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Editorial
. 2024 Jun;9(6):103483.
doi: 10.1016/j.esmoop.2024.103483. Epub 2024 Jun 3.

Systemic treatment of mismatch repair deficient/microsatellite instability-high metastatic colorectal cancer-single versus double checkpoint inhibition

Affiliations
Editorial

Systemic treatment of mismatch repair deficient/microsatellite instability-high metastatic colorectal cancer-single versus double checkpoint inhibition

D Marinelli et al. ESMO Open. 2024 Jun.
No abstract available

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Conflict of interest statement

Disclosure CC reports honoraria from Amgen, Bayer, Merck, Roche, and Servier; carries out consulting or advisory roles for Amgen, Bayer, MSD, and Roche; is on the speakers’ bureau for Servier; reports research funding from Bayer, Merck, and Servier; and reports travel, accommodations, and expenses covered by Roche and Servier. FP reports institutional research grants from BMS, Incyte, Agenus, Amgen, Lilly, and AstraZeneca, and personal fees from BMS, MSD, Amgen, Merck-Serono, Pierre-Fabre, Servier, Bayer, Takeda, Astellas, Johnson & Johnson, Rottapharm, Ipsen, AstraZeneca, GSK, Daiichi-Sankyo, Seagen, and BeiGene. DR has received honoraria from Amgen, MSD, Takeda, and Pierre-Fabre. DS is on the advisory board for Angen, Janssen, Astellas, Bayer, Servier, Novartis, MSD, Merck, Pfizer, and Ipsen. DM, AS, EB, FC, and VP have declared no conflicts of interest.

Figures

Figure 1
Figure 1
Progression-free survival (PFS) in patients with microsatellite instability-high (MSI-H)/mismatch repair deficient (dMMR) metastatic colorectal cancer (mCRC) treated with first-line immunotherapy or chemotherapy in the KEYNOTE-177 and CheckMate-8HW clinical trials. Chemo, chemotherapy; CI, confidence interval; CM, CheckMate; HR, hazard ratio; Ipi, ipilimumab; KN-177, KEYNOTE-177; Nivo, nivolumab.

References

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