Weekly Oncology Highlights | Oncology News, Updates and Spotlights

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Your go-to digest for the latest breakthroughs in cancer care.

This week’s digest spans across FDA approvals and NCCN guideline updates. 

Scroll down to read more on this week’s ONCOassist Spotlight Tool ! 

FLAME Trial: 10-Year Focal-Boost Radiotherapy Results in Prostate Cancer

The FLAME Phase III trial confirms that a focal boost (up to 95 Gy) to MRI-visible intraprostatic lesions alongside standard EBRT significantly increases 10-year biochemical disease-free survival (86% vs. 71%) in intermediate- to high-risk localized prostate cancer, without additional toxicity. Other disease-free metrics also favored the boost arm.
(Ref: Menne Guricová, K.et al (2025). Focal boost to the intraprostatic tumor in external beam radiotherapy for localized prostate cancer: 10-year outcomes of the FLAME trial. Journal of Clinical Oncology, Advance online publication.)

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Modeyso (Dordaviprone): First FDA-Approved Systemic Therapy for H3 K27M-Mutant DMG

The FDA granted accelerated approval to Modeyso (dordaviprone) for both adult and pediatric patients (≥1 year) with recurrent H3 K27M-mutant diffuse midline glioma. This marks the first systemic therapy approved for this aggressive brain tumor subtype. Clinical data show an objective response rate of approximately 22%, with a median duration of response of ~10.3 months.
(Ref:Jazz Pharmaceuticals. (2025, August 6). FDA grants accelerated approval to dordaviprone (Modeyso) for H3 K27M-mutant diffuse midline glioma [Press release].)

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Enhertu (T-DXd) Approved for HER2-Low and HER2-Ultralow Metastatic Breast Cancer

The FDA expanded approval of fam-trastuzumab deruxtecan-nxki (Enhertu) for hormone receptor–positive metastatic breast cancer expressing HER2-low (IHC 1+/2+, ISH−) or HER2-ultralow (IHC 0 with minimal staining), post-endocrine therapy. This extends targeted ADC treatment to previously underserved patient subsets.
(Ref: U.S. Food and Drug Administration. (2025, January 27). FDA approves fam-trastuzumab deruxtecan-nxki for HR-positive, HER2-low or HER2-ultralow metastatic breast cancer [Press release].)

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NCCN Guidelines Now Include LEMS Evaluation in SCLC Care Pathways

The updated NCCN Clinical Practice Guidelines for Small Cell Lung Cancer now recommend evaluation for Lambert-Eaton Myasthenic Syndrome (LEMS), including neurologic consultation, PQ- and N-type VGCC antibody testing, and consideration of amifampridine for symptomatic management.
(Ref: Catalyst Pharmaceuticals. (2025, August 6). LEMS antibody testing and treatment recommendations added to NCCN guidelines for SCLC [Press release].)

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Bacterial Decolonization with Mupirocin Ointment Reduces Severe AROM in NPC Radiotherapy

A Phase III randomized clinical trial in nasopharyngeal carcinoma patients undergoing definitive chemoradiotherapy compared a bacterial decolonization (BD) protocol using mupirocin nasal ointment with standard of care (SoC). The BD regimen significantly halved the rate of severe (grade ≥3) acute radiation oral mucositis (AROM)—from 47.7% to 22.7% (relative risk 0.48; P < .001). Secondary benefits included reduced oral pain, eased swallowing difficulty, and lower rates of nasal and oral Staphylococcus aureus colonization. Results suggest that mupirocin decolonization is a promising, cost-effective approach for alleviating AROM in nasopharyngeal cancer patients undergoing radiotherapy
(Ref: Liao, Z., Xiong, X., Zhao, L., et al. (2025). Bacterial decolonization with mupirocin ointment for acute radiation oral mucositis prevention: A Phase III randomized clinical trial. JAMA Oncology. Advance online publication.)

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ONCOassist Tool Spotlight: Metastatic Castrate Resistant Prostate Cancer Tool

Systemic treatment options for mCRPC include:For Reference 320 x 250 px 2000 x 2000 px 1

  • AR pathway inhibitors (ARPi)
  • Cytotoxic chemotherapy
  • Radioligand therapy
  • PARP inhibitors and others.

This tool is designed to show efficacy outcomes with novel treatment options in recent clinical trials for mCRPC patient.

Join the ONCOassist oncology community, the go-to CE‑approved app for oncology professionals worldwide !

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  •  Access essential tools like staging systems, toxicity scoring, drug calculators, prognostic scores and NCCN regimens,all in one place .
  • Stay informed with ONCOnews & ONCOvideos featuring expert insights, conference coverage and peer-tested protocols 

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Weekly Oncology Highlights | Oncology News, Updates and Spotlights

Screenshot 2025 07 25 at 1.32.03 PM

Your go-to digest for the latest breakthroughs in cancer care.

This week’s digest spans EU approvals in myeloma and lung cancer, precision-driven trials in breast and hematologic oncology, and a biomarker breakthrough in lung adenocarcinoma brain metastasis.

Leading voices. Big insights. Scroll down for Dr. Maria Barbu!

 

Sarclisa (Isatuximab) Gains EU Approval in Transplant-Eligible Newly Diagnosed Multiple Myeloma

On July 25, 2025, the European Commission approved Sarclisa combined with VRd (bortezomib, lenalidomide, dexamethasone) as induction therapy for transplant-eligible NDMM. The GMMG-HD7 Phase III trial showed significant MRD negativity and prolonged progression-free survival versus VRd alone.
Clinical insight: This approval broadens Sarclisa’s role to include early disease lines, regardless of transplant eligibility.
(Ref: Sanofi press release citing GMMG-HD7 results and EC approval, July 25, 2025)

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CHMP Recommends TEVIMBRA (Tislelizumab) for Resectable NSCLC (RATIONALE-315) Trial

On July 28, 2025, CHMP issued a positive opinion for TEVIMBRA plus platinum-based chemo as neoadjuvant therapy followed by adjuvant monotherapy in high-risk resectable NSCLC. In the Phase III RATIONALE‑315 trial, TEVIMBRA significantly improved MPR (56.2% vs 15.0%), pCR (40.7% vs 5.7%), and event-free survival (HR 0.56; P=0.0003).
Practice relevance: Could establish the first perioperative immunotherapy standard in early-stage NSCLC.
(Ref: BeOne Medicines CHMP recommendation release, July 28, 2025)

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TEODOR Trial Launched to Evaluate ct-DNA Guided  De-escalation in HR+ Breast Cancer

Natera and ABCSG have initiated the TEODOR Phase II RCT, investigating whether hormone receptor-positive, HER2-negative patients who are ctDNA-negative and endocrine-responsive can safely skip neoadjuvant chemotherapy in favor of endocrine therapy. Primary endpoints are pCR rate and modified PEPI score.
Innovative approach: Personalizes neoadjuvant decision-making via ctDNA and endocrine sensitivity metrics.
(Ref: Natera press release announcing TEODOR trial launch, July 29, 2025)

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Pirtobrutinib (Jaypirca) Meets Primary Endpoint Against Ibrutinib in First-Line CLL/SLL (BRUIN CLL-314)

On July 29, 2025, Lilly announced that pirtobrutinib demonstrated non-inferiority and statistical superiority, in overall response rate versus ibrutinib in treatment-naïve or BTKi-naïve CLL/SLL, in the head-to-head BRUIN CLL‑314 Phase III trial. PFS data is immature but trending favourably.
Clinical takeaway: This is first head-to-head evidence supporting a non-covalent BTK inhibitor in frontline CLL/SLL.
(Ref: Lilly press release with BRUIN trial topline results, July 29, 2025)

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Neuronatin (NNAT) Overexpression Predicts Brain Metastatis and Poor Survival in Lung Adenocarcinoma

A retrospective study of 200 lung adenocarcinoma patients (33 with brain metastasis) showed that nuclear NNAT immunopositivity corresponded with significantly shorter overall survival (7.6 vs 24.4 months) and independently predicted brain metastasis risk. NNAT-IRS positivity was similarly linked to diminished outcomes.
Translational insight: NNAT may serve as a valuable early prognostic biomarker to stratify high-risk patients for brain-directed surveillance and intervention.
(Ref: Basaran Goksen et al. Scientific Reports 2025;15:27653)

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This week’s Oncology Spotlight: Dr. Maria Barbu on Cancer Care in Romania!

In this week’s special segment from IUCS 2024, we speak with Dr. Maria Barbu, a medical oncologist from Bucharest, Romania. CLICK HERE TO WATCH!Oncology Spotlight 45 1Dr. Barbu shares her perspective on the evolving oncology landscape in Eastern Europe, particularly in the treatment of prostate cancer.Explore more stories & insights on ONCOassist. Your clinical edge, just a tap away. 

Join the ONCOassist oncology community, the go-to CE‑approved app for oncology professionals worldwide !

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  •  Access essential tools like staging systems, toxicity scoring, drug calculators, prognostic scores and NCCN regimens,all in one place .
  • Stay informed with ONCOnews & ONCOvideos featuring expert insights, conference coverage and peer-tested protocols 

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Weekly Oncology Highlights | Oncology News, Updates and Spotlights

Screenshot 2025 07 25 at 1.32.03 PM

Your go-to digest for the latest breakthroughs in cancer care.

This week’s updates spans EU precision approvals in prostate and breast cancer, immunotherapy-driven de-escalation in cSCC, and generic access gains, underscoring strides toward personalized, accessible oncology care.

Leading voices. Big insights. Scroll down to watch now Dr. Vinayak Maka’s Oncology Spotlight!

EU Approves Nubeqa (Darolutamide) for Metastatic Hormone-Sensitive Prostate Cancer 

On July 21, 2025, the European Commission approved Nubeqa (darolutamide) plus ADT in mHSPC, based on the Phase III ARANOTE trial showing a 46% reduction in radiographic progression or death (HR 0.54; 95% CI 0.41–0.71; P < 0.0001). The safety profile was consistent with published data, and the indication now supports use with or without chemotherapy.
Clinical insight: Offers flexibility to tailor therapy intensity in mHSPC patients.
(Ref: Bayer press release reporting ARANOTE outcomes and EC approval, July 21, 2025)

Blenrep (Belantamab Mafodotin) Combinations Approved in EU for Relapsed/Refractory Multiple Myeloma

In relapsed/refractory multiple myeloma after ≥ 1 prior therapy (including prior lenalidomide for BPd), the European Commission approved Blenrep + bortezomib + dexamethasone (BVd) and Blenrep + pomalidomide + dexamethasone (BPd) on July 24, 2025. Head-to-head Phase III DREAMM‑7 and DREAMM‑8 trials showed superior progression-free survival, with DREAMM‑7 also demonstrating a ~42% overall survival benefit compared to daratumumab-based triplets. Ocular events were common but manageable; discontinuation rates were ≤ 9%, and non‑ocular AEs included thrombocytopenia, neutropenia, diarrhoea and COVID‑19.
Practice shift: Blenrep becomes the first anti‑BCMA ADC combination approved in the EU, offering substantial PFS/OS gains and outpatient-friendly administration in the earliest relapsed setting, redefining options post–first relapse.
(Ref: GSK press releases and CHMP positive opinion based on DREAMM‑7/8 efficacy and safety data; Reuters on EU approval and global context)

EC Approves Itovebi™ (Inavolisib) for PIK3CA‑Mutated HR‑Positive, HER2‑Negative Advanced Breast Cancer 

On July 23, 2025, the European Commission approved Inavolisib combined with palbociclib and fulvestrant for adults with PIK3CA-mutated, ER-positive, HER2-negative advanced breast cancer relapsing within 12 months post-endocrine therapy. The INAVO120 Phase III data showed 57% PFS improvement (HR 0.43; median 15.0 vs 7.3 months; P < 0.001), 33% OS benefit (HR 0.67; P = 0.019), and delayed chemotherapy initiation by approximately two years.
Impact: First PI3K-targeted therapy delivering both PFS and OS benefit in this biomarker-defined subgroup, underscores upfront genomic testing.
(Ref: Roche and EMA documentation of INAVO120 final OS analysis and EC approval, July 2025
)

EC Approves DARZALEX® (Daratumumab SC) for High‑Risk Smouldering Multiple Myeloma

On July 23, 2025, the European Commission authorized subcutaneous daratumumab as first licensed monotherapy for high-risk smouldering multiple myeloma. The Phase III AQUILA study demonstrated a 51% reduction in progression to active MM or death versus observation.
Breakthrough: Establishes the first early-intervention, approved therapeutic for high-risk SMM.
(Ref: CHMP positive opinion and EC approval based on AQUILA outcomes as reported by Janssen in mid‑2025 )

ECUS FDA Tenatatively Approves Zydus Generic Ibrutinib Tablets for CLL/SLL 

On July 24, 2025, Zydus Lifesciences received tenatative U.S. FDA approval for generic Ibrutinib tablets in all three strenghts for CLL/SLL with 17p deletion and Waldenstrom’s macroglobulinemia. Branded Ibrutinib annual U.S. sales are estimated at USD 2.15 billion. Significance: Paves way for broader access and cost reduction in BTK- inhibitor therapy upon patent expiry. (Ref: FDA tenatative approval report and market analysis in targeted oncology news, July 24, 2025)

This week’s Oncology Spotlight: Dr. Vinayak Maka on using the ONCOassist app!

In this podcast, as one of our earliest users in India, Dr. Maka shares how the app transformed the way he accesses staging systems, toxicity grading, oncology calculators, and real-time updates at the point of care.Oncology Spotlight 45 2  Explore more stories & insights on ONCOassist. Your clinical edge, just a tap away.     

Join the ONCOassist oncology community, the go-to CE‑approved app for oncology professionals worldwide !

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  •  Access essential tools like staging systems, toxicity scoring, drug calculators, prognostic scores and NCCN regimens,all in one place .
  • Stay informed with ONCOnews & ONCOvideos featuring expert insights, conference coverage and peer-tested protocols 

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Weekly Oncology Highlights – Powered by ONCOassist

Weekly Oncology Highlights – Powered by ONCOassist

Your go-to digest for the latest breakthroughs in cancer care.

 

From breakthrough PARP/AR combo efficacy to transformative immunotherapy approvals and rare cancer strides, this week’s oncology updates spotlight how precision therapies and regulatory momentum are setting new benchmarks in survival and patient outcomes.

Leading voices. Big insights. Scroll down to watch now Dr. Akash Maniam’s Oncology Spotlight!

 

TALAPRO-2: Talazoparib + Enzalutamide Survival Breakthrough in mCRPC

A final overall survival analysis from the phase III TALAPRO‑2 trial showed that talazoparib plus enzalutamide in HRR-deficient metastatic castration-resistant prostate cancer reduced risk of death by 38% (HR 0.62; p = 0.0005), extending median OS to 45.1 vs 31.1 months compared to placebo + enzalutamide.

Safety profile consistent: grade 3+ anemia (43%), neutropenia (20%); no new safety signals. (Reference: Fizazi et al., The Lancet, 2025 Final OS Analysis)

TEVIMBRA® (Tislelizumab) Approved in EU for Nasopharyngeal Carcinoma Based on RATIONALE-309

The European Commission approved tislelizumab (TEVIMBRA®) with gemcitabine and cisplatin as first-line therapy for metastatic/recurrent nasopharyngeal carcinoma not suitable for curative treatment.

(Reference: BeOne Medicines Ltd., “European Commission Approves TEVIMBRA® in Combination with Chemotherapy as a First‑Line Treatment for Nasopharyngeal Carcinoma,” July 10, 2025)

ENGOT‑OV60/RAMP 201: Avutometinib + Defactinib in Recurrent Low‑Grade Serous Ovarian Cancer 

Results from the phase II ENGOT‑OV60/GOG‑3052/RAMP 201 study, published in JCO, showed that the oral combination of MEK inhibitor avutometinib plus FAK inhibitor defactinib induced a 31% confirmed ORR in 115 heavily pretreated patients with recurrent low-grade serous ovarian cancer (LGSOC), including complete and partial responses. Notably, KRAS-mutant tumors responded at 44%, compared with 17% in wild-type cases. Median progression-free survival was 12.9 months overall, extending to 22.0 months in the KRAS-mutant cohort versus 12.8 months in the wild-type group. The safety profile was manageable; common grade ≥3 AEs included elevated CPK (24%), diarrhea (8%), and anemia (5%), while approximately 10% discontinued due to toxicity. (Reference: Banerjee et al., JCO, 2025)

ICR Identifies New “Armour” Protein (SLC7A11) in Melanoma

The Institute of Cancer Research (UK) identified SLC7A11 as a protective protein that shields melanoma cells from oxidative stress and enhances invasive potential. Elevated SLC7A11 maintains cytoskeletal dynamics essential for amoeboid movement and metastasis. Notably, in vitro inhibition killed ~75% of melanoma cells within 72 hours, suggesting a promising therapeutic target. The researchers also caution that antioxidant supplements (e.g., glutathione) may reinforce this “armour” and should be used judiciously in melanoma patients. (Reference: ICR press release, July 15, 2025)

FDA grants Fast Track to ZEN-3694 + Abemaciclib for NUT Carcinoma

On July 14, the FDA awarded Fast Track designation to the BET inhibitor ZEN‑3694, in combination with abemaciclib, for treatment of metastatic or unresectable NUT carcinoma following prior chemotherapy. This ultra‑rare, aggressive cancer lacks approved systemic therapies. Preclinical and early clinical data support the combination’s potency, and FDA Fast Track status will facilitate expedited review via priority communication and potential accelerated approval mechanisms. (Reference: Zenith Epigenetics Ltd. press release, July 14, 2025)

This week’s Oncology Spotlight: Dr. Akash Maniam compares the Oncology Systems and Cancer Care of UK and the Caribbean

In this podcast, Dr. Akash Maniam contrasts cancer care in the UK with that in the Caribbean, spotlighting challenges from diagnostic delays to limited trial access and geographic barriers. Oncology Spotlight 45 1His insights underscore the urgent need for global oncology equity, especially in low‑resource settings where systemic gaps and lack of auditing hinder outcomes.   Explore more stories & insights on ONCOassist. Your clinical edge, just a tap away.     

Join the ONCOassist oncology community, the go-to CE‑approved app for oncology professionals worldwide !

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  •  Access essential tools like staging systems, toxicity scoring, drug calculators, prognostic scores and NCCN regimens,all in one place .
  • Stay informed with ONCOnews & ONCOvideos featuring expert insights, conference coverage and peer-tested protocols 

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Weekly Oncology Highlights – Powered by ONCOassist

Weekly Oncology Highlights – Powered by ONCOassist

Your go-to digest for the latest breakthroughs in cancer care.

 

From a landmark EU approval of perioperative immunotherapy in bladder cancer to strong CAR‑T durability and promising oral regimens in haematological malignancies, this week’s oncology updates show how targeted drugs and regulatory advances are driving better survival and improves patient outcomes.

Leading voices. Big insights. Scroll down to watch now Dr. Grant Jirka’s Oncology Spotlight!

 

Imfinzi (Durvalumab) Gains EU Approval in Muscle-Invasive Bladder Cancer Based on NIAGARA Trial Results

The European Commission has approved AstraZeneca’s Imfinzi (durvalumab) in combination with gemcitabine and cisplatin as neoadjuvant treatment, followed by Imfinzi as monotherapy adjuvant treatment after radical cystectomy, for adult patients with resectable muscle-invasive bladder cancer (MIBC).

This regulatory nod follows results from the Phase III NIAGARA trial, which demonstrated a 32% reduction in risk of disease progression, recurrence, or death (HR 0.68; 95% CI, 0.56–0.82; p<0.0001) and a 25% reduction in risk of death (HR 0.75; 95% CI, 0.59–0.93; p=0.0106) compared to neoadjuvant chemotherapy alone. At two years, 82.2% of patients treated with the Imfinzi regimen were alive, and 67.8% were event-free.

Imfinzi was well tolerated, with no new safety signals, and was consistent with known profiles in neoadjuvant and adjuvant settings. The ESMO Magnitude of Clinical Benefit Scale (MCBS) awarded this regimen the highest grade of “A” in the curative setting. Regulatory submissions are ongoing in Japan and other countries. (Reference: AstraZeneca. “Imfinzi Approved in the EU Based on NIAGARA Phase III Results.” July 2025)

 

STAMPEDE Trial: Metformin Shows No Significant Survival Benefit in mHSPC, But Reduces ADT-Related Metabolic Effects

In the latest arm of the STAMPEDE platform Phase III trial, the addition of metformin (850 mg BID) to standard of care (SOC) in non-diabetic patients with metastatic hormone-sensitive prostate cancer (mHSPC) did not significantly improve overall survival (HR 0.91; 95% CI, 0.80–1.03; p=0.15), although median survival was numerically longer: 67.4 months vs. 61.8 months in the SOC group.

However, metformin significantly reduced adverse metabolic effects commonly seen with androgen deprivation therapy (ADT), such as weight gain and metabolic derangements. Grade 3 or worse gastrointestinal side effects were higher in the metformin group (9% vs. 7%).

While not practice-changing, the findings underscore metformin’s metabolic safety benefits and its potential utility in settings where ARPI access is limited due to cost or comorbidities. (Reference: Gillessen S. et al. “STAMPEDE Trial: Metformin in Metastatic Prostate Cancer.” The Lancet Oncology, July 2025)

 

Taiho’s INQOVI (decitabine and cedazuridine) + Venetoclax Accepted by FDA for AML Review 

The U.S. FDA has accepted Taiho Oncology’s supplemental new drug application (sNDA) for INQOVI (decitabine and cedazuridine) in combination with venetoclax for the treatment of newly diagnosed acute myeloid leukemia (AML) in adults ineligible for intensive induction chemotherapy. A standard review has been assigned with a PDUFA action date of February 25, 2026.

The submission is supported by ASCERTAIN-V (AStx727-07), a Phase 2b trial involving 101 patients, where INQOVI was administered on days 1–5 of a 28-day cycle and venetoclax daily. The trial met its primary endpoint with a complete response (CR) rate of 46.5%, while CR + CRi was 63.4%. Median overall survival was 15.5 months; at 12 months, over 75% of patients who achieved CR remained in CR.

Safety was consistent with known profiles of both agents, with no new safety signals or drug-drug interactions reported. Grade ≥3 adverse events occurred in 98% of patients, with febrile neutropenia (49.5%), anemia (38.6%), and neutropenia (35.6%) being most common.

If approved, this would be the first all-oral regimen for patients with AML who are not eligible for standard induction therapy. (Reference: Taiho Oncology Press Release, July 9, 2025; data presented at ASCO & EHA 2025)

 

TRANSFORM 3-Year Update Confirms Durable Benefit of Lisocabtagene Maraleucel in Second-Line LBCL

The Phase III TRANSFORM trial (NCT03575351) evaluating lisocabtagene maraleucel (liso-cel) versus standard of care (SOC) in second-line relapsed/refractory large B-cell lymphoma (LBCL) with ≤12 months of relapse post first-line therapy has reported 3-year follow-up data.

Median event-free survival (EFS) was 29.5 months with liso-cel vs. 2.4 months with SOC (HR 0.375; 95% CI, 0.259–0.542). The 3-year progression-free survival (PFS) rates were 51% vs. 26.5%, respectively. While overall survival (OS) was not reached in either arm, a crossover-adjusted OS HR of 0.566 (95% CI, 0.359–0.895) favored liso-cel.

Safety remained consistent with earlier reports, with no new safety signals. These findings reinforce liso-cel’s curative potential as a second-line therapy in LBCL. (Reference: Kamdar M. et al. “Three-Year Results from the TRANSFORM Trial.” Journal of Clinical Oncology, July 2025)

 

Divarasib Shows Durable Activity in KRAS G12C+ NSCLC With Favourable Long-Term Safety

Updated data from a Phase I study (NCT04449874) of divarasib (GDC-6036) in KRAS G12C–mutated non-small cell lung cancer (NSCLC) showed long-term antitumor activity and sustained safety beyond 1 year.

Among 65 patients, the objective response rate (ORR) was 55.6%, and median duration of response (DoR) reached 18.0 months. The median progression-free survival (PFS) was 13.8 months overall, and 15.3 months at the 400 mg dose level.

Divarasib, a next-generation KRAS G12C inhibitor, exhibited a favorable safety profile and high selectivity. Its extended activity profile supports its promise as a potentially superior alternative to current KRAS G12C inhibitors. (Reference: Sacher A. et al. “Divarasib in KRAS G12C–Positive NSCLC: Long-Term Results.” Journal of Clinical Oncology, July 2025)

 

This week’s Oncology Spotlight: Dr.Grant Jirka shares his insights on ONCOassist’s Advanced Myelofibrosis Scoring Tool

In a recent video feature, Dr. Grant Jirka, Hematology/Oncology Fellow in Los Angeles, demonstrates how the ONCOassist Advanced Myelofibrosis Scoring Tool is streamlining clinical decision-making in one of hematology’s most challenging diseases. Oncology Spotlight 45By integrating five major prognostic models IPSS, DIPSS, DIPSS-Plus, MIPSS70, and MIPSS70-Plus, into a single, intuitive interface, the tool allows oncologists to input 12 variables and receive comprehensive risk stratification in under 90 seconds. From simplifying transplant discussions to supporting more confident, informed treatment planning, this tool is a game-changer in managing myelofibrosis.

 

 

Explore more stories & insights on ONCOassist. Your clinical edge, just a tap away.     

Join the ONCOassist oncology community, the go-to CE‑approved app for oncology professionals worldwide !
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  •  Access essential tools like staging systems, toxicity scoring, drug calculators, prognostic scores and NCCN regimens,all in one place .
  • Stay informed with ONCOnews & ONCOvideos featuring expert insights, conference coverage and peer-tested protocols 
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