Can Cancer Cause Fibromyalgia?

Cancer is characterized by the uncontrolled division and spread of abnormal cells, forming malignant tumors that disrupt normal bodily function. Fibromyalgia (FM), conversely, is a chronic pain disorder defined by widespread musculoskeletal pain, profound fatigue, sleep disturbances, and cognitive difficulties, with an unknown primary cause.

Medical consensus frames fibromyalgia as a disorder of central sensitization, meaning the nervous system processes pain signals abnormally, amplifying sensations. While the conditions appear separate, their co-occurrence in patients is frequent, suggesting a link based on correlation rather than simple, direct causation. This relationship often involves the systemic toll of the malignancy and its subsequent treatments, creating an environment susceptible to chronic pain syndromes.

The Link Between Cancer and Fibromyalgia

A cancer diagnosis does not directly cause primary fibromyalgia. However, studies have observed a higher prevalence of fibromyalgia among cancer patients and survivors compared to the general population. Fibromyalgia has been detected in a significant percentage of patients with lung cancer and is more common in breast cancer survivors.

This relationship is often described as secondary fibromyalgia, where the chronic disease state or the psychological and physical stress acts as a trigger. The prolonged pain, anxiety, and systemic inflammatory response associated with the malignancy can create an environment conducive to the development of chronic widespread pain. Cancer is considered a powerful trigger for the onset of fibromyalgia-like symptoms in susceptible individuals, contributing to the nervous system changes characteristic of FM.

Treatment-Induced Fibromyalgia-Like Syndromes

Oncology treatments are a major factor in the development of chronic pain and fatigue syndromes that closely mimic fibromyalgia. Chemotherapy is particularly associated with these iatrogenic effects. Chemotherapy-induced peripheral neuropathy (CIPN) involves damage to peripheral sensory nerves, leading to numbness, tingling, and chronic pain, often in the hands and feet.

Chemotherapy agents can also induce severe fatigue, cognitive dysfunction, and widespread musculoskeletal pain, which are nearly indistinguishable from the symptoms of FM. Furthermore, hormonal therapies, such as the estrogen blocker tamoxifen used for breast cancer, can precipitate severe fatigue and widespread body pain in survivors.

Surgery and radiation therapy also contribute to persistent pain states that can resemble FM symptoms. Radiation can cause late-effect toxicity, and surgical procedures, such as mastectomy, can result in persistent post-surgical pain syndromes. These complications introduce chronic nociceptive input and inflammation, which can ultimately lead to the central sensitization that characterizes fibromyalgia.

Shared Biological Pathways and Immune System Changes

Shared underlying biological pathways contribute to the co-existence of cancer survival and fibromyalgia. Chronic systemic inflammation is one such mechanism, where both conditions are associated with elevated levels of pro-inflammatory cytokines. This low-grade, persistent inflammation can increase pain sensitivity and contribute to the fatigue and mood disturbances seen in both patient populations.

Both conditions involve central sensitization, a heightened responsiveness of the central nervous system to pain signals. This state of nociplastic pain is linked to disruptions in neurotransmitter systems, specifically the serotonergic and dopaminergic pathways, which are responsible for pain modulation. Mitochondrial dysfunction and increased oxidative stress, which affect cellular energy production, are present in both post-cancer fatigue and fibromyalgia.

Managing Co-Existing Conditions

Managing a patient with a history of cancer who develops fibromyalgia symptoms presents significant diagnostic challenges. The widespread pain, fatigue, and cognitive issues must be carefully evaluated to rule out cancer recurrence or persistent, treatable effects of the oncology treatment, necessitating a comprehensive assessment.

A multidisciplinary, biopsychosocial approach is recommended for effective management of this complex co-morbidity. Treatment often involves tailored pharmacological strategies, including specific anti-depressants like duloxetine or nerve-pain medications such as pregabalin, which help modulate central pain signals. Non-pharmacological therapies are equally important and include:

  • Physical therapy, modified for the patient’s physical tolerance.
  • Cognitive behavioral therapy (CBT) to help manage the psychological impact of chronic pain and fatigue.
  • Focusing on improved sleep hygiene.
  • Gentle, consistent exercise modification to address the severe fatigue and deconditioning.