TY - JOUR
T1 - Oligometastatic Rectal Adenocarcinoma Treated With Short-Course Radiation Therapy and Chemotherapy With Nonoperative Intent of the Primary for Locoregional Complete Responders
AU - Schiff, Joshua P.
AU - Chin, Re I.
AU - Roy, Amit
AU - Mahapatra, Lily
AU - Stowe, Hayley B.
AU - Andruska, Neal
AU - Huang, Yi
AU - Mutch, Matthew
AU - Fields, Ryan C.
AU - Hawkins, William G.
AU - Doyle, Maria
AU - Chapman, Will
AU - Tan, Benjamin
AU - Henke, Lauren E.
AU - Badiyan, Shahed N.
AU - DeSelm, Carl
AU - Samson, Pamela P.
AU - Pedersen, Katrina
AU - Kim, Hyun
N1 - Funding Information:
Sources of support: This work had no specific funding. Disclosures: Dr Doyle report honoraria from Medtronics Advisory Board. Dr Henke reports grants from Varian Medical Systems; consulting fees from Varian Medical Systems, Radiologica; honoraria from Varian Medical Systems, ViewRay; and is on the advisory board of ViewRay. Dr Badiyan reports honoraria from Mevion Medical Systems. Dr Pedersen reports grants from AbbVie, Arcus, Array, BioLineRx, Boston Biomedical, BMS, Daiichi Sankyo, Ipsen, MedImmune, Nouscom, Novartis, Pfizer, Pierre Fabre, Rafael, Roche/Genentech, Natera, Arcus; royalties from UpToDate; consulting fees from Pfizer, Array; honoraria from Medscape, Clinical Care Options; support for travel from NCCN, Beigene, Array, NOUSCOM; is on the advisory board of Array, Bayer; and has a leadership position at NCCN Colon, Rectal, Anal, Small Bowel Guidelines Committee, ASCO Annual Meeting Scientific Program Committee. Dr Kim reports grants from Varian Medical Systems; and honoraria from ViewRay, Varian Medical Systems. All other authors have no disclosures to declare.
Publisher Copyright:
© 2022 American Society for Radiation Oncology
PY - 2022/9/1
Y1 - 2022/9/1
N2 - Purpose: Nonoperative management with short-course radiation therapy (SCRT) as a component of definitive therapy for oligometastatic rectal cancer has not been previously reported. This single-institution retrospective analysis evaluates treatment with SCRT in combination with chemotherapy (SCRT-CTX) with nonoperative intent for patients with a locoregional clinical complete response (cCR). Methods and Materials: Thirty-six patients with newly diagnosed oligometastatic rectal cancer were treated with SCRT-CTX between January 1, 2018, and May 31, 2020. Digital rectal examination, endoscopy, and imaging (computed tomography or magnetic resonance imaging) were used to determine cCR. Medically operable patients without cCR underwent surgical resection of the primary rectal tumor. Patients with cCR who experienced a local failure received salvage surgery. Rates of hospitalization related to primary tumor disease and pelvic symptoms were reviewed. Overall survival (OS) and progression free survival were evaluated. Results: Seventeen percent (6/36) of patients achieved cCR after SCRT-CTX. Eleven percent (4) of patients experienced a local failure. OS for all patients was 83% (71%-96%) at 12 months and 57% (41%-80%) at 24 months. Progression free survival for all patients was 56% (41%-74%) at 12 months and 10% (3.1%-35%) at 24 months. On multivariate analysis, having received more than 4 months of chemotherapy (hazard ratio = 0.21; 95% confidence interval, 0.06-0.71; P = .01) and definitive treatment of metastatic site (hazard ratio = 0.17; 95% confidence interval, 0.05-0.66; P = .01) predicted for improved OS. The number of patients requiring hospitalization due to obstruction (8/36, 22%), rectal bleeding (5/36, 14%), or need for permanent ostomy placement (5/36, 14%) was low, and there was a decrease in endorsement of obstructive symptoms and rectal bleeding after completion of SCRT-CTX. Conclusions: SCRT-CTX with nonoperative intent for patients with a locoregional cCR may be a reasonable treatment option for patients with newly diagnosed oligometastatic rectal adenocarcinoma and demonstrates excellent control of pelvic disease and symptoms. Increased duration of chemotherapy within the treatment paradigm may improve oncologic outcomes.
AB - Purpose: Nonoperative management with short-course radiation therapy (SCRT) as a component of definitive therapy for oligometastatic rectal cancer has not been previously reported. This single-institution retrospective analysis evaluates treatment with SCRT in combination with chemotherapy (SCRT-CTX) with nonoperative intent for patients with a locoregional clinical complete response (cCR). Methods and Materials: Thirty-six patients with newly diagnosed oligometastatic rectal cancer were treated with SCRT-CTX between January 1, 2018, and May 31, 2020. Digital rectal examination, endoscopy, and imaging (computed tomography or magnetic resonance imaging) were used to determine cCR. Medically operable patients without cCR underwent surgical resection of the primary rectal tumor. Patients with cCR who experienced a local failure received salvage surgery. Rates of hospitalization related to primary tumor disease and pelvic symptoms were reviewed. Overall survival (OS) and progression free survival were evaluated. Results: Seventeen percent (6/36) of patients achieved cCR after SCRT-CTX. Eleven percent (4) of patients experienced a local failure. OS for all patients was 83% (71%-96%) at 12 months and 57% (41%-80%) at 24 months. Progression free survival for all patients was 56% (41%-74%) at 12 months and 10% (3.1%-35%) at 24 months. On multivariate analysis, having received more than 4 months of chemotherapy (hazard ratio = 0.21; 95% confidence interval, 0.06-0.71; P = .01) and definitive treatment of metastatic site (hazard ratio = 0.17; 95% confidence interval, 0.05-0.66; P = .01) predicted for improved OS. The number of patients requiring hospitalization due to obstruction (8/36, 22%), rectal bleeding (5/36, 14%), or need for permanent ostomy placement (5/36, 14%) was low, and there was a decrease in endorsement of obstructive symptoms and rectal bleeding after completion of SCRT-CTX. Conclusions: SCRT-CTX with nonoperative intent for patients with a locoregional cCR may be a reasonable treatment option for patients with newly diagnosed oligometastatic rectal adenocarcinoma and demonstrates excellent control of pelvic disease and symptoms. Increased duration of chemotherapy within the treatment paradigm may improve oncologic outcomes.
UR - http://www.scopus.com/inward/record.url?scp=85131141126&partnerID=8YFLogxK
U2 - 10.1016/j.prro.2022.04.008
DO - 10.1016/j.prro.2022.04.008
M3 - Article
C2 - 35526826
AN - SCOPUS:85131141126
SN - 1879-8500
VL - 12
SP - e406-e414
JO - Practical Radiation Oncology
JF - Practical Radiation Oncology
IS - 5
ER -