ONN® - OncLive News Network®

2 experts are featured in this series.

The phase 2 ARASEC trial (NCT02799602) evaluated darolutamide (Nubeqa) plus androgen deprivation therapy (ADT) in patients with metastatic hormone-sensitive prostate cancer (mHSPC) in the United States, utilizing an innovative synthetic historical control design derived from the prospective, randomized phase 3 CHAARTED trial (NCT00309985). Neal D. Shore, MD, FACS, and Rana R. McKay, MD, FASCO, co-led the trial, which met its primary end point of radiographic progression-free survival, with an HR of 0.29 compared with the ADT monotherapy control arm, and demonstrated a statistically significant overall survival benefit (HR, 0.50). In this Investigator Perspectives program, Shore and McKay explore design, key findings, and significance of ARASEC.

The Moonlight Shift, with host Gina Mauro, features leading and early-career oncologists from the Tri-State corridor in peer-level conversations about where the field is going — and what it still has to work out.

The Moonlight Shift

The Moonlight Shift, with host Gina Mauro, features leading and early-career oncologists from the Tri-State corridor in peer-level conversations about where the field is going — and what it still has to work out.

Dr. Edwin Choy from the sarcoma oncology program and Dr. Sarah Bouberhan from gynecologic medical oncology at Massachusetts General Hospital discussed perivascular epithelioid cell tumors (PEComas), rare mesenchymal neoplasms affecting approximately 75% of patients with benign or uncertain malignant potential. PEComas occur predominantly in women aged 20 to 55 years, commonly affecting the uterus, kidney, retroperitoneum, gastrointestinal tract, liver, and lungs. Diagnosis requires expert pathological evaluation with specific immunohistochemical markers including melanocytic markers (HMB-45, Melan-A) and smooth muscle markers (SMA, desmin, caldesmon).

Molecular characterization reveals approximately 50% harbor TSC1 or TSC2 loss affecting mTOR pathway signaling, whereas others demonstrate TFE3 gene rearrangements. The AMPECT phase 2 trial established nab-sirolimus as FDA-approved first-line therapy for advanced disease, demonstrating 39% response rates with 10.6-month progression-free survival and 40.8-month overall survival. Patients with TSC2 mutations showed nearly 90% response rates versus 13% for non-TSC2 mutations.

Dr. Megan Melody from Tampa General Hospital Cancer Institute and Dr. Mark Roschewski from Memorial Sloan Kettering Cancer Center discussed how circulating tumor DNA (ctDNA) testing is transforming lymphoma care through enhanced risk stratification, treatment monitoring, and personalized patient management.

Key insights emphasized ctDNA as an emerging risk factor superior to baseline assessments, with most patients achieving undetectable levels after 2 cycles. Combined negative positron emission tomography and ctDNA results reduce relapse risk from 15% to 20% to single digits. However, ctDNA currently serves as a prognostic marker rather than treatment-guiding tool, with ongoing ALPHA3 trial investigating ctDNA-guided therapy using allogeneic CAR-T cells.

Clinical Implementation:

• Seventy-five percent concordance between ctDNA and PET imaging results

• Serial testing preferred over single time-point assessments for surveillance

• Technology varies across lymphoma subtypes, with phased variant assays showing superior sensitivity

• Quantitative values enable kinetic monitoring for individual patients with baseline controls

2 experts are featured in this series.

Dr. Helena Yu of Memorial Sloan Kettering Cancer Center and Dr. Sonam Puri of Moffitt Cancer Center discuss the phase 3 TOP study, presented at the European Lung Cancer Congress (ELCC) 2026, which evaluated osimertinib plus carboplatin/pemetrexed versus osimertinib monotherapy in non–small cell lung cancer (NSCLC) patients with EGFR mutations and concurrent TP53 alterations. The study showed a median progression-free survival (PFS) of 34.0 versus 15.6 months (hazard ratio [HR], 0.44), with consistent benefit across subgroups including central nervous system (CNS) and liver metastases. The experts contextualize TOP within FLAURA2 and MARIPOSA, address patient selection beyond TP53, walk through safety and toxicity management for combination regimens, and outline sequencing strategies at progression. They close with practical guidance for community oncologists and unanswered questions, including the role of circulating tumor DNA (ctDNA) dynamics as an emerging predictive biomarker.

Dr. Pedro Barata and Dr. Johann De Bono discuss recent advances in metastatic castration-resistant prostate cancer, with a focus on the evolving role of radiopharmaceuticals across the treatment landscape. They review key clinical updates from recent meetings, including emerging data on both established therapies and next-generation PSMA-targeted approaches, and examine how these findings are shaping treatment selection and sequencing strategies.

2 experts are featured in this series.

Dr. Mazyar Shadman from the University of Washington/Fred Hutchinson Cancer Center and Dr. Danielle Brander from Duke Cancer Institute discuss matching adjusted indirect comparisons (MIACs) for first-line chronic lymphocytic leukemia (CLL) treatment decisions. The discussion explores how these statistical methodologies help compare treatments from different clinical trials when direct head-to-head comparisons are unavailable, acknowledging their limitations while recognizing their value in rapidly evolving treatment landscapes.

Key analyses include zanubrutinib (SEQUIOA trial) comparisons with venetoclax-based fixed-duration regimens, CLL14 (venetoclax-obinutuzumab), and AMPLIFY (acalabrutinib-venetoclax). Results consistently favored continuous BTK inhibitor therapy for progression-free survival, particularly after 3 years, while demonstrating favorable safety profiles despite longer treatment exposure.

Clinical Considerations:

  • MIACs provide systematic comparisons beyond separate trial evaluations but cannot replace randomized head-to-head trials
  • Anchored analyses (shared control arms) offer stronger evidence than unanchored methodologies
  • Patient goals regarding treatment duration, efficacy priorities, and risk tolerance remain paramount in decision-making
  • Disease markers including IGHV mutation status and TP53 aberrations influence optimal treatment selection between continuous versus fixed-duration approaches

3 experts in this video

A panel of exerts focus on the management of advanced renal cell carcinoma, emphasizing why the first-line treatment decision is the most critical opportunity to influence patient outcomes. This initial treatment decision can shape the entire patient journey and remains central to achieving optimal outcomes. Experts explore the importance of early and effective disease control, including how tumor biology, disease burden, and patient fitness shape treatment selection and prognosis. We’ll also discuss key clinical considerations and real-world patterns, including the fact that some patients may not receive subsequent therapy. Finally, they will review emerging clinical data and consider how these insights can be applied to optimize outcomes for the patient in front of us.

1 expert is featured in this series.

Lori Wirth, MD, discusses the latest NCCN guideline updates in differentiated thyroid cancer. This program focuses on evolving strategies for managing patients with progressive, radioactive iodine–refractory disease, with particular emphasis on the growing role of next-generation sequencing (NGS) and precision oncology. Dr. Wirth highlights how identifying actionable molecular alterations such as kinase fusions have transformed first-line treatment decisions, enabling more targeted and effective therapies that are reshaping the standard of care.

Kathryn S. Nevel, MD and Michael Veronesi, MD, PhD provide an overview of the evolving imaging strategies in glioma and discuss the use of magnetic resonance imagining and amino acid PET imaging throughout the glioma patient journey.

1 panelist

Amer Zeidan, MBBS, reviews key updates in myelodysplastic syndromes (MDS) presented at the 2025 ASH Annual Meeting. The program highlights real-world and clinical trial data shaping care for patients with lower-risk MDS, including insights on treatment initiation and outcomes with luspatercept