🙃 Totally agree. The question isn't who is the best, but what is best for our patients. We have to keep working forward @ASCO@ESTRO_RT@ASTRO_org@Uroweb
Is there a name for that condition where people are incontinent of thoughts and words on Twitter?!! You see it on other platforms. Must be some meds or some sort of sphincter you can put on the post button. Or just focus on day job. THANK YOU FOR YOUR ATTENTION TO THIS MATTER 😀
Wonderful few days at #ASCO26 catching up with so many mates. And what a fantastic experience to do an @ASCO Plenary Discussion on the wonderful PROTEUS Trial! Amazing room. Massive trial, look forward to diving into details in @NEJM paper and more to come. Huge congrats to all
As #ASCO2026 wraps up, I can’t recommend the Early Career Lounge enough for residents attending next year! ✨
The workshops , mentoring meetings and talks from @ASCOTECAG were a real highlight. Apply to the Abstract Forum to present your work and get valuable feedback, take advantage of the Presentation Skills Webinar beforehand, and connect with fellow trainees along the way! 🤝 Thank you @NazliDizman & @cdanicas !
THE @ONCOALERT RoundUp🚨 DAY 3 of #ASCO26
🚨For the FULL NEWSLETTER 👉https://t.co/Ou3rJ6A8W6
🔹 #RASolute302: Daraxonrasib became the first RAS-targeted therapy to improve OS in previously treated metastatic pancreatic cancer (13.2 vs 6.6 mo).
🔹 #LIBRETTO: Adjuvant selpercatinib cut recurrence/progression risk by 83% in RET+ early-stage NSCLC.
🔹 #PROTEUS: Perioperative apalutamide improved pathologic response and long-term outcomes in high-risk localized prostate cancer.
🔹 #BREAKWATER: EC + FOLFIRI further expanded frontline options for BRAF V600E mCRC.
🔹 #HorizonCRC01: Trastuzumab rezetecan showed strong activity in refractory HER2+ mCRC.
🔹 #PLUDO: New data inform optimal sequencing of LuPSMA and docetaxel in mCRPC.
🔹 #OBX115: IL-15–engineered TIL therapy achieved a 67% ORR in heavily pretreated melanoma.
🔹 Ultra-low-dose nivolumab + metronomic chemotherapy improved survival and QoL in recurrent/metastatic HNSCC.
🔹 #SARC041: Abemaciclib became the first CDK4 inhibitor to improve PFS in dedifferentiated liposarcoma.
@GIMedOnc@DrChoueiri@jamecancerdoc@Rodrosb@YannickBuccella@HHorinouchi@MarioBalsaMD@g_mountzios@OncBrothers@lungoncdoc@diegoadiazg@AnaVManana@UOzkerim@declangmurphy@DrYukselUrun@DrSpratticus@tugbawitter@DrRishabhOnco@KalantriShreyas@josemarciofigu1@nataliagandur@DraMartinezLago@ozdogan_md
Validation of PSA ⏬ among Latin American (LA) subgroup of LIBERTAS - Ph 3 study APA + continuous vs intermittent ADT in mCSPC @urotoday#ASCO26
n=118 from LA
🌟Med PSA: 22.95 (vs 7.32 ITT)
@ 6 mos:
🌟PSA50: 96%
🌟PSA90: 83%
🌟PSA < 0.2: 61%
🌟n=62 randomized to Rx phase
#ASCO26 GU Oncology Spotlight 🚨
🔬 Abstract 5017 | PROTRACT
ctDNA-guided biomarker-directed therapy vs physician/patient choice in mCRPC progressing after abiraterone/prednisone
Presented by Corinne Maurice-Dror, MD
@ASCO@OncoAlert
This is a very relevant precision-oncology question in prostate cancer:
➡️ Can ctDNA help guide whether a patient should receive docetaxel or enzalutamide after progression on abiraterone?
PROTRACT tested a simple treatment-selection strategy:
🔵 Biomarker-directed arm
• ctDNA ≥2% → docetaxel
• ctDNA <2% → enzalutamide
vs
🟠 Physician/patient choice
• docetaxel or enzalutamide, based on clinical preference
Primary endpoint: PFS
Secondary endpoints included OS, PSA50 response, PFS2, safety, and ctDNA correlatives.
🔵 Why this matters
This trial directly addresses a common real-world problem:
After abiraterone progression in mCRPC, treatment choice is often based on clinical judgment, patient preference, fitness, access, and toxicity concerns.
But biology may matter.
A higher ctDNA fraction may reflect more aggressive disease biology and could potentially support moving toward chemotherapy rather than sequential AR pathway inhibition.
🔵 Feasibility signal
The study randomized 42 patients before early termination due to slow accrual.
Importantly:
➡️ 57% of patients had discordance between physician/patient preference and ctDNA-directed assignment.
That is the key signal.
ctDNA guidance would have changed the treatment direction for more than half of patients.
🟠 Important caveat
This was underpowered and stopped early.
So PROTRACT should not be read as a definitive efficacy trial.
But it is still highly informative because it shows how often biomarker-directed treatment selection may differ from usual clinical choice.
🔵 My take
PROTRACT is important not because it settles the sequencing question, but because it frames the next one:
➡️ Can ctDNA move from prognostic biomarker to treatment-selection tool in mCRPC?
The future algorithm may not simply ask:
“ARPI again or chemotherapy?”
It may ask:
What does the tumor biology suggest this patient needs next?
#ASCO26 #GUOnc #ProstateCancer #mCRPC #ctDNA #PrecisionOncology #Biomarkers #ClinicalTrials #TreatmentSequencing
@OncLive@TargetedOnc@CancerNetwork@ASCOPost@ecancer@VJOncology@curetoday