# The Impact COVID-19 Infection on Cancer Patients: A Tertiary Cancer Center Experience in Jordan

**Authors:** Kamal Al-rabi, Fadwa Al-Qadi, Akram Al-Ibraheem, Khalid Halahleh, Samer Salah, Hazim Ababneh, Mohammad Akkawi, Maher Sughayer, Lana Tafesh, Layan Abu Abed, Mohammad Ma'koseh

PMC · DOI: 10.7759/cureus.51310 · Cureus · 2023-12-29

## TL;DR

This study examines how COVID-19 affects cancer patients in Jordan, finding high mortality and treatment disruptions.

## Contribution

The study provides insights into the impact of COVID-19 on cancer patients in a low- to middle-income country context.

## Key findings

- 31.8% of cancer patients with COVID-19 required hospitalization, and 15.8% died.
- Low albumin and leucocytosis were strongly associated with higher mortality.
- Recent chemotherapy was linked to better survival in patients with active cancer.

## Abstract

Background: Cancer patients are at higher risk of serious complications of COVID-19. Few studies evaluated the impact of COVID-19 on cancer patients in low- and middle-income countries. Our study aims to evaluate the outcomes of COVID-19 infection in cancer patients treated at our institution.

Methods: Medical records of patients with a positive COVID-19 polymerase chain reaction (PCR) between April 2020 and October 2020 were reviewed. Fisher's exact test and logistic regression analysis were employed to correlate various variables with mortality. Survival estimates were generated using the Kaplan-Meier method.

Results: A total of 317 patients were included, with a median age was 55 years (range: 19-88). 82 (25.9%) had hematological neoplasms while the remainder had solid cancers. At the time of infection, 220 (69.4%) had active cancer, and 99 (31.2%) had received systemic anticancer treatment (SACT) within four weeks. Hospitalization was required for 101 (31.8%), 17 (5.3%) were admitted to the ICU and 50 (15.8%) died. Among patients with active cancer, SACT was delayed or discontinued in 140 (63.6%) patients.

In the entire patient cohort, low albumin (p=<0.001) and leucocytosis (p=<0.001) correlated with mortality within six months of COVID-19 infection. The six-month mortality rate in patients with active cancer was significantly higher in patients with hypertension (p=0.024), no recent SACT (0.017), hematological cancer (p=0.029), low albumin (p=<0.001), leucocytosis (p=0.002) and lymphocyte count of less than 500/µL (p=0.004). Recent chemotherapy was associated with better 6-month survival rates (78.8% vs 89.9%, p=0.012) in patients with active cancer, patients with solid cancers (95.9% vs 82.2%, p=0.006) and was non-inferior in patient with hematological neoplasms (72% vs 65.4%, p=0.519).

Conclusion: COVID-19 infection in our cancer patients was associated with significant morbidity and mortality and adversely affected their treatment. The decision to delay or discontinue SACT should be individualized, considering other risk factors for mortality.

## Linked entities

- **Diseases:** cancer (MONDO:0004992), COVID-19 (MONDO:0100096)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** impaired immunity (MESH:D020274), SACT (MESH:D016609), lymphoma (MESH:D008223), immunodeficiency (MESH:D007153), chronic kidney disease (MESH:D051436), lymphopenia (MESH:D008231), hypoxia (MESH:D000860), infectious (MESH:D003141), infection (MESH:D007239), cancer (MESH:D009369), hematologic malignancies (MESH:D019337), Coronavirus (MESH:D018352), lung cancer (MESH:D008175), hypoalbuminemia (MESH:D034141), COVID (MESH:D000086382), respiratory illness (MESH:D012140), lung adenocarcinoma (MESH:D000077192), -rabi (MESH:D011818), hypertension (MESH:D006973), Mortality (MESH:D003643), B cell aplasia (MESH:D015448), breast cancer (MESH:D001943), diabetes (MESH:D003920), lung squamous cell carcinoma (MESH:D002294)
- **Chemicals:** remdesivir (MESH:C000606551), Paxlovid (MESH:C000719967), Nirmatrelvir plus ritonavir (-), molnupiravir (MESH:C000656703), Bamlanivimab (MESH:C000711749), etesevimab (MESH:C000711968)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC10823193/full.md

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Source: https://tomesphere.com/paper/PMC10823193