For a number of years, investigators have reported stress- or trauma-related symptoms such as avoidant behaviors, intrusive thoughts, and heightened arousal in survivors of cancer.[1-4] These symptoms resemble those seen in individuals who have experienced traumatic events such as:[5]
These symptoms experienced by cancer survivors fall under the “Trauma- and Stressor-Related Disorders” category in the Diagnostic and Statistical Manual of Mental Disorders, fifth edition (DSM-5). The category includes acute stress disorder, adjustment disorders, and post-traumatic stress disorder (PTSD).[5]
Reviews note that post-traumatic stress (PTS) has been studied in a variety of cancers, including:[6]
Most of the studies to date have used the criteria of the DSM, fourth edition (DSM-IV) because they were conducted before publication of the DSM-5. This summary will primarily refer to the studies conducted using the DSM-IV criteria.
Studies have varied in the assessment of patients for the full syndrome of PTSD (i.e., all DSM criteria met) or only some of the PTSD-related symptoms (e.g., intrusive thoughts as measured by the Impact of Event Scale). As a result, incidence rates have varied.
Factors suggesting which patients might be at increased risk of developing PTS and PTSD have not been extensively studied; however, one study of women with early-stage breast cancer [7] found an association with PTSD-like symptoms in patients with the following characteristics:
Another study of men and women treated with bone marrow transplant [8] found that lower levels of social support and the use of avoidance coping correlated significantly to a higher number of PTSD-like symptoms. One German study [9] that evaluated patients with breast cancer for PTSD and acute stress disorder (ASD) concluded that patients with lifetime PTSD (8.7%) were much more likely to experience cancer-related ASD or PTSD (odds ratio, 14.1).
Although no specific therapies for PTS symptoms in the cancer setting have been developed, treatment modalities used with other people with PTSD can be useful in alleviating distress in cancer patients and survivors.
In this summary, unless otherwise stated, evidence and practice issues as they relate to adults are discussed. The evidence and application to practice related to children may differ significantly from information related to adults. When specific information about the care of children is available, it is summarized under its own heading.
Reviews of the literature [1] note that post-traumatic stress (PTS) has been studied in a variety of cancers, including:
The incidence of the full syndrome of post-traumatic stress disorder (PTSD) (meeting all Diagnostic and Statistical Manual of Mental Disorders [DSM] diagnostic criteria) ranges from 3% to 4% in patients recently diagnosed with early-stage disease to 35% in patients evaluated after treatment. When the incidence of PTSD-like symptoms (not meeting the full diagnostic criteria) is measured, rates are higher, ranging from 20% in patients with early-stage cancer to 80% in those with recurrent cancer.
The earliest research (predating the DSM, fourth edition [DSM-IV]) on PTS among cancer survivors concentrated on the prevalence and characteristics of the disorder in patients who had undergone or were undergoing treatment, adult and child cancer survivors, and/or their family members. A wide variety of cancer types was studied, including leukemia,[2] breast cancer, and head and neck cancers.[3] Much of the earlier research dealt with survivors of Hodgkin disease, probably because diagnoses at an early age and higher rates of survival resulted in a larger population available for study.[4] These survivors were found to have a particularly high prevalence of intrusive thoughts and avoidance behaviors, even though they were many years posttreatment.[5-7] Most of these studies investigated PTSD-like symptoms, rather than the complete mental disorder with all diagnostic criteria.
The first study of cancer patients using the DSM-IV diagnostic criteria looked at 27 patients (most with breast cancer), all at least 3 years postdiagnosis and no longer receiving any cancer treatments. A prevalence rate of 4% for current PTSD and 22% lifetime prevalence was found.[8] Those who met the criteria for lifetime prevalence were noted to have higher levels of general psychological distress, suggesting that individuals with a history of PTSD are at a substantial risk of continued emotional difficulties.
Studies using the Structured Clinical Interview for DSM (SCID) [9] found prevalence rates for PTSD between 3% and 10% in adult cancer patients. Most of these studies looked at women with early-stage breast cancer, who were evaluated a few months to a few years after their cancer treatments. Similarly, in a prospective study of 115 patients with all stages of breast cancer being treated in a comprehensive cancer center, 4% met the full diagnostic criteria for PTSD; 41% met the subsyndromal criteria for PTSD (experiencing intense fear, helplessness, or horror after being diagnosed with cancer). This set of subsyndromal criteria was a weak predictor of PTSD (12%) but an equally useful predictor of major depressive disorder, global anxiety disorder, and past major depressive disorder, and it may better serve as a marker for elevated distress.[10]
In a few studies of patients who underwent bone marrow transplants, slightly higher prevalence rates have been reported, ranging from 5% [11] to 12% to 19% [12] to as high as 35%.[13] The range in prevalence appears to be influenced by time of assessment (higher rates occur with more time since transplant) and the assessment method used. Studies reporting lower rates typically used a self-report questionnaire,[14] whereas those reporting higher rates [13] used the SCID and evaluated for symptoms at multiple times since diagnosis (i.e., lifetime prevalence). The changes to the fifth edition of the DSM (DSM-5) included removal of the subjective response of “intense fear, horror, or helplessness” that had been added to Criterion A in the DSM-IV.[15]
As an illustration of the distinction between these tools, a German study evaluated patients with breast cancer (n = 127) for PTSD immediately postsurgery and 6 months after the first assessment.[16] The assessments included screening instruments for acute stress disorder (ASD) and PTSD, such as the Impact of Event Scale-Revised (IES-R) and the PTSD Checklist-Civilian (PCL-C). The first assessment also included a semistructured interview using the SCID. On the basis of the SCID, 2.4% of participants met the criteria for mild-to-moderate cancer-related PTSD, and 2.4% were diagnosed with ASD. However, the IES-R and PCL-C screening instruments identified PTSD in 18.5% of participants at the first assessment and in 11.2% to 16.3% of participants at the second assessment. Authors of the study suggested that unlike the SCID, the IES-R and PCL-C screening instruments measure diffuse emotional distress and adjustment problems and not precise PTSD symptoms.
One of the main differences between symptom-based measures such as the PCL-C and an actual SCID-based diagnosis is the dysfunction caused by the symptoms. The symptoms are rather common, but only a very small percentage of people who have the symptoms are disabled by them.
A variety of sociodemographic, disease-related, psychosocial, and psychological variables have been investigated to determine their relationship to post-traumatic stress (PTS) related to cancer. At present, no clear picture emerges about who is at increased risk of developing PTS after a diagnosis of or treatment for cancer.
Few patient characteristics have been shown to predict the occurrence of PTS. High levels of psychological distress have been correlated with both stress symptoms [1-3] and full-syndrome post-traumatic stress disorder (PTSD) diagnoses in adult survivors.[1] In addition, trait anxiety was found to predict post-traumatic symptoms in the parents of survivors of childhood cancer.[4] Women who are survivors of cancer and who have a diagnosis of lifetime PTSD tend to have a history of exposure to trauma.[1,5] Demographic characteristics such as age, sex, and education level at time of diagnosis have not been reliable predictors of stress symptoms.[1,6,7]
Disease-related variables that have been associated with a higher incidence of PTSD in patients who underwent bone marrow transplant include more advanced disease and a longer hospital stay.[8] Other studies, however, have found no association between time since diagnosis and treatment, severity of disease, or type of cancer treatment received.[1,9,10] The relationship between disease stage and post-traumatic symptoms has not been adequately studied. Most studies have not found an association; however, they typically included a limited range of disease stages or studied early-stage cancer.[11]
The time since diagnosis and treatment has been shown to correlate with and predict post-traumatic symptoms in survivors of osteogenic sarcoma [2] and Hodgkin lymphoma.[7,12] Specifically, people who were further from diagnosis and treatment tended to exhibit fewer symptoms. This effect, however, has not been found in studies of patients with recent recurrences,[13] survivors of breast cancer,[1] or survivors of childhood cancers.[14] Duration of treatment, rather than time since treatment, has been shown to predict stress symptoms in survivors of childhood cancer.[14]
The presence of pain and other physical symptoms has been shown to correlate with levels of intrusive thoughts.[2] Cancer recurrence has also been shown to increase the likelihood of stress symptoms in patients.[13]
The experience of past traumatic events appears to be an important psychosocial risk factor associated with PTS symptoms,[5,15,16] as was found in both early-stage [17] and metastatic breast cancer.[18] Previous trauma in combination with recent stressful life events was significantly related to PTS symptoms.[19]
Other psychosocial risk factors such as premorbid psychopathology,[20,21] high levels of general psychological distress,[22] and dysfunctional coping and attributional styles [15,23,24] have been linked to a risk of PTSD in war veterans, Holocaust survivors, and other disaster victims. In addition, several investigators have linked predisposing genetic factors [25,26] and other biological factors (e.g., overly reactive hormonal systems and reduced hippocampal volume) to risk of PTSD.[27-29] Among social factors, the quality of the recovery environment, often measured in terms of social support, has been shown to affect risk of PTSD after exposure to combat [20] and burn injury.[30] The effect of threats to life and body integrity has been documented in samples of adults and families [1,4,12] but not children.[14]
Psychological variables that have been related to a higher incidence of PTSD include:
Greater perceived availability of social support is associated with fewer stress-response symptoms in patients with early-stage breast cancer [17,19] and in patients who have undergone bone marrow transplant.[32]
The availability and timeliness of accurate health-related information may also offer protection from stress-response symptoms. Women who met the diagnostic criteria for acute stress disorder reported significantly less satisfaction with the communication of their cancer diagnosis.[33] Similarly, women who were unaware of their cancer stage reported higher stress-response symptoms than those who knew more about the stage of their disease.[34] To the extent that adequacy of information reflects the quality of a patient’s relationship with medical staff, another protective factor may be the quality of those relationships. Difficult patient-staff relationships have been reported to predict stress-response symptoms in women with cancer.[35]
PTSD is precipitated by an intensely distressing event; however, this factor alone is not sufficient to explain the disorder. Not everyone exposed to a traumatic stressor develops the full-blown syndrome (or subsets of symptoms) or qualifies for the diagnosis. Attempts to explain these differences and to predict who is vulnerable have focused on the following:
Early studies of Vietnam War veterans suggested a two-factor learning theory to account for trauma-related pathology.[36,37] The same theory has also been applied to the development of PTSD in patients with cancer.[38-40]
PTSD symptoms develop as a function of both classical conditioning and instrumental learning. Classical conditioning accounts for the fear responses elicited by various stimuli that are associated with the original traumatic event. Neutral stimuli (e.g., smells, sounds, and visual images) previously paired with the aversive stimuli (e.g., chemotherapy or painful procedures) eventually evoke anxiety, arousal, and fear when presented alone, even after the trauma has ended. Higher-order conditioning and stimulus generalization account for the exacerbation and extension of symptoms to additional stimuli. Once established, PTSD symptoms are maintained through instrumental learning, that is, avoidant responses are reinforced because avoidance of the stimuli prevents unpleasant feelings and thoughts.
Estimates from epidemiological studies suggest that on average, 25% to 33% of individuals who are exposed to traumatic events, including cancer, develop PTSD or subsyndromal PTSD.[27,41] Although the disorder appears to be a result of learning processes, many factors have been suggested to explain why one person develops PTSD and another does not.
The diagnostic criteria for PTSD and ASD changed considerably in the fifth edition of the American Psychiatric Association’s Diagnostic and Statistical Manual of Mental Disorders (DSM-5). Changes from the fourth edition to the DSM-5 included the following:[1]
Criterion A, which is necessary for PTSD and ASD diagnoses, specifically states, “A life-threatening illness or debilitating medical condition is not necessarily considered a traumatic event. Medical incidents that qualify as traumatic events involve sudden, catastrophic events.” Thus, for the experience of cancer to meet Criterion A, it must entail acute and extreme adverse events in the context of cancer and/or cancer treatments. Events such as the cancer diagnosis, side effects of cancer treatments, and distress, worries, or negative thoughts about prognosis do not automatically qualify as trauma. Furthermore, patients with cancer can only be diagnosed with ASD or PTSD if they experience specific trauma-related symptoms, many of which are focused on or related to re-experiencing symptoms and intrusive memories. Fear of recurrence or worries about prognosis do not qualify as PTSD or ASD symptoms.
The four core clusters of symptoms for a PTSD diagnosis are as follows:
These symptoms must last for at least 1 month and cause clinically significant distress or impairment in social, occupational, or other important areas of functioning.
A timely, careful assessment of patients with cancer is critical to identify symptoms of cancer-related PTS, to note the deleterious impact of the symptoms on functioning, and to plan interventions targeted at the most distressing symptoms. It is also critical that the assessment distinguish between the full DSM PTSD syndrome (meets all required diagnostic criteria) and PTS-related symptoms only.
The most difficult aspect of PTS assessment in the cancer setting is the determination of precisely when to evaluate the patient. Diagnosis is complicated because cancer is not an acute or discrete event, but an experience marked by repeated trauma and indeterminate length. An individual may exhibit the symptoms of PTS at any point from diagnosis through treatment, to treatment completion and, possibly, to recurrence.[2] Patients such as Holocaust survivors, whose history of victimization can cause PTSD or its symptoms, can have symptoms activated by any number of stimuli encountered during their treatment (e.g., clinical procedures such as being inside magnetic resonance imaging or computed tomography scanners). While such patients may have more difficulty adjusting to cancer and cancer treatment, their symptomatology is likely to vary greatly according to their circumstances. The relative predominance of specific PTS symptoms may wax and wane throughout the cancer experience and beyond.[3]
The definition in the DSM-5 indicates that although PTSD symptoms usually begin within 3 months after trauma, there may be a delay of 4 or more months or even years before symptoms appear.[1] These findings support the necessity for long-term monitoring of cancer survivors and their family members.
At least one study found that individuals who have experienced a traumatic event may exhibit early symptoms without meeting the full criteria for a diagnosis of PTSD.[4] Nonetheless, the appearance of these early symptoms was found to predict later development of full PTSD syndrome. These results lend further credence to the need for both repeated and long-term follow-up of individuals exposed to the trauma of cancer. For more information, see Adjustment to Cancer: Anxiety and Distress.
The difficulty of properly diagnosing PTS may be compounded by the overlapping of PTS symptoms with those of other psychiatric disorders and by the time-related aspects of normal adjustment. For example, irritability, poor concentration, hypervigilance, excessive fear, and disturbed sleep are also symptoms of generalized anxiety disorder. Other arousal and avoidance symptoms are common to PTSD, phobias, and panic disorder, but loss of interest, sense of a foreshortened future, avoidance of other people, and sleep impairment might suggest both PTSD and depressive disorders. Even normal reactions to the diagnosis and treatment of life-threatening disease can consist of responses such as:
Clinicians and researchers must be particularly attuned to the causes, duration, and severity of PTSD-like symptoms when considering PTSD among several diagnoses. For instance, in a study of women with breast cancer, 41% reported experiencing “intense fear, helplessness, or horror”; however, on further comprehensive diagnostic interview, only 4% met the full PTSD criteria. Assessment must be able to distinguish between general psychological distress and symptoms of PTSD.[5]
The accurate diagnosis of PTSD also requires the use of reliable and valid instruments. Many studies have used the PTSD module of the Structured Clinical Interview for DSM-III-R–Nonpatient Edition.[6] This instrument is a clinician-administered, structured clinical interview that is time intensive and may not be feasible in settings without adequately trained mental health professionals. However, one study [7] investigated the utility of a cost-effective screening tool, the PTSD Checklist-Civilian Version (PCL-C).[8] In this study of 82 women diagnosed with breast cancer assessed 6 to 72 months after cancer treatment, use of the PCL-C resulted in a sensitivity of 0.60 and specificity of 0.99. Other cutoff scores for the PCL-C that could be used were discussed, depending on the clinical resources available in specific cancer treatment settings. Most research studies have used the Impact of Event Scale, a self-report of intrusive thoughts;[9] however, it is important to note that this tool can help evaluate PTS symptoms but is not designed to assess PTSD.
In attempting to diagnose PTSD, it is important to be aware that this disorder is often marked by comorbid psychopathology. Substance abuse, affective disorders, and other anxiety disorders are consistently encountered in samples of people with PTSD.[3,10-12] It has been reported that war veterans with PTSD exhibited substantial comorbid pathology that included:[13]
High rates of concurrent disorders have also been documented in other trauma victims. For example, 40% to 42% of disaster survivors with PTSD also qualified for a diagnosis of major depression, and 20% to 42% met the criteria for concurrent generalized anxiety disorder.[13,14] While this has not yet been studied in cancer patients or survivors, the presence of co-occurring psychiatric disorders in Vietnam War veterans and other trauma victims would indicate that cancer clinicians should be alert to identify and treat such related syndromes in their patients.
Conceptual and practical problems can arise in the application of PTS to cancer patients and survivors. The basic concept of an extreme traumatic stressor has been described variously as an event involving direct personal experience that involves actual or threatened death or serious injury.[15] This event can be protracted and continuous but is more frequently a single, time-limited event (e.g., rape, natural disaster). In this context, for the person who has experienced a diagnosis of cancer, the exact nature of the trauma is unclear. Is it the actual diagnosis, aspects of the treatment process, information given about recurrence, negative test results, or some other aspect of the cancer experience? Identifying a discrete stressor within the multiple crises that constitute a cancer experience is much more difficult than it is for other traumas. In one study of patients with breast cancer who underwent autologous bone marrow transplant, more PTSD-like symptoms were reported at the time of initial diagnosis.[16]
Another concern regarding conceptual fit is related to re-experiencing the trauma. In a study of women with early-stage breast cancer, researchers found that the traumatizing aspects of the cancer experience were receiving the diagnosis and waiting for test results from node dissection.[17] Arguing that these “information traumas” are future oriented and tend to cause intrusive worry about the future—not intrusive recollections of past events—the authors questioned whether cancer fits a conceptual model of PTSD trauma. Re-experiencing the trauma is often measured in terms of unwanted intrusive thoughts about the traumatic event. The cognitive processing of a current and ongoing health threat with uncertain outcome might differ significantly from unwanted intrusive thoughts about a single past event. Some researchers have argued that not all intrusive thoughts are negative or indicate re-experiencing a trauma; rather, they might represent appropriate vigilance and attention to potential symptoms that could result in appropriate help-seeking.[5,18]
Conversely, a unique study assessing the physiological reactivity of patients with breast cancer to a personalized imagery script of their most stressful experiences with the cancer found elevated physiologic responses that were comparable to those of PTSD patients who had experienced other (non–cancer-related) traumas. This finding suggests a good fit between patients with cancer and the PTSD trauma model, as it shows comparable symptoms of increased arousal in patients with cancer. Also, in a factor analytic study designed to confirm the presence of the three broad PTSD symptom clusters (re-experiencing, avoidance of reminders, and hyperarousal), researchers found some tentative support for the DSM-IV symptom clusters in a sample of breast cancer survivors.[19]
In a study of 74 women breast cancer survivors interviewed at 18 months postdiagnosis via the SCID, three groups were identified: one meeting the full criteria for PTSD (n = 12), another meeting partial but not full criteria for PTSD (i.e., subsyndromal, n = 5), and a no-PTSD group (n = 47). Further analyses investigated group differences. Some notable factors affecting the full-criteria PTSD group compared with the subsyndromal and no-PTSD groups included the following:[20]
Further research is needed to continue to investigate the important question of how well the conceptual model of PTSD as an anxiety response to a major life trauma fits the life experience of patients with cancer. Reviews have argued both in favor of [21] and against [18] the continued use of trauma models for conceptualizing the experience of cancer. Others have proposed alternate conceptual models.[5,22]
The chronic and sometimes devastating psychological and interpersonal sequelae of post-traumatic stress disorder (PTSD) necessitates timely and effective treatment .[1,2] The avoidant responses associated with PTSD often delay or prevent individuals from seeking professional assistance. While no specific therapies for PTSD in the cancer setting have been developed, treatment modalities used with other people with PTSD can help alleviate distress in cancer patients and survivors.[3,4]
Most clinicians recommend using a multimodal approach, choosing components to meet the specific needs of each patient and taking into account any concurrent psychiatric disorders such as depression or substance abuse. Multiple modalities are frequently considered in a crisis intervention approach to facilitating adjustment of patients with cancer.
The crisis intervention model comprises a broad range of therapies that can be helpful in the treatment of post-traumatic stress symptoms. The goals of this model are to reduce symptoms and restore patients to their usual levels of functioning. In this model, the therapist often takes an active, directive stance with the patient, focusing on the following: [5][Level of evidence: II]
Cognitive-behavioral techniques have proven especially helpful within the crisis intervention setting. Some of these methods include the following:[6]
In a single case study, a 10-session cognitive-behavioral intervention for a male cancer patient who was 3 years post–bone marrow transplant and had PTSD was found to be effective. This study used a combination of cognitive coping strategies, relaxation procedures, relapse prevention, and generalization techniques. Benefits were maintained at a 6-month follow-up.[7][Level of evidence: III] Behaviorally oriented approaches to sexual therapy may also be useful when the avoidance manifested by patients is decreased sexual activity and avoidance of intimate situations.
Support groups also appear to benefit people who experience post-traumatic symptoms. In the group setting, such patients can receive emotional support and encounter others with similar experiences and symptoms, thereby validating their own experiences and learning a variety of coping and management strategies.
For patients with particularly distressing or severe symptoms, psychopharmacology may provide an additional means of treatment. Several classes of medications have been used to treat individuals with PTSD.[8,9] For pharmacological treatments for PTSD, see the table below. For example:
| Medication | Dosing (mg/day) | Target Symptomsc | Evidence Basis |
|---|---|---|---|
| RCT = randomized controlled trial; SSRIs = selective serotonin reuptake inhibitors. | |||
| aAdapted from Berger et al.[10] and Asnis et al.[11] | |||
| bAll studies conducted in patients without cancer only. No studies have been reported on pharmacological treatments for PTSD conducted in patients with cancer. | |||
| cPTSD symptom clusters are as follows: cluster B, re-experiencing; cluster C, avoidance/numbing; cluster D, hyperarousal. | |||
| dConsidered first-line treatments for PTSD. | |||
| eFDA approved for the treatment of PTSD. | |||
| fUsed mainly as augmentation to SSRIs or serotonin-potentiating non-SSRIs. | |||
| SSRIsd | |||
| Sertralinee | 50–200 | All symptom clusters | Several RCTs |
| Paroxetinee | 20–50 | All symptom clusters | Several RCTs |
| Fluoxetine | 20–60 | All symptom clusters | Several RCTs |
| Fluvoxamine | 50–300 | All symptom clusters | Open label |
| Citalopram | 20–60 | All symptom clusters | Open label |
| Escitalopram | 10–20 | All symptom clusters | Open label |
| Serotonin-Potentiating Non-SSRIs | |||
| Venlafaxine | 37.5–225 | All symptom clusters | Open label |
| Duloxetine | 30–120 | All symptom clusters | Open label |
| Trazodone | 50–300 | Insomnia, possibly other clusters | Open label |
| Mirtazapine | 15–45 | Insomnia, possibly other clusters | Open label |
| Other Antidepressants | |||
| Imipramine | 50–225 | Possibly all clusters | One RCT |
| Other Agents Used as Augmentation Therapy Onlyf | |||
| Atypical Antipsychotics | |||
| Risperidone | 1–6 | Clusters B and D, possibly cluster C | Several RCTs |
| Olanzapine | 5–20 | Possibly all clusters | One RCT |
| Quetiapine | 25–300 | Possibly all clusters | Open label |
| Anticonvulsants | |||
| Lamotrigine | 50–400 | Clusters B and C | One RCT |
| Adrenergic-Inhibiting Agents | |||
| Prazosin | 2–6 | All symptom clusters (primary target symptom: nightmares) | Several RCTs |
The cancer treatment experience may be considered a significant traumatic event, given the nature of diagnosis, the number of invasive and painful procedures, and the often-long hospitalizations that children and their families must endure. On the basis of this exposure model, a number of studies have examined whether children treated for cancer are at a significantly higher risk for developing symptoms of post-traumatic stress disorder (PTSD). The results of these studies have been mixed.[1] One study reported that children and adolescents who were undergoing treatment reported some symptoms of post-traumatic stress (PTS). However, for most children, these symptoms did not meet the criteria for a diagnosis of PTSD, and the symptoms diminished over time.[2][Level of evidence: II]
Other studies suggest that survivors of childhood cancer have an increased risk for PTS symptoms and PTSD after treatment is finished. In a study of 78 adults aged 18 to 41 years who had been treated for childhood cancer, 20.5% met the criteria for a diagnosis of PTSD at some time since the end of their treatment. Clinically significant events of intrusive symptoms (9%) and avoidant symptoms (16.7%) were reported in the sample, and the symptoms were associated with elevated reports of anxiety and other measures of psychological distress.[3][Level of evidence: II] Survivors who report higher levels of uncertainty about their disease and future appear to be more likely to have elevated reports of PTS symptoms.[4][Level of evidence: II][5]
Similarly, a study of 182 adolescent and young adult cancer survivors who were more than 5 years from diagnosis and more than 2 years from completion of cancer treatment found that 16% met the criteria for PTSD. A relationship between PTSD and higher levels of other psychological problems was also reported.[6] When survivors meet the criteria for PTSD, they are more likely to experience depression and negative affect, lower satisfaction with life, and poorer reported health-related quality of life, as well as difficulty performing developmental tasks.[7][Level of evidence: II]
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Risk Factors, Protective Factors, and Hypothesized Mechanisms
Added Johnson et al. as reference 25.
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