TY - JOUR
T1 - Complete Pathologic Response to Neoadjuvant Chemoimmunotherapy and Oxaliplatin-Induced Fever Associated With IL-6 Release in a Patient With Locally Advanced Colon Cancer
AU - Copur, Mehmet Sitki
AU - Schroeder, Caleb
AU - Ly, Quan
AU - Wedel, Whitney
AU - Kelly, Jacqueline R.
AU - Rodriguez, Paul
AU - Tun, Soe Min
AU - Lintel, Nicholas
AU - Horn, Adam
AU - Riley, Bronson
N1 - Funding Information:
consultant/advisory role for Exelixis, Tempus, and OncLive. He also has received funding for travel, accommodations, and expenses from the following: AstraZeneca, Bristol Myers Squibb, Merck, Foundation Medicine, Guardant Health, Ipsen, and Janssen. AJF has served as a consultant and received research funding from iRhythm Technologies. MMS has no COIs. AAD has had travel expenses paid by Menarini Silicon Biosystems.
Funding Information:
do not report any conflicts of interest. This work was supported by a training grant from the National Center for advancing Translational Sciences, National Institutes of Health (uL1 Tr001860). The funding agency was not involved in the study design; the collection, analysis, and interpretation of data; the writing of the report; or the decision to submit the article for publication.
Publisher Copyright:
© 2022 UBM Medica Healthcare Publications. All rights reserved.
PY - 2022
Y1 - 2022
N2 - Neoadjuvant systemic therapy is a preferred treatment approach for a number of tumor types due to many potential advantages over upfront surgery, including tumor downstaging, early treatment of micrometastatic disease, and providing an in vivo test of tumor biology. For colon cancer, current standard of care is upfront surgery followed by adjuvant systemic therapy in high-risk patients. Concerns about inaccurate radiological staging and tumor progression during preoperative treatment, as well the lack of randomized data demonstrating benefit, are among the reasons for the limited use of neoadjuvant therapy in this disease. Locally advanced colon cancer, defined as primary colon cancer with direct invasion into the adjacent structures or extensive regional lymph node involvement, is not always amenable to pathological complete resection, and when attempted it comes with high incidence of postoperative morbidity and mortality because of the required multivisceral resection. Clinical trials of neoadjuvant chemotherapy for colon cancer to date have been promising with downstaging of disease and higher rates of R0 resection. Here, we report a case of a patient with locally advanced, unresectable, mismatch repair deficient sigmoid colon cancer who was treated with neoadjuvant chemoimmunotherapy followed by surgical resection leading to a complete pathologic response after preoperative systemic chemoimmunotherapy.
AB - Neoadjuvant systemic therapy is a preferred treatment approach for a number of tumor types due to many potential advantages over upfront surgery, including tumor downstaging, early treatment of micrometastatic disease, and providing an in vivo test of tumor biology. For colon cancer, current standard of care is upfront surgery followed by adjuvant systemic therapy in high-risk patients. Concerns about inaccurate radiological staging and tumor progression during preoperative treatment, as well the lack of randomized data demonstrating benefit, are among the reasons for the limited use of neoadjuvant therapy in this disease. Locally advanced colon cancer, defined as primary colon cancer with direct invasion into the adjacent structures or extensive regional lymph node involvement, is not always amenable to pathological complete resection, and when attempted it comes with high incidence of postoperative morbidity and mortality because of the required multivisceral resection. Clinical trials of neoadjuvant chemotherapy for colon cancer to date have been promising with downstaging of disease and higher rates of R0 resection. Here, we report a case of a patient with locally advanced, unresectable, mismatch repair deficient sigmoid colon cancer who was treated with neoadjuvant chemoimmunotherapy followed by surgical resection leading to a complete pathologic response after preoperative systemic chemoimmunotherapy.
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U2 - 10.46883/2022.25920944
DO - 10.46883/2022.25920944
M3 - Article
C2 - 35180339
AN - SCOPUS:85124931697
SN - 0890-9091
SP - 115
EP - 119
JO - Oncology
JF - Oncology
IS - 3602
ER -