Pathological Tumor Response Following Immune Checkpoint Blockade for Deficient Mismatch Repair Advanced Colorectal Cancer

Author:

Ludford Kaysia1ORCID,Cohen Romain2,Svrcek Magali3,Foo Wai Chin4,Colle Raphael2,Parc Yann5,Thomas Jane Varkey6,Morris Van Karlyle6,Kopetz Scott6,Chang George J7,Overman Michael6,Andre Thierry2

Affiliation:

1. Division of Cancer Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX, USA

2. Department of Medical Oncology, Hôpital Saint-Antoine, AP-HP, Sorbonne Université, F-7512 Paris, France

3. Department of Pathology, Hôpital Saint-Antoine, AP-HP, Sorbonne Université, F-7512 Paris, France

4. Division of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA

5. Department of Digestive Surgery, Hôpital Saint-Antoine, AP-HP, Sorbonne Université, F-7512 Paris, France

6. Department of Gastrointestinal Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA

7. Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA

Abstract

Abstract Immune checkpoint inhibition (CPI) for metastatic colorectal cancer (mCRC) with deficient mismatch repair (dMMR) demonstrates high clinical activity that appears durable, but the impact of CPI on pathological tumor response is unknown. In this retrospective analysis, our objective was to assess pathological response and clinical outcomes in dMMR mCRC patients treated with CPI prior to surgical resection of primary and/or metastatic tumor. Among 121 advanced dMMR mCRC patients treated with CPI at 2 institutions between November 2016 and December 2018, 14 underwent surgery. Pathologic complete response was noted in the resected specimens of 13 patients despite the presence of residual tumor on preoperative imaging in 12 of those patients. With median follow-up of 9 months, no patients have had disease relapse or progression. For this small retrospective study, the data suggest that residual radiographic tumor may not require systematic resection following response to anti-PD1–based therapy. However, larger prospective studies are warranted.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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