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NCT06745076
This phase II trial tests how well personalized reduction of chemotherapy (nivolumab, doxorubicin, vinblastine and dacarbazine) based on circulating tumor deoxyribonucleic acid (ctDNA) evaluation works for treating patients with Hodgkin lymphoma that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Chemotherapy drugs, such as nivolumab, doxorubicin, vinblastine and dacarbazine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Many types of tumors tend to lose cells or release different types of cellular products including their DNA, which is referred to as ctDNA, into the bloodstream before changes can be seen on scans. Health care providers can measure the level of ctDNA in blood or other bodily fluids and, based on the result, assign patients to a reduced number of chemotherapy treatments or the standard number of chemotherapy treatments. Using ctDNA to assign a personalized reduction of chemotherapy may be effective in treating patients with advanced Hodgkin lymphoma.
NCT07209059
This is a single-center, open-label, phase 2 pilot study evaluating the efficacy and safety of a response-adapted first-line treatment strategy for patients with classical Hodgkin lymphoma (cHL) and unfavorable prognostic factors. The FINISH protocol (First-line Immuno-chemotherapy Navigated by Interim PET for Stratification and Hazard minimization In Hodgkin lymphoma) integrates nivolumab into induction therapy and tailors subsequent treatment based on interim PET-CT response. The study also includes exploratory monitoring of circulating tumor DNA (ctDNA) to investigate its role in early response assessment and residual disease detection.
NCT06857500
Classical Hodgkin lymphoma (cHL) is commonly diagnosed in young adults and adults (YP\&A) defined by the National Cancer Institute as 18 to 59 years of age. Clinically, these patients often present with poor prognostic factors such as advanced stage. In phase III trials that primarily include patients aged 18 to 59 years, several international cooperative oncology groups have studied new initial treatments for Ann Arbor stage III and IV cHL. These treatments include traditional dose-dense/dose-intensity cytotoxic approaches (such as the FONDAZIONE ITALIANA LINFOMI FIL-ROUGE trial) or novel selectively active agents such as nivolumab (SWOG S1826 trial) or brentuximab vedotin (BV) (HD21 and ECHELON-1 trials). Among these, the most beneficial initial treatment schedule remains controversial, not only because of additional acute toxicities and additional drug-related expenses, but especially for long-term disease control. Brentuximab Vedotin is a monoclonal antibody conjugated with a protease-cleavable linker to the microtubule disrupting agent monomethylauristatin E, which targets CD30 on Reed-Sternberg cells. The global phase III ECHELON-1 study compared BV in combination with adriamycin, vinblastine, and dacarbazine (BV+AVD) versus adriamycin, bleomycin, vinblastine, and dacarbazine (ABVD) in patients with newly diagnosed stage III and IV cHL. Among the 1,334 patients included, the majority of cases (1,148; 86%) were YP\&A age. At the 51st National Congress of the Italian Society of Hematology, a post-hoc analysis of long-term follow-up data from ECHELON-1 was conducted to assess progression-free survival (PFS) in the subgroup aged 18 to 59 years. YP\&A patients received either BV+AVD (N= 580) or ABVD (N= 568): after 2 years of follow-up, the Kaplan-Mayer curve of PFS for BV+AVD flattened with a plateau that remained consistently at 87% up to 7 years with a number of events of 67 compared to the Kaplan-Mayer curve of PFS for ABVD that decreased during follow-up to 79% with a number of 91 events (HR 0.667; 95% CI: 0.486-0.914; P= 0.011 by log-rank test). Based on the study design, no patients in either arm received consolidation radiotherapy to residual nodal masses (RNM). Low rates of second malignancies (5% for BV+AVD vs. 6% for ABVD), no apparent effect on fertility (pregnancies: 92 for BV+AVD vs. 73 for ABVD), and resolution or improvement of peripheral neuropathy in the majority of patients were reported by the investigators. Additionally, the YP\&A subgroup showed a 7-year overall survival of 97% (number of events, 21) for BV+AVD vs. 92% (number of events, 39) for ABVD (HR, 0.489; 95% CI, 0.287-0.833; P= 0.007 by log-rank test) with a 51% reduction in the risk of death from any cause 13 . These data underscore the clinical benefit of BV+AVD for patients aged 18-59 years, mainly regarding disease cure, with no new safety signals. Therefore, BV+AVD is one of the standards of care for YP\&A with untreated advanced cHL. To date, there have been no studies outside of prospective clinical trials examining the efficacy and safety of BV+AVD for newly diagnosed advanced cHL in patients aged 18-59 years. In this study, involving 3 Italian oncology centers dedicated to the care of HL, we aim to examine a cohort of YP\&A with stage III-IV cHL with a median follow-up of two years after first-line treatment with BV+AVD, with the aim of understanding the outcome and specific side effects in a real-life experience.