Major Advances

Verified advances, grouped by theme. Categories with no verified content show an honest empty state — nothing is manufactured to fill them.

Treatment Innovations

FDA approves the first all-oral combination regimen for older adults with newly diagnosed acute myeloid leukemia

Evidence stage: Emerging ClinicalRegulatory status: FDA Approved
Cancer type
Leukemia
Published
August 13, 2026

In the single-arm Study ASTX727-07, an all-oral combination of decitabine/cedazuridine (Inqovi) plus venetoclax produced a complete remission rate of 41.6% (and a combined complete-remission-or-partial-hematologic-recovery rate of 52.5%) in older or…

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Early Detection & Diagnostics

FDA approves Cologuard Plus, a next-generation stool DNA test for colorectal cancer screening

Evidence stage: Later-Stage HumanRegulatory status: FDA Approved
Cancer type
Colorectal Cancer
Published
August 13, 2026

In the prospective, 20,176-participant BLUE-C study, Cologuard Plus (a next-generation multitarget stool DNA test) detected colorectal cancer with 95% sensitivity and correctly identified 94% of participants without colorectal cancer or…

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Clinical Research

Adding lenvatinib and pembrolizumab to TACE improves progression-free survival in liver cancer, but the trial’s overall-survival goal was not met

Evidence stage: Later-Stage HumanRegulatory status: Investigational
Cancer type
Liver Cancer
Published
August 13, 2026

In the randomized, double-blind, phase 3 LEAP-012 trial, adding lenvatinib and pembrolizumab to TACE significantly extended progression-free survival compared with TACE alone (14.6 months versus 10.0 months) in patients with…

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AMBASSADOR trial finds adjuvant pembrolizumab extends disease-free survival in high-risk bladder cancer — not yet FDA-approved for this use

Evidence stage: Later-Stage HumanRegulatory status: Investigational
Cancer type
Bladder Cancer
Published
August 13, 2026

In the randomized, phase 3 AMBASSADOR trial, adjuvant pembrolizumab after radical surgery significantly extended disease-free survival compared with observation alone in patients with high-risk muscle-invasive or locally advanced urothelial carcinoma.…

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Precision / Personalized Medicine

Six-year OlympiA data sustain the adjuvant olaparib survival benefit in BRCA-mutated, HER2-negative early breast cancer

Evidence stage: High-Certainty EvidenceRegulatory status: FDA Approved
Cancer type
Breast Cancer
Published
August 13, 2026

In the randomized, double-blind, placebo-controlled OlympiA trial, one year of adjuvant olaparib significantly improved invasive disease-free survival (primary publication) and, in a later analysis, significantly improved overall survival as well…

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Prevention & Risk Reduction

Patient Support & Survivorship

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AI & Technology in Cancer Care

Cancer Biology & Mechanisms

A lab-made “molecular glue” reprograms a lymphoma oncogene to trigger cancer-cell self-destruction, in early cell and mouse studies

Evidence stage: PreclinicalRegulatory status: Investigational
Cancer type
Lymphoma
Published
August 13, 2026

In laboratory cell-line and mouse studies, a Stanford-engineered small molecule that forces two proteins (the lymphoma oncogene BCL6 and the enzyme CDK9) into physical proximity reprogrammed BCL6 to switch ON…

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Screening

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Immunotherapy

FDA approves blinatumomab in the consolidation phase of B-cell precursor acute lymphoblastic leukemia, regardless of MRD status

Evidence stage: High-Certainty EvidenceRegulatory status: FDA Approved
Cancer type
Leukemia
Published
August 13, 2026

In the randomized, phase 3 ECOG-ACRIN E1910 trial, adding blinatumomab to consolidation chemotherapy significantly extended overall survival compared with chemotherapy alone in adults with MRD-negative B-cell precursor ALL — the…

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FDA approves talquetamab, a first-in-class bispecific antibody, for heavily pretreated multiple myeloma

Evidence stage: Later-Stage HumanRegulatory status: FDA Approved
Cancer type
Multiple Myeloma
Published
August 13, 2026

In the single-arm, open-label, phase 1/2 MonumenTAL-1 trial, talquetamab produced meaningful, durable responses in patients with heavily pretreated, relapsed or refractory multiple myeloma who had already exhausted the major available…

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FDA converts tarlatamab’s accelerated approval to full approval for small cell lung cancer, on a real survival benefit

Evidence stage: High-Certainty EvidenceRegulatory status: FDA Approved
Cancer type
Lung Cancer
Published
August 13, 2026

In the randomized, open-label, phase 3 DeLLphi-304 trial, tarlatamab significantly extended overall survival compared with chemotherapy in patients with extensive-stage small cell lung cancer that had progressed after platinum-based chemotherapy…

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Cancer Vaccines

Personalized mRNA cancer vaccine plus pembrolizumab reduces melanoma recurrence risk in randomized phase 2b trial

Evidence stage: Emerging ClinicalRegulatory status: Investigational
Cancer type
Melanoma / Skin Cancer
Published
August 13, 2026

In the randomized, phase 2b KEYNOTE-942 trial, adding a personalized mRNA cancer vaccine (manufactured for each patient's own tumor mutations) to pembrolizumab reduced the risk of melanoma recurrence or death…

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Targeted Therapies

Lunresertib plus camonsertib produces durable responses in advanced endometrial and ovarian cancer in early trial data

Evidence stage: Emerging ClinicalRegulatory status: Investigational
Cancer type
Endometrial (Uterine) Cancer
Published
August 13, 2026

In the gynecologic expansion cohort of the first-in-human, phase 1 MYTHIC trial, the combination of lunresertib (a PKMYT1 inhibitor) and camonsertib (an ATR inhibitor) produced durable objective responses in heavily…

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Luveltamab tazevibulin showed responses in platinum-resistant ovarian cancer in dose-optimization data; the trial was later terminated

Evidence stage: Emerging ClinicalRegulatory status: Investigational
Cancer type
Ovarian Cancer
Published
August 13, 2026

In the dose-optimization portion of the now-terminated phase 2/3 REFRaME-O1 trial, the antibody-drug conjugate luveltamab tazevibulin produced objective responses in patients with platinum-resistant ovarian cancer expressing folate receptor alpha, at…

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FDA approves zolbetuximab for CLDN18.2-positive gastric and gastroesophageal junction cancer

Evidence stage: High-Certainty EvidenceRegulatory status: FDA Approved
Cancer type
Stomach (Gastric) Cancer
Published
August 13, 2026

In two separate, randomized, double-blind, phase 3 trials (SPOTLIGHT and GLOW), adding zolbetuximab to first-line chemotherapy significantly extended both progression-free survival and overall survival, compared with chemotherapy alone, in patients…

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FDA converts tisotumab vedotin’s accelerated approval to full approval for recurrent or metastatic cervical cancer

Evidence stage: High-Certainty EvidenceRegulatory status: FDA Approved
Cancer type
Cervical Cancer
Published
August 13, 2026

In the randomized, open-label, phase 3 innovaTV 301 trial, tisotumab vedotin significantly extended both overall survival (11.5 months versus 9.5 months) and progression-free survival (4.2 months versus 2.9 months), compared…

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Cell Therapies

Genomics & Molecular Oncology

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Gene & Genetic Technologies

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Radiation Advances

Surgical Advances

Liquid Biopsy & Circulating Tumor Technologies

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Biomarkers