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
671P - LuMIERE: A phase I/II study evaluating safety, dosimetry, and preliminary activity of [177Lu]Lu-FAP-2286 in patients with advanced solid tumors
Presenter: Jonathan McConathy
Session: Poster session 01
672P - Inference failure with synthetic arms: Empirical application to phase III oncology trials
Presenter: Alexander Decruyenaere
Session: Poster session 01
673P - Project Optimus for dose optimization: Implementation strategies for your trial from the statistician’s standpoint
Presenter: Miguel Pereira
Session: Poster session 01
674P - Patient enrollment per month (accrual) in clinical trials leading to the FDA approval of new cancer drugs
Presenter: Sebastian Albers
Session: Poster session 01
675P - Evaluation of the safety and efficacy of JSKN003 in patients with advanced HER2-positive (IHC 3+) solid tumors (excluding breast cancer)
Presenter: Lin Shen
Session: Poster session 01
678TiP - A phase I, first-in-human, dose escalation and expansion study of oral pan-RAF/MEK molecular glue NST-628 in subjects with solid tumors harboring RAS-MAPK pathway alterations
Presenter: Charlotte Lemech
Session: Poster session 01
679TiP - Cancer Research UK phase I/IIa trial of the prostaglandin E2 (PGE2) receptor 4 (EP4) antagonist HTL0039732 as monotherapy and in combination with immunotherapy in patients (pts) with advanced solid tumors
Presenter: Debashis Sarker
Session: Poster session 01
680TiP - A phase I/IIa first-in-human clinical trial evaluating MDX2001, a multi-specific antibody in patients with advanced solid tumor malignancies
Presenter: Anna Minchom
Session: Poster session 01
681TiP - A phase I/II, open label, multi-center, non-randomized dose escalation and dose expansion study of AMXI-5001 in patients with advanced malignancies
Presenter: Lee Rosen
Session: Poster session 01