Abstract
Introduction
Some patients with cancer may present with progressive or persistent disease at a
limited number of sites following a period of treatment response. We evaluated the
safety and effectiveness of metastasis-directed radiotherapy (MRT) for oligoprogressive
or oligopersistent disease in patients receiving systemic treatment for metastatic
colorectal cancer (mCRC).
Patients and methods
Patients with mCRC who received 5-fluorouracil, leucovorin, and oxaliplatin; 5-fluorouracil,
leucovorin, and irinotecan; and/or capecitabine chemotherapy between 2011 and 2020
at a single institution were identified. Then, those who underwent MRT for five or
fewer lesion sites while receiving systemic treatment for other metastases were categorized.
The primary endpoint was time to change to systemic therapy. Secondary endpoints included
MRT-related toxicity, overall survival, and local control.
Results
Among 4157 patients included, 91 (2%) received MRT to limited lesion sites (55 oligoprogressive
and 36 oligopersistent) during systemic treatment following a period of treatment
response. The median time to change to next-line systemic therapy was 5 months in
the overall cohort (measured from the current chemotherapy session) and 9.5 (range,
6.0–40.6) months in the MRT group (measured from the MRT session). No severe toxicity
or systemic treatment interruption was observed following MRT. The 1-year local control
and overall survival rates were 69% and 99%, respectively.
Conclusion
In patients with oligoprogressive or oligopersistent mCRC, MRT may be performed safely
in conjunction with systemic treatment to maximize the benefit of systemic therapy
and to prolong the time to change to systemic therapy. Further prospective studies
should confirm these findings.
Keywords
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Article info
Publication history
Published online: November 18, 2021
Accepted:
October 7,
2021
Received in revised form:
October 6,
2021
Received:
August 26,
2021
Identification
Copyright
© 2021 Elsevier Inc. All rights reserved.