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Per RECIST 1.1, PD is defined as at least a 20% increase in the sum of diameters of target lesions. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of ≥5 mm. The appearance of one or more new lesions is also considered PD. DOR as assessed by the investigator per RECIST 1.1 will be presented.",{"measure":26,"description":27,"timeFrame":21},"Progression-free Survival (PFS) Per RECIST 1.1 as Assessed by the Investigator","PFS is defined as the time from the first dose of study treatment to the first documented PD or death due to any cause, whichever occurs first will be assessed by the investigator using RECIST 1.1. Per RECIST 1.1, PD was defined as ≥20% increase in the sum of diameters of target lesions. In addition to the relative increase of 20%, the sum must also demonstrate an absolute increase of ≥5 mm. The appearance of one or more new lesions is also considered PD. PFS as assessed by the investigator per RECIST 1.1 will be presented.",{"measure":29,"description":30,"timeFrame":21},"Overall Survival (OS) Per RECIST 1.1 as Assessed by the Investigator","OS is defined as the time from the first dose of study treatment to death due to any cause as assessed by the investigator per RECIST 1.1 will be presented.",{"measure":32,"description":33,"timeFrame":34},"Area Under the Concentration-Time Curve (AUC) of MK-3120 Antibody-Drug Conjugate (ADC)","Blood samples will be collected to determine the AUC of MK-3120 ADC.","At specified time points up to approximately 43 months",{"measure":36,"description":37,"timeFrame":34},"AUC of MK-3120 Total Antibody (TAb)","Blood samples will be collected to determine the AUC of MK-3120 TAb",{"measure":39,"description":40,"timeFrame":34},"AUC of MK-3120 Free Payload","Blood samples will be collected to determine the AUC of MK-3120 free payload.",{"measure":42,"description":43,"timeFrame":34},"Maximum Concentration (Cmax) 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