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New treatment identified for low grade and serous ovarian cancer

Susan HauWritten by Susan HauMedically ReviewedUpdated May 25, 20224 min read
New treatment identified for low grade and serous ovarian cancer
In this article
  1. Potential New Standard of Care
  2. Clinical Trial Results: Trametinib vs. Standard Care
  3. Addressing the Treatment Gap in Low-Grade Serous Cancer
  4. How CancerFax Helps

Potential New Standard of Care

May 2022: Trametinib may become a new standard of care for recurring, low-grade serous ovarian cancer (Mekinist). According to study findings published in the February 2022 issue of The Lancet, trametinib beat both chemotherapy and anti-estrogens like tamoxifen by around 52 percent, adding six months of progression-free (period during which the cancer did not advance) survival for patients.

Clinical Trial Results: Trametinib vs. Standard Care

In 260 women with recurrent serous ovarian tumours who had previously received chemotherapy, researchers from the United States and the United Kingdom compared once-daily oral trametinib to one of five standard of care regimens (either chemotherapy or anti-estrogen medications). When compared to usual treatment, trametinib participants showed a fourfold higher response to therapy after 15 months. Trametinib outperformed all other treatments, slowing disease progression for 13 months (versus seven months for standard treatment). Skin rash, anaemia, high blood pressure, diarrhoea, and weariness are some of the potentially dangerous adverse effects of trametinib treatment.

Addressing the Treatment Gap in Low-Grade Serous Cancer

Low-grade serous ovarian cancer is a difficult-to-treat invasive form of ovarian cancer marked by strong hormone receptor activation, genetic alterations, and poor chemotherapy response. Until now, the cancer toolbox lacked effective therapeutic options for patients with low-grade serous ovarian cancer. According to an editorial accompanying the report, 70% of these women will recur, with only 5% responding to further chemotherapy.

How CancerFax Helps

CancerFax is a specialist cancer access and patient-navigation platform. We help patients and families understand their options, organise medical records, coordinate hospital communication, and support cross-border treatment planning where appropriate.

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Medical Record Review

We help collect and organise reports, scans, pathology, biomarker results, and treatment history for structured case review.

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Eligibility Coordination

We communicate with hospitals or trial teams to assess whether a case may be suitable for further screening.

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Hospital Communication

We support appointment coordination, document submission, translation, and direct communication with international departments.

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Travel & Admission Support

For international patients, we help with practical coordination — travel planning, hospital admission guidance, and local support.

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Treatment & Trial Navigation

If this option is not suitable, we help explore other relevant treatments, clinical trials, or advanced care pathways.

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End-to-end Coordination

From inquiry through to follow-up, our coordinators provide a single point of contact for the family.

CancerFax does not guarantee treatment access, eligibility, or clinical outcome. Our role is to help patients access accurate information, structured review, and appropriate specialist pathways.

Susan Hau

About Susan Hau

Susan Hau is a distinguished researcher in the field of cancer cell therapy, with a particular focus on T cell-based approaches and cancer vaccines. Her work spans several innovative treatment modalities, including CAR T-cell therapy, TIL (Tumor-Infiltrating Lymphocyte) therapy, and NK (Natural Killer) cell therapy. Hau's expertise lies in cancer cell biolo…

✓ Reviewed for medical accuracy by the CancerFax review panel.

Medical Disclaimer

This article is for educational purposes only and should not replace medical advice, diagnosis, or treatment from a qualified oncology specialist. Every patient's case is different. Treatment decisions should always be made after a review of complete medical records by the treating medical team.

Treatment availability, eligibility, timelines, and access can change. Any clinical trial participation depends on detailed review and approval by the trial hospital or investigator.