AI Article Synopsis

  • The study evaluated the effectiveness of panitumumab in frail or elderly patients with RAS wild-type unresectable colorectal cancer who had not received prior chemotherapy.
  • Among the 36 enrolled patients, those with left-sided tumors (LSTs) had a median overall survival of 19.3 months, while those with right-sided tumors (RSTs) had 12.3 months, indicating a significant survival advantage for LSTs.
  • The findings suggest that panitumumab may be a beneficial treatment for this patient group, particularly for those with left-sided tumors.

Article Abstract

Background: We previously reported the response rate of a phase II OGSG1602 study on panitumumab in chemotherapy-naive frail or elderly patients with RAS wild-type unresectable colorectal cancer (CRC) [Terazawa T, Kato T, Goto M, et al. Oncologist. 2021;26(1):17]. Herein, we report a survival analysis.

Methods: Patients aged ≥65 years and considered unsuitable for intensive chemotherapy or aged ≥76 years were enrolled. Primary tumors located from the cecum to the transverse colon were considered right-sided tumors (RSTs); those located from the splenic flexure to the rectum were considered left-sided tumors (LSTs).

Results: Among the 36 enrolled patients, 34 were included in the efficacy analysis, with 26 and 8 having LSTs and RSTs, respectively. The median progression-free survival (PFS) and overall survival (OS) were 6.0 [95% CI, 5.4-10.0] and 17.5 months (95% CI, 13.8-24.3), respectively. Although no significant differences existed in PFS between patients with LST and RST {6.6 (95% CI, 5.4-11.5) vs. 4.9 months [95% CI, 1.9-not available (NA), P = .120]}, there were significant differences in OS [19.3 (95% CI, 14.2-NA) vs.12.3 months (95% CI, 9.9-NA), P = .043].

Conclusion: Panitumumab showed favorable OS in frail or elderly patients with RAS wild-type CRC and no prior exposure to chemotherapy. Panitumumab may be optimal for patients with LSTs (UMIN Clinical Trials Registry Number UMIN000024528).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322121PMC
http://dx.doi.org/10.1093/oncolo/oyac145DOI Listing

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