Published online Jul 24, 2024. doi: 10.5306/wjco.v15.i7.796
Revised: May 5, 2024
Accepted: May 22, 2024
Published online: July 24, 2024
Processing time: 151 Days and 11.9 Hours
Bone metastases from lung cancer account for 8.5%, with those located in the hyoid bone being extremely rare. In this editorial, we made a review about Hsu et al case report highlighted the importance of palliative radiotherapy, even with an unusual but effective scheme in pain control in a patient with non-small cell lung cancer in stage IV.
Core Tip: Bone metastases from lung cancer account for 8.5%, with those located in the hyoid bone being extremely rare. This editorial remarks the importance of radiotherapy in palliative care, specially in pain control, always accompanied of systemic therapy in oncological patients.
- Citation: Montijano M, Ocanto A, Couñago F. Hyoid metastasis an unusual location from lung cancer. World J Clin Oncol 2024; 15(7): 796-798
- URL: https://www.wjgnet.com/2218-4333/full/v15/i7/796.htm
- DOI: https://dx.doi.org/10.5306/wjco.v15.i7.796
The treatment of choice in patients with metastatic non-small cell lung cancer (NSCLC) is systemic treatment[1], and around 20%-50% of patients with NSCLC present olig
Bone metastases of pulmonary origin are common in the evolution of the disease, with osteolytic metastases being the most related to lung cancer and produce by cell adhesion molecules, chemokine receptors of tumor cells and cell surface receptors that attach to the bone matrix and establish growth in bone[4], this type of lesions are exceptional in the hyoid bone, in fact in solid tumors only a few case reports have been described in this location, therefore their clinical mana
Nowadays in the stage IV lung adenocarcinoma, the targetable oncogenic driver mutations, immune checkpoints (programmed cell death protein 1/programmed cell death ligand 1/cytotoxic T lymphocyte-associated protein 4) and translocations conducted to development of specific drugs (tyrosine kinase or immune checkpoints inhibitors) with impressive response and survival rates[5]. An example is this case report[3], the patient was treated with a platinum-based chemo-immunotherapy along with pembrolizumab, which is recognized as the standard first-line in this stage. The data from KEYNOTE-189[6], published in 2018, suggested that introducing pembrolizumab as a first-line therapy in untreated metastatic non-squamous NSCLC without epidermal growth factor receptor or anaplastic lymphoma kinase mutations improve overall survival across all programmed cell death ligand 1 categories. In this case report epidermal growth factor receptor and anaplastic lymphoma kinase mutations are not evaluated or mentioned, which can change the therapeutic management. For this group of patients, an increase in survival justify local therapies including RT.
There are several phase 2 clinical trials that have shown an increase in progression free survival in oligometastatic patients with NSCLC treated with Stereotactic Body Radiotherapy (SBRT) compared to those undergoing maintenance therapy[7-10]. These trials demonstrated that patients most likely to benefit from RT are those whose disease responds to systemic therapy. Most trials recommend SBRT, either alone, conventionally, hypofractioned RT or chemoradiotherapy to the primary lesion. In fact, the most radical approximation in patients oligometastatic is a combination of primary tumor treatment with metastases directed to therapy.
Palliative RT could achieve a significant pain response in up to 80% of patients with a median response duration of 18-21 months. It is broadly accepted as the standard of care RT in metastatic bone pain, despite the absence of randomized trials comparing RT with pain killing strategies such as opioids or surgical options[11]. Based on all the available evide
Metastases bone in hyoid are exceptional with a management not clear until the date. In patients oligometastatic the key is the ablative therapy and in palliative stage the RT is the best option with good results in pain control despite the scheme used. RT must to be accompanied of systemic therapy according targetable oncogenic driver mutations/translocations and immune checkpoints.
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