What do oncologists think of the OlympiA trial (LYNPARZA®)?
OlympiA — Adjuvant gBRCAm, HER2-negative, high-risk early breast cancer (1 year of olaparib)
FDA APPROVED · Mar 2022FDA-approved March 11, 2022, for the adjuvant treatment of adults with deleterious or suspected deleterious germline BRCA-mutated, HER2-negative, high-risk early breast cancer who have been treated with neoadjuvant or adjuvant chemotherapy; patients are selected by an FDA-approved companion diagnostic.
Physician voices — verbatim
Full physician voice list (13)
Full conference coverage and trial data: KOL Pulse trial profile coming soon.
What do oncologists think of the OlympiaN trial (LYNPARZA®)?
OlympiaN — Neoadjuvant, chemotherapy-free olaparib +/- durvalumab in gBRCAm, ER-negative/low, HER2-negative early-stage breast cancer (INVESTIGATIONAL)
INVESTIGATIONAL · neoadjuvant BRCAm early BCInvestigational. OlympiaN is a phase 2 study of neoadjuvant, chemotherapy-free olaparib — alone or with durvalumab — in germline BRCA-mutated, ER-negative/low, HER2-negative early (stage I-II) breast cancer. This neoadjuvant use is not FDA-approved. Presented at SABCS 2025.
Physician voices — verbatim
Full physician voice list (5)
Full conference coverage and trial data: KOL Pulse trial profile coming soon.
LYNPARZA® — FDA status
FDA APPROVEDLYNPARZA® (olaparib) is an FDA-approved PARP inhibitor used across several cancers — including germline BRCA-mutated, HER2-negative breast cancer (both high-risk early and metastatic disease), BRCA- and HRR-mutated advanced prostate cancer, BRCA-mutated advanced ovarian cancer and ovarian-cancer maintenance, and BRCA-mutated metastatic pancreatic cancer. For the full, current list of FDA indications and prescribing information, see lynparza.com or FDA label (DailyMed). KOL Pulse indexes the physician conversation; the label is owned and maintained by the manufacturer.
LYNPARZA® sentiment — FAQ
OlympiA
What do oncologists think of the OlympiA trial (LYNPARZA®)?
Across 13 verified physician voices in KOL Pulse's index for OlympiA, 0% expressed positive sentiment, 0% were nuanced (praising the result while flagging a caveat), 100% were neutral, and 0% were critical. Positive voices highlight the sustained invasive- and distant-disease-free-survival and overall-survival benefit of one year of adjuvant olaparib on long-term follow-up, and the move of a PARP inhibitor into the curative-intent adjuvant setting; nuanced and critical voices flag long-term tolerability, patient selection and germline testing access, and open questions such as PALB2 and combination/sequencing with immunotherapy.
Where can I find the OlympiA trial data for LYNPARZA® (olaparib)?
OlympiA is registered as NCT02032823 and studied LYNPARZA® (olaparib) in Adjuvant gBRCAm, HER2-negative, high-risk early breast cancer (1 year of olaparib). KOL Pulse's OlympiA trial profile is coming soon.
OlympiaN
What do oncologists think of the OlympiaN trial (LYNPARZA®)?
Across 5 verified physician voices in KOL Pulse's index for OlympiaN, 40% expressed positive sentiment, 20% were nuanced (praising the result while flagging a caveat), 40% were neutral, and 0% were critical. Positive voices highlight the high pathologic-complete-response rates achieved with a chemotherapy-free neoadjuvant PARP-inhibitor regimen in early BRCA-mutated breast cancer, and the prospect of de-escalating chemotherapy; nuanced and critical voices flag the small, non-randomized phase 2 design, the immaturity of event-free and survival outcomes, and how many patients are needed before this is practice-ready.
Where can I find the OlympiaN trial data for LYNPARZA® (olaparib)?
OlympiaN is registered as NCT05498155 and studied LYNPARZA® (olaparib) in Neoadjuvant, chemotherapy-free olaparib +/- durvalumab in gBRCAm, ER-negative/low, HER2-negative early-stage breast cancer (INVESTIGATIONAL). KOL Pulse's OlympiaN trial profile is coming soon.
Regulatory
Is LYNPARZA® (olaparib) FDA approved?
LYNPARZA® is FDA-approved. KOL Pulse organizes this page by clinical trial and links out to the manufacturer's brand site and the FDA label for the full, current list of FDA indications and prescribing information — the label is owned and updated by the manufacturer, so we point to it rather than reproducing it.