Research Summaries

FDA Alert
FDA Alert
05/18/2026
Anthony Calabro, MA
The FDA approved Enhertu for neoadjuvant treatment of adults with HER2-positive stage II or III breast cancer and adjuvant treatment of patients with residual invasive disease after neoadjuvant therapy. ...
05/18/2026
FDA Alert
FDA Alert
05/15/2026
Anthony Calabro, MA
The FDA approved Bizengri for adults with advanced, unresectable, or metastatic NRG1 fusion-positive cholangiocarcinoma after prior systemic therapy, providing a new targeted option for an ultra-rare and...
05/15/2026
Research Summary
Research Summary
05/14/2026
Ashton L. Stahl
Phase 3 data evaluated whether relacorilant plus nab-paclitaxel improves survival in platinum-resistant ovarian cancer.
05/14/2026
Research Summary
Research Summary
05/14/2026
Anthony Calabro, MA
In an open-label, multicenter phase 2 study, frontline mantle cell lymphoma, MRD-driven acalabrutinib-lenalidomide anti-CD20 therapy produced high molecular complete response rates.
05/14/2026
Research Summary
Research Summary
05/14/2026
Anthony Calabro, MA
In phase 1/2 BRUIN, most patients with CLL/SLL or MCL had stable or improved PROs during pirtobrutinib treatment.
05/14/2026
FDA Approval
FDA Approval
05/14/2026
Ashton L. Stahl
The FDA has approved sonrotoclax for adults with relapsed or refractory mantle cell lymphoma who have received prior BTK inhibitor therapy.
05/14/2026
FDA Approval
FDA Approval
05/04/2026
Anthony Calabro, MA
On May 1, the FDA approved vepdegestrant (Veppanu), a heterobifunctional protein degrader, for adults with estrogen receptor–positive, human epidermal growth factor receptor 2–negative, ESR1-mutated...
05/04/2026
FDA Alert
FDA Alert
04/23/2026
Anthony Calabro, MA
On March 25, the FDA has approved relacorilant (Lifyorli), in combination with nab-paclitaxel for adults with platinum-resistant ovarian and related gynecologic cancers who have received prior systemic...
04/23/2026
Research Summary
Research Summary
04/20/2026
Ashton L. Stahl
In a multicenter cohort, post-oophorectomy HRT was not linked to higher breast cancer risk in women with BRCA variants.
04/20/2026
FDA Approval
FDA Approval
04/15/2026
Anthony Calabro, MA
The FDA has granted full approval for the use of brexucabtagene autoleucel in adults with relapsed or refractory mantle cell lymphoma, based on confirmatory ZUMA-2 data.
04/15/2026