Neoadjuvant Immunotherapy–Based Systemic Treatment in MMR-Deficient or MSI-High Rectal Cancer: Case Series

Author:

Demisse Rahel12,Damle Neha1,Kim Edward1,Gong Jun3,Fakih Marwan4,Eng Cathy5,Oesterich Leslie1,McKenny Madison6,Ji Jingran1,Liu James1,Louie Ryan7,Tam Kit1,Gholami Sepideh8,Halabi Wissam9,Monjazeb Arta10,Dayyani Farshid11,Cho May1

Affiliation:

1. 1UC Davis Comprehensive Cancer Center, Sacramento, California;

2. 2Loma Linda University Health, Loma Linda Medical Center, Loma Linda, California;

3. 3Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Health System, Los Angeles, California;

4. 4City of Hope National Medical Center, Duarte, California;

5. 5Vanderbilt-Ingram Cancer Center, Nashville, Tennessee;

6. 6Department of Diagnostic Radiology, UC Davis Medical Center, Sacramento, California;

7. 7UC Davis Medical Center, California;

8. 8Department of Surgical Oncology and

9. 9Department of Colorectal Surgery, UC Davis Medical Center, Sacramento, California;

10. 10Department of Radiation Oncology, UC Davis Comprehensive Cancer Center, Sacramento, California; and

11. 11Division of Hematology/Oncology, Department of Medicine, University of California Irvine, Orange, California.

Abstract

Treatment options for locally advanced rectal cancer have continued to consist largely of chemotherapy, chemoradiation, and/or surgical resection. For patients who are unable to undergo these therapeutic modalities or who do not to experience a response to them, treatment options are limited. We report 3 cases of mismatch repair–deficient (dMMR) locally advanced adenocarcinoma of the rectum that showed significant response with neoadjuvant immunotherapy–based systemic treatment. The first patient was not eligible for standard therapy because of a history of radiotherapy to the prostate with concurrent comorbidities and therefore received single-agent pembrolizumab. The second patient did not respond to total neoadjuvant chemoradiation and subsequently received combined nivolumab and ipilimumab. The third patient had a known family history of Lynch syndrome and presented with locally advanced rectal cancer and a baseline carcinoembryonic antigen level of 1,566 ng/mL. She was treated using neoadjuvant pembrolizumab and FOLFOX (folinic acid, fluorouracil, oxaliplatin). In this small series, we suggest that single-agent and combined-modality neoadjuvant immunotherapy/chemotherapy appear to be safe and effective treatment options for patients with (dMMR) locally advanced rectal cancer. Our findings encourage further studies to investigate the role of neoadjuvant immunotherapy as a viable treatment strategy in this population.

Publisher

Harborside Press, LLC

Subject

Oncology

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