| Literature DB >> 35455816 |
Alin Popescu1, Marius Craina1, Stelian Pantea2, Catalin Pirvu2, Daniela Radu2, Iosif Marincu3, Felix Bratosin3, Iulia Bogdan3, Samer Hosin4, Cosmin Citu1, Elena Bernad1, Radu Neamtu1, Catalin Dumitru1, Adelina Geanina Mocanu1, Adrian Gluhovschi1.
Abstract
Being one of the most common malignancies in young women, cervical cancer is frequently successfully screened around the world. Early detection enables for an important number of curative options that allow for more than 90% of patients to survive more than three years without cancer relapse. Unfortunately, the COVID-19 pandemic put tremendous pressure on healthcare systems and access to cancer care, determining us to develop a study on the influence the pandemic had on surgical care of cervical cancer, and to assess changes in its management and outcomes. A retrospective study design allowed us to compare cervical cancer trends of the last 48 months of the pre-pandemic period with the first 24 months during the COVID-19 pandemic, using the database from the Timis County Emergency Clinical Hospital. New cases of cervical cancer presented to our clinic in more advanced stages (34.6% cases of FIGO stage III during the pandemic vs. 22.4% before the pandemic, p-value = 0.047). These patients faced significantly more changes in treatment plans, postponed surgeries, and postponed radio-chemotherapy treatment. From the full cohort of cervical cancer patients, 160 were early stages eligible for curative intervention who completed a three-year follow-up period. The disease-free survival and overall survival were not influenced by the surgical treatment of choice, or by the SARS-CoV-2 infection (log-rank p-value = 0.449, respectively log-rank p-value = 0.608). The individual risk factors identified for the three-year mortality risk were independent of the SARS-CoV-2 infection and treatment changes during the COVID-19 pandemic. We observed significantly fewer cases of cervical cancer diagnosed per year during the first 24 months of the COVID-19 pandemic, blaming the changes in healthcare system regulations that failed to offer the same conditions as before the pandemic. Even though we did not observe significant changes in disease-free survival of early-stage cervical cancers, we expect the excess of cases diagnosed in later stages to have lower survival rates, imposing the healthcare systems to consider different strategies for these patients while the pandemic is still ongoing.Entities:
Keywords: COVID-19; SARS-CoV-2; cervical cancer; disease-free survival; hysterectomy
Year: 2022 PMID: 35455816 PMCID: PMC9024750 DOI: 10.3390/healthcare10040639
Source DB: PubMed Journal: Healthcare (Basel) ISSN: 2227-9032
Characteristics of new patients with cervical cancer presenting at gynecology and general surgery clinics for investigations and treatment over a course of six years before and during the COVID-19 pandemic.
| Variables * | Pre-Pandemic | During Pandemic | |
|---|---|---|---|
| Age, years (mean ± SD) | 38.6 ± 8.1 | 37.4 ± 8.6 | 0.324 |
| BMI, kg/m2 (mean ± SD) | 23.3 ± 4.4 | 23.8 ± 5.2 | 0.457 |
|
| 0.248 | ||
| <2 cm | 133 (39.2%) | 16 (30.3%) | |
| ≥2 cm | 207 (60.8%) | 36 (69.2%) | |
|
| 0.047 | ||
| I | 135 (39.7%) | 11 (21.1%) | |
| II | 82 (24.1%) | 13 (25.0%) | |
| III | 76 (22.4%) | 18 (34.6%) | |
| IV | 47 (13.8%) | 10 (19.2%) | |
|
| 0.942 | ||
| Grade 1 | 191 (56.2%) | 29 (55.7%) | |
| Grade 2 | 105 (30.9%) | 17 (32.7%) | |
| Grade 3 | 44 (12.9%) | 6 (11.6%) | |
|
| 0.755 | ||
| Squamous-cell | 268 (78.8%) | 40 (76.9%) | |
| Adenocarcinoma | 72 (21.2%) | 12 (23.1%) | |
|
| |||
| Change in treatment plan | 41 (12.1%) | 12 (23.1%) | 0.030 |
| Postponed surgery | 32 (9.4%) | 11 (21.2%) | 0.011 |
| Postponed radio-chemotherapy | 44 (12.9%) | 15 (28.8%) | 0.002 |
| ICU hospitalization | 23 (6.8%) | 6 (11.5%) | 0.220 |
| Mortality | 20 (5.9%) | 4 (7.7%) | 0.612 |
* Data reported as n(%) unless specified differently.
Characteristics of patients with early-stage cervical cancer under follow-up based on their COVID-19 status.
| Characteristics * | SARS-CoV-2 Negative ( | SARS-CoV-2 Positive ( | |
|---|---|---|---|
| Age, years | 38.0 ± 9.4 | 39.2 ± 9.1 | 0.516 |
| BMI, kg/m2 | 26.4 ± 3.5 | 27.8 ± 4.4 | 0.057 |
| Overall survival | 108 (84.4%) | 28 (87.5%) | 0.657 |
| DFS **, months, (median[IQR]) | 34 [31–36] | 33 [30–36] | 0.531 |
| Follow-up, months, (median[IQR]) | 34 [28–36] | 34 [29–36] | 0.948 |
|
| 0.076 | ||
| Robot surgery | 16 (12.5%) | 8 (25.0%) | |
| Open surgery | 112 (87.5%) | 24 (75.0%) | |
|
| 0.871 | ||
| <2 cm | 50 (39.1%) | 12 (37.5%) | |
| ≥2 cm | 78 (60.9%) | 20 (62.5%) | |
|
| 0.141 | ||
| 0 | 94 (73.4%) | 18 (56.3%) | |
| 1 | 12 (9.4%) | 6 (18.7%) | |
| >1 | 22 (17.2%) | 8 (25.0%) | |
|
| 0.490 | ||
| IA2 | 40 (31.3%) | 8 (25.0%) | |
| IB1 | 88 (68.7%) | 24 (75.0%) | |
|
| 0.967 | ||
| Grade 1 | 74 (57.8%) | 18 (56.3%) | |
| Grade 2 | 40 (31.2%) | 10 (31.3%) | |
| Grade 3 | 14 (11.0%) | 4 (12.4%) | |
|
| 0.868 | ||
| Local | 16 (12.4%) | 3 (9.4%) | |
| Regional | 8 (6.3%) | 2 (6.3%) | |
| Distant | 8 (6.3%) | 1 (3.2%) | |
| Total | 32 (25.0%) | 6 (18.8%) | |
|
| 0.223 | ||
| Squamous-cell | 111 (86.7%) | 25 (78.1%) | |
| Adenocarcinoma | 17 (13.3%) | 7 (21.9%) | |
|
| 0.762 | ||
| Radiotherapy-only | 20 (15.6%) | 8 (25.0%) | |
| Chemotherapy-only | 5 (3.9%) | 3 (9.4%) | |
| Radio-chemotherapy | 6 (4.7%) | 4 (12.4%) | |
|
|
|
| 0.031 |
| No complications | 45 (35.2%) | 20 (62.5%) | |
| Score 1 | 52 (40.6%) | 8 (25.0%) | |
| Score 2 | 24 (18.8%) | 2 (6.25%) | |
| Score 3 | 7 (5.4%) | 2 (6.25%) |
* Data reported as n(%) unless specified differently; ** DFS—Disease-Free Survival.
Figure 1Kaplan–Meyer plot of the three-year disease-free survival in patients with early-stage cervical cancer based on the surgical treatment type.
Figure 2Kaplan–Meyer plot of the three-year survival probability in patients with newly-diagnosed cervical cancer based on SARS-CoV-2 infection status.
Multivariate regression analysis for the three-years mortality in patients with early-stage cervical cancer.
| Factor | Odds Ratio | Confidence Interval | |
|---|---|---|---|
| Tumor Size (≥2 cm) | 1.8 | 1.4–2.5 | 0.022 |
| Relapse | 4.2 | 3.1–5.8 | <0.001 |
| High Grade | 5.1 | 3.3–7.2 | <0.001 |
| SARS-CoV-2 infection | 1.3 | 0.7–1.9 | 0.246 |
| Lymph Nodes (≥2) | 2.9 | 1.6–3.6 | 0.003 |
| Clavien–Dindo (≥3) | 1.5 | 0.9–1.9 | 0.085 |
| Change in treatment plan | 1.3 | 0.9–1.6 | 0.104 |
| Postponed surgery * | 1.1 | 0.8–1.3 | 0.417 |
| Postponed radio-chemotherapy * | 1.3 | 0.8–1.7 | 0.115 |
* Between 1 and 8 weeks.
Existing studies describing the COVID-19 pandemic impact on cervical cancer survival.
| First Author (Year) | Conclusions |
|---|---|
| Gupta et al. (2021) [ | A 2.52% to 3.80% increase in cervical cancer-related deaths with treatment delays ranging from 9 weeks to 6 months. |
| Kregting et al. (2021) [ | An increase of 2.0, 0.3, and 2.5 cancer deaths per 100,000 individuals in 10 years. |
| Matsuo et al. (2021) [ | Wait-time of 6.1–9.8 weeks for cervical cancer treatment was not associated with increased risk of all-cause mortality compared to a wait-time of 6 weeks. |
| Matsuo et al. (2021) [ | In women with early-stage cervical cancer, an 8-week delay for hysterectomy may not be related with short-term disease recurrence and shorter DFS. |
| Davies et al. (2022) [ | Over the next 3 years, there is anticipated considerable rise in newly-diagnosed cervical cancer cases. Increased surgical capacity might alleviate this burden with no significant morbidity or mortality increase. |
| Matsuo et al. (2021) [ | Postponing hysterectomy for 6–8 weeks is appropriate for women with early-stage cervical cancer in centers or areas with a high prevalence of COVID-19 illness and has no detrimental effect on survival. |