🔥The final outcomes of SOFT and TEXT are out in @Annals_Oncology
Ovarian function suppression (OFS) + tamoxifen ⬇️ recurrence risk compared to tamoxifen Further reduction in recurrence is seen with exemestane + OFS vs. tamoxifen
https://t.co/cpHhlv21vo
🔥 More is not always the best
REDUCE trial demonstrated that every 12 weeks denosumab is not inferior to standard every 4 weeks
✅ Non inferior efficacy
✅ Improved safety profile
✅ Reduce cost
I love this type of trials!
Congratulations to all investigators
#ASCO26
OPTIMA does not teach us a completely new biology; it reinforces the Oncotype DX-era message with Prosigna/PAM50 at a phase III level.
What makes it important is the population: clinically high-risk ER+/HER2− EBC, frequent nodal positivity, 19% pN2 disease, and 37% premenopausal patients. Yet 68% had low ROR scores, and chemotherapy omission was non-inferior for 5-year IBCFS.
Clinical risk ≠ genomic risk
‼️median follow-up is only 3.9 years, which is still early for HR+ disease.
Alongside #ASCO26, the new ESMO metastatic breast cancer guidelines have just been published in @Annals_Oncology
Congrats to all co-authors, and a special mention to @myESMO mentor @E_de_Azambuja for this well-deserved recognition! 👏🏼
@OncoAlert
Link: https://t.co/AlUMSY6iTZ
🚨 THE 15 MOST IMPORTANT TRIALS OF #ASCO26
May 29 - June 2 | Chicago
Which trial are you watching most closely?
🌟 PLENARY GAME-CHANGERS
1️⃣ PROTEUS
Perioperative apalutamide + ADT in high-risk localized prostate cancer
2️⃣ LIBRETTO-432
Adjuvant selpercatinib in RET+ NSCLC
3️⃣ HARMONi-6
Ivonescimab + chemo vs tislelizumab + chemo in squamous NSCLC
4️⃣ RASolute 302
Daraxonrasib (RMC-6236) in metastatic pancreatic cancer
5️⃣ SARC041
Abemaciclib in dedifferentiated liposarcoma
⚡ FRONTLINE & PERIOPERATIVE SHIFTS
6️⃣ KEYNOTE-B15 / EV-304
EV + pembrolizumab vs chemo in MIBC
7️⃣ LITESPARK-022
Pembrolizumab + belzutifan in adjuvant ccRCC
8️⃣ AMBITION
Paclitaxel/bevacizumab ± atezolizumab in HR+ breast cancer
9️⃣ NeoADAURA
Neoadjuvant osimertinib in EGFR+ NSCLC
🔟 A-DREAM
ADT interruption strategies in mCSPC
🧬 PRECISION, ADCs & NEXT-GEN IMMUNOLOGY
1️⃣1️⃣ DESTINY-Breast06
T-DXd expands into HER2-ultralow disease
1️⃣2️⃣ CROWN (7-year update)
Lorlatinib durability in ALK+ NSCLC
1️⃣3️⃣ DeLLphi-312
Tarlatamab in frontline SCLC
1️⃣4️⃣ COMMIT
Atezolizumab + FOLFOX/Bev in MSI-H mCRC
1️⃣5️⃣ IMvigor011
ctDNA-guided adjuvant atezolizumab in bladder cancer
#OncoTwitter #MedTwitter #ASCO26 #CancerResearch @OncoAlert@ASCO@JCOPO_ASCO@OncBrothers
A wonderful experience in Berlin.
Behind every trial is the persistent work of researchers striving to change the future of patients with cancer.
Deep respect to all who continue to move breast cancer care forward.
This is my overview #ESMOBreast26@myESMO. @OncoAlert
2nd Line Treatment Options in Mets Breast Cancer
Post Progression after AI + Cdk 4/6 inhibitors use in 1st Line
Mandatory = Organise NGS testing
See the Wonderful options
Trial evidence and Efficacy snd Salient Toxicity
🚨 FDA’s take on SERENA-6 is basically this:
“Nice data… but are we helping patients?”
Let’s break it down 👇
🧠 Problem 1: Wrong question
Trial asks:
👉 Switch early vs don’t switch
But real-world question is:
👉 Switch early vs switch later
FDA:
❌ “You didn’t answer the real question.”
⏱️ Problem 2: The PFS illusion
PFS looks great (16 vs 9.2 months)
But… it starts from:
👉 ESR1 mutation detection (not progression)
FDA:
❓ “What does this PFS even mean clinically?”
🧬 Problem 3: Biology mismatch
We assume: ESR1 mutation = resistance
FDA says:
👉 Not so fast
Patients may still benefit from AI + CDK4/6i
even AFTER mutation appears
👉 Early switch = stopping a working drug
🔁 Problem 4: No second chance
Control arm never got camizestrant later ❌
So we don’t know:
👉 Early vs delayed use
FDA:
❌ “This comparison is incomplete”
📉 Problem 5: Where is survival benefit?
OS = immature
Final data → years away
FDA:
👉 “Without OS, paradigm shift is risky”
⚠️ Problem 6: Not risk-free
QT prolongation
Bradycardia
Rare TdP
👉 Not a harmless switch
🎯 FDA’s real message:
“Just because we can act early…
doesn’t mean we should.”
🔖 Save this - this is how regulators think
📖 Full FDA briefing in comment ⬇️
#OncoTwitter #MedTwitter #BreastCancer #ESMOBreast26
@OncoAlert@myesmo@esmo_open@asco@OncBrothers
HR+/HER2- metastatic breast cancer is driven by diverse biology & evolving resistance. @DrDebuTripathy et al discuss precision treatment advances through targeted therapies, genomic profiling, & patient-centered decision making: https://t.co/DU86kXa5qB
@OncoAlert#BCSM#TNBCDay
PATINA is now out in @nejm. Among pts with HR+/HER2+ MBC progression-free after chemo induction, adding palbociclib to 1L ET+HER2-blockade maintenance prolonged PFS from 29 mo to an astonishing 44 months (HR 0.75, p=0.02). Congrats @Otto_DFCI & coauthors! https://t.co/YoE3Pje9Be
HER2+ eBC: Do we still need carboplatin in neoadjuvant TCHP?
New phase III neoCARHP suggests: maybe not 👀
🧠 Core idea:
Taxane + trastuzumab + pertuzumab (THP) can achieve similar pCR to TCHP, with less toxicity.
🧪 Trial snapshot (stage II-III HER2+ early BC, n=774)
🟦 THP × 6 cycles (taxane + H + P)
🟥 TCHP × 6 cycles (taxane + carbo + H + P)
📌 Primary endpoint: pCR (noninferiority met)
✅ pCR 64.1% (THP) vs 65.9% (TCHP)
Δ -1.8%, OR 0.93, P(noninferiority)=0.0089
🧬 Subgroups stayed consistent
HR+ 👉 56% vs 59%
HR- 👉 78% vs 78%
⚠️ Safety win (biggest headline)
Grade 3-4 AEs: 20.7% (THP) vs 34.6% (TCHP)
Serious AEs: 1.3% vs 4.7%
Less anemia, N/V, neutropenia, thrombocytopenia with THP ✅
🎯 Clinical takeaway:
For lower or moderate-risk HER2+ disease, carboplatin-free THP may be a strong de-escalation strategy…
…but we still need EFS/OS maturity, especially for stage III.
🔖 Save this for tumor board debates.
📖 Full paper in comment ⬇️
#OncoTwitter #MedTwitter #BreastCancer #HER2positive
@OncoAlert@myesmo@esmo_open@ASCO
🚨 HER2CLIMB 05 just made “maintenance” exciting in HER2+ MBC
#SABCS25
Finish THP induction, then instead of “wait and watch,” you lock in control with tucatinib plus HP in 1L maintenance.
✨ Big picture
💙 Median PFS: 24.9 vs 16.3 months
💙 Extra 8.6 months without progression
💙 HR 0.64 (0.51 to 0.79), p < 0.0001
🧬 Works in both HR negative and HR positive
🟦 HR negative
• PFS 24.9 vs 12.6 months
• HR 0.55 (0.40 to 0.76), p = 0.0002
• +12.3 months gain
🟧 HR positive
• PFS 25.0 vs 18.1 months
• HR 0.73 (0.55 to 0.98), p = 0.0389
• +6.9 months gain
😌 Toxicity that oncologists can live with
Mostly low grade diarrhea, nausea and mild LFT rise, no new scary signals.
💡 Clinic takeaway
Tucatinib plus HP in 1L maintenance turns a good THP responder into a long controller, buying extra chemo free time across HR subsets.
🔖 Save this for your next breast board
#OncoTwitter #MedTwitter #BreastCancer #HER2 @OncoAlert@myesmo@esmo_open@ASCO@SABCSSanAntonio
DESTINY-Breast05 makes one thing clear, at this pace, T-DXd is rapidly becoming the backbone across most HER2-positive disease settings.
It cut invasive recurrence from 12.5% to 6.2% (↓ 53% ) & raised 3-year IDFS from 83.7% to 92.4% in pts with residual high-risk disease. ILD (9.6%) is the one safety signal that still deserves close attention.
@OncoAlert https://t.co/pfdgRBGK9j
#SABCS25
We learned from the lidERA study that oral SERDs may also be used in the early-stage setting. We saw that, as monotherapy, they are superior to endocrine therapy. However, for their combination with CDK4/6 inhibitors—or for sequential use after 2–3 years of AI plus CDK4/6 therapy—we will need to wait for additional data. We also need to keep cost in mind: these are expensive drugs, and the target population is very large. I doubt that even the most developed countries can absorb such financial burdens.