Neoadjuvant immune checkpoint blockade in women with mismatch repair deficient endometrial cancer: a phase I study

Neoadjuvant immune checkpoint blockade (ICB) has shown unprecedented activity in mismatch repair deficient (MMRd) colorectal cancers, but its effectiveness in MMRd endometrial cancer (EC) remains unknown. In this investigator-driven, phase I, feasibility study (NCT04262089), 10 women with MMRd EC of any grade, planned for primary surgery, received two cycles of neoadjuvant pembrolizumab (200 mg IV) every three weeks. A pathologic response (primary objective) was observed in 5/10 patients, with 2 patients showing a major pathologic response. No patient achieved a complete pathologic response. A partial radiologic response (secondary objective) was observed in 3/10 patients, 5/10 patients had stable disease and 2/10 patients were non-evaluable on magnetic resonance imaging. All patients completed treatment without severe toxicity (exploratory objective). At median duration of follow-up of 22.5 months, two non-responders experienced disease recurrence. In-depth analysis of the loco-regional and systemic immune response (predefined exploratory objective) showed that monoclonal T cell expansion significantly correlated with treatment response. Tumour-draining lymph nodes displayed clonal overlap with intra-tumoural T cell expansion. All pre-specified endpoints, efficacy in terms of pathologic response as primary endpoint, radiologic response as secondary outcome and safety and tolerability as exploratory endpoint, were reached. Neoadjuvant ICB with pembrolizumab proved safe and induced pathologic, radiologic, and immunologic responses in MMRd EC, warranting further exploration of extended neoadjuvant treatment.

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Publication Details

Journal
Nature Communications
Published
2024-09-03
DOI
https://doi.org/10.1038/s41467-024-52098-8
Citations
24
Primary Topic
Endometrial and Cervical Cancer Treatments
Type
article
Field-Weighted Citation Impact
13.99

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article

Neoadjuvant immune checkpoint blockade in women with mismatch repair deficient endometrial cancer: a phase I study

Viktor Hendrik Koelzer, Annegé Vledder, Anneke L. Eerkens, Dominik Loiero et al.
24 citations
Nature Communications
Endometrial and Cervical Cancer Treatments
13.99
article

Neoadjuvant immune checkpoint blockade in women with mismatch repair deficient endometrial cancer: a phase I study

Viktor Hendrik Koelzer, Annegé Vledder, Anneke L. Eerkens, Dominik Loiero, Anna K.L. Reyners, Refika Yigit, Koen Brummel, Tjalling Bosse, Mathilde Jalving, Arja ter Elst, Thijs Roelofsen, Joost Bart, Hans W. Nijman, Diana C.J. Spierings, David N. Church, Marta Requesens, Rie Klomp, Nienke van Rooij, Natascha M. de Lange, René Wardenaar, Marco de Bruyn, Floris Foijer, Patty Klok, Floris-Jan Haan, Annechien Plat, Sterre T. Paijens
article en
24 citations

Abstract

Neoadjuvant immune checkpoint blockade (ICB) has shown unprecedented activity in mismatch repair deficient (MMRd) colorectal cancers, but its effectiveness in MMRd endometrial cancer (EC) remains unknown. In this investigator-driven, phase I, feasibility study (NCT04262089), 10 women with MMRd EC of any grade, planned for primary surgery, received two cycles of neoadjuvant pembrolizumab (200 mg IV) every three weeks. A pathologic response (primary objective) was observed in 5/10 patients, with 2 patients showing a major pathologic response. No patient achieved a complete pathologic response. A partial radiologic response (secondary objective) was observed in 3/10 patients, 5/10 patients had stable disease and 2/10 patients were non-evaluable on magnetic resonance imaging. All patients completed treatment without severe toxicity (exploratory objective). At median duration of follow-up of 22.5 months, two non-responders experienced disease recurrence. In-depth analysis of the loco-regional and systemic immune response (predefined exploratory objective) showed that monoclonal T cell expansion significantly correlated with treatment response. Tumour-draining lymph nodes displayed clonal overlap with intra-tumoural T cell expansion. All pre-specified endpoints, efficacy in terms of pathologic response as primary endpoint, radiologic response as secondary outcome and safety and tolerability as exploratory endpoint, were reached. Neoadjuvant ICB with pembrolizumab proved safe and induced pathologic, radiologic, and immunologic responses in MMRd EC, warranting further exploration of extended neoadjuvant treatment.

Nature CommunicationsVol. 15(1)
Leiden University (NL), University Medical Center Groningen (NL), Centre for Human Genetics (GB), University of Groningen (NL), University of Zurich (CH), John Radcliffe Hospital (GB), University of Oxford (GB), University Hospital of Zurich (CH), Treant Zorggroep (NL), Oxford BioMedica (United Kingdom) (GB), Isala (NL), Erasmus University Rotterdam (NL)
KWF Kankerbestrijding, Universitair Medisch Centrum Groningen
Gender equality
Openalex Percentile: Top 1%
Endometrial and Cervical Cancer Treatments
13.99
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