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ANCO - Education and Empowering the Northern California Cancer Community

Oncology News & Updates

Get the latest oncology updates each month from several organizations all in one location here.


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  • 05/03/2023 3:30 PM | Anonymous member (Administrator)
    ANCO and MOASC STATEMENT ON CANCER CARE DRUG SHORTAGE

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    FDA Approvals

    Genentech is pleased to announce the US Food and Drug Administration (FDA) approval of POLIVYĒį (polatuzumab vedotin-piiq) in combination with a rituximab product, cyclophosphamide, doxorubicin, and prednisone (R-CHP) for the treatment of adult patients who have previously untreated diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS) or high-grade B-cell lymphoma (HGBL) and who have an International Prognostic Index score of 2 or greater.

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    The Food and Drug Administration granted approval to epcoritamab-bysp (EPKINLY, Genmab) as the first and only T-cell engaging bispecific antibody for the treatment of adult patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL), not otherwise specified (NOS), including DLBCL arising from indolent lymphoma, and high-grade B cell lymphoma, after two or more lines of systemic therapy.

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    The Food and Drug Administration approved olaparib (Lynparza, AstraZeneca Pharmaceuticals LP) with abiraterone and prednisone (or prednisolone) for adult patients with deleterious or suspected deleterious BRCA-mutated (BRCAm) metastatic castration-resistant prostate cancer (mCRPC), as determined by an FDA-approved companion diagnostic test.

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    Coding and Reimbursement Updates

    On May 1, the Center for Medicare & Medicaid Innovation (CMMI) updated its information and calculations relative to the forthcoming (July 1) Enhancing Oncology Model (EOM). This communication describes updates to the EOM payment methodology, specifically concerning the calculation of episode expenditures for performance period episodes.

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    View the May E-Reimbursement Newsletter

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    CMS & Noridian Updates

    MolDX: Molecular Diagnostic Tests (MDT) (L35160) – R16 – Effective May 04, 2023
    This Local Coverage Determination (LCD) has been revised under contractor numbers: 01112 (NCA), 01182 (SCA), 01212 (AS, GU, HI, and NMI), and 01312 (NV).

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    Top Denials and Solutions – Q2 Webinar – June 19, 2023
    This event includes: Claim Denials, Electonic Data Interchange (EDI), Medical Necessity, Medicare Secondary Payer, Duplicate claims, Medical Review

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  • 04/03/2023 3:31 PM | Anonymous member (Administrator)
    State and National Legislative & Regulatory Issues

    Late stage cancer rates could rise if ACA ruling stands, experts worry
    A federal judge’s recent ruling on the Affordable Care Act means that patients would have to pay for some cancer screenings that are currently free—a ruling that, if it holds, could make the potentially life-saving tests unaffordable for many, experts say.

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    President Biden Prioritizes Cancer Research, Access to Care in FY 2024 Budget Proposal
    The proposal allocates $48.3 billion for the National Institutes of Health (NIH)—an $811 million increase compared to FY 2023; $7.8 billion for the National Cancer Institute (NCI)—a $500 million increase compared to FY 2023; and $2.5 billion for the Advanced Research Projects Agency for Health (ARPA-H)—a $1 billion increase compared to FY 2023. The request also specifically allocates $1 billion for the Cancer Moonshot initiative.

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    CMS & Noridian Updates

    Hospital In-Patient, Long-Term Care Proposed Rule Aims to Advance Equity, Support Underserved Communities
    On April 10, 2023, the Centers for Medicare & Medicaid Services (CMS) issued the fiscal year (FY) 2024 Medicare Hospital Inpatient Prospective Payment System (IPPS) and Long-Term Care Hospital (LTCH) Prospective Payment System (PPS) proposed rule.

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    On April 5, 2023, the Centers for Medicare & Medicaid Services (CMS) released the 2024 Medicare Advantage and Part D Final Rule, which will revise regulations governing Medicare Advantage (MA), the Medicare Prescription Drug Benefit (Part D), Medicare cost plans, and Programs of All-Inclusive Care for the Elderly (PACE). The rule makes changes related to prior authorization, health equity, marketing and communications, and other areas.

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    CMS Proposes Policies to Improve Patient Safety and Promote Health Equity

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    Reduced Beneficiary Coinsurance for 20 Part B Drugs in Effect April 1; Includes Cancer Drugs
    On January 1, a provision of the Inflation Reduction Act (IRA) went into effect requiring drug companies to pay rebates to Medicare when prescription drug prices increase faster than the rate of inflation for certain drugs given to people enrolled in the program. The provision also provides for lower Medicare Part B beneficiary cost sharing on such drugs beginning April 1, 2023.

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    FDA Approvals

    31 Patient and Provider Groups Warn that Mifepristone Ruling Threatens All FDA-approved Drugs

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    Coding and Reimbursement Updates

    The California Medical Association (CMA) has submitted a letter in strong opposition to Cigna’s decision to re-release its costly, burdensome modifier 25 policy. The policy – Modifier 25-Significant, Separately Identifiable Evaluation and Management Service by the Same Physician on the Same Day of the Procedure or Other Service – will require the submission of medical records with all Evaluation and Management (E/M) claims with CPT 99212-99215 and modifier 25 when a minor procedure is billed. It is scheduled to become effective nationwide on May 25, 2023.

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