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O'Donnell, Conor D J

0009-0009-6291-846X

Mayo Clinic

Division of Oncology, Mayo Clinic, Jacksonville, FL 32224, USA.

Citations 12

Circulating Tumor DNA Predicts Early Recurrence Following Locoregional Therapy for Oligometastatic Colorectal Cancer
O'Donnell, C. , Naleid, Nikolas , Siripoon, Teerada , Zablonski, Kevin , Storandt, Michael H. , Hallemeier, Christopher L. , Conces, Madison , Bajor, David L. , Starlinger, Patrick , Atwell, Thomas D. , Mitchell, Jessica L. , Mahipal, Amit , Jin, Zhaohui , O'Donnell, Conor D J , Zablonski, Kevin G , Starlinger, Patrick , Mitchell, Jessica , Mahipal, Amit , Jin, Zhaohui , Selfridge, Jennifer Eva , Hallemeier, Christopher Leigh , Jethwa, Krishan R. , Thiels, Cornelius A. , Warner, Susanne G.

Cancers | July 1, 2024 | Volume: 16 | Issue: 13 | Pages: 2407

10.3390/cancers16132407 Get It

(1) Background: Local therapies offer a potentially curative approach for patients with oligometastatic colorectal cancer (CRC). An evidence-based consensus recommendation for systemic therapy following definitive locoregional therapy is lacking. Tumor-informed circulating tumor DNA (ctDNA) might provide information to help guide management in this setting. (2) Methods: A multi-institutional retrospective study was conducted, including patients with CRC that underwent curative-intent locoregional therapy to an isolated site of metastatic disease, followed by tumor-informed ctDNA assessment. The Kaplan–Meier method and log-rank tests were used to compare disease-free survival based on ctDNA results. ctDNA test performance was compared to carcinoembryonic antigen (CEA) test results using McNemar’s test. (3) Results: Our study cohort consisted of 87 patients treated with locoregional interventions who underwent ctDNA testing. The initial ctDNA test post-intervention was positive in 28 patients and negative in 59 patients. The median follow-up time was 14.0 months. Detectable ctDNA post-intervention was significantly associated with early disease recurrence, with a median disease-free survival (DFS) of 6.63 months compared to 21.30 months in ctDNA-negative patients (p < 0.001). ctDNA detected a numerically higher proportion of recurrences than CEA (p < 0.097). Post-intervention systemic therapy was not associated with improved DFS (p = 0.745). (4) Conclusions: ctDNA results are prognostically important in oligometastatic CRC, and further prospective studies are urgently needed to define its role in guiding clinical decisions.
Updates on the Management of Colorectal Cancer in Older Adults
O'Donnell, C. , Hubbard, Joleen M. , Jin, Zhaohui , O'Donnell, Conor D J , Hubbard, Joleen , Jin, Zhaohui

Cancers | May 10, 2024 | Volume: 16 | Issue: 10 | Pages: 1820

10.3390/cancers16101820 Get It

Colorectal cancer (CRC) poses a significant global health challenge. Notably, the risk of CRC escalates with age, with the majority of cases occurring in those over the age of 65. Despite recent progress in tailoring treatments for early and advanced CRC, there is a lack of prospective data to guide the management of older patients, who are frequently underrepresented in clinical trials. This article reviews the contemporary landscape of managing older individuals with CRC, highlighting recent advancements and persisting challenges. The role of comprehensive geriatric assessment is explored. Opportunities for treatment escalation/de-escalation, with consideration of the older adult’s fitness level. are reviewed in the neoadjuvant, surgical, adjuvant, and metastatic settings of colon and rectal cancers. Immunotherapy is shown to be an effective treatment option in older adults who have CRC with microsatellite instability. Promising new technologies such as circulating tumor DNA and recent phase III trials adding later-line systemic therapy options are discussed. Clinical recommendations based on the data available are summarized. We conclude that deliberate efforts to include older individuals in future colorectal cancer trials are essential to better guide the management of these patients in this rapidly evolving field.