On December 31, 2019 a cluster of cases of pneumonia were first described in Wuhan, caused by a novel type of coronavirus called SARS-CoV-2. This virus causes various clinical manifestations encompassed under the term COVID-19 [1]. On March 11, 2020 the World Health Organization declared COVID-19 a global pandemic [2]. In Spain, the most critical period was between February 15 and May 15, 2020. During this time, various different case definitions were provided [3], [4]. Initial data showed that patients with cancer are at highest risk of developing severe COVID-19 disease [5].
In this pandemic context, risks and benefits of receiving cancer treatment should be carefully weighted. Treatment RT delays and interruptions can negatively impact outcome and long-term survival. Another fact to consider is that in a ROD protective measures among staff and changes in its regular workflow must be implemented when treating COVID-19 patients [6].
The objectives of this study are to analyze the incidence of COVID-19 in patients referred to RODs in Spain, subsequent treatment modifications and to determine death-related risk factors due to COVID-19.
Material and methods
A retrospective, observational multicenter study was carried out by 66 ROD in Spain throughout a nationwide survey between February 15 and May 15, 2020. All patients scheduled for or in treatment were registered as well as those with a confirmed/suspected case of COVID-19 according to case definitions at the time [3].
Demographic data and information regarding COVID-19 infection, tumor and RT treatment was collected. SPSS statistical software package (v.22.0; IBM-SPSS; Chicago, IL; USA) was used. The study was approved by the Clinical Research Ethics Committee and is in compliance with Regulation (EU) 2016/679 on the protection of data.
Results
Between February 15 and May 15 2020, 39.848 patients were registered in all 66 RODs 329 cases of COVID-19 were declared, which represents an incidence of 0.8%. The highest incidences were recorded in Madrid (2.2%) and the Basque Country (2%). Geographical distribution can be seen in the supplementary material.
Complete data for 235 COVID-19 patients was provided and analyzed. Patient characteristics are shown in Table 1 . Patients mean age was 65 ± 14 years. The most common symptoms were fever (63,4%), cough (42,6%) and dyspnea (31,6%). Chest radiographs were performed on 82% of patients, demonstrating pneumonia in 52%, bilateral in 37%. Reverse-transcription polymerase chain reaction assay was performed in 214 patients, with positive results in 146 patients (62%). Cases were classified as: confirmed (66,4%), discarded (15,7%), probable (8,1%) and suspicious (9,8%).
Table 1.
Characteristics of COVID-19 cancer patients.
| n | % | n | % | ||||
|---|---|---|---|---|---|---|---|
| Sex | Male | 149 | 63,4 | Previous treatments | Surgery | 89 | 38 |
| Female | 86 | 36,6 | Chemotherapy | 73 | 31 | ||
| comorbidities | Cardiovascular | 88 | 37,4 | RT treatment intent | Adjuvant | 60 | 25,5 |
| HTA | 90 | 38,4 | Palliative | 68 | 28,9 | ||
| Diabetes | 47 | 20 | Radical | 107 | 45,5 | ||
| Pulmonary | 63 | 26,8 | RT type | EBRT | 230 | 97,9 | |
| Hepatic | 15 | 6,4 | BT | 2 | 0,9 | ||
| Renal | 21 | 8,9 | EBRT + BT | 3 | 1,3 | ||
| Obesity | 35 | 14,9 | Systemic treatment | Total | 130 | 61,3 | |
| Primary tumour | Upper Gastrointestinal | 17 | 7,2 | Chemotherapy | 98 | 41,7 | |
| Lower Gastrointestinal | 13 | 5,5 | Hormone therapy | 36 | 15,3 | ||
| Gynecological | 14 | 6 | Immunotherapy | 11 | 4,7 | ||
| Haematological | 16 | 6,8 | Targeted treatments | 2 | 0,9 | ||
| Breast | 24 | 10,2 | Timing of RT-systemic treatment | Concomitant | 77 | 32,8 | |
| Head and Neck | 36 | 15,3 | Sequential | 31 | 13,2 | ||
| Prostate | 34 | 14,5 | Both | 41 | 17,4 | ||
| Lung | 52 | 22,1 | Palliative treatments | Bone metastases | 42 | 17,9 | |
| Central Nervous System | 13 | 5,5 | Spinal compression | 12 | 5,1 | ||
| Urological (non-prostate) | 8 | 3,4 | Brain metastases | 22 | 9,4 | ||
| Others | 8 | 3,4 | |||||
| Tumor Stage | I | 29 | 12,3 | Moment of COVID-19 Diagnosis | Before RT | 94 | 40 |
| II | 34 | 14,5 | During RT | 118 | 50,2 | ||
| III | 68 | 28,9 | After RT | 23 | 9,8 | ||
| IV | 100 | 42,6 | |||||
The original treatment scheme was modified in 166 patients (70,6%). These treatment changes were: hypofractionation (6%), reduction of dose and/or total fractions (3%), suspension of systemic treatment (2%), RT suspension (15,3%), RT interruption (20,4%) and initiation delay (23,8%). 118 patients (50,2%) completed treatment with no incidents, 33 (14%) completed RT with a higher overall treatment time, 42 (17,8%) patients completed RT treatment before expected (due to infection, toxicity or death). 10 patients (4,2%) successfully cured from COVID-19 but died due to tumor progression.
151 patients (64.3%) required hospital admission due to COVID-19 related complications, only 4 of which (2.6%) were admitted to the Intensive Care Units. 52 patients (mortality 22.1%) died due to COVID-19 or secondary complications.
The incidence of COVID-19 in our study was 0.8%, 64,3% required hospital admission and COVID-19 mortality were 22,1%. In our study, death-related risk factors were advanced age, liver comorbidities, upper GI tract primary tumors, presence of brain metastases, palliative radiotherapy, dyspnea, pneumonia and elevated LDH levels. COVID-19 infection modified cancer treatment in 70,6%. In the univariant analysis (supplementary material), various prognostic factors for death were identified. The multivariate analysis is shown in Table 2 .
Table 2.
Multivariant analysis of prognostic factors for COVID-19-related death.
| Variant | Cure | Death | p | OR | IC 95% | |
|---|---|---|---|---|---|---|
| Age | 63,8 ± 14 years | 69,77 ± 13 years | 0,000 | 1,069 | 1,031–1,106 | |
| hepatic comorbity | Yes | 8 (53,3%) | 7 (46,7%) | 0,042 | 0,263 | 0,072–0,954 |
| No | 175 (79,5%) | 45 (20,5%) | ||||
| Upper GI tumor | Yes | 5 (38,5%) | 8 (61,5%) | 0,004 | 7,300 | 1,903–28,000 |
| No | 178 (80,2%) | 44 (19,8%) | ||||
| brain metastases | Yes | 11 (50%) | 11 (50%) | 0,006 | 0,222 | 0,075–0,653 |
| No | 172 (80,8%) | 41 (19,2%) | ||||
| RT treatment | Adjuvant/radical | 142 (85%) | 25 (15%) | 0,041 | 0,320 | 0,107–0,955 |
| Palliative | 41 (60,3%) | 27 (39,7%) | ||||
| Dyspnea | Yes | 47 (60,3%) | 31 (39,7%) | 0,000 | 0,251 | 0,115–0,545 |
| no | 136 (86,6%) | 21 (13,4% | ||||
| Pneumonia | si | 80 (65,6%) | 42 (34,4%) | 0,008 | 0,221 | 0,073–0,669 |
| no | 68 (93,2%) | 5 (6,8%) | ||||
| LDH | 317,9 ± 184,19 | 558,8 ± 553,8 | 0,029 | 1,003 | 1,000–1,006 | |
Discussion
COVID-19 incidence in cancer patients compared to the general population has been reported in various studies in China 1% vs 0,29% [7], in a Wuhan hospital 0,79% vs 0,37% [8] and in Madrid 4,2% vs 0,63% [9]. The prevalence of COVID-19 among cancer patients has been reported as 2.0% [10].
Patients with recent cancer diagnosis were at significantly increased risk for COVID-19 infection (OR, 7.14) and had significantly worse outcomes with higher rates of hospitalization 47.46% and death 14.93% [11].
The probability of death from COVID-19 in patients with cancer published in different studies is 25.6% [12], 28% [13], [14], 30.6% [15]. In the study by Mehta et al. [13] the risk factors for death were older age, higher composite comorbidity score, ICU admission, and elevated inflammatory markers (d-dimer, lactate, and LDH). In a prospective study [14] death-related risk factors were male, advanced age, hypertension and cardiovascular disease. Leukemia (OR 2.25) was also identified a death related risk factor in another study [15]. In our study there are very few hematological tumors (only 16 patients) and in the multivariate analysis, upper digestive tumors are those with the highest risk of death (OR 7.3).
The ESTRO Radiation Therapist Committee [16] published a series of recommendations to adapt routine clinical practice in an RT department in a pandemic situation.
Given the severity of COVID-19 infection in these patients, it is important to avoid unnecessary visits to the hospital and promote remote visits when possible, a careful selection of patients that will benefit from radiotherapy as well as those in which treatment may be delayed or even omitted, and shortening of radiation therapy [17], [18]. Multiple studies have proposed different hypofractionation schemes [19]. In our study, only 6% of treatments were modified to a hypofractionation scheme, probably due to the fact that most guidelines and hypofractionation recommendations appeared after our inclusion period had concluded [20], [21], [22].
Conclusions
Cancer patients are at higher risk of developing more severe cases of COVID-19 with increased mortality. Therefore, it is important optimize patient and treatment selection. In patients that will benefit from RT treatment and present mild symptoms, treatment shall be continued using hypofractionated schemes and proper protective measures.
Acknowledgments
Thanks for the cooperation and for providing the data of the patients under treatment in the study period, to: Jose Begara (GenesisCare Malaga y Benalmadena. Andalucia), Joaquín Gómez Oliveros (GenesisCare Córdoba), José A. González Ferreira (GenesisCare Sevilla. Andalucia), Fátima Ginés Santiago (Hospital Universitario Reina Sofía. Andalucia), Julia Montañés Uceda (Quironsalud Infanta Luisa. Andalucia), Ricardo Esco (Quironsalud Floresta. Aragon), Germán Juan Rijo (Hospital de JOVE y Hospital Universitario Central de Asturias), Maria Victoria Villas (Hospital General Universitario de Albacete. Castilla La Mancha), José Reyes Rodrígez Garrido (CAULE, Castilla-León), Maria Jesús Vega Chicote (Complejo Asistencial de Zamora, Castilla-León), Rocío Cantalapiedra (Hospital de Campo Grande, Castilla-León), Virginia Ruiz (Hospital Universitario de Burgos, Catilla-León), Meritxell Mollà Armadà (Hospital Clinic Barcelona, Cataluña), Manuel Algara (Hospital del Mar, Cataluña), Jordi Giralt (Hospital Universitario Vall D'Hebron, Cataluña), Benjamin Guix (Institut Imor, Cataluña), Almudena Zapatero (Hospital Universitario de La Princesa, Comunidad de Madrid), Natalia Carballo (MD Anderson, Comunidad de Madrid), Rosa M Cañón (H QuironSalud Torrevieja, Comunidad Valenciana), Gabriel Vazquez (Hospital de San Juan Alicante, Comunidad Valenciana), José López Torrecilla (Hospital General Valencia, Comunidad Valenciana), Meritxell Vila (Hospital IMED Elche, Comunidad Valenciana), Pablo Soler (Hospital IMED Valencia, Comunidad Valenciana), Magdalena Martí (Hospital IVO Alcoy, Comunidad Valenciana), Enrique Garcia Miragall (Hospital General Universitario de Elche, Comunidad Valenciana), (Clínica Radioterapia Cáceres, Extremadura), Joaquín Cabrera Rodríguez (Hospital Universitario de Badajoz, Extremadura), (Hospital Virgen del Puerto, Plasencia, Extremadura), Arturo (Centro Oncológico de Galicia), Victor M Muñoz Garzon (Hospital Meixoeiro (CHUVI), Galicia), Marta Casasús (Hospital Juaneda Miramar, Islas Baleares), Fernando Otón (H Universitario de Canarias, Islas Canarias), Juan Ignacio Rodríguez Melcón (Hospital Universitario de Gran Canaria Dr. Negrín, Islas Canarias), Pedro C Lara (Hospital universitario San Roque, Islas Canarias), Juan Salinas Ramos (Hospital GU Santa Lucia de Cartagena, Murcia), y Clara Eíto (Clinica IMQ, Pais Vasco).
Footnotes
Supplementary data to this article can be found online at https://doi.org/10.1016/j.radonc.2021.06.001.
Appendix A. Supplementary data
The following are the Supplementary data to this article:
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