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Salivary Gland Cancer: Patient Guide

Salivary Gland Cancer: what it is, diagnosis and staging, treatment options, and questions to ask your cancer team.

NCI source:National Cancer Institute — Salivary Gland Cancer

Review status: AI-assisted, source checked. Not reviewed by a clinician. How we check pages

The short answer

Salivary Gland Cancer means a group of uncommon cancers beginning in salivary-gland tissue. The exact diagnosis matters because many pathology subtypes exist and may behave differently.

  • Salivary Gland Cancer means a group of uncommon cancers beginning in salivary-gland tissue.

  • A typical evaluation may include head-and-neck examination, imaging, tissue sampling, pathology, and staging.

  • Treatment categories may include surgery, radiation, systemic treatment in selected cases, and clinical trials.

  • Planning depends on gland, subtype, grade, facial-nerve involvement, stage, and resectability.

Choose how you want to read this

The whole article, with every detail and caution.

This page is for people facing a salivary gland tumor, and for the people helping them. It covers where these tumors start, the main subtypes, symptoms, staging, and treatment.

The smaller the gland, the worse the odds

You have three pairs of major salivary glands. The parotid glands sit in front of and just below each ear. The submandibular glands sit below the jawbone. The sublingual glands sit under the tongue, in the floor of the mouth. Many small minor glands also sit in the lining of the mouth, throat, larynx (voice box), and sinuses.

Now the fact that shapes everything else. A lump is more likely to be cancer when it sits in a smaller gland. NCI gives the share of tumors that are malignant (cancer):

  • Parotid: 20 to 25 percent of tumors are malignant
  • Submandibular: 35 to 40 percent
  • Palate, which holds minor glands: about 50 percent
  • Sublingual: more than 90 percent

Most parotid lumps are benign (not cancer). A lump under the tongue is much more likely to be cancer, so have it checked.

These are uncommon cancers. The age-adjusted rate from 2018 to 2022 was 1.3 cases per 100,000 people a year. That is about 3 to 5 percent of all head and neck cancers.

The subtype changes the story

Salivary glands produce an unusually long list of tumor types. Four account for most malignancies.

Mucoepidermoid carcinoma is the most common, at 29 to 34 percent of malignant tumors. It is graded on a point system. Zero to 4 points is low grade. Five to 6 is intermediate. Seven to 14 is high grade. That number belongs on your pathology report.

Adenoid cystic carcinoma makes up about 7.5 percent of epithelial malignancies. NCI calls it slow growing but aggressive. NCI says it has a remarkable capacity to come back. Ten-year survival is reported to be less than 50 percent.

Acinic cell carcinoma is about 17 percent of primary malignant salivary tumors. More than 80 percent of them start in the parotid.

Carcinoma ex pleomorphic adenoma accounts for 4.6 percent. It grows inside a tumor that used to be benign. That is one reason benign salivary tumors get removed rather than watched for years.

Two outliers frame the range. Squamous cell carcinoma of a salivary gland does badly. Survival is 24 percent at 5 years and 18 percent at 10 years. Polymorphous low-grade adenocarcinoma does remarkably well. Overall survival is 80 percent at 25 years.

What actually brings people in

The usual first sign is a lump, and NCI stresses that it is usually painless. It may sit near the ear, in the cheek, along the jaw, on the lip, or inside the mouth.

Other symptoms carry more weight. They suggest the tumor is doing more than sitting there:

  • Fluid draining from the ear
  • Trouble swallowing, or trouble opening the mouth wide
  • Numbness or weakness in the face
  • Face pain that does not go away

Facial weakness deserves its own line. The facial nerve runs directly through the parotid gland. NCI notes that nerve involvement affects the outlook, and that pain and facial paralysis are common in adenoid cystic carcinoma. Report a drooping eyelid or a lopsided smile right away. Do not wait for the next visit.

The list of known risk factors is short. Exposure to ionizing radiation is the main one. Four job exposures also appear: rubber products manufacturing, asbestos mining, plumbing, and some kinds of woodworking.

How it gets diagnosed

The workup starts with a physical exam and health history. Imaging follows, using MRI, CT, or PET. Endoscopy, a look inside with a thin lighted tube, is used at times.

Fine needle aspiration biopsy is the most common way to get tissue. A thin needle draws cells from the lump for examination. When that is not enough, an incisional biopsy takes a small piece. Sometimes the surgeon removes the tumor first and the pathologist examines it afterward.

How it is staged

For the major glands, the stages run this way:

  • Stage 0: abnormal cells confined to gland ducts, called carcinoma in situ
  • Stage I: tumor 2 cm or smaller, confined to the gland
  • Stage II: tumor larger than 2 cm but not more than 4 cm, still confined
  • Stage III: tumor larger than 4 cm, spread to soft tissue, or both. One lymph node may be involved
  • Stage IV (A to C): progressively wider spread to skin, bone, nerves, lymph nodes, or distant organs. Your team can tell you which letter applies

What predicts the outcome

Here NCI says something that surprises people. For adenoid cystic carcinoma, NCI says clinical stage may be a better predictor than histological grade (how abnormal the cells look under a microscope), and tumors larger than 4 cm had a worse course. Early-stage, low-grade tumors are usually cured by surgery alone.

Things NCI says affect the outlook include the gland involved, the histology, the grade, the stage, nerve involvement, and spread to lymph nodes or distant sites.

Perineural invasion means cancer traveling along nerves. NCI says it can occur, particularly in high-grade adenoid cystic carcinoma, and should be specifically identified and treated.

Treatment

Surgery is the main treatment. NCI says early-stage, low-grade tumors are usually curable by adequate surgery alone.

Large bulky or high-grade tumors carry a poorer outlook. NCI says they may best be treated with surgery plus radiation afterward. Radiation may raise local control and survival when clear margins cannot be achieved. Clear margins mean no cancer is found at the edge of the removed tissue. That is often hard in an area crowded with nerves.

NCI says two radiation options have been effective for tumors that cannot be removed or that come back. One is fast neutron-beam radiation therapy. The other is an accelerated hyperfractionated photon-beam schedule. Ask your team whether either is an option for you. NCI also says tumors that cannot be removed, or that come back, may respond to chemotherapy.

Questions to bring to your surgeon

  • Which gland is involved, and what is the exact histologic subtype?
  • What grade is it, and for mucoepidermoid carcinoma, what was the point score?
  • Is the facial nerve involved, and can it be preserved?
  • Was perineural invasion found, and were margins clear?
  • Does my case call for radiation after surgery, and why?
  • Is fast neutron therapy relevant here, and is there a center that offers it?
  • Given adenoid cystic histology, how long will surveillance continue?

Sources

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Common questions

What is salivary gland cancer?

It is a group of uncommon cancers beginning in salivary-gland tissue.

How is it diagnosed?

The evaluation may include head-and-neck examination, imaging, tissue sampling, pathology, and staging; the exact sequence depends on the situation.

How is treatment planned?

Teams consider gland, subtype, grade, facial-nerve involvement, stage, and resectability.

Should I seek a specialist opinion?

For an uncommon diagnosis, specialist pathology or treatment review can confirm a plan and clarify alternatives.

Questions to ask your doctor

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Written from National Cancer Institute material and compared with the source cited below.

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Sources last checked: 2026-08-13 what this meansLast updated: 2026-10-02Next planned review: 2027-07-22

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Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes, and this is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.

Editorial status: Source checked — This page was written with AI assistance and then compared with the sources listed on it, looking for statements those sources do not back up. That check is not a sentence-by-sentence record and can miss errors. It is not a medical review, and it does not confirm the page is complete or right for your situation.

Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.

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