ASCO is the world's largest oncology professional society; its annual meeting each June is where most practice-changing trials are first presented.
The American Society of Clinical Oncology, based in Alexandria, Virginia, is the world's largest oncology professional society, and its Annual Meeting each June, with around forty thousand attendees, is where most practice-changing trials are first presented. It publishes the Journal of Clinical Oncology and its JCO sister journals, runs the TAPUR basket trial and CancerLinQ, and issues clinical practice guidelines including the 2021 guideline on immune-related side effects. OnCo connects it to bottlenecks on hidden failures and incentives that reward marginal gains, and to ideas such as a guideline fast track for repurposed drugs and independent validation of surrogate endpoints. Whether a society funded partly by industry can police value is the fair question. Its guidelines collection has its own page.
Clifford Hudis is a breast oncologist who has run ASCO since 2016.
Prostate cancer trialist who helped bring abiraterone and sipuleucel-T to patients, and led ASCO in 2025-26.
Head and neck cancer leader who established organ-preserving chemoradiation and led ASCO in 2021-22.
At Harlem Hospital in the 1950s she showed methotrexate could shrink breast and skin cancers, tested drugs on patients' own tumour cells, and in 1964 was the only woman among the seven founders of ASCO.
Lori Pierce is a breast radiation oncologist and ASCO past president focused on equity in cancer care.
Lynn Schuchter is a melanoma oncologist who led ASCO in 2023-24.
Community oncologist who led ASCO in 2024-25 with a focus on bringing trials to patients close to home.
Confirms that the TROP2 antibody-drug conjugates are given without a TROP2 test and that PD-L1 remains the one selection assay in metastatic triple-negative disease, which is why assay harmonisation matters.
Shows how quickly the standard moved: the 2021 guideline and its reversal are 15 months apart.
Checkpoint inhibitors are now given to hundreds of thousands of patients a year, many in community clinics and emergency departments, so a common, explicit playbook for their autoimmune side effects saves lives. The guideline standardised when to stop, when to give steroids and when to escalate, and made multidisciplinary toxicity teams routine. It does not remove the judgement needed for rare events or for patients whose cancer is responding.
The last major guideline written before KEYNOTE-522 changed the standard; the 2022 rapid update reversed the immunotherapy line within a year.
Sets the surgical and systemic rules for the one in nine to one in six triple-negative patients who carry a germline BRCA variant (11 to 17 percent by cohort); the adjuvant gap it named was filled by OlympiA the following year.
The document that made biomarker testing part of routine pancreatic cancer care in the United States; the 2018 version it built on fixed the second-line chemotherapy sequence still used in most guidelines.
The formal adoption of PRODIGE 24 into practice; every later debate about giving chemotherapy before rather than after surgery starts from this recommendation.
Triple-negative is a laboratory definition; this guideline wrote the oestrogen and progesterone half of it, and the 1 to 10 percent low-positive band it created is still argued over.
Shares Micro-learning pushed to community oncologists within 30 days of a practice change, Cap public prices for new cancer drugs to tiers of the ESMO and ASCO value scales, End the abstract-to-paper gap: require full results with any conference presentation, Give negative trials plenary slots at the big cancer conferences.
Shares Offline decision support for generalists treating common cancers in low-resource settings, ASCO clinical practice guidelines, A guideline fast track for repurposed drugs with phase 3 evidence but no manufacturer, Living guidelines published as versioned, computable rules.
Shares ASCO clinical practice guidelines, A guideline fast track for repurposed drugs with phase 3 evidence but no manufacturer, Living guidelines published as versioned, computable rules, Weak real-world evidence and registries.
Shares ASCO clinical practice guidelines, Default-inclusive eligibility: sponsors must justify every exclusion criterion, Living, machine-readable guidelines pushed to the point of care in every country, Older and multimorbid patients are excluded and undertreated.
Shares Micro-learning pushed to community oncologists within 30 days of a practice change, End the abstract-to-paper gap: require full results with any conference presentation, Real-time guideline-concordance feedback for every cancer centre, Living, machine-readable guidelines pushed to the point of care in every country.
Shares Every payer covers routine care costs for trial participants, in every country, Lay trial navigators funded per centre, evaluated in a randomised trial, Stop excluding people with a prior cancer, controlled HIV, or treated hepatitis, A public equity index for trial sites and sponsors, tied to funding.
Shares Exempt oncologists who follow the pathway from prior authorisation, Living guidelines published as versioned, computable rules, Patients lack understanding, navigation and agency, Knowledge reaches practice too slowly.
Shares Power trials to detect a benefit patients would value, not the smallest detectable one, An independent programme that validates surrogate endpoints, setting by setting, Patients lack understanding, navigation and agency, Regulatory divergence between regions.