on the incidence rates in the general population, corresponding to a standardized morbidity ratio of 1.97 (1.50–2.54) [39].

The MHRA has advised caution while using ChAdOx1 nCoV-19 in people of any age who are at higher risk of blood clots because of underlying medical conditions [40]. This guidance could impact patients with cancer, considering that malignancy itself is associated with an increased risk of thromboembolism [41]. Some countries have restricted the use of this vaccine to older age groups, even though the EMA and MHRA opine that based on data available on 26 May 2021, the benefits outweigh the risks in the majority of people.

According to the US FDA, 15 cases of thrombosis with thrombocytopenia have been reported up to 24 April 2021 among recipients of the Ad.26.COV2.S vaccine [42]. All of these cases occurred in women between the ages of 18 and 59 (median 37 years), with the onset of symptoms between 6 and 15 days after vaccination.

Thrombocytopenia following administration of mRNA vaccines BNT162b2 and mRNA-1273 has been reported in 20 patients (median age 41 years; 11 female) [43]. Of these, 17 had no pre-existing thrombocytopenia, while 14 reported bleeding symptoms prior to hospitalization.

Efficacy of COVID-19 vaccines in patients with cancer

Currently, there are limited data about the efficacy of COVID-19 vaccines in patients with cancer.

In the SOAP-02 study described above, measurement of anti-S protein immunoglobulin levels 21 days following the first dose of the BNT162b2 vaccine showed that 97% (31/32) of HCs, 39% (21/54) of patients with solid cancer, and only 13% (5/39) of patients with hematological cancer had developed an adequate level of immune protection. However, some of these serological non-responders demonstrated an increase in T cells secreting IFN-γ and/or IL-2. Notably, among patients with solid cancers who received the boost dose at day 21, 95% (18/19) showed protective levels of anti-SARS-CoV-2 antibodies at week 5.

As a response to the current shortage of COVID-19 vaccine supply, some countries have adopted a policy of increasing the interval between vaccine doses. As an example, in the UK and British Columbia, Canada, the prime-boost gap is currently 8 and 16 weeks, respectively. Emerging data show that increased gap improves the immunogenicity and efficacy of the ChAdOx1 nCoV-19 vaccine [44]. While this approach may be suitable for the general population with an intact immune system, results from the SOAP-02 and other studies raise the concern that a prolonged prime-boost interval may leave patients with cancer vulnerable to COVID-19 [45].

While waiting for additional trial and real-world data to accrue, it may be prudent for policymakers to consider tailored time points for vaccinating patients with cancer or other causes of immunodeficiency.

Vulnerable patients with cancer could be further protected by vaccinating their caregivers and all care-home staff on priority.

Emerging variants

Mutant variants of the wild-type (Wuhan) SARS-CoV-2 virus have been documented in most geographies of the world, and are tracked by online databases such as https://www.gisaid.org/hcov19-variants/. Knowledge regarding these variants is rapidly evolving. Currently, the variants of concern include B.1.1.7 (alpha), B.1.351 (beta), P.1 (gamma), and B.1.617.2 (delta), which were first identified in the UK, South Africa, Brazil, and India, respectively. Such viral variants may differ with respect to transmissibility, lethality, and response to vaccines [46].

In a study of 2026 adults in South Africa, the ChAdOx1 nCoV-19 vaccine did not confer any significant protection against mild-to-moderate COVID-19 due to the B.1.351 variant [47]. A post hoc analysis found that efficacy against symptomatic COVID-19 of ChAdOx1 nCoV-19 was 70.4% for the B.1.1.7 variant and 81.5% for non-B.1.1.7 variants [48].

A population-scale study from Qatar showed that the effectiveness of the BNT162b2 vaccine was 89.5% (95% CI, 85.9–92.3) against the B.1.1.7 variant and 75.0% (95% CI, 70.5–78.9) against the B.1.351 variant [49].

There is rising concern that patients with an immunocompromised state, such as those with cancer, could develop long-lasting or persistent SARS-CoV-2 infection, which could accelerate viral evolution and emergence of variants [50]. Patients with cancer have been shown to carry significantly higher intra-host viral genetic diversity than their non-cancer counterparts [51]

The clinical impact of SARS-CoV-2 variants on patients with cancer is currently unknown.

Future considerations

Currently, most COVID-19 vaccines employ a two-dose schedule, a notable exception being Ad.26.COV2.S. which is given as a single dose. Some patients with cancer may have incomplete immune reconstitution following anticancer therapy, or may have an immunocompromised status as a result of their disease, and hence they may generate a suboptimal protective response following a two-dose schedule. Three-dose schedules of COVID-19 vaccines are currently in clinical trials (e.g., NCT04368728) in healthy volunteers, and similar trials are needed for patients with cancer as well.

The VOICE study (ClinicalTrials.gov identifier, NCT04715438, target sample size 873) aims to recruit patients with cancer being treated with chemotherapy, immunotherapy, or combination chemo-immunotherapy, and HCs, in order to assess side effects and the kinetics and strength of immune responses to COVID-19 vaccination. Results from this and similar studies from other countries will be valuable in designing future vaccination strategies for patients with cancer.

Several registries have been set up for collecting real-world COVID-19 data related to patients with cancer, and are generating valuable data and contributing to the scientific understanding of the ongoing pandemic [60].

Future late-phase COVID-19 vaccine trials should allow an adequate number of patients with cancer to participate as well [7].

References

  1. Osuchowski MF, Winkler MS, Skirecki T, et al. The COVID-19 puzzle: deciphering pathophysiology and phenotypes of a new disease entity. Lancet Respir Med. 2021. https://doi.org/10.1016/S2213-2600(21)00218-6.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Saini KS, de Las HB, de Castro J, et al. Effect of the COVID-19 pandemic on cancer treatment and research. Lancet Haematol. 2020;7(6):e432–5. https://doi.org/10.1016/S2352-3026(20)30123-X.

    Article  PubMed  PubMed Central  Google Scholar 

  3. Saini KS, de Las HB, Plummer R, et al. Reimagining global oncology clinical trials for the postpandemic era: a call to arms. JCO Glob Oncol. 2020;6:1357–62. https://doi.org/10.1200/GO.20.00346.

    Article  PubMed  Google Scholar 

  4. Meattini I, Franco P, Belgioia L, et al. Radiation therapy during the coronavirus disease 2019 (covid-19) pandemic in Italy: a view of the nation’s young oncologists. ESMO Open. 2019. https://doi.org/10.1136/esmoopen-2020-000779.

    Article  Google Scholar 

  5. Lambertini M, Toss A, Passaro A, et al. Cancer care during the spread of coronavirus disease (COVID-19) in Italy: young oncologists’ perspective. ESMO Open. 2019. https://doi.org/10.1136/esmoopen-2020-000759.

    Article  PubMed  PubMed Central  Google Scholar 

  6. de Las HB, Saini KS, Boyle F, et al. Cancer treatment and research during the COVID-19 pandemic: experience of the first 6 months. Oncol Ther. 2020;8(2):171–82. https://doi.org/10.1007/s40487-020-00124-2.

    Article  Google Scholar 

  7. Corti C, Crimini E, Tarantino P, et al. SARS-CoV-2 vaccines for cancer patients: a call to action. Eur J Cancer Oxf Engl. 1990;2021(148):316–27. https://doi.org/10.1016/j.ejca.2021.01.046.

    CAS  Article  Google Scholar 

  8. Saini KS, Lanza C, Romano M, et al. Repurposing anticancer drugs for COVID-19-induced inflammation, immune dysfunction, and coagulopathy. Br J Cancer. 2020;123(5):694–7. https://doi.org/10.1038/s41416-020-0948-x.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  9. Wang X, Sahu KK, Cerny J. Coagulopathy, endothelial dysfunction, thrombotic microangiopathy and complement activation: potential role of complement system inhibition in COVID-19. J Thromb Thrombolysis. 2021;51(3):657–62. https://doi.org/10.1007/s11239-020-02297-z.

    CAS  Article  PubMed  Google Scholar 

  10. Saini KS, Tagliamento M, Lambertini M, et al. Mortality in patients with cancer and coronavirus disease 2019: a systematic review and pooled analysis of 52 studies. Eur J Cancer Oxf Engl. 1990;2020(139):43–50. https://doi.org/10.1016/j.ejca.2020.08.011.

    CAS  Article  Google Scholar 

  11. Tagliamento M, Agostinetto E, Bruzzone M, et al. Mortality in adult patients with solid or hematological malignancies and SARS-CoV-2 infection with a specific focus on lung and breast malignancies: a systematic review and meta-analysis. Crit Rev Oncol Hematol. 2021. https://doi.org/10.1016/j.critrevonc.2021.103365.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Zhang H, Han H, He T, et al. Clinical characteristics and outcomes of COVID-19-infected cancer patients: a systematic review and meta-analysis. J Natl Cancer Inst. 2021;113(4):371–80. https://doi.org/10.1093/jnci/djaa168.

    CAS  Article  PubMed  Google Scholar 

  13. Sahu KK, Ailawadhi S, Malvik N, Cerny J. Challenges of cellular therapy during the COVID-19 pandemic. Adv Exp Med Biol. 2021;1318:657–72. https://doi.org/10.1007/978-3-030-63761-3_36.

    Article  PubMed  Google Scholar 

  14. Leclerc M, Maury S. A rationale to prioritise vaccination of HSCT patients against COVID-19. Lancet Haematol. 2021;8(3):e163–4. https://doi.org/10.1016/S2352-3026(21)00008-9.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Ribas A, Sengupta R, Locke T, et al. Priority COVID-19 vaccination for patients with cancer while vaccine supply is limited. Cancer Discov. 2021;11(2):233–6. https://doi.org/10.1158/2159-8290.CD-20-1817.

    CAS  Article  PubMed  Google Scholar 

  16. Poland GA, Ovsyannikova IG, Kennedy RB. SARS-CoV-2 immunity: review and applications to phase 3 vaccine candidates. Lancet Lond Engl. 2020;396(10262):1595–606. https://doi.org/10.1016/S0140-6736(20)32137-1.

    CAS  Article  Google Scholar 

  17. World Health Organization (2021). Draft landscape and tracker of COVID-19 candidate vaccines. https://www.who.int/publications/m/item/draft-landscape-of-covid-19-candidate-vaccines. Accessed 26 MAy 2021.

  18. Thompson MG, Burgess JL, Naleway AL, et al. Interim estimates of vaccine effectiveness of BNT162b2 and mRNA-1273 COVID-19 vaccines in preventing SARS-CoV-2 infection among health care personnel, first responders, and other essential and frontline workers - eight U.S. Locations, December 2020-March 2021. Morb Mortal Wkly Rep. 2021;70(13):495–500.

    CAS  Article  Google Scholar 

  19. Kyriakidis NC, López-Cortés A, González EV, Grimaldos AB, Prado EO. SARS-CoV-2 vaccines strategies: a comprehensive review of phase 3 candidates. NPJ Vacc. 2021;6(1):28. https://doi.org/10.1038/s41541-021-00292-w.

    CAS  Article  Google Scholar 

  20. Garassino MC, Vyas M, de Vries EGE, et al. The ESMO Call to Action on COVID-19 vaccinations and patients with cancer: vaccinate monitor educate. Ann Oncol Off J Eur Soc Med Oncol. 2021. https://doi.org/10.1016/j.annonc.2021.01.068.

    Article  Google Scholar 

  21. Hwang JK, Zhang T, Wang AZ, Li Z. COVID-19 vaccines for patients with cancer: benefits likely outweigh risks. J Hematol OncolJ Hematol Oncol. 2021;14(1):38. https://doi.org/10.1186/s13045-021-01046-w.

    CAS  Article  Google Scholar 

  22. Brodziak A, Sigorski D, Osmola M, et al. Attitudes of patients with cancer towards vaccinations-results of online survey with special focus on the vaccination against COVID-19. Vaccines. 2021;9(5):411. https://doi.org/10.3390/vaccines9050411.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  23. Yusuf A, Sarfati D, Booth CM, et al. Cancer and COVID-19 vaccines: a complex global picture. Lancet Oncol. 2021. https://doi.org/10.1016/S1470-2045(21)00244-8.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Tagliamento M, Spagnolo F, Poggio F, et al. Italian survey on managing immune checkpoint inhibitors in oncology during COVID-19 outbreak. Eur J Clin Invest. 2020;50(9):e13315. https://doi.org/10.1111/eci.13315.

    CAS  Article  PubMed  Google Scholar 

  25. Saini KS, Punie K, Twelves C, et al. Antibody-drug conjugates, immune-checkpoint inhibitors, and their combination in breast cancer therapeutics. Expert Opin Biol Therapy. 2021. https://doi.org/10.1080/14712598.2021.1936494.

    Article  Google Scholar 

  26. Keech C, Albert G, Cho I, et al. Phase 1–2 trial of a SARS-CoV-2 recombinant spike protein nanoparticle vaccine. N Engl J Med. 2020;383(24):2320–32. https://doi.org/10.1056/NEJMoa2026920.

    CAS  Article  PubMed  Google Scholar 

  27. Li J-X, Zhu F-C. Adjuvantation helps to optimise COVID-19 vaccine candidate. Lancet Infect Dis. 2021. https://doi.org/10.1016/S1473-3099(21)00094-3.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Waissengrin B, Agbarya A, Safadi E, Padova H, Wolf I. Short-term safety of the BNT162b2 mRNA COVID-19 vaccine in patients with cancer treated with immune checkpoint inhibitors. Lancet Oncol. 2021. https://doi.org/10.1016/S1470-2045(21)00155-8.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Monin L, Laing AG, Muñoz-Ruiz M, et al. Safety and immunogenicity of one versus two doses of the COVID-19 vaccine BNT162b2 for patients with cancer: interim analysis of a prospective observational study. Lancet Oncol. 2021. https://doi.org/10.1016/S1470-2045(21)00213-8.

    Article  PubMed  PubMed Central  Google Scholar 

  30. See I, Su JR, Lale A, et al. US case reports of cerebral venous sinus thrombosis with thrombocytopenia after Ad26COV2S vaccination , March 2 to April 21, 2021. JAMA. 2021. https://doi.org/10.1001/jama.2021.7517.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Nazy I, Sachs UJ, Arnold DM, et al. Recommendations for the clinical and laboratory diagnosis of VITT against COVID-19: communication from the ISTH SSC subcommittee on platelet immunology. J Thromb Haemost JTH. 2021. https://doi.org/10.1111/jth.15341.

    Article  PubMed  Google Scholar 

  32. Bussel JB, Connors JM, Cines DB, et al. Thrombosis with thrombocytopenia syndrome (also termed vaccine-induced thrombotic thrombocytopenia). https://www.hematology.org/covid-19/vaccine-induced-immune-thrombotic-thrombocytopenia. Accessed 26 May 2021.

  33. Cines DB, Bussel JB. SARS-CoV-2 vaccine-induced immune thrombotic thrombocytopenia. N Engl J Med. 2021. https://doi.org/10.1056/NEJMe2106315.

    Article  PubMed  PubMed Central  Google Scholar 

  34. Oldenburg J, Klamroth R, Langer F, et al. Diagnosis and management of vaccine-related thrombosis following AstraZeneca COVID-19 vaccination: guidance statement from the GTH. Hamostaseologie. 2021. https://doi.org/10.1055/a-1469-7481.

    Article  PubMed  Google Scholar 

  35. Schultz NH, Sørvoll IH, Michelsen AE, et al. Thrombosis and thrombocytopenia after ChAdOx1 nCoV-19 vaccination. N Engl J Med. 2021. https://doi.org/10.1056/NEJMoa2104882.

    Article  PubMed  PubMed Central  Google Scholar 

  36. Østergaard SD, Schmidt M, Horváth-Puhó E, Thomsen RW, Sørensen HT. Thromboembolism and the Oxford-AstraZeneca COVID-19 vaccine: side-effect or coincidence? Lancet Lond Engl. 2021. https://doi.org/10.1016/S0140-6736(21)00762-5.

    Article  Google Scholar 

  37. CDC Health Alert Network (2021) Cases of cerebral venous sinus thrombosis with thrombocytopenia after receipt of the Johnson and Johnson COVID-19 Vaccine. https://emergency.cdc.gov/han/2021/han00442.asp. Accessed 26 May 2021.

  38. Medicines and healthcare products regulatory agency, UK (2021). Coronavirus vaccine - weekly summary of yellow card reporting. https://www.gov.uk/government/publications/coronavirus-covid-19-vaccine-adverse-reactions/coronavirus-vaccine-summary-of-yellow-card-reporting. Accessed 26 May 2021.

  39. Pottegård A, Lund LC, Karlstad Ø, et al. Arterial events, venous thromboembolism, thrombocytopenia, and bleeding after vaccination with Oxford-AstraZeneca ChAdOx1-S in Denmark and Norway: population based cohort study. BMJ. 2021;373:n1114. https://doi.org/10.1136/bmj.n1114.

    Article  PubMed  Google Scholar 

  40. Medicines and Healthcare products Regulatory Agency (2021) Press Release: MHRA issues new advice, concluding a possible link between COVID-19 Vaccine AstraZeneca and extremely rare, unlikely to occur blood clots. https://www.gov.uk/government/news/mhra-issues-new-advice-concluding-a-possible-link-between-covid-19-vaccine-astrazeneca-and-extremely-rare-unlikely-to-occur-blood-clots. Accessed 26 May 2021.

  41. Aapro M, Lyman GH, Bokemeyer C, et al. Supportive care in patients with cancer during the COVID-19 pandemic. ESMO Open. 2021;6(1):100038. https://doi.org/10.1016/j.esmoop.2020.100038.

    CAS  Article  PubMed  Google Scholar 

  42. US Food and Drug Administration. FDA News Release (2021) FDA and CDC lift recommended pause on Johnson and Johnson (Janssen) COVID-19 vaccine use following thorough safety review. https://www.fda.gov/news-events/press-announcements/fda-and-cdc-lift-recommended-pause-johnson-johnson-janssen-covid-19-vaccine-use-following-thorough. Accessed 26 May 2021.

  43. Lee E-J, Cines DB, Gernsheimer T, et al. Thrombocytopenia following Pfizer and Moderna SARS-CoV-2 vaccination. Am J Hematol. 2021;96(5):534–7. https://doi.org/10.1002/ajh.26132.

    CAS  Article  PubMed  Google Scholar 

  44. Voysey M, Costa Clemens SA, Madhi SA, et al. Single-dose administration and the influence of the timing of the booster dose on immunogenicity and efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine: a pooled analysis of four randomised trials. Lancet Lond Engl. 2021;397(10277):881–91. https://doi.org/10.1016/S0140-6736(21)00432-3.

    CAS  Article  Google Scholar 

  45. Palich R, Veyri M, Marot S, et al. Weak immunogenicity after a single dose of SARS-CoV-2 mRNA vaccine in treated cancer patients. Ann Oncol Off J Eur Soc Med Oncol. 2021. https://doi.org/10.1016/j.annonc.2021.04.020.

    Article  Google Scholar 

  46. Neuzil KM. Interplay between emerging SARS-CoV-2 variants and pandemic control. N Engl J Med. 2021. https://doi.org/10.1056/NEJMe2103931.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Madhi SA, Baillie V, Cutland CL, et al. Efficacy of the ChAdOx1 nCoV-19 Covid-19 vaccine against the B.1.351 variant. N Engl J Med. 2021. https://doi.org/10.1056/NEJMoa2102214.

    Article  PubMed  PubMed Central  Google Scholar 

  48. Emary KRW, Golubchik T, Aley PK, et al. Efficacy of ChAdOx1 nCoV-19 (AZD1222) vaccine against SARS-CoV-2 variant of concern 202012/01 (B.1.1.7): an exploratory analysis of a randomised controlled trial. Lancet Lond Enl. 2021. https://doi.org/10.1016/S0140-6736(21)00628-0.

    Article  Google Scholar 

  49. Abu-Raddad LJ, Chemaitelly H, Butt AA, National Study Group for COVID-19 Vaccination. Effectiveness of the BNT162b2 Covid-19 Vaccine against the B117 and B1351 Variants. N Engl J Med. 2021. https://doi.org/10.1056/NEJMc2104974.

    Article  Google Scholar 

  50. Choi B, Choudhary MC, Regan J, et al. Persistence and evolution of SARS-CoV-2 in an immunocompromised host. N Engl J Med. 2020;383(23):2291–3. https://doi.org/10.1056/NEJMc2031364.

    Article  Google Scholar 

  51. Siqueira JD, Goes LR, Alves BM, et al. SARS-CoV-2 genomic analyses in cancer patients reveal elevated intrahost genetic diversity. Virus Evol. 2021;7(1):vea013. https://doi.org/10.1093/ve/veab013.

    Article  Google Scholar 

  52. Shaw RH, Stuart A, Greenland M, Liu X, Van-Tam JSN, Snape MD. Heterologous prime-boost COVID-19 vaccination: initial reactogenicity data. The Lancet. 2021. https://doi.org/10.1016/S0140-6736(21)01115-6.

    Article  PubMed  Google Scholar 

  53. Callaway E. Mix-and-match COVID vaccines trigger potent immune response. Nature. 2021;593(7860):491. https://doi.org/10.1038/d41586-021-01359-3.

    CAS  Article  PubMed  Google Scholar 

  54. Food and Drug Administration (2021) Conduct of clinical trials of medical products during the COVID-19 public health emergency. guidance for industry, investigators, and institutional review boards. https://www.fda.gov/media/136238/download. Accessed 26 May 2021.

  55. Desai A, Gainor JF, Hegde A, et al. COVID-19 vaccine guidance for patients with cancer participating in oncology clinical trials. Nat Rev Clin Oncol. 2021;15:1–7. https://doi.org/10.1038/s41571-021-00487-z.

    CAS  Article  Google Scholar 

  56. Korompoki E, Gavriatopoulou M, Kontoyiannis DP. COVID-19 vaccines in patients with cancer-a welcome addition, but there is need for optimization. JAMA Oncol. 2021. https://doi.org/10.1001/jamaoncol.2021.1218.

    Article  PubMed  Google Scholar 

  57. Tu W, Gierada DS, Joe BN. COVID-19 vaccination-related lymphadenopathy: what to be aware. Radiol Imaging Cancer. 2021;3(3):e210038. https://doi.org/10.1148/rycan.2021210038.

    Article  PubMed  PubMed Central  Google Scholar 

  58. Lehman CD, Lamb LR, D’Alessandro HA. Mitigating the impact of coronavirus disease (COVID-19) vaccinations on patients undergoing breast imaging examinations: a pragmatic approach. AJR Am J Roentgenol. 2021. https://doi.org/10.2214/AJR.21.25688.

    Article  PubMed  Google Scholar 

  59. US CDC (2021) Interim clinical considerations for use of COVID-19 vaccines currently authorized in the United States. https://www.cdc.gov/vaccines/covid-19/info-by-product/clinical-considerations.html#Coadministration. Accessed 26 May 2021.

  60. Lee AJX, Purshouse K. COVID-19 and cancer registries: learning from the first peak of the SARS-CoV-2 pandemic. Br J Cancer. 2021. https://doi.org/10.1038/s41416-021-01324-x.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Funding

No funding or sponsorship was received for this study or publication of this article.

Authorship

All named authors meet the International Committee of Medical Journal Editors (ICMJE) criteria for authorship for this article, take responsibility for the integrity of the work as a whole, and have given their approval for this version to be published.

Authors contributions

Kamal S. Saini conceptualized the manuscript; all authors provided significant inputs; Kamal S. Saini wrote the manuscript; all authors reviewed, edited, and approved the final manuscript.

Disclosures

Kamal S. Saini reports consulting fees from the European Commission outside the submitted work.

Diogo Martins-Branco declares honoraria and advisory board fees from Janssen, Pfizer, Merck Sharp & Dohme, Angelini, AstraZeneca, and Novartis, and meeting/travel grants from LEO Farmacêuticos, Merck Sharp & Dohme, Ipsen, Janssen, Roche, Laboratórios Vitória, and Novartis, outside the submitted work.

Marco Tagliamento declares travel, accommodations, expenses supported by Roche, Bristol-Myers Squibb, AstraZeneca, and Takeda, and activity as medical writer supported by Novartis and Amgen outside the submitted work.

Kevin Punie reports honoraria for advisory/consultancy roles for AstraZeneca, Eli Lilly, Gilead Sciences, Novartis, Pfizer, Pierre Fabre, Hoffmann/La Roche and Vifor Pharma (paid to institution, outside the submitted work); speaker fees for Eli Lilly, Medscape, MSD, Mundi Pharma, Novartis, Pfizer and Hoffmann/La Roche (paid to institution, outside the submitted work); research funding from Sanofi (paid to institution, outside the submitted work); and travel support from AstraZeneca, Novartis, Pfizer, PharmaMar, and Hoffmann/La Roche outside the submitted work.

Giuseppe Curigliano reports personal fees for consulting, advisory role, and speakers’ bureau from Roche/Genentech, Novartis, Pfizer, Lilly, Foundation Medicine, Samsung, and Daichii-Sankyo; honoraria from Ellipses Pharma; and fees for travel and accommodation from Roche/Genentech, and Pfizer outside the submitted work.

Evandro de Azambuja reports honoraria and advisory board fees from Roche/GNE, Novartis, Seattle Genetics, Eli Lilly, Zodiacs, Libbs, and Pierre Fabre; travel grants from Roche/GNE, GSK, and Novartis; and research grants to institution from Roche/GNE, AstraZeneca, GSK, Novartis, and Servier outside the submitted work.

Matteo Lambertini acted as consultant for Roche, Lilly, AstraZeneca, and Novartis, and received speaker honoraria from Roche, Takeda, Lilly, Novartis, Pfizer, and Sandoz outside the submitted work.

The other authors do not report any conflicts of interest.

Compliance with ethics guidelines

This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.

Consent to publish

All authors have reviewed the final version of this manuscript and provided their consent to publish.

Data availability

All data and references mentioned in this manuscript are from publicly available sources. Data sharing is not applicable to this article as no datasets were generated or analyzed during the current study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kamal S. Saini.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Saini, K.S., Martins-Branco, D., Tagliamento, M. et al. Emerging issues related to COVID-19 vaccination in patients with cancer. Oncol Ther 9, 255–265 (2021). https://doi.org/10.1007/s40487-021-00157-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s40487-021-00157-1

Keywords

  • Cancer
  • COVID-19
  • Efficacy
  • mRNA
  • SARS-CoV-2
  • Toxicity
  • Vaccine
  • Viral vector