key: cord-0825760-bmwkiol9
authors: Barry, Aisling; Apisarnthanarax, Smith; O'Kane, Grainne M; Sapisochin, Gonzalo; Beecroft, Robert; Salem, Riad; Yoon, Sang Min; Lim, Young-Suk; Bridgewater, John; Davidson, Brian; Scorsetti, Marta; Solbiati, Luigi; Diehl, Adam; Schuffenegger, Pablo Munoz; Sham, Jonathan G; Cavallucci, David; Galvin, Zita; Dawson, Laura A; Hawkins, Maria A
title: Management of primary hepatic malignancies during the COVID-19 pandemic: recommendations for risk mitigation from a multidisciplinary perspective
date: 2020-06-06
journal: Lancet Gastroenterol Hepatol
DOI: 10.1016/s2468-1253(20)30182-5
sha: f72c6fbc65eed0c149730422378f0e49e84de693
doc_id: 825760
cord_uid: bmwkiol9

Around the world, recommendations for cancer treatment are being adapted in real time in response to the pandemic of COVID-19. We, as a multidisciplinary team, reviewed the standard management options, according to the Barcelona Clinic Liver Cancer classification system, for hepatocellular carcinoma. We propose treatment recommendations related to COVID-19 for the different stages of hepatocellular carcinoma (ie, 0, A, B, and C), specifically in relation to surgery, locoregional therapies, and systemic therapy. We suggest potential strategies to modify risk during the pandemic and aid multidisciplinary treatment decision making. We also review the multidisciplinary management of intrahepatic cholangiocarcinoma as a potentially curable and incurable diagnosis in the setting of COVID-19.

Since early 2020, global recommendations for cancer treatment have been adapted in real time in response to the COVID-19 pandemic. Cancer continues to result in a substantial number of deaths on average per day; 1 thus, maintaining cancer treatment while minimising the risk of exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) must be balanced carefully. Multidisciplinary cancer collaborations are occurring worldwide, [2] [3] [4] [5] [6] [7] [8] [9] with the shared goal of developing shortterm to medium-term treatment strategies to circumvent procedural, staffing, and resource shortages, while limiting the potential negative outcomes for patients 10 and staff. 11 Therefore, treatment strategies must align with region-specific resource limitations. Currently, many centres are at different timepoints along the pandemic curve (eg, rises, peaks or surges, declines, and second waves), with each timepoint presenting its own specific challenges. During the rise, departments prepare for the peak stage by reducing cancer care services and treatments and planning for potential staff shortages due to illness and redeployment. As the pandemic peaks and surges, priority might be given to cancer emergencies, such as spinal cord compression, and patients for whom cancer therapy is likely to be curative and therefore the benefits of treatment outweigh the possible risk of SARS-CoV-2 infection and the use of the health-care system's resources. As the decline of the pandemic begins for many centres, the return of routine diagnostics will result in an increase in new cancer diagnoses and the return of existing patients with cancer whose treatments might have been deferred. The decline phase might also be a challenging time for many departments who are continuing to manage ongoing staff shortages and the risk of SARS-CoV-2 infection, in addition to anticipating a potential second wave. As we navigate these difficult times, the point at which each centre is located along this curve and the resources available must be considered when deciding on the most appropriate treatments for patients with cancer.

However, considering the down stream implications of treatment choices is also an imperative. To guide our own departments and other cancer centres and clinics, multidisciplinary repre sentatives from academic hospitals in multiple countries at different stages of the COVID-19 pandemic, including some hospitals in the epicentres of the pandemic, have collaborated to synthesise these recommendations on the safe and effective management of patients with primary hepatic malignancies during the pandemic.

This Rapid Review was done as part of an international collaborative effort to combine and develop guidelines for the management of patients with liver cancer during the COVID-19 pandemic. This collaboration consisted of 19 multidisciplinary liver specialists from highvolume liver malignancy academic centres in seven countries (ie, Canada, the USA, the UK, Italy, Australia, South Korea, and Chile) and five continents (ie, North America, Europe, Australia, Asia, and South America) at different stages of the pandemic. A Delphi-type methodology was not feasible because of the timeliness of response that was needed. 12 Instead, institutional guidelines from the authors' centres were used to form the basis of the collaborative recommendations. We rapidly reviewed the published literature and comprehensively searched professional society guidelines, including recom mendations related to COVID-19 and patients with liver cancer (appendix), to ensure that the evidence and recommendations incorporated into the initial draft of the manuscript were up to date. [3] [4] [5] [6] 13, 14 Each specialist was invited to provide their opinions and recommendations regarding hepatocellular carcinoma, staged by the Barcelona Clinic Liver Cancer (BCLC) 15 classification system as either 0, A, B, or C, and intrahepatic cholangiocarcinoma, whether potentially curable or incurable. Once all opinions were collected, specialists were invited to provide individual feedback at

The management of primary intrahepatic malignancies, such as hepatocellular carcinoma and intrahepatic cholangiocarcinoma, requires a multidisciplinary approach involving hepatology, surgical oncology, transplant surgery, medical oncology, diagnostic and interventional radiology, and radiation oncology. Worldwide, primary hepatic malignancies are the fourth leading cause of deaths from cancer. 16 Tumour burden (eg, size, location, number of lesions, and vascular invasion) and patient factors (eg, age, underlying liver disease, liver function, and portal hypertension) are taken into consideration when clinicians decide on appropriate treatment pathways for primary hepatic malignancies.

Each discipline involved in this treatment pathway is uniquely and adversely affected by the COVID-19 pandemic. In addition to the effect on cancer services, including access to the operating room, chemotherapy day care, radiation therapy, diagnostic imaging, staffing, and shortages of personal protective equipment, patients with cancer are undergoing rigorous, individual risk-benefit assessments of their treatment options with the scarce and rapidly changing data available on the effect of COVID-19. Despite the paucity of evidencebased data, it has become routine to discuss with patients the risk of infection with SARS-CoV-2 17 because the combination of cancer diagnoses and comorbidities (eg, underlying liver disease, diabetes, 18 cardiovascular disease, and immunosuppressive states) might result in a possible increase in the morbidity and mortality related to COVID-19. 10 Liver disease is commonly associated with comorbidities; therefore, these patients are particularly susceptible. 19 Published data have shown that patients with comorbidities, such as diabetes, a high body-mass index (eg, >30 kg/m²), and malignancies, are at an increased risk for admission to intensive care units, the need for mechanical ventilatory support, and death if infected with SARS-CoV-2. [20] [21] [22] Notably, chronic viral hepatitis has not been shown to be a particular risk factor for negative outcomes after SARS-CoV-2 infection; 23 however, patients with nonalcoholic fatty liver disease might have hypertension, diabetes, and obesity, and are probably at an increased risk of negative outcomes. 5 Recipients of solid organ transplants might be at an increased risk of developing severe SARS-CoV-2 infections, 24 or secondary bacterial coinfections, or both, and might see higher rates of complications and mortality due to COVID-19 compared with immunocompetent patients. 25, 26 How ever, transplant recipients do not seem to require a reduction in immunosuppression to protect against complications from SARS-CoV-2 infection. 5 Many of the treatment options available for intrahepatic malignancies involve invasive procedures.

Screening guidelines for COVID-19 among the institutions involved in this Rapid Review vary; however, all patients with concerning symptoms and risk factors for COVID-19 are being screened. Additionally, all patients have a naso pharyngeal swab tested for SARS-CoV-2 24-72 h before planned surgery. Surgeons in some institutions are only operating on patients who are negative for SARS-CoV-2, and when patients are positive for SARS-CoV-2, after delays of a minimum of 7-14 days, they require at least one negative swab for SARS-CoV-2 before surgery. In many centres, asymptomatic patients undergoing interventional radio logy procedures will have SARS-CoV-2 testing done, if they require general anaesthesia, or even if they require conscious sedation, before having locoregional therapies to mitigate the risk of exposure to staff. In most chemotherapy and radiotherapy depart ments, all patients are screened and swabbed before treatment. For patients who test positive for SARS-CoV-2, continuation or initiation of chemo therapy or radiotherapy should be considered if required for the urgent control of the cancer, or, when possible, deferred until the patient has had at least two tests negative for SARS-CoV-2. 27 Regardless of the variability in testing for SARS-CoV-2, all institutions had individual recommendations. As the COVID-19 pandemic continues to evolve, we recom mend that all centres routinely review their own policies on the basis of the rapidly changing data on SARS-CoV-2 infection and the availability of personal protective equipment.

For many patients, the COVID-19 pandemic has also affected the availability of clinical trials. Patients should continue to be reassessed and considered for trials when trials are available; modifications to clinical trial assessments and follow-up procedures might be required to allow for physical distancing when possible (eg, telemedicine follow-up visits).

For patients with hepatocellular carcinoma, we have made our recommendations on the basis of the commonly used BCLC classification system (table 1, figure) . 15 Surgical intervention (ie, resection and transplantation) for hepato cellular carcinoma confined to the liver is associated with the best outcomes, is the most probable chance for a cure, and, in general, is the treatment of choice for well selected patients. [28] [29] [30] [31] Liver transplants and hepatobiliary surgical programmes require substantial resources to provide presurgical assessments and care, to do the surgeries, and to provide care after surgery, including the supply of personal protective equipment. During the COVID-19 pandemic, these essential cancer care services have been substantially affected, with reduced (or suspended)

transplant activity at most institutions and scarce operating room resources for liver-related surgeries. These reductions are mainly to facilitate staff redeployment to areas of more acute need, such as intensive care units and so-called COVID wards, and to ensure the increased access and availability of much needed intensive care beds. We should, however, continue to advocate for surgery in selected patients who are most likely to be cured, when resources and personnel are available, and when aligned with the overall priorities of the cancer centre. This recommendation is particularly relevant in the setting of smaller, unifocal disease that is amenable to straightforward resection with the anticipation that intensive care units will hardly be used. The surgeon should select patients for whom they have no preoperative expectation of prolonged inpatient hospitalisation, require ment of blood trans fusion, or prolonged admission to intensive care units, because ventilators and blood products are already in short supply in many areas. 32 For centres with experience of minimally invasive hepa tectomy, the use of laparoscopic or robotic approaches to achieve these goals can be considered, 33 but must be balanced against the theoretical aerosol dissemination of SARS-CoV-2 to staff. Preop eratively screening patients for SARS-CoV-2 and universal personal protective equipment might mitigate this risk. Postoperative follow-up should use telemedicine options as allowable by local regulatory bodies. As resources become more scarce, surgery might not be an immediate option for many patients with primary hepatic malig nancies in many regions during the COVID-19 pandemic. Regardless, we would encourage patients to be referred to tertiary liver cancer centres to allow a process of treatment optimisation based on expert multidisciplinary rounds, an awareness of the best evidence-based care available during the COVID-19 pandemic, and the ability to provide patient consultations via telehealth.

For patients whose cancers are resectable but resection is not available, alternative local therapies, such as thermal ablation (ie, radiofrequency ablation and microwave ablation), stereotactic body radiotherapy, or proton beam therapy, can be used instead as upfront, definitive, or neoadjuvant therapies to bridge patients while they wait for surgery, reserving resection for the time of progression or after the pandemic. For patients on the transplant list, the aforementioned local therapies, together with regional therapies, such as transarterial chemoembo lisation, transarterial embolisation, or transarterial radio embolisation, can be more frequently used to bridge patients, attempting to ensure disease control while waiting times become further delayed. 34 For patients who received transarterial chemoembolisation, radiofrequency ablation, or stereotactic body radiotherapy in the bridging setting, Sapisochin and colleagues 35 described no difference in waiting list drop-out rates, postoperative complications, or 5-year overall survival from the time of listing, between the bridging methods used. Patients who would have had their cancers resected or been considered for a liver transplant before the COVID-19 pandemic, but who are treated with alternative local therapies, systemic therapies, or both during the pandemic, should undergo restaging and be considered once again for surgical resection or transplantation when operating facilities are re-established. Alternatively, further local and regional therapies can be reconsidered at the time of follow-up.

In patients with solitary or a few, small, accessible tumour masses, the use of locally ablative therapies, such as radiofrequency ablation, microwave ablation, 36, 37 and yittrium-90 in the form of radiation segmentectomy, stereotactic body radiotherapy, or proton beam therapy, will depend on the centre's local expertise and the availability of particular technologies. When If a liver transplant or surgical resection is unavailable, consider bridging with locoregional therapies (eg, radiofrequency ablation, microwave ablation, stereotactic body radiotherapy, proton beam therapy, TACE, or TARE); if surgical resection is unavailable, consider surveillance †; consider locoregional ablation with radiofrequency ablation, microwave ablation, stereotactic body radiotherapy, proton beam therapy, TACE, or TARE (by use of a same-day model that does not use technetium-99-labelled macroaggregated albumin), and surveillance † Recommendations are presented in the order that they should be considered. BCLC=Barcelona Clinic Liver Cancer. TACE=transarterial chemoembolisation. TAE=transarterial embolisation. TARE=transarterial radioembolisation. *These recommendations are to be considered when standard therapies are not available. †Surveillance involves blood tests every 1-3 months (eg, for α-fetoprotein in secreting tumours) and diagnostic imaging every 3 months. [38] [39] [40] [41] In many centres, procedures, such as thermal ablation and transarterial embolisation, require specialisation in anaesthetics, and the need for anaesthesia introduces a greater likelihood of patients undergoing aerosol generating procedures (as opposed to those that generate respiratory droplets). This likelihood places patients and health-care workers at greater risk of exposure to SARS-CoV-2. In centres that do these procedures with consciously sedated patients, an aerosol generating procedure is avoided, which is valuable in reducing the possible exposure of health-care workers to SARS-CoV-2. Many centres screen for COVID-19 before the procedure to detect potentially infectious asymptomatic carriers of SARS-CoV-2. 42 Still, other local methods, such as stereotactic body radiotherapy and proton beam therapy, have their own disadvantages. Radiotherapy treatments generally require patients to attend multiple outpatient visits, potentially increasing the risk of SARS-CoV-2 exposure. Reducing the number of radiotherapy fractions delivered and the use of breathing control devices, 43 and the use of non-invasive tumour motion techniques (eg, avoiding insertion on fiducial markers) should strongly be considered.

In a resource-limited setting with no access to locoregional therapies and surgery, the use of (preferably outpatient) oral systemic therapies as a bridge to more definitive therapy could be considered if the pace of disease progression in a surveillance strategy would result in a tumour no longer amenable to locoregional therapies at the time these therapies became available. There are no strong data to support this recommendation. A small case series reported the ability of sorafenib to downstage advanced hepato cellular carcinoma to a resectable state, but typically, sorafenib yields stable disease at best. 44 However, if stable disease would be adequate, first-line, oral tyrosine kinase inhibitors, such as sorafenib or lenvatinib, could be used. At the American Society of Clinical Oncology's annual meeting in 2019, early results from a phase 2 trial of perioperative checkpoint inhibitor therapy with nivolumab monotherapy or nivolumab-ipilimumab combination therapy for resectable hepato cellular carcinoma showed that 6 weeks of checkpoint inhibitor therapy before resection was able to produce a pathological complete response in three of the eight patients treated thus far. 45 However, this is not standard care and the combination of nivolumab and ipilimumab has been associated with high requirements for corticosteroids; thus, this combination is not recom mended as a treatment of choice when alternative therapies are available. 46 In the COVID-19 era, oral systemic therapies are preferable to those requiring infusion or day care because oral therapies are well suited for telemedicine, allowing virtual outpatient assessments and fewer visits to the hospital or clinic. Presently, shortages in chemotherapeutic and targeted agents because of import and travel restrictions, and increased patient referrals because of shifting treatment frameworks, have placed undue pressure on medical oncologists. Additionally, there are increased pressures to consider alternatives to standard-of-care systemic therapy during the COVID-19 pandemic because factors such as drug-induced immuno suppression and in-hospital visits might potentially increase the risk of COVID-19 infection. We suggest, when systemic therapy is required, using oral and out-of-hospital therapies while leveraging telemedicine resources to assess toxicity at the discretion of the medical oncologist.

After doing a multidisciplinary review of patients who are candidates for definitive surgery, and depending on the availability of locoregional therapies, deferred treatment and surveillance is a further potential option during the COVID-19 pandemic. Access to, and the availability of, diagnostic imaging and pathology at this time might substantially affect standard surveillance guidelines. 47 For patients who could potentially be cured and who are not treated with upfront local therapy, follow-up blood tests (eg, α-fetoprotein in secreting disease, liver function tests, and platelet count) every 1-3 months and imaging (eg, ultrasound, triphasic liver CT, or triphasic liver MRI) every 3 months should be considered for those with very early or early stage disease (ie, BCLC 0 or BCLC A). Frequent surveillance imaging and blood tests might identify patients in whom there is tumour progression (and who therefore require earlier treatment) and those in which the tumour burden is stable and can be safely watched. 48 Patients whose treatments are deferred must be carefully monitored to ensure that their treatment options are subsequently reviewed. For patients who are treated upfront, the frequency of follow-up can be reduced to every 4-6 months to reduce resource use. However, the frequency of these tests and procedures will probably vary according to the phase of the pandemic that a centre is experiencing (eg, the tests and procedures should not overlap with the estimated peak or surge of the pandemic whenever possible) and should be related to the suitability and availability of salvage or next-line therapies. Follow-up visits should be led by a single discipline and done with the use of telemedicine whenever feasible to reduce travel and in-person hospital visits. 49 We also recommend the regular continuation of virtual tumour boards and multi disciplinary team meetings to help review patient care, especially for the review of patients who have had their definitive therapy deferred. 50 Because a low risk of radiation pneumonitis has been reported, macro aggregated albumin scans to estimate lung shunt fractions and lung dose are not required. 50 The availability of these procedures might also depend on the stage of the pandemic each centre is at, and if the centres do such procedures as inpatient or outpatient visits. Therefore, if certain interventional resources are diminished or unavailable, the use of radiotherapy in tumours equal to and less than 10 cm in diameter (ie, those most likely to be controlled) 51 could be considered, so long as liver dose-volume constraints are met.

Identifying patients with intermediate hepatocellular carcinoma refractory to locoregional therapies but with preserved liver function has been increasingly recognised as being important and allows these patients access to systemic therapies. 52 Furthermore, in patients who are unsuitable for locoregional therapies, systemic treatment is a first-line option. The REFLECT study 53 showed that lenvatinib resulted in higher responses rates than sorafenib; therefore, in a resource-limited setting, lenvatinib could be considered a bridge to locoregional therapies, such as transarterial chemoembolisation or transarterial radioembolisation, if these therapies are not immediately available. In these circumstances, virtual appointments for monitoring tolerance are feasible and could be spaced to one appointment every 4 weeks, depending on tolerance.

Oral therapy with tyrosine kinase inhibitors is often complicated by side-effects, the management of which might require more contact with health-care staff than would be desired during the COVID-19 pandemic. To limit the risk of side-effects from oral tyrosine kinase inhibitors while bridging to locoregional therapies, reducing the dose of the inhibitor can be considered. 54 Consider testing for SARS-CoV-2 24-48 h before the radiotherapy simulation is done; if the patient is not urgent and tests positive for SARS-CoV-2, delay the procedure for 7-14 days until the patient has at least one test negative for SARS-CoV-2; in cases of pending or positive SARS-CoV-2 testing, standard personal protective equipment and respiratory protocols should be instituted DEB=drug-eluting beads. SARS-CoV-2=severe acute respiratory syndrome coronavirus 2. TACE=transarterial chemoembolidation. TAE=transarterial embolisation. TARE=transarterial radioembolisation. 

decompensation. Radiotherapy has also been shown to lead to the recanalisation of hepatocellular carcinomas with macrovascular invasion, but this recanalisation can take months. 56 Despite excellent cancer control with local therapies, most patients with macro vascular invasion will ultimately develop intrahepatic progression. Macrovascular invasion is associated with diffuse occult vascular invasion and a high risk of diffuse hepatocellular carcinoma that will ultimately progress when only local therapy is used.

The combination of atezolizumab and bevacizumab 19 is now recognised as the preferred first-line treatment option for advanced hepatocellular carcinoma over sorafenib; however, during the COVID-19 pandemic, oral tyrosine kinase inhibitors are the preferred therapeutic strategy. 53 As previously emphasised, these strategies minimise hospital exposure and the use of infusion clinics, especially with the use of telemedicine and, for patients with a poor performance status, substantial comorbidities, or both, upfront dose reductions. Furthermore, the use of atezolizumab-bevacizumab would require patients to have upper endoscopies to assess varices, given the risk of bleeding association with the drug combination shown by the IMbrave150 trial. 19 However, upper endoscopies are considered to be highrisk, aerosol generating procedures and have been restricted during the COVID-19 pandemic, requiring full personal protective equipment in some countries. 57 The use of immune checkpoint inhibitors comes with the risk of immune-related adverse events, most notably pneumonitis, which might present a diagnostic challenge in communities with a high prevalence of SARS-CoV-2 infection. Moreover, there is theoretical concern that immune-mediated pneumonitis and lung injury induced by SARS-CoV-2 could have synergistic lung toxicity. Whether immune checkpoint inhibitors, through their mechanism of action, amplify the immune hyperactivation and cytokine storm characteristic of severe COVID-19 disease is unknown. 58 For these reasons, choosing an oral tyrosine kinase inhibitor rather than an immune checkpoint inhibitor in the first-line setting might be prudent. In the second-line setting, after disease pro gression on sorafenib or lenvatinib, there are several potential considerations. For those patients who tolerated their first-line tyrosine kinase inhibitor and who have Child-Pugh class A disease, the oral tyrosine kinase inhibitors regorafenib and cabozantinib are a treatment option. For those patients intolerant to their first-line tyrosine kinase inhibitor and who have an α-fetoprotein concentration of equal to or more than 400 ng/mL, ramucirumab has an excellent toxicity profile, but requires intravenous administration every 2 weeks and so uses more resources. El Kouheiry and colleagues 46 showed the efficacy of administering 1 mg/kg nivolumab and 3mg/kg ipilimumab every 3 weeks for four doses, followed by nivolumab (240 mg every 2 weeks or 480 mg every 4 weeks), in patients who had progressed on sorafenib. Although this regimen has been granted approval by the US Food and Drug Administration, 25 (51%) of 49 patients required systemic corticosteroids for adverse events related to treatment, and this regimen would therefore not be recommended if there is a high risk of COVID-19 exposure. Best supportive care or palliation are alternative options, especially for patients at high risk of having drug-related toxic effects, including patients with Child-Pugh B, or worse, liver function (table 1) .

Combined modality therapies, such as external beam radiotherapy and transarterial chemoembolisation, or sorafenib and transarterial radioembolisation, have been studied in patients with hepatocellular carcinoma and macrovascular invasion with some success. 59, 60 Other combinations are being investigated in randomised trials, including sorafenib with or without stereotactic body radiotherapy (NCT01730937). However, combined modality treatment might not be practical during the COVID-19 pandemic, and systemic therapy alone is generally preferred. Although not standard of care, in selected patients who are not good candidates for systemic therapy or who are refractory to systemic therapy, radiotherapy or trans arterial radio embolisation alone can be used, deferring systemic therapy until the time of progression. 61

In patients diagnosed with intrahepatic cholangiocarcinoma, resection is standard of care when possible, and neoadjuvant systemic therapy has been used to reduce tumour size to make the cancer resectable (table 3) . 62 When resource availability permits, surgery should be considered in the setting of small, easily resectable lesions with minimal anticipated postoperative morbidity and resource use. However, given the decreased access to operating theatres seen during the COVID-19 pandemic, alternative strategies might be necessary. For patients requiring downstaging for resectability, neoadjuvant systemic therapy can be used for extended periods until resources become available. For patients who do not require downstaging before definitive therapy, but for whom surgery is not an option because of scarce resources, we would favour the use of other available locoregional therapies rather than neoadjuvant chemotherapy.

As an alternative to resection for small, unresectable intrahepatic cholangiocarcinoma, radiofrequency ablation or microwave ablation can be considered; retrospective cohort studies have suggested that ablation provides good local tumour control in patients with lesions less than or Rapid Review equal to 5 cm in diameter that are located away from segmental bile ducts, the liver surface, and major vessels. [63] [64] [65] Stereotactic body radiotherapy and proton beam therapy can be considered for peripheral lesions and hypofractionated radiotherapy (ie, with 15 fractions) can be considered for more centrally located disease. For larger, localised intrahepatic cholangio carcinoma, neoadjuvant chemo therapy, radiotherapy, or transarterial radio embo lisation 66 can be considered when surgery is not possible. Tao and colleagues 67 reported long-term survival rates with definitive radiotherapy in localised, inoperable intrahepatic cholangiocarcinoma (median tumour size 7·9 cm [range 2·2-17·0]) that compare favourably with resection. Close surveillance is also an option for such patients upon multidisciplinary review and frequent surveillance is particularly needed if a plan is made to treat only if there is evidence of disease progression. In settings where surgery and locoregional therapies are unavailable, bridging chemotherapy is a reasonable option until resources are renewed. The most commonly used neoadjuvant regimens include intra venous gemcitabinebased chemotherapy (typically gemcitabine-cisplatin) and are not ideal to administer during the COVID-19 pandemic because of the added risks of immunosuppression and exposure to health-care settings (eg, multiple visits to infusion centres and to clinics or hospitals to manage toxic effects). Unfortu nately, where surgery and locoregional therapies are unavailable, there is not enough evidence to recommend the use of any oral chemotherapies. In the adjuvant setting, oral capecitabine, as reported by the BILCAP trial, 68 has shown an overall survival advantage compared with resection alone and we would recommend that adjuvant capecitabine continues to be instituted for all patients that undergo resection for intrahepatic cholangiocarcinoma. In the BILCAP trial, 68 adjuvant capecitabine was either started within 12 weeks after surgery or within 16 weeks after surgery. Therefore, in times of scarce resources or elevated COVID-19 prevalence, it might be reasonable to postpone adjuvant chemotherapy for up to 16 weeks after surgery to minimise the patient's exposure to health-care settings. For patients with margin-positive disease after resection, we typically recommend the addition of chemoradiation in the course of adjuvant therapy; however, chemo radiation can be done 5-6 months after adjuvant capecitabine monotherapy, thereby delaying the intensive exposure to health-care settings and the use of resources needed for radiotherapy.

A regimen of cisplatin-gemcitabine is the current standard-of-care for palliative chemotherapy for intrahepatic cholangiocarcinoma. In the midst of serious resource constraints and a high prevalence of COVID-19 in the community, the cisplatin-gemcitabine regimen could be modified from dosing on day 1 and day 8 of a 21 day cycle to dosing on day 1 and day 14 of a 28 day cycle. 69 This modification could reduce the number of visits to infusion centres, the immunosuppressive effects of the chemotherapy, and the development of cytopenias when blood transfusions are in short supply. There is less justification for the use of second-line chemo therapies when the benefit is more modest. 70 For specific patient cohorts selected on a molecular basis, oral targeted therapies are both effective and non-immuno suppressive and can be considered. 71 Ghassan K Abou-Alfa and colleagues 7 2 published a phase 3 randomised, controlled study of ivosidenib versus placebo in IDH1-mutant chemotherapy-refractory cholangiocarcinoma. The study showed a significant improvement in progression-free survival in the ivosidenib group compared with placebo (median 2·7 months [95% CI 1·6-4·2] vs 1·4 months [1·4-1·6]; hazard ratio 0·37 [95% CI 0·25-0·54]; onesided p<0·0001). 72 During this time of drug shortages and the potential for SARS-CoV-2 transmission to patients, consideration can also be given to surveillance and best supportive care or palliative, single-fraction radiotherapy for symptomatic disease, if needed. 73 For patients with intrahepatic cholangiocarcinoma who have or are at high risk of biliary obstruction requiring decompression, the method of biliary stenting should be individualised on the basis of tumour and patient factors. Both endoscopically assisted procedures and percutaneous biliary drainage are possible, but additional risk factors, such as the use of aerosol generating procedures, should be considered. When possible, in patients who are not (2) local ablative therapies (eg, stereotactic body radiotherapy, hypofractionated radiotherapy, radiofrequency ablation, or microwave ablation); (3) TARE (by use of a same-day model that does not use technetium-99-labelled macroaggregated albumin) with deferred resection; (4) surveillance † Incurable, metastatic, or both First, consider systemic therapy; but, for localised, non-metastatic disease, a combination of systemic therapy and radiotherapy, or TARE, can be used Consider (1) systemic therapy; (2) surveillance †; (3) best supportive care; (4) palliative radiotherapy (with a single fraction) for symptomatic liver disease or metastatic disease; and (5) targeted therapies for selected subgroups Rapid Review candidates for surgical resection, metal stents would be preferable to plastic stents to avoid the need for potential restenting in the future. Given the challenges in doing endoscopic procedures, for patients positive for SARS-CoV-2 who require stenting, a percutaneous transhepatic drain can be placed while the patient is consciously sedated. The position along the COVID-19 pandemic curve where each institution lies will influence the timing of when biliary stents are replaced.

COVID-19 is directly affecting all multidisciplinary aspects of cancer care in institutions at all stages of the pandemic curve and could potentially negatively affect patients with hepatocellular carcinoma or intrahepatic cholangiocarcinoma quite substantially. During these challenging times, clinicians must continue to work together, advocate for our patients with liver cancer, be flexible in considering alternative interventions that carry less of a risk to patients and health-care workers, and use telemedicine and virtual tumour board resources when needed. These recommendations are based on the most up-to-date available evidence, aim to provide guidance for centres across the world in the management of intrahepatic malignancies during the COVID-19 pandemic in the short-term and medium-term, and should be used flexibly according to the dynamic state of COVID-19 in each centre.

AB, LAD, and MAH drafted the outline and planned this Rapid Review. AB, SA, LAD, and MAH contributed to the initial drafting of the manuscript. All authors who contributed opinions based on their individual expertise and the expertise and policies of their centres critically reviewed the manuscript. AB, SA, LAD, MAH, and PMS drafted the figures and the tables. All authors agreed to submit the final version of the manuscript.

RS is a consultant for Boston Scientific, Cook, Sirtex, Eisai, Genentech, and Becton Dickinson. PMS is on the Advanced Radiotherapy Committee for the International Association for the Study of Lung Cancer. LAD has a licensing agreement with Raysearch for image registration software in a system for radiation treatment planning. GMK is a consultant for Eisai. GS declares research funding from Roche and Bayer, outside the submitted work. AD declares funding from the

We searched MEDLINE and PubMed using the search terms "COVID-19, coronavirus, novel coronavirus, SARS-CoV-2", "cancer, tumour, malignancy", and "liver, hepatocellular carcinoma, intrahepatic cholangiocarcinoma, intrahepatic*, cholangio*" to identify articles for this Rapid Review published between Dec 1, 2019, and April 28, 2020. We also identified publications through searches of our own files, providing additional references on the basis of specialist interests. We reviewed only articles published in English. We selected up-to-date and evolving management guidelines related to the liver, original research articles, letters, and reviews on the basis of their clinical relevance to each section of this Rapid Review.

Clinical Research Division at Fred Hutchinson Cancer Research Center, outside the submitted work. MAH and JB declare funding from the NIHR Biomedical Research Centre at University College London Hospitals National Health Service Foundation Trust, outside the submitted work. All other authors declare no competing interests.

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Radiotherapy as a bridge to liver transplantation for hepatocellular carcinoma

Stereotactic body radiotherapy vs. TACE or RFA as a bridge to transplant in patients with hepatocellular carcinoma. An intention-to-treat analysis

Radiofrequency ablation of hepatocellular carcinoma as first-line treatment: long-term results and prognostic factors in 162 patients with cirrhosis

Phase 2 study of combined sorafenib and radiation therapy in patients with advanced hepatocellular carcinoma

Stereotactic body radiation therapy as an alternative treatment for small hepatocellular carcinoma

Consensus report from the Miami Liver Proton Therapy conference

Stereotactic body radiation therapy vs. radiofrequency ablation in Asian patients with hepatocellular carcinoma

Outcomes after stereotactic body radiotherapy or radiofrequency ablation for hepatocellular carcinoma

Presumed asymptomatic carrier transmission of COVID-19

Concerns for activated breathing control (ABC) with breast cancer in the era of COVID-19: maximizing infection control while minimizing heart dose

Liver resection after downstaging hepatocellular carcinoma with sorafenib

Randomized, open-label, perioperative phase II study evaluating nivolumab alone versus nivolumab plus ipilimumab in patients with resectable HCC

Safety profile of nivolumab (NIVO) plus ipilimumab (IPI) combination therapy in patients with advanced hepatocellular carcinoma (HCC) in the CheckMate 40 study

Hepatocellular carcinoma surveillance: an evidencebased approach

Hepatocellular carcinoma demonstrates heterogeneous growth patterns in a multi-center cohort of patients with cirrhosis

President Trump expands telehealth benefits for medicare beneficiaries during COVID-19 outbreak

Streamlining radioembolization in UNOS T1/T2 hepatocellular carcinoma by eliminating the lung shunt study

High-dose stereotactic body radiotherapy correlates increased local control and overall survival in patients with inoperable hepatocellular carcinoma

Deterioration of liver function after transarterial chemoembolization (TACE) in hepatocellular carcinoma (HCC): an exploratory analysis of OPTIMIS-an international observational study assessing the use of sorafenib after TACE

Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial

Starting dose of sorafenib for the treatment of hepatocellular carcinoma: a retrospective, multiinstitutional study

Survival benefit of liver resection for hepatocellular carcinoma associated with portal vein invasion

Treatment of portal vein tumor thrombosis of hepatoma patients with either stereotactic radiotherapy or three-dimensional conformal radiotherapy

British Society of Gastroenterology. Endoscopy activity and COVID-19: BSG and JAG guidance

Controversies about COVID-19 and anticancer treatment with immune checkpoint inhibitors

Efficacy and safety of transarterial chemoembolization plus external beam radiotherapy vs sorafenib in hepatocellular carcinoma with macroscopic vascular invasion: a randomized clinical trial

Efficacy and safety of selective internal radiotherapy with yttrium-90 resin microspheres compared with sorafenib in locally advanced and inoperable hepatocellular carcinoma (SARAH): an open-label randomised controlled phase 3 trial

Stereotactic body radiation therapy for hepatocellular carcinoma with macrovascular invasion

Neoadjuvant chemotherapy for initially unresectable intrahepatic cholangiocarcinoma

Management of unresectable intrahepatic cholangiocarcinoma: how do we decide among the various liver-directed treatments?

Radiofrequency ablation for the treatment of primary intrahepatic cholangiocarcinoma

Radiofrequency ablation in the treatment of unresectable intrahepatic cholangiocarcinoma: systematic review and metaanalysis

Treatment of unresectable intrahepatic cholangiocarcinoma with yttrium-90 radioembolization: a systematic review and pooled analysis

Ablative radiotherapy doses lead to a substantial prolongation of survival in patients with inoperable intrahepatic cholangiocarcinoma: a retrospective dose response analysis

Capecitabine compared with observation in resected biliary tract cancer (BILCAP): a randomised, controlled, multicentre, phase 3 study

Biweekly cisplatin and gemcitabine in patients with advanced biliary tract cancer

ABC-06 | A randomised phase III, multi-centre, open-label study of active symptom control (ASC) alone or ASC with oxaliplatin / 5-FU chemotherapy (ASC+mFOLFOX) for patients (pts) with locally advanced / metastatic biliary tract cancers (ABC) previously-treated with cisplatin/gemcitabine (CisGem) chemotherapy

Pemigatinib for previously treated, locally advanced or metastatic cholangiocarcinoma: a multicentre, open-label, phase 2 study

Ivosidenib in IDH1-mutant, chemotherapy-refractory cholangiocarcinoma (ClarIDHy): a multicentre, randomised, double-blind, placebocontrolled, phase 3 study

Phase II trial of palliative radiotherapy for hepatocellular carcinoma and liver metastases