The oncology KOL conversation on X today is led by Lung Cancer, Breast Cancer, GI Cancers, GU Cancers, Multiple Myeloma, Leukemia & Lymphoma. The KOL Pulse Daily Digest of what verified physician (KOL) voices are discussing on X across lung, breast, GI, GU, multiple myeloma, and leukemia & lymphoma, ranked by engagement over the last 48 hours.
The thoracic oncology community is discussing a post-hoc analysis of the PACIFIC trial, which found baseline PPI use was associated with shorter PFS and OS in patients receiving durvalumab for stage III NSCLC. Additionally, results from the phase 3 CheckMate 73L trial showed that nivolumab-based consolidation failed to improve outcomes versus standard durvalumab in the same setting. New real-world data on Trastuzumab Deruxtecan (T-DXd) in HER2-mutant NSCLC from the TRACER HERTras study is also being shared.

“Post-hoc analysis of the PACIFIC trial: baseline PPI use was associated with significantly shorter PFS and OS in patients receiving durvalumab after chemoradiotherapy for unresectable stage III NSCLC.”
— @Dr_ElvinaA · PACIFIC trial and PPIs · View post ↗
“Great summary by @UOzkerim / @OncoAlert highlighting this week’s key #LungCancer updates including: 🫁 PACIFIC post hoc analysis in @TheLancetOncol 🧬 KRAScendo-1 industry update”
— @BRicciutiMD · This week in lung cancer · View post ↗
“TRACER HERTras study just out in @JTOonline , the biggest RWD cohort on T-DXd in #HER2mut #NSCLC:”
— @g_mountzios · TRACER HERTras RWD study · View post ↗The breast oncology community is discussing real-world data on post-progression outcomes for patients receiving first-line aromatase inhibitor plus ribociclib. A study from the Flatiron database (n=5649) found that first-line ribociclib was associated with longer PFS2 and chemo-free survival. Separately, there is discussion around the ongoing ASCENT-03 and ASCENT-04 trials, which are evaluating sacituzumab govitecan with or without pembrolizumab in first-line metastatic TNBC.

“The use of first line ribociclib (vs AI alone) was associated with longer PFS2 and chemo-free survival, including among patients aged ≥65 years.”
— @PTarantinoMD · Real-world ribociclib outcomes · View post ↗
“Early (immediate) separation of curves is a sign of selection bias: the patients receiving ribo+AI and AI alone are not the same! ➡️ a causal conclusion cannot be drawn! Classical bias: ‘Detecting Selection Bias in Observational Studies—When Interventions Work Too Fast’ in JAMA Internal Medicine”

“This would be true if the intervention was ‘coffee intake.’ But in this case, the intervention is a drug, ribociclib, that works rapidly, substantially improves ORR, PFS (from the first scan) and OS. Which makes this adjusted real world analysis solid.”

“Thanks for the reply. The fact that ribociclib works rapidly in RCTs like MONALEESA-2 does not eliminate selection bias in this observational analysis. Early curve separation is exactly the pattern expected when fitter patients are preferentially given the combination. IPTW cannot correct for unmeasured confounding.”
The GI oncology community is discussing new data from ESMO GI 2026, led by the KRYSTAL-10 trial, where adagrasib plus cetuximab failed to improve PFS or OS versus chemotherapy in second-line KRAS G12C-mutated mCRC, despite a higher ORR. Another prominent topic is the use of post-surgical ctDNA to determine which patients with resected colorectal cancer benefit from adjuvant chemotherapy. An exploratory analysis from the ATOMIC study is also being discussed, questioning the necessary amount of chemotherapy in adjuvant MSI-H CRC.

“Ivonescimab plus gemcitabine and cisplatin as first-line therapy for advanced biliary tract cancer: a multicenter, open-label phase 2 trial - Journal of Hepatology”
— @Erman_Akkus · Ivonescimab 1L biliary tract cancer (Ph 2) · View post ↗
“👉ORR with 40% higher, but no PFS & OS benefit for combination over CTx”
— @ArndtVogel · KRYSTAL-10 trial results · View post ↗
“For patients undergoing upfront surgery for colorectal liver metastases, postsurgical 🧬 ctDNA identifies who will derive overall survival benefit from (m)adjuvant chemotherapy, and who can safely avoid it.”
— @DrYukselUrun · ctDNA-guided therapy · View post ↗
“⛔️EMERALD1 – int HCC TACE + durva + bev improved PFS & ORR vs TACE, but no OS benefit”
— @GillSharlene · EMERALD-1 trial results · View post ↗The GU oncology community is discussing new data for the HIF-2α inhibitor casdatifan in refractory metastatic ccRCC from the ARC-20 trial, which showed an ORR of 31–35%. Additionally, the ARTO trial demonstrated an overall survival benefit (HR 0.55) for adding SBRT to abiraterone and ADT in oligometastatic mCRPC after a median follow-up of 53 months. New ESTRO consensus recommendations are also being shared on how to implement focal boosts for prostate cancer following the positive FLAME trial.

“SBRT + Abiraterone + ADT vs Abiraterone + ADT in oligometastatic mCRPC. Arto Trial. First Ph II randomised trial to show Mets directed SBRT May improve OS in mCRPC. Consistent benefit: PSA response, biochemical PFS, radiological PFS, overall survival.”
— @roxboxfix · ARTO trial · long-term OS analysis · View post ↗
“New "1 in 1000" prostate cancer discovered: of 4534 men with aggressive prostate cancer, 5 carried an inherited CDK12 mutation.”
— @DrMHofman · Germline CDK12 mutation · View post ↗
“⚡️ Casdatifan (HIF-2α inhibitor) in refractory metastatic ccRCC (ARC-20, n=127): ORR 31–35%, median PFS not estimable at >12 months follow-up in the 100 mg QD cohort.”
— @drenriquegrande · Casdatifan in ccRCC · View post ↗
“🚨 Big #prostatecancer paper in @Nature claimed NSD2 inhibition could reverse lineage plasticity + resensitize CRPC/NEPC models to enzalutamide. Now retracted. 🐭Reason: animal welfare protocol breaches in mouse control arms - tumor burden/bodyweight data confirmed protocol”
— @Adam_Weiner535 · Nature NSD2/CRPC paper retracted · View post ↗
“I explained why I believe what you said is misinformation. In an academic discussion, if you think I’m wrong, you can certainly refute my argument and point out the flaws in my reasoning.”

“Your reply is a non sequitur. My point was that perioperative ADT is not standard of care, and your post does not address that.”

“What I would say is that I’ll concede that the Proteus Trial compared two methods of systemic intensification against each other, showing Apalutamide to improve outcomes. I think you would acknowledge there is no comparator arm in this trial that is solely the current standard of care.”

“How do you propose delivering risk-adapted local therapy when perioperative ADT masks PSA, which remains our best biomarker for identifying patients who need salvage local treatment? My point is simple: PROTEUS did not test overall systemic treatment escalation against best standard-of-care management. It tested apalutamide added to perioperative ADT, not a modern local-first strategy with PSA-guided salvage therapy. That is not misinformation. It is a critique of the control arm and the clinical inference being drawn from the trial. The highlighted statement overstates what PROTEUS proves and, in my view, risks circumventing the robust data supporting local-first treatment with risk-adapted salvage therapy. In this population, I would have expected substantially higher salvage RT utilization. By shifting toward PSMA DMFS while suppressing PSA with ADT, we may be delaying recognition of salvageable local failures until distant disease is detected. So to be clear: PROTEUS supports intensification within a perioperative ADT framework. It does not establish that broad perioperative systemic escalation is superior to best standard-of-care local-first management with PSA-guided salvage therapy. At this point, I think we are talking past each other, so I’m comfortable agreeing to disagree and moving on. I would only suggest avoiding ad hominem framing and trying to steelman the opposing view rather than labeling disagreement as misinformation.”
The myeloma/hematology community is discussing a new proposal to revise the definition of light-chain smoldering myeloma based on serum FLC values and other criteria. Additionally, there is continued focus on clinical trials, including results from MajesTEC-9 suggesting teclistamab outperforms PVd and Kd in the relapsed setting, and updates on trials in newly diagnosed disease (EQUATE, EAA241) and smoldering myeloma (DETER-SMM).

“New proposal to revise the definition of light-chain smoldering myeloma to abnormal serum FLC values, absence of detectable intact immunoglobulin on SPEP and immunofixation, and BMPC > 10% without myeloma-defining events:”
— @Myeloma_Doc · Light-chain smoldering myeloma definition · View post ↗
“MajesTEC-9 Results : Teclistamab Outperforms PVd & Kd in Relapsed #Myeloma:”
— @MyelomaTeacher · MajesTEC-9 results · View post ↗
“EAA241 - Ph 2 RCT Dara-Bor-Dex vs Cy-Bor-Dex in the treatment of Newly Diagnosed Multiple Myeloma with Light Chain Cast Nephropathy (LCCN)”
— @mtmdphd · EAA241 trial · View post ↗The hematology community is discussing new EBMT guidelines for autologous and allogeneic transplantation in adult Hodgkin lymphoma. There is also conversation around specific lymphoma classifications, including CD20-negative large B-cell lymphomas and immunodeficiency-associated primary CNS lymphomas. Additionally, the primary analysis of the EPCORE DLBCL-3 trial, evaluating epcoritamab in first-line DLBCL, is being shared.

“Can PRISM-AML help decide who should undergo allogeneic transplant after azacitidine + venetoclax? The answer is yes… but with caution.”
— @HenrychihangFu1 · PRISM-AML and transplant decisions · View post ↗
“📝 CD20 Negative Large B-Cell Lymphomas: - Plasmablastic Lymphoma - Primary Effusion Lymphoma - HHV8 Associated Lymphoma - ALK Positive LBCL”
— @UyanikMehmetS · CD20 Negative LBCL · View post ↗
“#Hematology Autologous and allogeneic haematopoietic cell transplantation in adult patients with #Hodgkin #lymphoma: recommendations from the @TheEBMT Practice Harmonisation and Guidelines Committee and Lymphoma Working Party”
— @DrRaulCordoba · Hodgkin Lymphoma transplant guidelines · View post ↗