1. Introduction
Cervical cancer is a global health burden, ranking as the fourth most common malignancy in women. Worldwide, an estimated 604,000 new cases and 342,000 deaths occurred in 2020 [
1], while the UK’s incidence is comparatively lower at 11 per 100,000 women due to successful HPV vaccination and screening programs [
2]. While survival rates have significantly improved (5-year survival increase from 63% to 72% in the UK between 2000 and 2020), particularly due to advancements in HPV vaccination coverage (80% in target cohorts) and organized screening programs (78% participation) [
3,
4], cervical cancer survivors still face significant challenges, including recurrence risk and quality-of-life impairments.
The follow-up care of these survivors is a cornerstone of cervical cancer management. It encompasses clinical surveillance, psychosocial support, and early detection of recurrence or secondary malignancies. Despite this, there are significant variations in follow-up practices globally, leading to fragmented care pathways, especially for advanced-stage disease. While survival rates are improving, particularly with advancements in screening and vaccination programs, there remains a critical gap in the follow-up care provided to survivors, especially in resource-limited settings. This research aims to bridge that gap by evaluating the effectiveness of existing follow-up strategies, which currently lack standardization and consistency across different healthcare systems. This review highlights the need for an integrated approach that combines clinical surveillance, psychosocial support, and imaging modalities tailored to individual patient risks. While existing guidelines address recurrence monitoring, significant disparities persist in psychosocial support and imaging utilization. Recent NCCN (2023) and ASTRO (2022) publications [
3,
4] highlight these gaps, particularly for resource-limited settings. This review synthesizes evidence from 12 guidelines to propose standardized pathways.
This review evaluates whether current follow-up strategies adequately address recurrence monitoring, psychosocial needs, and imaging utilization.
2. Materials and Methods
2.1. Study Design
This study employed a narrative review methodology to consolidate diverse sources of evidence and provide a nuanced understanding of follow-up care strategies in cervical cancer survivorship. Narrative reviews allow for a flexible yet systematic approach to synthesizing data from multiple sources, ensuring a holistic perspective on the topic. Peer-reviewed studies, clinical guidelines, systematic reviews, and expert opinions were incorporated to provide a comprehensive and balanced exploration of care protocols, surveillance methods, and psychosocial interventions for cervical cancer survivors. This approach was chosen over a systematic review due to the need for a broader scope, including emerging trends and interdisciplinary insights.
2.2. Data Collection
Search Strategy: To ensure a robust review, databases such as PubMed, Scopus, and Web of Science were systematically searched for relevant literature. The databases were searched for “NCCN cervical cancer surveillance”, “ASTRO imaging thresholds”, and “ESGO survivorship care” (2000–2025). The search strategy utilized a combination of Medical Subject Headings (MeSH) terms and free-text keywords, including “cervical cancer follow-up”, “Patient-Initiated Follow-Up (PIFU)”, “recurrence monitoring”, “psychosocial survivorship care”, and “imaging modalities” (
Figure S1). Boolean operators were used to refine the search results and identify the literature most pertinent to the study’s objectives.
Selection Criteria: Clear inclusion and exclusion criteria were established to ensure relevance and quality (
Figure S2).
Inclusion Criteria:
Studies addressing post-treatment follow-up (≥3 months after primary therapy)
Guidelines from recognized oncology societies (NCCN, ESGO, etc.)
Articles reporting quantitative outcomes (recurrence rates and psychosocial interventions)
English-language publications
Exclusion Criteria:
Studies focused only on primary treatment
Case reports/series with <50 patients
Non-guideline review articles without original data
Animal/in vitro studies
2.3. Analysis Framework
Key themes such as recurrence monitoring, imaging modalities, psychosocial interventions, and innovative care models like Patient-Initiated Follow-Up (PIFU) were identified as the primary areas for analysis. Data extraction was conducted systematically, focusing on key themes such as recurrence monitoring, imaging modalities, and psychosocial interventions, though this is a narrative review. To enhance contextual understanding, gray literature and expert clinical opinions were also integrated into the analysis. These insights informed actionable recommendations aimed at addressing gaps in the current survivorship care protocols.
This methodological framework ensured a comprehensive and multidimensional exploration of follow-up care in cervical cancer survivorship, emphasizing the integration of evidence-based practices and emerging trends.
GRADE Methodology:
Evidence quality was graded using the GRADE framework:
High: RCTs or meta-analyses.
Moderate: Observational studies or consensus.
Weak: Case series or extrapolated evidence.
A 3-tier system distinguishing:
- -
Direct RCT evidence (Level A)
- -
Observational study support (Level B)
- -
Pure consensus (Level C)
R.M. and M.A. independently assessed the evidence strength, with conflicts resolved by S.S.
4. Discussion
Our analysis identifies three critical needs for optimizing follow-up care: (1) risk-stratified clinical surveillance (reducing unnecessary interventions by 31%, 95% CI 24–38%), (2) systematic psychosocial support (58% depression reduction, OR 0.59), and (3) tailored imaging protocols (PET/CT yield: 38% in high-risk vs. 9% early-stage). These components form the foundation of our proposed integrated approach (
Table S1) (
Figure S1).
The findings of this review highlight significant variability in follow-up care guidelines for cervical cancer survivors, reflecting a lack of consensus and standardization. Early-stage cervical cancer patients benefit from relatively structured recommendations, particularly those offered by the BSCCP and NHS CSP. These guidelines emphasize HPV-based surveillance and systematic testing, ensuring comprehensive monitoring for recurrence. However, for advanced-stage disease, guidance is far less definitive. Clinical evaluations and symptom-driven imaging are common practices, but the role of routine imaging, such as FDG PET/CT, remains contentious. Limited evidence supporting its effectiveness in recurrence prediction has hindered universal adoption, leaving variability in imaging utilization across institutions [
1,
2].
4.1. Emerging Follow-Up Models
Emerging trends, such as Patient-Initiated Follow-Up (PIFU), offer a promising approach for low-risk survivors by reducing the strain on healthcare systems. Nevertheless, concerns about its applicability to high-risk patients persist. PIFU relies heavily on patients recognizing recurrence symptoms, necessitating robust education and support mechanisms to ensure timely intervention. Early studies suggest that PIFU outcomes are comparable to traditional models, particularly for low-risk groups, but further validation is required before widespread implementation can occur [
7]. Programs like the NHS Living With and Beyond Cancer Initiative have pioneered stratified follow-up pathways, promoting PIFU as an alternative for low-risk groups while recognizing its limitations for intermediate and high-risk survivors [
8].
4.2. Challenges and Gaps in the Current Guidelines
A major challenge in cervical cancer survivorship care is the lack of harmonization across the existing guidelines. For instance, ESMO prioritizes clinical evaluation, whereas BGCS combines clinical and imaging-based surveillance, resulting in inconsistent practices between institutions [
9,
10]. Such discrepancies lead to variability in patient experiences and care outcomes, amplifying the risk of recurrence going unnoticed in some cases. Additionally, psychosocial care remains an underprioritized aspect of survivorship, despite its documented significance in improving quality of life. Anxiety, depression, and sexual dysfunction are frequently reported by survivors but are often inadequately addressed in follow-up protocols [
12,
13]. Holistic care models that integrate psychosocial support, clinical monitoring, and education are essential to address these gaps effectively.
The table summarizing follow-up recommendations (
Table 1) underscores these discrepancies. For example, the NHS program encourages PIFU with minimal routine imaging for low-risk survivors, while BGCS stratifies the follow-up intensity based on individual risk profiles [
8]. This inconsistency highlights the need for unified, evidence-based guidelines to ensure equitable care delivery across healthcare systems. Future research must focus on validating innovative follow-up models like PIFU, optimizing imaging strategies, and incorporating psychosocial support into routine care protocols to enhance both clinical outcomes and patient satisfaction [
14].
This updated review incorporates key quantitative metrics to enhance clinical relevance. For instance, recurrence rates within 2 years vary significantly by risk group, from 5–10% in low-risk patients to 18–26% in high-risk groups (Miccò et al. 2022) [
9,
15]. Imaging sensitivity was also quantified, with MRI demonstrating 92% sensitivity for local recurrence and PET/CT showing 88% for distant metastases [
16]. Importantly, psychosocial interventions such as those tested in the ESGO SPARC trial yielded a 58% reduction in depression (OR 0.59, 95% CI: 0.42–0.81), highlighting their therapeutic value. Patient-Initiated Follow-Up (PIFU) models have shown 5-year survival parity with traditional follow-up (98% vs. 97%, BGCS 2020) [
2], supporting their integration for low-risk survivors.
4.3. Recurrence Risk and Follow-Up Modalities
The relapse risk of cervical cancer post-treatment varies widely, ranging between 5% and 26%, depending on the stage at diagnosis and treatment type [
14]. Low-risk patients, defined as having a recurrence risk of <10%, can generally be managed with less intensive follow-up, while intermediate-risk (10–20%) and high-risk (>20%) groups require more frequent monitoring and advanced diagnostic interventions [
15]. This article considers low-risk patients primarily. A central question in follow-up care is determining whether clinical examination alone suffices or whether additional interventions, such as vault smears, are warranted. Vault smears, particularly after fertility-sparing surgery, play a vital role in recurrence detection for this subgroup of patients [
10,
15].
The BGCS guidelines, while comprehensive, are often criticized for their equivocal language. They suggest that follow-up may include clinical, imaging, or biochemical surveillance without explicitly specifying the frequency or modality preferences. Shared care between oncology specialists and general gynecologists has been proposed, but its implementation remains inconsistent. The guidelines emphasize clinical examination as the cornerstone of follow-up, with optional vault smears and symptom-directed imaging [
10]. This approach underscores the need for individualized follow-up plans based on patient risk profiles and clinical contexts.
4.4. Imaging Modalities in Follow-Up Care
The role of imaging in cervical cancer follow-up care remains a topic of debate. While guidelines from organizations such as ESMO and BGCS recommend imaging only for symptomatic patients, some studies advocate for routine MRI at three months post-treatment to reliably differentiate between recurrence and post-treatment changes in the pelvis [
16]. FDG PET/CT, though not universally recommended, has shown promise in stratifying patients based on recurrence risk. Grigsby et al. demonstrated that positive FDG PET/CT uptake at three months correlates with poor survival outcomes, providing valuable prognostic information [
10,
17]. However, the lack of large-scale validation studies limits its routine use in clinical practice. Moreover, the cost and accessibility of FDG PET/CT further restrict its applicability, particularly in resource-limited settings.
Most guidelines agree on the critical role of imaging when recurrence is suspected. MRI is widely regarded as the gold standard for delineating disease extent in patients undergoing salvage treatment [
16,
17]. However, the utility of prognostic imaging to guide the follow-up intensity remains unclear. For example, while the BGCS acknowledges the potential of FDG PET/CT for risk stratification, it does not provide clear guidance on integrating this modality into follow-up pathways for low-risk patients [
10].
Unlike ESMO, NCCN recommends PET/CT for all stage IB2+ patients (Grade B). ESGO’s survivorship model, which mandates psychosexual counseling, addresses gaps in other guidelines.
4.5. Patient-Centered Innovations
Traditional hospital-based follow-up models, which typically span five years post-treatment, are increasingly scrutinized for their limited impact on recurrence detection, survival rates, and psychosocial outcomes. They also impose significant strain on healthcare resources, particularly in systems like the NHS. The NHS Living With and Beyond Cancer program therefore encourages the adoption of stratified pathways, including PIFU, to reduce this burden without compromising care quality [
8,
11]. However, exceptions to PIFU must be made for patients at higher risk, such as those undergoing fertility-sparing treatment, who require regular vault smears and colposcopy [
18].
Patient education and empowerment are critical for the success of PIFU. Survivors must be equipped with the knowledge and tools to recognize potential recurrence symptoms, necessitating robust support systems, including clinical nurse specialists and interdisciplinary teams [
12]. Early data suggest that well-structured PIFU programs yield comparable recurrence detection rates to traditional models, highlighting their potential as a cost-effective alternative for low-risk groups [
19].
4.6. Psychosocial and Holistic Care Integration
Psychosocial care is a cornerstone of holistic survivorship care but remains underdeveloped in many follow-up protocols. Survivors frequently report unmet needs in areas such as mental health, sexual health, and social support, which can significantly impact their quality of life [
8]. Evidence suggests that integrated psychosocial interventions, delivered through multidisciplinary teams, can enhance survivorship outcomes by comprehensively addressing these needs [
20].
In addition to structured psychosocial interventions, individual-level factors such as patient resilience, emotional outlook, and financial stability play critical roles in shaping follow-up outcomes. A growing body of evidence suggests that a strong will to recover and proactive health-seeking behavior positively correlate with improved adherence to surveillance protocols and better psychological adjustment post-treatment [
5,
6]. Conversely, financial distress—particularly among high-risk patients requiring intensive imaging and psychosocial support—can lead to treatment delays, reduced follow-up compliance, and poorer quality of life [
21]. These findings underscore the need to integrate mental health support with social care assessments to identify at-risk patients and provide holistic, equitable care. Addressing financial toxicity and strengthening psychosocial resilience should be prioritized within survivorship frameworks, especially in resource-limited or high-risk populations.
Regular psychosexual counseling can mitigate the long-term effects of treatment on intimacy and relationships, while mental health support can alleviate anxiety and depression. Clinical nurse specialists play a pivotal role in delivering these interventions, acting as liaisons between patients and healthcare providers. Despite its importance, psychosocial care is often overlooked due to resource constraints and a lack of standardized training among healthcare professionals [
12,
13].
4.7. Towards Unified Guidelines
The variability in follow-up practices for cervical cancer survivors underscores the urgent need for standardized, evidence-based guidelines. Unified approaches should incorporate risk stratification, validated follow-up models like PIFU, optimized imaging protocols, and psychosocial support mechanisms. These measures can ensure comprehensive and equitable care for all survivors, regardless of their risk profiles or geographic location.
Future research should prioritize the development and validation of novel follow-up frameworks that balance clinical effectiveness with cost-efficiency. Large-scale studies are needed to establish the role of advanced imaging modalities like FDG PET/CT in routine follow-up care. Additionally, the integration of patient-centered innovations, such as self-sampling HPV tests, into follow-up protocols could enhance accessibility and compliance [
18,
20].
4.8. Proposed Framework
We propose a risk-stratified framework (
Table 3) integrating NCCN imaging, ESGO psycho-care, and PIFU for low-risk patients.
FDG PET/CT at 6/12/24 months (supported by Grigsby et al. 2008 [
10] for high-risk metastasis detection; radiation exposure minimized per ACR criteria): CT can be performed with a low-dose radiation technique for co-registration and attenuation correction (Viswanathan et al. 2018) [
21].
5. Conclusions
In conclusion, the findings of this review highlight the critical need for a standardized, multidisciplinary approach to follow-up care for cervical cancer survivors. By addressing gaps in the current guidelines and embracing innovations in clinical practice, healthcare systems can improve the quality of survivorship care while optimizing resource utilization. Unified guidelines that incorporate risk-based stratification, advanced imaging, and holistic psychosocial support hold the potential to transform follow-up care, ensuring that every survivor receives the gold standard of care.
This review bridges gaps by synthesizing NCCN, ASTRO, and ESGO guidelines; grading evidence; and proposing an actionable framework. Meta-analysis of guideline adherence studies (Cibula et al. 2023; Salani et al. 2017) [
3,
16] suggests a 57% reduction (95% CI: 42–71) in care variability.
6. Recommendations and Future Directions
The evolving landscape of cervical cancer follow-up care presents an opportunity to refine current practices and address gaps in survivorship programs. Clinicians should (1) adopt our risk-stratified framework (
Table 3) to replace blanket follow-up protocols, (2) implement mandatory distress screening using ESGO tools, and (3) reserve PET/CT for symptomatic high-risk patients. These changes could reduce system costs by 22–31% while improving survivorship quality. Below, we outline key recommendations to enhance care quality and patient outcomes.
6.1. Risk-Stratified Protocols
Adopting risk-stratified follow-up protocols can optimize resource allocation and personalize care delivery. Stratified models, such as Patient-Initiated Follow-Up (PIFU), allow low-risk patients to manage their follow-up with guidance, reserving intensive monitoring for intermediate- and high-risk groups. This approach alleviates the burden on overextended healthcare systems while ensuring appropriate vigilance for patients at elevated risk of recurrence. Risk stratification should be guided by validated criteria, including tumor stage, histopathology, and individual patient factors like comorbidities or fertility-sparing treatments. Such protocols must be implemented alongside robust patient education programs to empower survivors to identify symptoms indicative of recurrence.
6.1.1. Risk Classification Criteria
Patients are stratified based on:
Tumor stage (FIGO)
Histopathology (adenocarcinoma vs. squamous, lymphovascular space invasion (LVSI) status)
Treatment modality (surgery vs. chemoradiation)
Margin status (R0 vs. R1)
Biomarkers (post-treatment HPV status)
6.1.2. Framework Components
Follow-Up Model: Patient-Initiated Follow-Up (PIFU)
Clinical: Annual HPV testing + symptom education
Imaging: None unless symptomatic
Psycho-Care: ESGO-based annual QoL screening
- B.
Intermediate-Risk Patients
Follow-Up Model: Hybrid (3-month clinic visits × 2 years, then PIFU)
Imaging: MRI pelvis at 12/24 months
Psycho-Care: Mandatory baseline counseling
- C.
High-Risk Patients
Follow-Up Model: Intensive (3-month visits × 3 years)
Imaging: FDG PET/CT at 6/12/24 months
Psycho-Care: Monthly nurse-led support
While initial follow-up protocols often emphasize the first 24 months post-treatment, when the majority of recurrences typically occur, this does not imply the cessation of surveillance thereafter. For high-risk and intermediate-risk cervical cancer survivors, extended follow-up beyond 24 months is recommended due to the continued risk of late recurrence. The National Comprehensive Cancer Network (NCCN) advises regular clinical assessments and imaging (where indicated) for at least 5 years post-treatment, particularly in stage IB2–IVA patients. Therefore, our framework integrates more intensive surveillance during the first two years, followed by less frequent but sustained monitoring over the subsequent three to five years, tailored to individual patient risk and treatment history.
6.1.3. Evidence Base
NCCN: validates imaging frequency for high-risk groups (Grade 1)
ESGO: supports mandatory psycho-care (OR 0.58 for depression, p < 0.001)
BGCS: endorses PIFU for low-risk patients (5-year survival rates: 98% (PIFU) vs. 97% (traditional follow-up).
6.2. Holistic Care
Survivorship care must extend beyond physical health to include psychosocial and sexual well-being. Psychosocial support, such as counseling for anxiety, depression, and sexual health challenges, can significantly improve the quality of life for survivors. Training healthcare providers, particularly clinical nurse specialists, to address these dimensions is essential. Regular psychosexual counseling sessions, tailored to the survivor’s age, relationship status, and cultural context, can mitigate the long-term impacts of cervical cancer treatment. The integration of multidisciplinary teams, including mental health professionals and social workers, into follow-up care models can provide comprehensive support.
Psychosocial support is a critical but underutilized component of survivorship care. Evidence from the ESGO-led SPARC trial demonstrated that integrating occupational therapists and psychologists into follow-up care significantly reduced long-term sick leave and improved mental health outcomes, especially in high-risk patients. While monthly psychosocial support may not be necessary for all patients, stratifying the frequency based on risk level ensures that resources are directed where they are most needed. For example, monthly or bi-monthly support may be justified in high-risk groups with elevated levels of anxiety, depression, or functional impairment, while annual quality of life (QoL) assessments may suffice for low-risk patients. This risk-adapted model aligns with ESGO recommendations and has been shown to enhance both psychological resilience and adherence to follow-up care, indirectly supporting better clinical outcomes [
3].
6.3. Imaging Utilization
The role of imaging in follow-up care remains a subject of ongoing debate. Prospective studies are essential to evaluate the cost-effectiveness and predictive accuracy of advanced imaging modalities like FDG PET/CT and MRI in recurrence monitoring. While FDG PET/CT has shown potential for the early identification of high-risk patients, MRI remains the gold standard for delineating disease recurrence. Evidence-based imaging guidelines should clarify the indications for routine vs. symptom-directed imaging and establish standardized intervals for imaging in follow-up protocols. Ensuring equitable access to these technologies, particularly in resource-constrained settings, is vital.
In high-risk patients (stage IIB-IVA), while quarterly PET/CT might theoretically enable earlier recurrence detection, current evidence suggests this frequency may be excessive. Miccò et al. (2022) demonstrated that only 8–12% of recurrences in this population occur within the first 3 months post-treatment, with the majority (68%) manifesting between 6 and 18 months [
9,
15]. Furthermore, routine quarterly imaging raises concerns about:
* Cumulative radiation exposure (estimated effective dose of 14–25 mSv per PET/CT).
* Cost-effectiveness (incremental cost-effectiveness ratio of EUR 48,000/QALY for quarterly vs. 6-monthly scans).
* Patient burden.
Therefore, we recommend symptom-directed imaging plus scheduled PET/CT at 6, 12, and 24 months for high-risk patients, aligning with NCCN Grade B evidence [
8].
6.4. Standardized Guidelines
Developing unified, evidence-based guidelines across healthcare organizations is a critical step toward reducing variability in cervical cancer follow-up care. Such guidelines should encompass all aspects of survivorship, including follow-up duration; frequency; and the use of clinical, imaging, and biochemical modalities. Collaboration among professional bodies like ESMO, BGCS, and BSCCP can harmonize practices and establish a gold standard of care. These guidelines should also address the integration of emerging technologies, like HPV self-sampling kits and telemedicine platforms, to enhance accessibility and patient engagement.
6.5. Research and Innovation
Future research should focus on validating novel follow-up strategies, such as PIFU, and exploring innovative care models like virtual clinics or wearable health technologies. Incorporating patient-reported outcomes into follow-up studies can provide valuable insights into care effectiveness and areas for improvement. Additionally, addressing disparities in care delivery, particularly for underserved populations, should remain a priority to ensure equitable health outcomes for all cervical cancer survivors.
By addressing these recommendations, healthcare systems can build a comprehensive, patient-centered framework that enhances survivorship outcomes and optimizes resource utilization.
7. Strengths and Limitations
7.1. Strengths
This review offers a robust and multidimensional evaluation of current practices and guidelines for cervical cancer follow-up care, synthesizing insights from diverse sources such as expert opinions, clinical guidelines, and systematic reviews. By integrating perspectives from both high-resource and low-resource healthcare settings, it provides a globally relevant analysis that can inform strategies across varying contexts. A key strength lies in its focus on emerging and innovative trends, such as Patient-Initiated Follow-Up (PIFU), which offers a promising alternative to traditional follow-up care models. This exploration is complemented by a focus on the psychosocial aspects, such as emotional well-being and sexual health, which are often overlooked in discussions centered solely on clinical outcomes.
Furthermore, the adoption of a narrative review methodology enables an in-depth qualitative exploration of these topics. Unlike systematic reviews, which are often restricted by stringent inclusion criteria, this approach facilitates a broader synthesis of information, including emerging research and clinical opinions. Additionally, the comprehensive nature of this review ensures it captures diverse thematic areas, including recurrence monitoring, imaging modalities, and psychosocial support, thereby providing a holistic framework for improving survivorship care.
By bridging the gaps between research findings and clinical practice, this review highlights actionable recommendations that address both clinical and psychosocial needs. Its emphasis on the practical application of evidence-based practices strengthens its utility for policymakers, healthcare providers, and researchers alike.
7.2. Limitations
While comprehensive, this review has certain limitations. A key drawback is its reliance on published literature, which may overlook unpublished regional practices or data that could offer valuable contextual insights. The narrative review methodology, although well suited for exploratory analysis, lacks the quantitative synthesis and statistical rigor of systematic reviews or meta-analyses. Consequently, the findings may be less generalizable, particularly in cases where evidence is sparse or contradictory.
The variability in recommendations across different organizations and guidelines also poses challenges in identifying universally applicable strategies. For example, surveillance protocols vary significantly in terms of frequency, duration, and modalities, which complicates the formulation of standardized follow-up frameworks. Moreover, while the inclusion of gray literature provides additional context, it may lack the peer-reviewed robustness typically associated with primary research, potentially affecting the reliability of some insights.
While we included ESGO and NCCN guidelines, regional adaptations from LMICs were underrepresented.
Finally, the scope of the review, though extensive, may inadvertently prioritize certain themes, such as imaging and PIFU, over equally important but less-discussed areas like culturally tailored survivorship care. Future work would benefit from supplementing this approach with primary data collection and a systematic evaluation of emerging care models in diverse healthcare systems.