OnCo

The state of the war on cancer, 2026

Generated from the OnCo corpus: what was approved, what read out, where the roadmaps stand, and what is still unsolved. Every figure below is a count over the objects on this site, so it is auditable and it is incomplete in exactly the ways the corpus is.

Three things defined 2026 in oncology as recorded here. First, antibody-drug conjugates moved from rescue therapy to first choice: two TROP2 ADCs were approved for first-line triple-negative breast cancer, trastuzumab deruxtecan reached early-stage HER2-positive disease, and the first bispecific ADC succeeded in phase 3. Second, immunotherapy grew a new limb: a personalised mRNA vaccine met its phase 3 endpoints in melanoma, an oncolytic virus was approved after an earlier rejection, and a blood test for residual disease decided, for the first time, who receives adjuvant immunotherapy. Third, targeted protein degradation arrived, with the first PROTAC approved for ESR1-mutant breast cancer.

The failures matter as much. TIGIT blockade did not add to PD-1 inhibition; a CD47 antibody was abandoned; a second TOP1-payload ADC given straight after a first works poorly. Pancreatic cancer and glioblastoma remain the deadliest common cancers, though the first pan-RAS inhibitor is in a pivotal trial and tumour treating fields earned the first pancreatic approval in decades.

The corpus at a glance

Approved 306Positive 296Standard of care 100Established 96Emerging 70Phase 3 54Phase 2 41Negative 40Mixed 30Recruiting 26Phase 1 20Withdrawn 14Preclinical 12Active 10Completed 6Concept 4Historic 3

Approvals recorded in 2026

34 label actions · 10 first-ever approvals
ProductRegionIndication
Acalabrutinib
Calquence
USFixed-duration acalabrutinib + venetoclax, previously untreated CLL/SLL without del(17p)/TP53 (AMPLIFY)
ArteraAI BreastUSRisk stratification in early-stage HR+/HER2- invasive breast cancerfirst approval
Atezolizumab
Tecentriq / Tecentriq Hybreza (SC)
USAdjuvant muscle-invasive bladder cancer, ctDNA-positive after cystectomy
Belzutifan
Welireg
USAdjuvant clear-cell RCC with pembrolizumab
Camizestrant
Etcamah
USHR+/HER2- advanced breast cancer with an emergent ESR1 mutation on AI + CDK4/6, with a CDK4/6 inhibitor (accelerated, 4 Sep 2026)first approval
Capivasertib
Truqap
USPTEN-deficient metastatic prostate cancer with abiraterone
Daratumumab
Darzalex / Darzalex Faspro (SC)
USWith teclistamab after ≥1 line (MajesTEC-3); high-risk smouldering myeloma (AQUILA)
Daraxonrasib
Rasonque
USMetastatic pancreatic cancer (previously treated)first approval
Datopotamab deruxtecan
Datroway
USFirst-line unresectable/metastatic TNBC, PD-1/PD-L1 inhibitor ineligible
Decitabine + cedazuridine (oral)
Inqovi
USNewly diagnosed AML, unfit for intensive induction, with venetoclax (ASCERTAIN-V)
Durvalumab
Imfinzi
USHigh-risk NMIBC with BCG
Encorafenib
Braftovi
USFirst-line BRAF V600E mCRC with cetuximab and chemotherapy
Gedatolisib
Revtorpyk
USHR+/HER2- advanced breast cancer after CDK4/6 inhibitor (July 2026)first approval
Isatuximab
Sarclisa / Sarclisa Escena (SC)
USSubcutaneous formulation (Sarclisa Escena)
Lutetium-177 vipivotide tetraxetan
Pluvicto
USLabel expansion (July 2026)
Nivolumab
Opdivo / Opdivo Qvantig (SC)
USUntreated advanced classical Hodgkin lymphoma with AVD, age ≥12
Optune / Optune Pax (TTFields)
Optune
USLocally advanced pancreatic cancer with chemotherapy
Palbociclib
Ibrance
USHR+/HER2+ advanced breast cancer maintenance with anti-HER2 and endocrine therapy
Pembrolizumab
Keytruda / Keytruda Qlex (SC)
USPlatinum-resistant PD-L1+ ovarian cancer; adjuvant RCC with belzutifan; with sacituzumab govitecan in 1L TNBC
Piflufolastat F-18 / Pylarify TruVu
Pylarify
USPylarify TruVu formulation
Pivekimab sunirine
Decnupaz
USBlastic plasmacytoid dendritic cell neoplasmfirst approval
Relacorilant
Lifyorli
USPlatinum-resistant ovarian, fallopian tube, or primary peritoneal cancer with nab-paclitaxelfirst approval
Rusfertide
Mimrylo
USErythrocytosis in adults with polycythaemia verafirst approval
Sacituzumab govitecan
Trodelvy
USFirst-line metastatic TNBC: monotherapy (PD-1 ineligible) or with pembrolizumab (PD-L1 CPS ≥10)
Selpercatinib
Retevmo
USLabel update (July 2026)
Sonrotoclax
Beqalzi
USRelapsed/refractory mantle cell lymphoma after ≥2 lines including a BTK inhibitor (accelerated)
Teclistamab
Tecvayli
USRelapsed/refractory myeloma after ≥1 prior therapy
Tovorafenib
Ojemda
EURelapsed/refractory paediatric low-grade glioma (conditional)
Trastuzumab deruxtecan
Enhertu
USEarly-stage HER2+ breast cancer (neoadjuvant and post-neoadjuvant)
Vepdegestrant
Veppanu
USESR1-mutated ER+/HER2- advanced or metastatic breast cancer after endocrine therapyfirst approval
Vusolimogene oderparepvec
Tudriqev
USUnresectable/metastatic melanoma after anti-PD-1, with nivolumab (accelerated)first approval
Zenocutuzumab
Bizengri
USNRG1-fusion cholangiocarcinoma
Zidesamtinib
Jideytro
USROS1+ NSCLC (July 2026)first approval
Zongertinib
Hernexeos
USFirst-line HER2-mutant non-squamous NSCLC

Trials reported in 2026

13 positive
  • NegativeAMPLIFY-7PPrimary DFS endpoint not met.
  • PositiveASCERTAIN-VCR 41.6%; median time to CR 2 months.
  • PositiveAZUR-1Primary endpoint (sustained cCR at 12 months) met; rates pending congress presentation.
  • PositiveBL-B01D1-307PFS and OS significantly improved at interim analysis (numbers presented ASCO 2026).
  • PositiveCLARITY-Gastric 01Co-primary endpoints including OS met (July 2026); numbers pending.
  • NegativeDREAM3RStopped early; primary endpoint not met.
  • PositiveEMERALD-3PFS HR ~0.70 (interim); OS immature.
  • MixedEPCORE DLBCL-1PFS HR 0.74; OS HR 0.96 (NS).
  • NegativeFianlimab + cemiplimab phase 3 (first-line melanoma)Primary PFS endpoint not met; numerical +5.1 months median PFS at the high dose.
  • PositiveFOURLIGHT-1PFS improved (HR not yet published in detail).
  • MixedHARMONi-3Interim PFS not statistically significant (May 2026); final readouts pending.
  • PositiveHERIZON-GEA-01PFS 12.4 vs 8.1 months (HR 0.63-0.65); OS significantly improved.
  • PositiveINSIGHTPFS favouring ripretinib in the ctDNA-defined subgroup (2026).
  • PositiveINTerpath-001 (V940-001)RFS and DMFS significantly improved (HRs pending presentation).
  • PositiveKrascendo 1Superior PFS and OS vs approved G12C inhibitors (topline, July 2026).
  • NegativeLITESPARK-012Primary endpoint not met (ASCO GU 2026).
  • PositiveLITESPARK-022DFS significantly improved vs pembrolizumab (interim; HR presented ASCO GU 2026).
  • PositivePANKU-Esophagus01 (BL-B01D1-305)OS and PFS significantly improved at interim analysis; numbers per ASCO 2026 presentation.
  • NegativepersevERAPFS 33.1 vs 28.2 months, not significant.
  • PositiveRASolute 302OS 13.2 vs 6.7 months, HR 0.40.
  • NegativeXPORT-EC-042 / ENGOT-EN20 / GOG-3083Primary PFS endpoint not met; mPFS 12.75 vs 7.43 months (mITT) not significant.

Negative, mixed, and withdrawn

failures are data
Trials
Programmes and targets

Where the roadmaps stand

Current (19 steps)
Emerging (19 steps)

Late-stage pipeline

41 products in phase 3 · 36 trials recruiting or active

Frontier technologies

64
ADC payload neutralisersAI-driven drug & target discoveryAlpha-emitter nanogenerators and daughter trappingAntibody-oligonucleotide conjugatesArmoured, logic-gated & next-gen CARsAuger-electron therapyBacteriophage-based tumour deliveryBispecific ADCBreath and volatile-organic-compound detectionCachexia-directed therapy (GDF-15 blockade)Cancer interception vaccinesCancer neuroscience: cutting the nerve supplyCAR-NK & CAR-macrophageCAR-T against stroma: fibroblasts and myeloid cellscfDNA fragmentomicsChronotherapy: timing treatment to the body clockContinuous and near-continuous ctDNA monitoringDe novo designed protein bindersDegrader-antibody conjugate (DAC)Digital twins and virtual control armsDNA origami nanorobotsDual-payload ADCEngineered bacteria as living cancer drugsEngineered exosomes as drug carriersEpigenetic editing (durable gene silencing)FLASH radiotherapyHistotripsy as an immune primerHypoxia-activated prodrugsImmune-stimulating antibody conjugate (ISAC)In situ vaccinationIn vivo base and prime editing for cancerIn vivo CAR-TIntratumoural gene electrotransfer (IL-12 plasmid)Lattice and GRID radiotherapyLogic-gated therapeutics (AND, NOT gates)Magnetic nanoparticle hyperthermiaMasked / conditionally active ADCMetabolic therapy: starving the tumour of a nutrientMicrobiome modulation to unlock immunotherapyMolecular glue discovery platformsN-of-1 and rapid platform trialsOligonucleotide therapeuticsOrganoid-guided therapy at scalePathology & radiology foundation modelsPhotothermal (plasmonic) nanoparticle ablationProgrammable DNA-targeting therapeuticsProton arc therapyQuantum-dot and molecular ultrasound imaging agentsRadio-antibody & radio-ADCRadiodynamic therapy and radiosensitising nanoparticlesRadioligand plus DNA-repair inhibitor combinationsSelf-amplifying and circular RNA therapeuticsSenolytics and senescence-directed therapySonodynamic therapySpatial-omics-guided treatment selectionSTING & innate immune agonistsSystematic drug repurposingTargeted alpha therapyTargeting the tumour's own microbesTargeting tumour mechanics and pressureTotal-body PET for screening and ultra-low-dose imagingTrained innate immunityTROP2 PETVery-high-energy electron therapy

Open problems, two per cancer

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