Cancer pain

Tumors cause pain by crushing or infiltrating tissue, triggering infection or inflammation, or releasing chemicals that make normally non-painful stimuli painful.

Invasion of bone by cancer is the most common source of cancer pain. It is usually felt as tenderness, with constant background pain and instances of spontaneous or movement-related exacerbation, and is frequently described as severe.[17][18] Rib fractures are common in breast, prostate and other cancers with rib metastases.[19]

The vascular (blood) system can be affected by solid tumors. Between 15 and 25 percent of deep vein thrombosis is caused by cancer (often by a tumor compressing a vein), and it may be the first hint that cancer is present. It causes swelling and pain in the legs, especially the calf, and (rarely) in the arms.[19] The superior vena cava (a large vein carrying circulating, de-oxygenated blood into the heart) may be compressed by a tumor, causing superior vena cava syndrome, which can cause chest wall pain among other symptoms.[19][20]

When tumors compress, invade or inflame parts of the nervous system (such as the brain, spinal cord, nerves, ganglia or plexa), they can cause pain and other symptoms.[17][21] Though brain tissue contains no pain sensors, brain tumors can cause pain by pressing on blood vessels or the membrane that encapsulates the brain (the meninges), or indirectly by causing a build-up of fluid (edema) that may compress pain-sensitive tissue.[22]

Pain from cancer of the organs, such as the stomach or liver (visceral pain), is diffuse and difficult to locate, and is often referred to more distant, usually superficial, sites.[18] Invasion of soft tissue by a tumor can cause pain by inflammatory or mechanical stimulation of pain sensors, or destruction of mobile structures such as ligaments, tendons and skeletal muscles.[23]

Pain produced by cancer within the pelvis varies depending on the affected tissue. It may appear at the site of the cancer but it frequently radiates diffusely to the upper thigh, and may refer to the lower back, the external genitalia or perineum.[17]

Some diagnostic procedures, such as lumbar puncture (see post-dural-puncture headache), venipuncture, paracentesis, and thoracentesis can be painful.[24]

Chemotherapy drugs

Potentially painful cancer treatments include:

• immunotherapy which may produce joint or muscle pain;
• radiotherapy, which can cause skin reactions, enteritis, fibrosis, myelopathy, bone necrosis, neuropathy or plexopathy;
• chemotherapy, often associated with chemotherapy induced peripheral neuropathy, mucositis, joint pain, muscle pain, and abdominal pain due to diarrhea or constipation;
• hormone therapy, which sometimes causes pain flares;
• targeted therapies, such as trastuzumab and rituximab, which can cause muscle, joint or chest pain;
• angiogenesis inhibitors like bevacizumab, known to sometimes cause bone pain;
• surgery, which may produce post-operative pain, post-amputation pain or pelvic floor myalgia.

The chemical changes associated with infection of a tumor or its surrounding tissue can cause rapidly escalating pain, but infection is sometimes overlooked as a possible cause. One study[25] found that infection was the cause of pain in four percent of nearly 300 people with cancer who were referred for pain relief. Another report described seven people with cancer, whose previously well-controlled pain escalated significantly over several days. Antibiotic treatment produced pain relief in all of them within three days.[17][26]

The way a person responds to pain affects the intensity of their pain (moderately), the degree of disability they experience, and the impact of pain on their quality of life. Strategies employed by people to cope with cancer pain include enlisting the help of others; persisting with tasks despite pain; distraction; rethinking maladaptive ideas; and prayer or ritual.[29]

Some people in pain tend to focus on and exaggerate the pain's threatening meaning, and estimate their own ability to deal with pain as poor. This tendency is termed "catastrophizing".[30] The few studies so far conducted into catastrophizing in cancer pain have suggested that it is associated with higher levels of pain and psychological distress. People with cancer pain who accept that pain will persist and nevertheless are able to engage in a meaningful life were less susceptible to catastrophizing and depression in one study. People with cancer pain who have clear goals, and the motivation and means to achieve those goals, were found in two studies to experience much lower levels of pain, fatigue and depression.[29]

People with cancer who are confident in their understanding of their condition and its treatment, and confident in their ability to (a) control their symptoms, (b) collaborate successfully with their informal carers and (c) communicate effectively with health care providers experience better pain outcomes. Physicians should therefore take steps to encourage and facilitate effective communication, and should consider psychosocial intervention.[29]

Psychosocial interventions affect the amount of pain experienced and the degree to which it interferes with daily life;[3] and the American Institute of Medicine[31] and the American Pain Society[32] support the inclusion of expert, quality-controlled psychosocial care as part of cancer pain management. Psychosocial interventions include education (addressing among other things the correct use of analgesic medications and effective communication with clinicians) and coping-skills training (changing thoughts, emotions, and behaviors through training in skills such as problem solving, relaxation, distraction and cognitive restructuring).[3] Education may be more helpful to people with stage I cancer and their carers, and coping-skills training may be more helpful at stages II and III.[29]

A person's adjustment to cancer depends vitally on the support of their family and other informal carers, but pain can seriously disrupt such interpersonal relationships, so people with cancer and therapists should consider involving family and other informal carers in expert, quality-controlled psychosocial therapeutic interventions.[29]

The WHO guidelines[6] recommend prompt oral administration of drugs when pain occurs, starting, if the person is not in severe pain, with non-opioid drugs such as paracetamol, dipyrone, non-steroidal anti-inflammatory drugs or COX-2 inhibitors.[6] Then, if complete pain relief is not achieved or disease progression necessitates more aggressive treatment, mild opioids such as codeine, dextropropoxyphene, dihydrocodeine or tramadol are added to the existing non-opioid regime. If this is or becomes insufficient, mild opioids are replaced by stronger opioids such as morphine, while continuing the non-opioid therapy, escalating opioid dose until the person is painless or the maximum possible relief without intolerable side effects has been achieved. If the initial presentation is severe cancer pain, this stepping process should be skipped and a strong opioid should be started immediately in combination with a non-opioid analgesic.[27] However, a 2017 Cochrane Review found that there is no high-quality evidence to support or refute the use of non-steroidal anti-inflammatories (NSAIDs) alone or in combination with opioids for the three steps of the three-step WHO cancer pain ladder and that there is very low-quality evidence that some people with moderate or severe cancer pain can obtain substantial levels of benefit within one or two weeks.[33]

Some authors challenge the validity of the second step (mild opioids) and, pointing to their higher toxicity and low efficacy, argue that mild opioids could be replaced by small doses of strong opioids (with the possible exception of tramadol due to its demonstrated efficacy in cancer pain, its specificity for neuropathic pain, and its low sedative properties and reduced potential for respiratory depression in comparison to conventional opioids).[27]

More than half of people with advanced cancer and pain will need strong opioids, and these in combination with non-opioid pain medicine can produce acceptable analgesia in 70–90 percent of cases. Morphine is effective in relieving cancer pain [34] although oxycodone shows superior tolerability and anlgesic effect, though cost may limit its value in certain healthcare systems.[35] Side effects of nausea and constipation are rarely severe enough to warrant stopping of treatment.[34] Sedation and cognitive impairment usually occur with the initial dose or a significant increase in dosage of a strong opioid, but improve after a week or two of consistent dosage. Antiemetic and laxative treatment should be commenced concurrently with strong opioids, to counteract the usual nausea and constipation. Nausea normally resolves after two or three weeks of treatment but laxatives will need to be aggressively maintained.[27] Buprenorphine is another opioid with some evidence of its efficacy but only low quality evidence comparing it to other opioids.[36]

Analgesics should not be taken "on demand" but "by the clock" (every 3–6 hours), with each dose delivered before the preceding dose has worn off, in doses sufficiently high to ensure continuous pain relief. People taking slow-release morphine should also be provided with immediate-release ("rescue") morphine to use as necessary, for pain spikes (breakthrough pain) that are not suppressed by the regular medication.[27]

Oral analgesia is the cheapest and simplest mode of delivery. Other delivery routes such as sublingual, topical, transdermal, parenteral, rectal or spinal should be considered if the need is urgent, or in case of vomiting, impaired swallow, obstruction of the gastrointestinal tract, poor absorption or coma.[27] Current evidence for the effectiveness of fentanyl transdermal patches in controlling chronic cancer pain is weak but they may reduce complaints of constipation compared with oral morphine.[37]

Liver and kidney disease can affect the biological activity of analgesics. When people with diminishing liver or kidney function are treated with oral opioids they must be monitored for the possible need to reduce dose, extend dosing intervals, or switch to other opioids or other modes of delivery.[27] The benefit of non-steroidal anti-inflammatory drugs should be weighed against their gastrointestinal, cardiovascular, and renal risks.[16]

Not all pain yields completely to classic analgesics, and drugs that are not traditionally considered analgesics but which reduce pain in some cases, such as steroids or bisphosphonates, may be employed concurrently with analgesics at any stage. Tricyclic antidepressants, class I antiarrhythmics, or anticonvulsants are the drugs of choice for neuropathic pain. Such adjuvants are a common part of palliative care and are used by up to 90 percent of people with cancer as they approach death. Many adjuvants carry a significant risk of serious complications.[27]

Anxiety reduction can reduce the unpleasantness of pain but is least effective for moderate and severe pain.[38] Since anxiolytics such as benzodiazepines and major tranquilizers add to sedation, they should only be used to address anxiety, depression, disturbed sleep or muscle spasm.[27]

If the analgesic and adjuvant regimen recommended above does not adequately relieve pain, additional options are available.[39]

Radiotherapy is used when drug treatment is failing to control the pain of a growing tumor, such as in bone metastasis (most commonly), penetration of soft tissue, or compression of sensory nerves. Often, low doses are adequate to produce analgesia, thought to be due to reduction in pressure or, possibly, interference with the tumor's production of pain-promoting chemicals.[40] Radiopharmaceuticals that target specific tumors have been used to treat the pain of metastatic illnesses. Relief may occur within a week of treatment and may last from two to four months.[39]

A neurolytic block is the deliberate injury of a nerve by the application of chemicals (in which case the procedure is called "neurolysis") or physical agents such as freezing or heating ("neurotomy").[41] These interventions cause degeneration of the nerve's fibers and temporary interference with the transmission of pain signals. In these procedures, the thin protective layer around the nerve fiber, the basal lamina, is preserved so that, as a damaged fiber regrows, it travels within its basal lamina tube and connects with the correct loose end, and function may be restored. Surgically cutting a nerve severs these basal lamina tubes, and without them to channel the regrowing fibers to their lost connections, a painful neuroma or deafferentation pain may develop. This is why the neurolytic is preferred over the surgical block.[42]

A brief "rehearsal" block using local anesthetic should be tried before the actual neurolytic block, to determine efficacy and detect side effects.[39] The aim of this treatment is pain elimination, or the reduction of pain to the point where opioids may be effective.[39] Though the neurolytic block lacks long-term outcome studies and evidence-based guidelines for its use, for people with progressive cancer and otherwise incurable pain, it can play an essential role.[42]

Cross-section of the spinal cord showing the dorsal column and the anterolateral spinothalamic tracts

Surgical cutting or destruction of peripheral or central nervous tissue is now rarely used in the treatment of pain.[39] Procedures include neurectomy, cordotomy, dorsal root entry zone lesioning, and cingulotomy.

Cutting through or removal of nerves (neurectomy) is used in people with cancer pain who have short life expectancy and who are unsuitable for drug therapy due to ineffectiveness or intolerance. Because nerves often carry both sensory and motor fibers, motor impairment is a possible side effect of neurectomy. A common result of this procedure is "deafferentation pain" where, 6–9 months after surgery, pain returns at greater intensity.[43]

Cordotomy involves cutting nerve fibers that run up the front/side (anterolateral) quadrant of the spinal cord, carrying heat and pain signals to the brain.

Pancoast tumor pain has been effectively treated with dorsal root entry zone lesioning (destruction of a region of the spinal cord where peripheral pain signals cross to spinal cord fibers); this is major surgery that carries the risk of significant neurological side effects.

Cingulotomy involves cutting nerve fibers in the brain. It reduces the unpleasantness of pain (without affecting its intensity), but may have cognitive side effects.[43]

Hypophysectomy is the destruction of the pituitary gland, and has reduced pain in some cases of metastatic breast and prostate cancer pain.[43]

Cross section of the spinal cord showing the subarachnoid cavity, dura mater and spinal nerve roots including the dorsal root ganglion

Intrathecal pump

An external or implantable intrathecal pump infuses a local anesthetic such as bupivacaine and/or an opioid such as morphine and/or ziconotide and/or some other nonopioid analgesic as clonidine (currently only morphine and ziconotide are the only agents approved by the US Food and Drug Administration for IT analgesia) directly into the fluid-filled space (the subarachnoid cavity) between the spinal cord and its protective sheath, providing enhanced analgesia with reduced systemic side effects. This can reduce the level of pain in otherwise intractable cases.[39][43][44]

Long-term epidural catheter

The outer layer of the sheath surrounding the spinal cord is called the dura mater. Between this and the surrounding vertebrae is the epidural space filled with connective tissue, fat and blood vessels and crossed by the spinal nerve roots. A long-term epidural catheter may be inserted into this space for three to six months, to deliver anesthetics or analgesics. The line carrying the drug may be threaded under the skin to emerge at the front of the person, a process called "tunneling", recommended with long-term use to reduce the chance of any infection at the exit site reaching the epidural space.[39]

Electrical stimulation of the dorsal columns of the spinal cord can produce analgesia. First, the leads are implanted, guided by fluoroscopy and feedback from the patient, and the generator is worn externally for several days to assess efficacy. If pain is reduced by more than half, the therapy is deemed to be suitable. A small pocket is cut into the tissue beneath the skin of the upper buttocks, chest wall or abdomen and the leads are threaded under the skin from the stimulation site to the pocket, where they are attached to the snugly fitting generator.[43] It seems to be more helpful with neuropathic and ischemic pain than nociceptive pain, but current evidence is too weak to recommend its use in the treatment of cancer pain.[45][46]

Due to the poor quality of most studies of complementary and alternative medicine in the treatment of cancer pain, it is not possible to recommend integration of these therapies into the management of cancer pain. There is weak evidence for a modest benefit from hypnosis; studies of massage therapy produced mixed results and none found pain relief after 4 weeks; Reiki, and touch therapy results were inconclusive; acupuncture, the most studied such treatment, has demonstrated no benefit as an adjunct analgesic in cancer pain; the evidence for music therapy is equivocal; and some herbal interventions such as PC-SPES, mistletoe, and saw palmetto are known to be toxic to some people with cancer. The most promising evidence, though still weak, is for mind-body interventions such as biofeedback and relaxation techniques.[10]

Despite the publication and ready availability of simple and effective evidence-based pain management guidelines by the World Health Organization (WHO)[6] and others,[7] many medical care providers have a poor understanding of key aspects of pain management, including assessment, dosing, tolerance, addiction, and side effects, and many do not know that pain can be well controlled in most cases.[27][47] In Canada, for instance, veterinarians get five times more training in pain than do physicians, and three times more training than nurses.[48] Physicians may also undertreat pain out of fear of being audited by a regulatory body.[10]

Systemic institutional problems in the delivery of pain management include lack of resources for adequate training of physicians, time constraints, failure to refer people for pain management in the clinical setting, inadequate insurance reimbursement for pain management, lack of sufficient stocks of pain medicines in poorer areas, outdated government policies on cancer pain management, and excessively complex or restrictive government and institutional regulations on the prescription, supply, and administration of opioid medications.[10][27][47]

People with cancer may not report pain due to costs of treatment, a belief that pain is inevitable, an aversion to treatment side effects, fear of developing addiction or tolerance, fear of distracting the doctor from treating the illness,[47] or fear of masking a symptom that is important for monitoring progress of the illness. People may be reluctant to take adequate pain medicine because they are unaware of their prognosis, or may be unwilling to accept their diagnosis.[8] Failure to report pain or misguided reluctance to take pain medicine can be overcome by sensitive coaching.[27][47]