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Tropomodulin 3 Overexpression as a Marker for Platinum Resistance and Immune Infiltration in Ovarian Cancer
Published on: August 2, 2024
A phase II trial of intraperitoneal interleukin-2 in patients with platinum-resistant or platinum-refractory ovarian
Anda M Vlad1, Raluca A Budiu, Diana E Lenzner
1Department of Obstetrics, Gynecology, and Reproductive Sciences, University of Pittsburgh School of Medicine, 300 Halket Str, Pittsburgh, PA 15213, USA.
Abstract:
Ovarian cancer patients with persistent (platinum-resistant) or progressive (platinum-refractory) disease respond poorly to second line chemotherapy and have low survival expectancy. New and improved therapeutic approaches are needed and immune biologics are one possibility. Interleukin-2 (IL-2) is a T-cell growth factor believed to be important in anti-tumor immunity. We performed a phase II clinical trial with intraperitoneal (IP) recombinant IL-2 administered in weekly infusions of 6 x 10(5) IU/m2. Thirty-one subjects were sequentially entered into the study and clinical responses were surgically confirmed in 24 patients. The primary end point of this study was clinical response with immunologic measurements as secondary end points. The IP regimen was generally well tolerated. Of the 24 patients assessed for response, there were 6 (4 complete, 2 partial) responses for an overall response rate of 25.0% [95% confidence interval (CI) of 11-45]. The median survival of the 31 patient cohort was 2.1 years (95% CI of 1.3-4.4), but for the 6 patients with responses the median survival has not been reached (range 24-120+ months). Eosinophil and lymphocyte numbers were continuously monitored during treatment. Peripheral blood eosinophils were markedly increased at the completion of treatment (p < 0.0001) and associated with increased circulating eotaxin (p = 0.03). We also found significant associations between changes in CD3 counts and survival (p = 0.05) and between IFNγ- secreting CD8 T cells at early time points and survival (p = 0.04). This study provides important evidence for IP IL-2 in platinum-resistant ovarian cancer and identifies several immune correlates of survival.
Insights
Intraperitoneal recombinant Interleukin-2 (IL-2) shows promise for platinum-resistant ovarian cancer, offering a new therapeutic avenue. This immunotherapy approach demonstrated a 25% response rate and improved survival in a phase II trial.
Area of Science:
- Oncology
- Immunotherapy
- Clinical Trials
Background:
- Platinum-resistant ovarian cancer has poor prognosis and limited treatment options.
- Interleukin-2 (IL-2), a T-cell growth factor, plays a role in anti-tumor immunity.
- Novel therapeutic strategies, including immune biologics, are needed.
Purpose of the Study:
- To evaluate the efficacy and safety of intraperitoneal (IP) recombinant IL-2 in patients with platinum-resistant ovarian cancer.
- To assess clinical responses and identify immune correlates of survival.
Main Methods:
- Phase II clinical trial involving weekly IP infusions of recombinant IL-2 (6 x 10^5 IU/m2).
- Thirty-one patients with persistent or progressive platinum-resistant ovarian cancer were enrolled.
- Clinical responses were surgically confirmed; immunologic markers were secondary endpoints.
Main Results:
- An overall response rate of 25.0% (6/24 patients) was observed, including 4 complete and 2 partial responses.
- Median survival for the entire cohort was 2.1 years; median survival was not reached for responders.
- Treatment led to increased peripheral blood eosinophils and circulating eotaxin; changes in CD3 counts and IFNγ-secreting CD8 T cells correlated with survival.
Conclusions:
- IP recombinant IL-2 is a generally well-tolerated and potentially effective treatment for platinum-resistant ovarian cancer.
- The study provides evidence supporting IL-2 immunotherapy and identifies immune biomarkers associated with improved survival outcomes.
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