Abstract 729P
Background
Botswana’s cervical cancer (CaCx) post-treatment guidelines recommend survivorship care every 6 months for the first 2 years and annually for the next 3-5 years following the end of curative or definitive treatment. The aims were to present patterns of survivorship care of CaCx patients in Botswana with or without human immunodeficiency virus (HIV) and evaluate factors associated with retention in survivorship care.
Methods
Between 2015-2022, women in Botswana with CaCx were prospectively enrolled in an observational cohort study and treated with curative or definitive intent RT or surgery-based treatment. Factors associated with retention in survivorship care were analyzed using multivariable logistic regression modeling (aOR). The ordinal chi-square test was used to assess impact of COVID-19 on follow-up rates.
Results
We evaluated 830 patients, of which 668 should have ≥1 office visit for the first 2 years and 442 for the next 3-5 years of survivorship care, respectively. Among the cohort (n=830), the median age was 47.7 years; 67.8% (n=563) were HIV-positive with 95.4% (n=537) on antiretroviral treatment. In accordance with the first 2 years of survivorship care, 16.3% (n=109) completed follow-up every 6 months. On multivariable analysis for the first 2 years, traveling ≥100 km (aOR 0.44, p<0.001) vs. <100 km for treatment and receiving surgery-based treatment (aOR 0.40, p<0.001) vs. RT were associated with decreased adherence. In accordance with the next 3-5 years of survivorship care, 10.9% (n=48) completed follow-up annually. On multivariable analysis for the next 3-5 years, traveling ≥100 km (aOR 0.47, p=0.016) vs. <100 km for treatment was associated with decreased adherence. HIV status was not associated with adherence for either period. Follow-up rates did not significantly decrease after the onset of the COVID-19 pandemic (April 1, 2020) during the first 2 year period (61.4% vs. 38.6%, p=0.079).
Conclusions
Majority of CaCx patients in Botswana are not adhering to the recommended survivorship care plan, with increased distance from treatment facilities serving as a primary barrier. Future interventions should aim to reduce barriers to care and improve adherence.
Clinical trial identification
IRB Protocol: 820659.
Editorial acknowledgement
Legal entity responsible for the study
University of Pennsylvania; Botswana UPENN Partnership.
Funding
National Cancer Institute (NCI).
Disclosure
K. Rendle: Financial Interests, Institutional, Research Grant: NIH/NCI, Pfizer/Lung Cancer Research Foundation, AstraZeneca/NCCN; Financial Interests, Personal, Speaker, Consultant, Advisor, One time scientific advisory fee paid to me: Merck; Financial Interests, Personal, Financially compensated role, Honoraria & travel grant from MJH Life Sciences to present at conference: MJH Life Sciences. S. Grover: Financial Interests, Personal, Speaker, Consultant, Advisor: Lumonus. All other authors have declared no conflicts of interest.
Resources from the same session
621P - Phase II trial of encorafenib and binimetinib (E+B) in patients (pts) with BRAF-altered advanced solid tumors: Results of E+B cohort in the BELIEVE trial (NCCH1901)
Presenter: Yoshitaka Honma
Session: Poster session 01
622P - Safety and efficacy of ifebemtinib (IN10018) combined with D-1553 in solid tumors with KRAS G12C mutation: Results from a phase Ib/II study
Presenter: Zhengbo Song
Session: Poster session 01
624P - Belvarafenib in patients (pts) with BRAF class II or III alteration-positive tumours: TAPISTRY study
Presenter: Rafal Dziadziuszko
Session: Poster session 01
625P - Initial results from the phase I, first-in-human study of the covalent, PI3Kα inhibitor TOS-358 in patients with solid tumors, expressing PI3Kα mutations or amplifications
Presenter: Marwan Fakih
Session: Poster session 01
626P - Roginolisib (IOA-244), a first oral allosteric modulator of phosphoinositide 3-kinase inhibitor delta (PI3Kδ) in patients with metastatic uveal melanoma
Presenter: Anna Di Giacomo
Session: Poster session 01
627P - Long-term efficacy and safety of larotrectinib in non-primary central nervous system (CNS) TRK fusion cancer
Presenter: Alexander Drilon
Session: Poster session 01
628P - Efficacy and safety of larotrectinib as first-line treatment for patients (pts) with TRK fusion cancer: An updated analysis
Presenter: David Hong
Session: Poster session 01
629P - Phase I study of pamiparib and cabozantinib in patients with metastatic solid tumors harboring homologous recombination deficiency (HRD)
Presenter: Siqing Fu
Session: Poster session 01