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Outcomes favoring robotic surgery for CRC may be influenced by patient selection factors, including clinical stability.
Robotic Surgery Exhibits Benefit in Select Colorectal Cancer Procedures

August 17th 2025

Outcomes favoring robotic surgery for CRC may be influenced by patient selection factors, including clinical stability.

Data suggest that sotorasib plus panitumumab may represent a valuable new treatment option in this KRAS G12C-mutated colorectal cancer population.
Sotorasib Combo Improves Patient-Reported Outcomes in KRAS G12C+ CRC

August 17th 2025

An update of phase 1 data from the CTMX-2051-101 study is expected to be available by the first quarter of 2026.
Safety Review Committee Supports CX-2051 Trial Continuation in Solid Tumors

August 15th 2025

Phase 2 CRDF-004 results revealed that the addition of onvansertib to chemotherapy/bevacizumab was well-tolerated, with no unexpected toxicities observed.
Onvansertib Exhibits Encouraging Responses in RAS-Mutant Metastatic CRC

July 30th 2025

Data from the phase 3 BEACON CRC trial support the approval of encorafenib plus cetuximab for this colorectal cancer population in China.
Encorafenib Combo Earns Chinese Approval in BRAF V600E+ Metastatic CRC

July 13th 2025

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Improving the Toxicity of Irinotecan/5-FU/ Leucovorin: A 21-Day Schedule

September 1st 2003

Irinotecan (CPT-11, Camptosar) is one of the new generation ofchemotherapeutic agents that has activity in advanced colorectal cancer.It has antitumor efficacy as a single agent, and also has beencombined with fluorouracil (5-FU) and leucovorin (IFL) to treat thesepatients. Randomized studies have confirmed the superiority of IFL to5-FU and leucovorin alone with regard to patient survival, time toprogression, and tumor response rate. The optimal schedule for combiningthese agents remains uncertain, but in the United States, theschedule of IFL weekly for 4 consecutive weeks repeated every 6 weeks,according to the schedule reported by Saltz et al, has been widely used,although with some toxicity (especially myelosuppression and diarrhea).In an attempt to improve the tolerability of IFL, some haveadvocated modifying the schedule of IFL to weekly for 2 weeks, withrepeated cycles every 21 days. Twenty-three patients with advancedcolorectal cancer have been treated on this schedule at a single institution.Therapy was well tolerated, with 35% of patients experiencinggrade 3/4 neutropenia, two of whom had episodes of febrile neutropenia,and 9% with grade 3/4 diarrhea. The median relative dose intensityof irinotecan administered in the first 18 patients treated with thisregimen was 94%. These data support the hypothesis that modifying theschedule of administration of IFL improves the tolerability and abilityto deliver the regimen, but must be confirmed by randomized prospectivestudies, which may also attempt to evaluate the role of bolus 5-FUin the treatment of advanced colorectal cancer.