EV305/#1276  Individualised PARP inhibitor dosing: does flexibility impact patient care

<h3>Introduction</h3> A significant limitation of PARPi, that are used as maintenance treatment in ovarain cancer, is their toxicity profile. Many patients require discontinuation or dose modifications. To optimise patient longevity on treatment, clinical practices may consider individualised dosing for certain patients. Initiating reduced dosages, with or without dose escalation, may improve longterm toxicity and maximise duration of therapy. Little data is available on the impact of individualised dosing. <h3>Methods</h3> A retrospective chart review was performed on 21 patients undergoing PARPi treatment in Cork between 2018 and 2023. Two cohorts were compared: those who received standard dose and those that received reduced-dose in the initial setting. Multiple toxicity profiles were assessed (haematological &amp; non-haematological). Patient outcomes, hospitalisations, and dose reductions/interruptions/escalations were compared between the two subgroups. <h3>Results</h3> Patients undergoing individualised treatment may have an improved toxicity profile compared to those prescribed standard regimens. The impact on progression-free survival between groups was indeterminate due to inter-sample variability. Patients undergoing individualised treatment had fewer events of vomiting (P = 0.476), severe nausea (P &gt; 0.999), anaemia (P &gt; 0.999) and leukopaenia (P &gt; 0.999). Individualised treatment regimens showed a reduction in overall severe toxicities compared to the standard group (83% vs. 33%). Individualised treatment did not improve the proportion of patients experiencing thrombocytopenia. <h3>Conclusion/Implications</h3> Individualised PARP inhibitor therapy may have a non-inferior impact on toxicity and progression-free survival in patients, however the statistical power of this study was limited by a small sample size and various confounding elements. Further research is needed support the results achieved herein.

Authors

Institutions

Publication Details

Published
2024-10-01
DOI
https://doi.org/10.1136/ijgc-2024-igcs.424
Primary Topic
Economic and Financial Impacts of Cancer
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

EV305/#1276  Individualised PARP inhibitor dosing: does flexibility impact patient care

Séamus O’Reilly, Vicki Cleary, Eileen Kennedy, Ciarán Murphy et al.
Economic and Financial Impacts of Cancer
article

EV305/#1276  Individualised PARP inhibitor dosing: does flexibility impact patient care

Séamus O’Reilly, Vicki Cleary, Eileen Kennedy, Ciarán Murphy, Dearbhaile Catherine Collins
article en

Abstract

<h3>Introduction</h3> A significant limitation of PARPi, that are used as maintenance treatment in ovarain cancer, is their toxicity profile. Many patients require discontinuation or dose modifications. To optimise patient longevity on treatment, clinical practices may consider individualised dosing for certain patients. Initiating reduced dosages, with or without dose escalation, may improve longterm toxicity and maximise duration of therapy. Little data is available on the impact of individualised dosing. <h3>Methods</h3> A retrospective chart review was performed on 21 patients undergoing PARPi treatment in Cork between 2018 and 2023. Two cohorts were compared: those who received standard dose and those that received reduced-dose in the initial setting. Multiple toxicity profiles were assessed (haematological &amp; non-haematological). Patient outcomes, hospitalisations, and dose reductions/interruptions/escalations were compared between the two subgroups. <h3>Results</h3> Patients undergoing individualised treatment may have an improved toxicity profile compared to those prescribed standard regimens. The impact on progression-free survival between groups was indeterminate due to inter-sample variability. Patients undergoing individualised treatment had fewer events of vomiting (P = 0.476), severe nausea (P &gt; 0.999), anaemia (P &gt; 0.999) and leukopaenia (P &gt; 0.999). Individualised treatment regimens showed a reduction in overall severe toxicities compared to the standard group (83% vs. 33%). Individualised treatment did not improve the proportion of patients experiencing thrombocytopenia. <h3>Conclusion/Implications</h3> Individualised PARP inhibitor therapy may have a non-inferior impact on toxicity and progression-free survival in patients, however the statistical power of this study was limited by a small sample size and various confounding elements. Further research is needed support the results achieved herein.

Cork University Hospital (IE)
Openalex Percentile: Top 72%
Economic and Financial Impacts of Cancer
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.