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Humana Medicaid adds ChemoFx coverage for gynecologic cancers

3 hours ago
By AI, Created 19:54 UTC, Oct 13, 2026, AGP -

DataMeds AI said its Helomics lab won a Medicaid coverage determination for the ChemoFx assay in gynecologic cancers after review by Humana’s Medicaid Coverage Policy Adoption forum. The decision could expand access to the tumor-response test for certain Medicaid members and support broader adoption of the assay under CPT codes 81535 and 81536.

Why it matters: - Humana’s Medicaid policy can widen access to ChemoFx for patients with gynecologic cancers who may need chemotherapy guidance. - Coverage may also improve reimbursement prospects for DataMeds AI’s Helomics subsidiary and support commercial volume for the assay. - The policy decision matters because the test is positioned as a treatment-selection tool in cancers where options can be limited or difficult to optimize.

What happened: - DataMeds AI said Helomics Corporation received a Medicaid coverage determination for the ChemoFx Assay in gynecologic cancers. - Humana’s Medicaid Coverage Policy Adoption forum reviewed the medical coverage policy and incorporated ChemoFx into its Coverage Determination for Pharmacogenomics Testing. - The policy number is HUM-SC-2240-003. - The effective date is July 22, 2026.

The details: - ChemoFx is a commercially available chemoresponse test that measures how a patient’s live tumor cells respond to chemotherapy agents. - The assay is billed under CPT codes 81535 and 81536. - Under Humana’s Medicaid policy, members may be eligible for ChemoFx if they have gynecologic cancer such as cervical, endometrial, fallopian tube, gynecologic sarcoma, ovarian or primary peritoneal cancer. - The policy lists several qualifying situations, including rare cancer with no established treatment guidelines, use during initial biopsy or surgery, recurrent cancer, treatment-refractory disease, or inability to tolerate recommended treatment. - The assay is not currently covered under all Humana plans. - Helomics is a CLIA-certified clinical laboratory in Pittsburgh and is a wholly owned subsidiary of DataMeds AI. - DataMeds AI said Helomics previously invested in lab automation to improve commercial readiness. - DataMeds AI said ChemoFx has peer-reviewed clinical utility data supporting treatment outcomes in gynecologic cancers. - The company also pointed to a 2021 peer-reviewed publication on ChemoFx in gynecologic cancer and a 2015 peer-reviewed cost-savings study in epithelial ovarian cancer. - The company said ChemoFx has not been cleared or approved by the U.S. Food and Drug Administration because it is a laboratory-developed test. - Helomics’ innovation division, Predictive Oncology, combines annotated biobanks from more than 130 tumor types with artificial intelligence and multi-omic data to support drug discovery and development. - For more information, see the company profile and the Helomics website.

Between the lines: - The coverage win gives DataMeds AI a payer-policy milestone that can matter as much as clinical validation in driving test adoption. - The policy language suggests Humana is targeting patients where therapy selection is especially uncertain, including rare, recurrent and treatment-refractory cases. - DataMeds AI is also signaling a broader commercialization push by linking the coverage decision to label expansion and additional publication plans. - The company framed ChemoFx as potentially cost-effective in recurrent epithelial ovarian cancer, including scenarios where assay-guided therapy reduces treatment costs versus empiric selection.

What's next: - DataMeds AI said it is preparing additional data for publication to support label expansion. - The company said it sees an opportunity to evaluate ChemoFx in other difficult-to-treat cancers. - Broader payer adoption remains a key test for whether the Humana Medicaid decision translates into wider coverage beyond this policy.

The bottom line: - Humana’s Medicaid coverage decision gives ChemoFx a notable reimbursement foothold in gynecologic cancers and could help DataMeds AI push the assay further into routine oncology decision-making.

Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.

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