Panelists discuss how treatment decisions for advanced endometrial cancer (EC) patients after progressing on immune-oncology (IO) therapy are guided by clinical trial data, real-world evidence, biomarker status, initial therapy response, and patient-specific factors to personalize subsequent treatment strategies.
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Summary for Physicians: Data Guiding Treatment Decisions Post-IO in Advanced EC
Treatment decisions for patients with advanced EC after progressing on IO therapy are primarily guided by clinical data, including results from clinical trials, real-world studies, and biomarkers. Key factors include:
Clinical Trial Data:
Data from clinical trials, especially those investigating second-line or combination therapies, are crucial in guiding treatment after IO failure. For instance, studies evaluating pembrolizumab combined with lenvatinib have shown promising results for patients with mismatch repair deficient (dMMR) or microsatellite instability-high (MSI-H) tumors, influencing the decision to continue or change treatment.
The effectiveness of other IO combinations, such as combining immune checkpoint inhibitors with antiangiogenic agents, informs whether these strategies could be applied in patients who have progressed on IO monotherapy.
Real-World Evidence:
Real-world data, such as studies on the use of IO therapies in advanced or recurrent EC, help clinicians understand how treatments work outside the controlled environment of clinical trials. This data is valuable in guiding treatment decisions, particularly when assessing long-term outcomes and adverse events associated with IO therapy in routine practice.
Research from studies such as S. Huepenbecker et al. (2024) provides insights into how IO therapies are being used in clinical settings, helping physicians to weigh the potential benefits and risks for their patients.
Biomarker Data:
Biomarkers such as MMR status, MSI, and tumor mutational burden play an essential role in guiding treatment decisions post-IO therapy. For example, patients with dMMR or MSI-H tumors may still benefit from further IO treatments, while others without these biomarkers may require alternative therapies.
New data on biomarker-guided therapy is helping to refine which patients are more likely to respond to second-line IO or combination therapies.
Response to Initial IO Therapy:
The initial response to IO therapy significantly influences decisions regarding subsequent treatment. If a patient had a positive response to IO therapy, there may be a rationale to continue with IO or pursue a different combination therapy.
For patients who did not respond to IO therapy or who experienced progression during treatment, the data from trials investigating chemotherapy, targeted therapies, or other combination strategies inform whether switching to these treatments might be more effective.
Patient-Specific Factors:
Patient performance status and overall health status, including comorbidities, are also considered when deciding on treatment after IO therapy. These factors may guide whether more aggressive treatments, such as chemotherapy or experimental agents, are appropriate.
Physician experience and judgment, along with patient preferences, can also influence the treatment approach when the available data offer multiple options.
In summary, treatment decisions after IO therapy in advanced EC are guided by clinical trial results, real-world evidence, biomarker data, and the patient's initial response to IO therapy. These combined factors help clinicians personalize treatment plans to optimize patient outcomes and select the most appropriate therapies in the post-IO setting.