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Featured Image: General views at the American Society for Clinical Oncology (ASCO) annual meeting. Courtesy: © ASCO/Max Gersh 2015. Used with permission.

Advances, Sequencing Challenges, and Real-World Integration of ADCs in Breast Cancer:...

Advances, Sequencing Challenges, and Real-World Integration of ADCs in Breast Cancer: Insights from ASCO 2026
General images of ESMO 2019 Congress being held in Barcelona, Spain, September 27 - October 1, 2019. Courtesy European Society for Medical Oncology (ESMO). Used with Permission.

ESMO 2025: Salubris Presents Favorable Safety and PK profile, with Encouraging...

Data from the dose escalation portion of the Phase 1/2 study of JK06 in patients with unresectable locally advanced or metastatic cancer, including non-small cell lung cancer (NSCLC) and breast cancer, is being presented at the European Society for Medical Oncology (ESMO) Congress, being held October 17 - 21, 2025, in Berlin, Germany.[1]

New Molecular Degraders Offer Hope for ‘Undruggable” Aggressive Breast Cancer

In a major stride toward tackling aggressive breast cancer, researchers from The Hebrew University of Jerusalem have developed druglike molecules that degrade a previously “undruggable” cancer-driving protein.

ASCO 2025: Sacituzumab Govitecan + Pembrolizumab Reduces Risk of Disease progression...

The combination of sacituzumab govitecan (Trodelvy®; Gilead Sciences; See ADC Drugmap)* + pembrolizumab (Keytruda®; Merck & Co/MSD) reduced the risk of disease progression or death by 35% (HR: 0.65) versus standard of care (SoC) pembrolizumab plus chemotherapy in first-line treatment for patients with PD-L1+ (CPS ≥10) metastatic triple-negative breast cancer (TNBC).
Featured Image - Laboratory. Courtesy 2019 Fotolia

Disitamab Vedotin Gains Approval in China for its Third Indication

Disitamab Vedotin Gains Approval in China for its Third Indication

Trastuzumab deruxtecan Followed by THP Before Surgery Showed Statistically Significant and...

Now positive topline results from a new study, the DESTINY-Breast11 phase 3 trial (NCT05113251), confirmed that trastuzumab deruxtecan (Enhertu®; Daiichi Sankyo and AstraZeneca)**, followed by paclitaxel, trastuzumab and pertuzumab (THP), demonstrated a statistically significant and clinically meaningful improvement in pCR rate versus Standard-of-Care (SoC; dose-dense doxorubicin and cyclophosphamide followed by THP [ddAC-THP]) when used in the neoadjuvant setting in patients with high-risk, locally advanced HER2-positive early-stage breast cancer.

Emiltatug Ledadotin (XMT-1660) Encouraging Data in mTNBC; Receives Fast Track Designation

The U.S. Food and Drug Administration (FDA) recently granted an additional Fast Track designation to emiltatug ledadotin (XMT-1660; see ADC Drugmap), an antibody-drug conjugate (ADC) targeting B7-H4 (VTCN1), an immune-suppressive plasma membrane protein that is overexpressed in multiple tumor types, including in breast, ovarian, and endometrial cancers, with relatively little or no expression in normal, or healthy, tissues.

SABCS 2024: Disitamab Vedotin Demonstrates Clinically Meaningful Results in the Treatment...

In 2022, with an estimated 2.3 million new cases and nearly 700.000 deaths globally, breast cancer emerged as the most prevalent cancer after lung...
Speakers and attendees during the morning sessions on Wednesday December 11, 2019. during the San Antonio Breast Cancer Symposium being held at the Henry B. Gonzalez Convention Center in San Antonio, TX. This year is the 42nd Anniversary of the meeting where over 7,500 physicians, researchers, patient advocates and healthcare professionals from over 90 countries attended the meeting which features the latest research on breast cancer treatment and prevention. Photo Courtesy 2019 © MedMeetingImages/Todd Buchanan

SABCS: Updated Data of Izalontamab Brengitecan/BL-B01D1 in Breast Cancer

The current study results presented at the 2024 San Antonio Breast Cancer Symposium (SABCS) confirm the encouraging efficacy seen in previously treated patients with metastatic and locally advanced breast cancer subtypes, particularly in earlier lines of therapy. The safety and tolerability of Izalontamab Brengitecan are consistent with previously published data.

FDA Grants Fast Track Designation to Rinatabart Sesutecan for Patients with...

The U.S. Food and Drug Administration (FDA) has granted Fast Track designation for rinatabart sesutecan (Rina-S; PRO1184), a folate receptor alpha (FRα / FOLR1)...