In June 2026, China's National Medical Products Administration (NMPA) approved iza-bren (brand name: Yizekang®; generic name: Loncastuximab Eglonatamab), a first-in-class EGFR×HER3 bispecific antibody-drug conjugate (ADC) independently developed by Biokin Pharmaceutical. The approval is for the treatment of patients with relapsed or metastatic nasopharyngeal carcinoma (NPC) following prior therapy.

At the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, Professor Ciara Catherine O'Sullivan from Mayo Clinic, representing the I-SPY 2.2 collaborator group, announced the neoadjuvant treatment results of Rilvegostomig (an anti-PD-1/TIGIT bispecific antibody) combined with Trastuzumab Deruxtecan (T-DXd) for early-stage high-risk HER2-negative breast cancer. Based on innovative Response Predictive Subtypes (RPS), the study aims to improve the pathological complete response (pCR) rate through precise drug combinations and explore the possibility of reducing traditional cytotoxic chemotherapy.

At a recent international academic conference on breast cancer, Professor Claudio Vernieri from the University of Milan and the Fondazione IRCCS Istituto Nazionale dei Tumori shared the latest results of the multicenter, real-world study PALMARES-2. The study focuses on patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer (ABC). It explores the clinical benefits and patient characteristics associated with continuing the original treatment regimen ("Treatment Beyond Progression," TBP) after experiencing disease progression (PD) on first-line endocrine therapy (ET) combined with a CDK4/6 inhibitor (CDK4/6i), providing an important reference for the TBP strategy in clinical practice.

In the evolution of treatment for Multiple Myeloma (MM), moving highly effective therapies forward to the early stages of the disease has become a current research hotspot. For patients with High-Risk Smoldering Multiple Myeloma (HR SMM), whether early active intervention can delay or even prevent its transformation into active myeloma is a focus of clinical attention. At a recent international academic conference, Professor Cyrille Touzeau from the University Hospital of Nantes in France shared the preliminary results of the ERASMM (EMN34) study. This study aimed to evaluate the safety and efficacy of the BCMA×CD3 bispecific antibody Elranatamab in patients with HR SMM. This journal has specially compiled the highlights of the conference for our readers.

In the field of relapsed/refractory classical Hodgkin lymphoma (R/R cHL), although the application of immune checkpoint inhibitors (such as anti-PD-1) and antibody-drug conjugates (such as Brentuximab Vedotin, BV) has significantly improved patient prognosis, clinical challenges remain severe for patients who fail multiple lines of therapy. Recently, at an international academic conference, Professor Enrico Derenzini, on behalf of the PRIMAVERA research team, shared the Phase I study results of the PRMT5 inhibitor AZD3470 in patients with R/R cHL. This journal has summarized the key points of the meeting to provide a deep analysis of this innovative therapy targeting MTAP deficiency and utilizing the "synthetic lethality" mechanism, representing a latest breakthrough in the field of hematologic malignancies.

At a recent international oncology symposium, Professor François-Clément Bidard from Institut Curie shared the updated results from the third data cut-off (DCO3) of the Phase III SERENA-6 study. The study focuses on patients with HR+/HER2- advanced breast cancer (ABC). During first-line treatment with an aromatase inhibitor (AI) combined with a CDK4/6 inhibitor (CDK4/6i), once a new-onset ESR1 mutation is detected via circulating tumor DNA (ctDNA) monitoring, the AI is immediately switched to Camizestrant, a novel oral selective estrogen receptor degrader (SERD), to assess clinical benefit. This report highlights key secondary endpoints—the final progression-free survival 2 (PFS2) and core data such as ctDNA kinetics analysis.

Diffuse Large B-Cell Lymphoma (DLBCL) is the most common subtype of Non-Hodgkin Lymphoma (NHL). Although the R-CHOP regimen has established its position as the cornerstone of first-line treatment, approximately 40% of high-risk patients still face the dilemma of refractory or relapsed disease. At a recent academic conference, Professor Georg Lenz from University Hospital Münster, Germany, on behalf of the research team, released the latest data from the frontMIND study (NCT04824092), exploring the clinical benefits of the anti-CD19 monoclonal antibody Tafasitamab (Tafa) combined with Lenalidomide (Len) and the R-CHOP regimen in patients with previously untreated high-risk DLBCL.

At the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting, Professor Ida Wong-Sefidan (MD) from the AIDS Malignancy Consortium (AMC), on behalf of the research team, shared a milestone study. This study aimed to evaluate the clinical benefits of the Bruton's tyrosine kinase (BTK) inhibitor Ibrutinib in combination with dose-adjusted R-EPOCH (R-da-EPOCH) for the treatment of Human Immunodeficiency Virus-associated Diffuse Large B-cell Lymphoma (HIV-DLBCL). The study results not only confirmed the safety of the regimen but also provided critical data support in terms of efficacy and subgroup survival analysis.