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Bispecific Toxicity Management in DLBCL Care

Robert Mancini, PharmD, discusses bispecific therapy advancements and strategies to manage adverse effects in diffuse large B-cell lymphoma (DLBCL) care, offering insights on toxicity phases, monitoring, and patient care.

Zahra mahmoudjafariAamir aliRobert manciniPractice pearlsBispecific antibodiesClinical trialsResponse ratesDuration of responseProgression free survivalToxicity profilesTrial designPatient cohortsBiospecific treatmentsLymphoma therapyStep up dosingOutpatient administration

Implementing Bispecific Treatments

Panelists explore the challenges, implementations, and decision-making processes surrounding bispecific treatments in DLBCL (diffuse large B cell lymphoma).

Emerging roleBispecific antibodiesDiffuse largeb cell lymphoma managementClinical trialsResponse ratesDuration of responseProgression free survivalToxicity profilesTrial designPatient cohortsBiospecific treatmentsLymphoma therapyStep up dosingOutpatient administrationPatient educationSide effect management

Patient Education and Monitoring in DLBCL Treatment

Health care experts provide insights into patient education, shared decision-making, and treatment monitoring in DLBCL (diffuse large B cell lymphoma) therapies, reviewing education strategies and response monitoring.

Emerging roleBispecific antibodiesDiffuse largeb cell lymphoma managementClinical trialsResponse ratesDuration of responseProgression free survivalToxicity profilesTrial designPatient cohortsBiospecific treatmentsLymphoma therapyStep up dosingOutpatient administrationPatient educationSide effect management

Real-World Study Shows Patients Treated with IMBRUVICA® (ibrutinib) Were Less Likely to Initiate a Next-Line Treatment than Patients on Acalabrutinib in First-line Chronic Lymphocytic Leukemia

Real-World Study Shows Patients Treated with IMBRUVICA® (ibrutinib) Were Less Likely to Initiate a Next-Line Treatment than Patients on Acalabrutinib in First-line Chronic Lymphocytic Leukemia
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United statesBryan jacobsImran khanChristie corbettNone of the janssen pharmaceutical companiesAtrium health levine cancer instituteJanssen biotech incAmerican society of hematology annual meetingDrug administrationJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonExchange commissionAmerican society of hematologyDivision of lymphoma therapy researchCompanies of johnson

Johnson & Johnson : Real-World Study Shows Patients Treated with IMBRUVICA® (ibrutinib) Were Less Likely to Initiate a Next-Line Treatment than Patients on Acalabrutinib in First-line Chronic Lymphocytic Leukemia

NEW ORLEANS, December 12, 2022 - The Janssen Pharmaceutical Companies of Johnson & Johnson today announced results of a real-world study showing that patients with chronic. | December 12, 2022

United statesBryan jacobsImran khanChristie corbettNone of the janssen pharmaceutical companiesAtrium health levine cancer instituteJanssen biotech incAmerican society of hematology annual meetingDrug administrationJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonExchange commissionAmerican society of hematologyDivision of lymphoma therapy researchCompanies of johnson