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ANCO - Education and Empowering the Northern California Cancer Community

September 2026

08/31/2026 2:40 PM | Anonymous

Call for Nominations:  ANCO's Board of Directors

  • In accordance with the by-laws of the Association of Northern California, the ANCO Board of Directors hereby issues a call for a nominations for members of the Board of Directors. (Read the job description).

    To nominate (or self-nominate) a candidate for the ANCO's Board of Directors, please use the form below by 11:00pm, October 15, 2026.

    Click here for a complete list of the current board of directors.

Submit a Nomination


Institutional Member News

  • UC Davis Comprehensive Cancer Center - Clinical Trials

    PHII-254 – Sinonasal Squamous Cell Carcinoma (Head & Neck) Randomized Phase 2 study adding Cemiplimab to chemotherapy before surgery Compares chemo (carboplatin + paclitaxel) with vs. without cemiplimab given before surgery in patients with sinonasal squamous cell cancer, to see if it's more effective at stopping cancer growth/spread than chemo alone. Website: https://clinicaltrials.gov/study/NCT07281417 Contact: UC Davis Comprehensive Cancer Center, Office of Clinical Research — OCRReferral@health.ucdavis.edu | 916-382-6970

    D7630C00001 – Breast Cancer (TNBC) Phase III study of Dato-DXd ± durvalumab vs. chemo + pembrolizumab Compares Dato-DXd with durvalumab against standard chemotherapy plus pembrolizumab in patients with PD-L1 positive, locally recurrent inoperable or metastatic triple-negative breast cancer, looking at progression-free survival, overall survival, and quality of life. Website: https://clinicaltrials.gov/study/NCT06103864 Contact: UC Davis Comprehensive Cancer Center, Office of Clinical Research — OCRReferral@health.ucdavis.edu | 916-382-6970

    NRG-GI012 – Hepatocellular Cancer (HCC) Phase III study of IO-based systemic treatment ± liver SBRT (HELIO-RT) Evaluates whether adding liver SBRT to first-line immunotherapy-based systemic treatment improves outcomes in patients with advanced hepatocellular carcinoma with macrovascular invasion. Website: https://clinicaltrials.gov/study/NCT07166406 Contact: UC Davis Comprehensive Cancer Center, Office of Clinical Research — OCRReferral@health.ucdavis.edu | 916-382-6970

Practice Management & Operations

  • Mednet has a new AI-powered tool, TrialMatch, helps oncologists quickly match patients with actively enrolling clinical trials using natural language searches.

Read More
  • A recent NCCN survey highlights persistent generic chemotherapy shortages impacting cancer centers nationwide, affecting critical agents like carboplatin and cisplatin—read more here.
Read More


The NCCN Policy & Advocacy

NCCN Oncology Clinical Trials Survey

NCCN is studying how policy and practice changes can strengthen collaboration between academic and community oncologists to improve representative enrollment in clinical trials.

  • Survey Link: Take the Survey

  • Time Commitment: ~10 minutes

  • Deadline: October 12, 2026

  • Confidentiality: All responses are confidential, unlinked to your identity, and approved by the Pearl Institutional Review Board.

  • Questions? Contact Ashley Orr (orr@nccn.org) or Taneal Carter (carter@nccn.org), both cc’ed on this email.

National Press Club for our expanded two-day summit, featuring a welcome reception on night one!

  • Schedule & Locations:

    • Monday, Oct 5 (Evening): Welcome Networking Reception at the JW Marriott

    • Tuesday, Oct 6: Policy Summit at the National Press Club

  • Keynote Speakers:

    • Dr. Anthony Letai, Director of the NCI

    • Captain Jacqueline Miller, MD, Acting Division Director, CDC Division of Cancer Prevention and Control

  • In-Person Attendance for SOSF Members: We have a few remaining slots available to fully cover registration, travel, and lodging for SOSF members. Please reply to this email if you are interested in attending in person.

  • Virtual Attendance: Free virtual registration is available to all using promo code GD2026.

  • Agenda: View the full schedule and speaker lineup here.

Corporate Member News

  • Bristol Myers Squibb invites you to an educational discussion on Patient Outcomes with a CELMoD (ZENBEXUS™) led by Dr. Saeed Sadeghi (UCLA). Topics include the CELMoD mechanism, clinical efficacy and safety data in RRMM, patient selection, and real-world management. Date & Time: Thursday, October 1, 2026 @ 6:30 PM PT
  • The FDA granted accelerated approval to camizestrant (Etcamah, AstraZeneca), an estrogen receptor antagonist, in combination with a CDK4/6 inhibitor (abemaciclib, palbociclib, or ribociclib) for adults with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative locally advanced or metastatic breast cancer upon detection of estrogen receptor-1 (ESR1) mutation during aromatase inhibitor and CDK4/6 inhibitor therapy, based on an FDA-authorized test.

Read More

  • The FDA approved imlunestrant (Inluriyo) in combination with abemaciclib (Verzenio), for adults with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, estrogen receptor 1 (ESR1)-mutated advanced or metastatic breast cancer, as detected by an FDA-authorized test, with disease progression following at least one line of endocrine therapy. Inluriyo and Verzenio are manufactured by Eli Lilly and Company.
  • The FDA granted accelerated approval to sevabertinib (Hyrnuo, Bayer Healthcare Pharmaceuticals Inc.), a kinase inhibitor, for adult patients with locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) whose tumors have HER2 (ERBB2) tyrosine kinase domain (TKD) activating mutations, as detected by an FDA-authorized test.
  • The FDA approved Mimrylo (rusfertide), a new treatment for adults with polycythemia vera, a rare blood disorder that causes the body to make too many red blood cells. 

Read More

  • The FDA approved Ziihera® (zanidatamab-hrii) with and without Tislelizumab plus Chemotherapy in first-Line HER2+ Advanced Gastroesophageal Adenocarcinoma.

Read More

  • The FDA approved BESREMi® (ropeginterferon alfa-2b-njft) for the treatment of adults with essential thrombocythemia (ET).

Read More

  • Revolution Medicine invites you to their upcoming National Broadcast on September 30th 2026 at 6pm in San Francisco.
Click Here For More Details


Reibursement Updates

  • In this month’s edition of E-Reimbursement, Bobbi Rubell breaks down essential Q4 HCPCS coding updates, key takeaways from the FY 2027 Inpatient Prospective Payment System (IPPS) final rule, and critical industry shifts. Stay ahead of regulatory changes, billing updates, and rising audit risks.
Read More

  

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