key: cord-0852839-52xyuwum
authors: Jones, C.M.; Hawkins, M.; Mukherjee, S.; Radhakrishna, G.; Crosby, T.
title: Considerations for the Treatment of Oesophageal Cancer With Radiotherapy During the COVID-19 Pandemic
date: 2020-04-09
journal: Clin Oncol (R Coll Radiol)
DOI: 10.1016/j.clon.2020.04.001
sha: cd3ab6c63292c015217fee1eab1ca745dfe4d9dc
doc_id: 852839
cord_uid: 52xyuwum

nan

The coronavirus disease 2019 (COVID-19) pandemic is a public health emergency caused by widespread infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) [1] . For patients with cancer, COVID-19 presents a significant challenge. Many are immunosuppressed, both as a direct result of the malignant disease and as a consequence of anti-cancer treatment. As such, they may be more likely to contract SARS-CoV-2 [2] . Given that hospitals are thought to act as a reservoir from which this virus spreads, the risk of COVID-19 is further exacerbated by the requirement for patients with cancer to frequently attend hospital for follow-up visits, imaging and intensive treatment [2e4] . In a small study in Wuhan, China, the suspected source of the COVID-19 outbreak, patients with cancer seemed to be at a higher risk of SARS-CoV-2 infection than the wider community, and both recurrent hospital visits and hospital admission conferred greater risk still [2] . A cancer diagnosis and recent anticancer treatment have additionally been linked to greater COVID-19 severity [3, 4] .

The impact of healthcare service pressures on the care of patients with cancer is also a concern. In the UK, as in other countries, a surge in critically unwell patients with COVID-19 is expected to significantly diminish bed availability within high-dependency (HDU) and intensive care units (ICUs). Widespread disease transmissibility will also impact on the availability of frontline clinical staff. Together, these service pressures and the shift in the risk:benefit ratio caused by the widespread transmission of SARS-CoV-2 necessitates e at least in the short to medium term e re-consideration of treatment pathways for patients with cancer. This is of particular pertinence to oesophageal cancer, which is typically treated using an intensive multimodality approach that involves thoracic radiotherapy, and for which significant delays in treatment are precluded by disease biology and symptoms such as dysphagia.

In light of this we convened an expert group of UK clinicians with expertise in oesophageal cancer. Consensus was sought for evidence-based approaches to the management of oesophageal cancer that would maintain benefit, minimise risk to the patient, accommodate for service pressures and limit hospital attendance. Guiding principles relevant to radiotherapy provision are described here. As the pandemic progresses, guidance for acting on these will be updated at www.uppergicancer.com.

Advice for stratifying and prioritising surgery and systemic treatments has been published elsewhere, as has practical advice for radiotherapy departments and practitioners [5e7]. Wherever possible, hospital attendances should be reduced or avoided. This includes through the provision of telephone-based consultations and either delaying treatment or modifying it to reduce the number of days on which patients must attend for radiotherapy and to limit the chance of acute admission. Departments should also institute measures to limit the spread of infection.

There are to our knowledge no data at present to indicate whether thoracic radiotherapy increases the severity of the COVID-19 disease course. A pragmatic approach is for patients diagnosed with COVID-19 or experiencing symptoms consistent with it to avoid or delay thoracic radiotherapy, although this will need to be reviewed as further data emerge.

Standard treatment approaches for potentially curable oesophageal cancer typically comprise neoadjuvant chemotherapy or chemoradiotherapy (CRT) followed by either resection or definitive CRT (dCRT), with some patients receiving postoperative chemotherapy or CRT dependent on resection margins and performance status. Guidance for adapting this therapy is provided here based on treatment intention and is summarised in Table 1 .

Elective surgery carried out with the expectation of cure is categorised as surgical priority level 2 by the National Health Service. There is concern that the expected increase in HDU/ICU bed occupancy and the risk of postoperative SARS-CoV-2 infection will severely limit or preclude surgical intervention. It is important that consideration is given to the prospects of surgical treatment. For patients who have started or completed neoadjuvant therapy, surgical intervention should be expedited where possible. If there is uncertainty related to surgical capacity, we would suggest that dCRT with no neoadjuvant or induction component is the most appropriate option to provide an upfront definitive treatment approach while limiting infection risk. In the absence of robust head-to-head data, dCRT and neoadjuvant treatment followed by surgery are typically viewed as delivering equivalent outcomes for oesophageal squamous cell carcinoma [8] . The evidence for equivalent outcomes from dCRT is less robust for oesophageal adenocarcinoma but good outcomes were seen for this group in SCOPE1 [9, 10] .

Despite the theoretical advantages of hypofractionated regimens during the COVID-19 pandemic, there is to our knowledge no robust evidence to advocate for a hypofractionated dCRT approach. Careful patient selection for dCRT using standard 50 Gy/25 fractions fractionation with concurrent chemotherapy is therefore imperative and patients should be counselled regarding the risk:benefit ratio of treatment. Patients at a higher risk include those with comorbidities and who are more likely to require acute admission, such as those with high-grade dysphagia when starting treatment [11] . Risks may also be mitigated through the use of weekly carboplatinepaclitaxel in place of 3weekly cisplatinefluoropyrimidine-based chemotherapy, given the more favourable toxicity profile. In a recently presented phase III trial and in a multicentre retrospective analysis from the UK, weekly carboplatinepaclitaxel-based dCRT has shown 2-and 3-year overall survival of 50 and 40%, respectively [12, 13] . The regimen was well tolerated and resulted in 10% grade 3 or above haematological toxicity, compared with 28% for cisplatinefluoropyrimidine-based treatment in SCOPE1 [9, 12, 13] . We also suggest considering lowering the threshold for prophylactic enteral nutrition where there is capacity to place enteral feeding tubes, as this would potentially minimise the need for unplanned hospitalisation [14] . Follow-up of patients managed with dCRT should, if service pressures allow, include endoscopy and cross-sectional imaging at 8 weeks post-treatment, with a low threshold for surgery if indicated [15] . It is hoped that HDU and ICU access may be somewhat better in the timeframe for 5e6 months, where such surgery might be considered.

In patients for whom the risks of dCRT are considered too great, or in instances where there is limited chemotherapy provision, consider definitive hypofractionated radiotherapy for locally advanced disease. Tumours of up to 5 cm Table 1 A summary of recommendations for the radiotherapy-based management of patients with oesophageal cancer during the coronavirus disease 2019 (COVID-19) pandemic. The impact of radiotherapy on disease severity in patients with a diagnosis of COVID-19 is unknown and it may be appropriate to avoid radiotherapy in such patients

Definitive treatment Expedite planned surgical resection before the expected surge in higher-level care bed occupancy. Consider dCRT as the most appropriate curative option for both OSCC and OAC.

Patients who are at high risk for readmission, such as those with high-grade dysphagia, may not be appropriate for dCRT. Consider use of weekly carboplatinepaclitaxel in place of cisplatinefluoropyrimidine-based chemotherapy to limit toxicity. Where dCRT is unavailable or inappropriate, consider hypofractionated dRT of 50 Gy/16 fractions for tumours of up to 5 cm in length or 55 Gy/10 fractions for tumours of up to 10 cm in length. Consider a low threshold for prophylactic enteral nutrition if there is capacity to place feeding tubes.

If neoadjuvant treatment is considered appropriate, consider hypofractionated dCRT 40 Gy/15 fractions with weekly carboplatin epaclitaxel.

Use a single 8 Gy/1 fraction or 20 Gy/5 fractions for relief of dysphagia or disease control in the palliative setting.

CRT, chemoradiotherapy; dCRT, definitive chemoradiotherapy; dRT, definitive radiotherapy; OAC, oesophageal adenocarcinoma; OSCC, oesophageal squamous cell carcinoma.

in length may be treated with 50 Gy/16 fractions and tumours of up to 10 cm in length with 50e55 Gy/20 fractions. In a recent single-centre retrospective series, this regimen resulted in reasonable median overall survival of 26 months that compared with 29 months for a dCRT cohort from the same centre that had fewer comorbidities but more advanced disease [16] . Time-to-stent insertion was also similar and grade 3 or above toxicity with definitive radiotherapy was favourable at 16.4%.

Where neoadjuvant CRT (nCRT) with a view to surgery is still considered to be a viable option, we suggest use of hypofractionated CRT consisting of 40 Gy/15 fractions with weekly carboplatin and paclitaxel; as modified from the Walsh regimen [17] . There is evidence to suggest that the benefits conferred by nCRT for pathological complete response and overall survival are seen at doses of 39.6 Gy, but it is less certain that higher doses deliver additional benefit [18] . Beyond the pandemic peak when surgical capacity begins to be restored but where services remain stretched, nCRT may again represent an appropriate treatment option. Neoadjuvant chemotherapy may also be considered with prophylactic growth factor support, although in both instances (neoadjuvant chemotherapy or nCRT) multidisciplinary teams need to consider whether such patients are likely to proceed to surgical resection within a reasonable timeframe.

Where performance status allows, patients with oesophageal cancer are typically considered for adjuvant chemotherapy or CRT. Decisions relating to the provision of adjuvant therapy are likely to be nuanced and dependent both on performance status, postoperative resection margins, disease stage and the likely additional benefit of such intervention, especially if neoadjuvant therapy has been given. If treatment is favoured, a delay of 12 weeks should be considered to avoid starting treatment during the peak of COVID-19.

Indications for radiotherapy for oesophageal cancer in the non-curative setting include disease control, haemostasis and the relief of dysphagia. Given the anticipated pressure on palliative care teams and a reduction in endoscopy capacity for procedures such as endoluminal stenting, radiotherapy will probably be an important option for symptom relief [19] . The risks of standard fractionation schedules in this setting of 30 Gy/10 fractions or 40 Gy/15 fractions will probably outweigh any benefits during the COVID-19 pandemic, and add further pressure to radiotherapy departments. As such, we suggest use of single 8 Gy/1 fraction or 20 Gy/5 fractions treatment schedules.

There is little evidence that dose escalation above 20 Gy achieves additional symptomatic benefit [20] .

The COVID-19 pandemic represents an unprecedented challenge for healthcare services. The recommendations here should serve to support clinicians in as far as possible mitigating the impact of this crisis on patients with oesophageal cancer and those who care for them.

The authors declare the following financial interests/ personal relationships which may be considered as potential competing interests: TC is an Advisory Board member for Bristol Myers-Squibb and Astra Zeneca, and has received conference funding from Roche. SM receives research funds from Celgene that do not relate to the published work.

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