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The Challenges of Treating Patients with Cancer Pain

Peer Viewpoint

The Challenges of Treating Patients with Cancer Pain

Sloan Beth Karver MD, FAAHPM

,
and Jessalyn H. Berger   [Author vitae]


Available online 25 January 2011.

Refers to:
Cancer Breakthrough Pain in the Presence of Cancer-Related Chronic Pain: Fact versus Perceptions of Health-Care Providers and Patients
The Journal of Supportive Oncology, Volume 8, Issue 6, November-December 2010, Pages 232-238,
Michelle I. Rhiner, Charles F. von Gunten
PDF (503 K)
  |      

Article Outline

References

Vitae

Breakthrough pain (BTP) is a temporary spike in pain that occurs in otherwise well-controlled persistent cancer pain.1 BTP may be described as either incident pain that is related to movement, nonincident pain that is unpredictable in nature, or end-of-dose pain that occurs after insufficient dosing of persistent pain.[1], [2] and [3] The authors analyzed a group of patients and found that half described pain related to particular activities. A significant number of patients with cancer experience these pain flares. In a single-population evaluation of cancer pain (n = 159), it was reported that of those patients with continuous pain, 57 (75%) experienced BTP. More than half (54%) of those patients who experienced cancer pain reported it being related to particular activities, while a little over one-quarter of patients (26%) experienced pain idiopathic in nature and 16% of patients experienced end-of-dose pain.3 In a survey of 545 cancer patients experiencing fluctuations in pain conducted by the American Pain Foundation, 96% of patients with cancer experienced episodes of BTP at least once a month, more than 70% experienced BTP episodes at least once a week, and more than one-fifth (22%) experienced BTP more than once a day.4

Fears relating to good pain management include a lack of technical knowledge about pain management and pain assessment. Attitudes about opioid addiction and regulatory guidelines influence the manner in which opioids are prescribed. Patients harbor a variety of fears and misconceptions such as opioid addiction, tolerance, side effects, and the meaning of pain, which can create a barrier to effective communication with health-care providers regarding cancer pain management and specifically BTP. Identifying these issues gives health-care professionals and patients an opportunity to develop strategies that can improve the treatment of BTP.

Many physicians lack the knowledge of proper around-the-clock (ATC) dosing. ATC treatment maintains drug concentrations and prevents peaks and troughs that can increase the risk of toxicity and result in lack of efficacy.

The authors recommend oral transmucosal delivery of opioids as an option for these challenges. Three formulations of the opioid fentanyl are available for transmucosal delivery: oral transmucosal fentanyl citrate (OTFC),5 fentanyl buccal tablets (FBTs),6 and fentanyl buccal soluble film (FBSF).7 OTFC is a fentanyl lozenge that has demonstrated an analgesic effect within 15 minutes of administration. Despite its rapid onset of action, the amount of fentanyl administered with the OTFC lozenge depends on the education provided to the patient on the use of this medication and the ability of the patient to actively use this product.5 While FBT (a tablet that utilizes an effervescent reaction to improve absorption) does not require substantial patient participation, its use has been associated with application-site side effects.6 Like OTFC and FBT, FBSF offers a rapid onset of action but does not require active patient participation and has minimal oral adverse side effects.7 These oral transmucosal fentanyl products should be administered only to opioid-tolerant patients, to avoid the risk of life-threatening respiratory depression. The reviewers stress that these products should be used only in opioid-tolerant patients.

Many physicians are quite aware when they have reached their “comfort level” of working with opioids. It is usually at that point that they will refer patients for consultation to the palliative care team or pain services. Patients may believe that pain is part of the cancer diagnosis and is to be expected. Some patients believe that use of opioids signifies the “end of life” is near. They may believe the side effects related to opioids are unavoidable and the burden of use of opioids outweighs the benefits.8

In summary, the article by Rhiner and von Gunten speaks to the challenges that we encounter in treating cancer patients' pain. BTP is often not recognized and at times not adequately treated. This article serves as a good review of the challenges of treating patients with cancer pain and offers suggestions on how to improve the management of cancer pain with our patients.

 

 

References1

1 R.K. Portenoy, D. Payne and P. Jacobsen, Breakthrough pain: characteristics and impact in patients with cancer pain, Pain 81 (1999), pp. 129–134. Article |

PDF (49 K)
| View Record in Scopus | Cited By in Scopus (301)

2 T. Gutgsell, D. Walsh, D.S. Zhukovsky, F. Gonzales and R. Lagman, A prospective study of the pathophysiology and clinical characteristics of pain in a palliative medicine population, Am J Hosp Palliat Care 20 (2003), pp. 140–148. View Record in Scopus | Cited By in Scopus (16)

3 S.S. Hwang, V.T. Chang and B. Kasimis, Cancer breakthrough pain characteristics and responses to treatment at a VA medical center, Pain 101 (2003), pp. 55–64. Article |

PDF (98 K)
| View Record in Scopus | Cited By in Scopus (71)

4 American Pain Foundation, Breakthrough Cancer Pain Survey Fact Sheet http://www.painfoundation.org/learn/programs/spotlight-on-cancer-pain/breakthrough-pain/btcp-fact-sheet.pdf (2009).

5 Actiq (oral transmucosal fentanyl citrate lozenge) prescribing information. Cephalon, Inc. Revised 2007.

6 Fentora (fentanyl buccal tablet) prescribing information. Cephalon, Inc. Revised 2007.

7 , Onsolis (fentanyl buccal soluble film) prescribing information, Meda Pharmaceuticals, Inc (2009).

8 K. Forbes, Opioids: beliefs and myths, J Pain Palliat Care Pharmacother 20 (2006), pp. 33–35. Full Text via CrossRef | View Record in Scopus | Cited By in Scopus (8)

Commentary on “Cancer Breakthrough Pain in the Presence of Cancer-Related Chronic Pain: Fact versus Perceptions of Health-Care Providers and Patients” by Michelle I. Rhiner, RN, MSN, ACHPN, and Charles F. von Gunten, MD, PhD (page 232)

Conflicts of interest: Dr. Karver serves on Speaker's Bureaus for Meda Pharmaceutical and Pfizer Pharmaceutical.

Correspondence to: Sloan Karver, MD, 12902 Magnolia Drive, Tampa, FL 33612; telephone: (813) 745-8483


1 PubMed ID in brackets

Vitae

Dr. Karver is an assistant professor of oncologic sciences, University of South Florida, Tampa, Florida.

Ms Berger is a masters candidate in health education and behavior, University of Florida, Gainesville, Florida.


The Journal of Supportive Oncology
Volume 8, Issue 6, November-December 2010, Pages 239-240
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Peer Viewpoint

The Challenges of Treating Patients with Cancer Pain

Sloan Beth Karver MD, FAAHPM

,
and Jessalyn H. Berger   [Author vitae]


Available online 25 January 2011.

Refers to:
Cancer Breakthrough Pain in the Presence of Cancer-Related Chronic Pain: Fact versus Perceptions of Health-Care Providers and Patients
The Journal of Supportive Oncology, Volume 8, Issue 6, November-December 2010, Pages 232-238,
Michelle I. Rhiner, Charles F. von Gunten
PDF (503 K)
  |      

Article Outline

References

Vitae

Breakthrough pain (BTP) is a temporary spike in pain that occurs in otherwise well-controlled persistent cancer pain.1 BTP may be described as either incident pain that is related to movement, nonincident pain that is unpredictable in nature, or end-of-dose pain that occurs after insufficient dosing of persistent pain.[1], [2] and [3] The authors analyzed a group of patients and found that half described pain related to particular activities. A significant number of patients with cancer experience these pain flares. In a single-population evaluation of cancer pain (n = 159), it was reported that of those patients with continuous pain, 57 (75%) experienced BTP. More than half (54%) of those patients who experienced cancer pain reported it being related to particular activities, while a little over one-quarter of patients (26%) experienced pain idiopathic in nature and 16% of patients experienced end-of-dose pain.3 In a survey of 545 cancer patients experiencing fluctuations in pain conducted by the American Pain Foundation, 96% of patients with cancer experienced episodes of BTP at least once a month, more than 70% experienced BTP episodes at least once a week, and more than one-fifth (22%) experienced BTP more than once a day.4

Fears relating to good pain management include a lack of technical knowledge about pain management and pain assessment. Attitudes about opioid addiction and regulatory guidelines influence the manner in which opioids are prescribed. Patients harbor a variety of fears and misconceptions such as opioid addiction, tolerance, side effects, and the meaning of pain, which can create a barrier to effective communication with health-care providers regarding cancer pain management and specifically BTP. Identifying these issues gives health-care professionals and patients an opportunity to develop strategies that can improve the treatment of BTP.

Many physicians lack the knowledge of proper around-the-clock (ATC) dosing. ATC treatment maintains drug concentrations and prevents peaks and troughs that can increase the risk of toxicity and result in lack of efficacy.

The authors recommend oral transmucosal delivery of opioids as an option for these challenges. Three formulations of the opioid fentanyl are available for transmucosal delivery: oral transmucosal fentanyl citrate (OTFC),5 fentanyl buccal tablets (FBTs),6 and fentanyl buccal soluble film (FBSF).7 OTFC is a fentanyl lozenge that has demonstrated an analgesic effect within 15 minutes of administration. Despite its rapid onset of action, the amount of fentanyl administered with the OTFC lozenge depends on the education provided to the patient on the use of this medication and the ability of the patient to actively use this product.5 While FBT (a tablet that utilizes an effervescent reaction to improve absorption) does not require substantial patient participation, its use has been associated with application-site side effects.6 Like OTFC and FBT, FBSF offers a rapid onset of action but does not require active patient participation and has minimal oral adverse side effects.7 These oral transmucosal fentanyl products should be administered only to opioid-tolerant patients, to avoid the risk of life-threatening respiratory depression. The reviewers stress that these products should be used only in opioid-tolerant patients.

Many physicians are quite aware when they have reached their “comfort level” of working with opioids. It is usually at that point that they will refer patients for consultation to the palliative care team or pain services. Patients may believe that pain is part of the cancer diagnosis and is to be expected. Some patients believe that use of opioids signifies the “end of life” is near. They may believe the side effects related to opioids are unavoidable and the burden of use of opioids outweighs the benefits.8

In summary, the article by Rhiner and von Gunten speaks to the challenges that we encounter in treating cancer patients' pain. BTP is often not recognized and at times not adequately treated. This article serves as a good review of the challenges of treating patients with cancer pain and offers suggestions on how to improve the management of cancer pain with our patients.

 

 

References1

1 R.K. Portenoy, D. Payne and P. Jacobsen, Breakthrough pain: characteristics and impact in patients with cancer pain, Pain 81 (1999), pp. 129–134. Article |

PDF (49 K)
| View Record in Scopus | Cited By in Scopus (301)

2 T. Gutgsell, D. Walsh, D.S. Zhukovsky, F. Gonzales and R. Lagman, A prospective study of the pathophysiology and clinical characteristics of pain in a palliative medicine population, Am J Hosp Palliat Care 20 (2003), pp. 140–148. View Record in Scopus | Cited By in Scopus (16)

3 S.S. Hwang, V.T. Chang and B. Kasimis, Cancer breakthrough pain characteristics and responses to treatment at a VA medical center, Pain 101 (2003), pp. 55–64. Article |

PDF (98 K)
| View Record in Scopus | Cited By in Scopus (71)

4 American Pain Foundation, Breakthrough Cancer Pain Survey Fact Sheet http://www.painfoundation.org/learn/programs/spotlight-on-cancer-pain/breakthrough-pain/btcp-fact-sheet.pdf (2009).

5 Actiq (oral transmucosal fentanyl citrate lozenge) prescribing information. Cephalon, Inc. Revised 2007.

6 Fentora (fentanyl buccal tablet) prescribing information. Cephalon, Inc. Revised 2007.

7 , Onsolis (fentanyl buccal soluble film) prescribing information, Meda Pharmaceuticals, Inc (2009).

8 K. Forbes, Opioids: beliefs and myths, J Pain Palliat Care Pharmacother 20 (2006), pp. 33–35. Full Text via CrossRef | View Record in Scopus | Cited By in Scopus (8)

Commentary on “Cancer Breakthrough Pain in the Presence of Cancer-Related Chronic Pain: Fact versus Perceptions of Health-Care Providers and Patients” by Michelle I. Rhiner, RN, MSN, ACHPN, and Charles F. von Gunten, MD, PhD (page 232)

Conflicts of interest: Dr. Karver serves on Speaker's Bureaus for Meda Pharmaceutical and Pfizer Pharmaceutical.

Correspondence to: Sloan Karver, MD, 12902 Magnolia Drive, Tampa, FL 33612; telephone: (813) 745-8483


1 PubMed ID in brackets

Vitae

Dr. Karver is an assistant professor of oncologic sciences, University of South Florida, Tampa, Florida.

Ms Berger is a masters candidate in health education and behavior, University of Florida, Gainesville, Florida.


The Journal of Supportive Oncology
Volume 8, Issue 6, November-December 2010, Pages 239-240

Peer Viewpoint

The Challenges of Treating Patients with Cancer Pain

Sloan Beth Karver MD, FAAHPM

,
and Jessalyn H. Berger   [Author vitae]


Available online 25 January 2011.

Refers to:
Cancer Breakthrough Pain in the Presence of Cancer-Related Chronic Pain: Fact versus Perceptions of Health-Care Providers and Patients
The Journal of Supportive Oncology, Volume 8, Issue 6, November-December 2010, Pages 232-238,
Michelle I. Rhiner, Charles F. von Gunten
PDF (503 K)
  |      

Article Outline

References

Vitae

Breakthrough pain (BTP) is a temporary spike in pain that occurs in otherwise well-controlled persistent cancer pain.1 BTP may be described as either incident pain that is related to movement, nonincident pain that is unpredictable in nature, or end-of-dose pain that occurs after insufficient dosing of persistent pain.[1], [2] and [3] The authors analyzed a group of patients and found that half described pain related to particular activities. A significant number of patients with cancer experience these pain flares. In a single-population evaluation of cancer pain (n = 159), it was reported that of those patients with continuous pain, 57 (75%) experienced BTP. More than half (54%) of those patients who experienced cancer pain reported it being related to particular activities, while a little over one-quarter of patients (26%) experienced pain idiopathic in nature and 16% of patients experienced end-of-dose pain.3 In a survey of 545 cancer patients experiencing fluctuations in pain conducted by the American Pain Foundation, 96% of patients with cancer experienced episodes of BTP at least once a month, more than 70% experienced BTP episodes at least once a week, and more than one-fifth (22%) experienced BTP more than once a day.4

Fears relating to good pain management include a lack of technical knowledge about pain management and pain assessment. Attitudes about opioid addiction and regulatory guidelines influence the manner in which opioids are prescribed. Patients harbor a variety of fears and misconceptions such as opioid addiction, tolerance, side effects, and the meaning of pain, which can create a barrier to effective communication with health-care providers regarding cancer pain management and specifically BTP. Identifying these issues gives health-care professionals and patients an opportunity to develop strategies that can improve the treatment of BTP.

Many physicians lack the knowledge of proper around-the-clock (ATC) dosing. ATC treatment maintains drug concentrations and prevents peaks and troughs that can increase the risk of toxicity and result in lack of efficacy.

The authors recommend oral transmucosal delivery of opioids as an option for these challenges. Three formulations of the opioid fentanyl are available for transmucosal delivery: oral transmucosal fentanyl citrate (OTFC),5 fentanyl buccal tablets (FBTs),6 and fentanyl buccal soluble film (FBSF).7 OTFC is a fentanyl lozenge that has demonstrated an analgesic effect within 15 minutes of administration. Despite its rapid onset of action, the amount of fentanyl administered with the OTFC lozenge depends on the education provided to the patient on the use of this medication and the ability of the patient to actively use this product.5 While FBT (a tablet that utilizes an effervescent reaction to improve absorption) does not require substantial patient participation, its use has been associated with application-site side effects.6 Like OTFC and FBT, FBSF offers a rapid onset of action but does not require active patient participation and has minimal oral adverse side effects.7 These oral transmucosal fentanyl products should be administered only to opioid-tolerant patients, to avoid the risk of life-threatening respiratory depression. The reviewers stress that these products should be used only in opioid-tolerant patients.

Many physicians are quite aware when they have reached their “comfort level” of working with opioids. It is usually at that point that they will refer patients for consultation to the palliative care team or pain services. Patients may believe that pain is part of the cancer diagnosis and is to be expected. Some patients believe that use of opioids signifies the “end of life” is near. They may believe the side effects related to opioids are unavoidable and the burden of use of opioids outweighs the benefits.8

In summary, the article by Rhiner and von Gunten speaks to the challenges that we encounter in treating cancer patients' pain. BTP is often not recognized and at times not adequately treated. This article serves as a good review of the challenges of treating patients with cancer pain and offers suggestions on how to improve the management of cancer pain with our patients.

 

 

References1

1 R.K. Portenoy, D. Payne and P. Jacobsen, Breakthrough pain: characteristics and impact in patients with cancer pain, Pain 81 (1999), pp. 129–134. Article |

PDF (49 K)
| View Record in Scopus | Cited By in Scopus (301)

2 T. Gutgsell, D. Walsh, D.S. Zhukovsky, F. Gonzales and R. Lagman, A prospective study of the pathophysiology and clinical characteristics of pain in a palliative medicine population, Am J Hosp Palliat Care 20 (2003), pp. 140–148. View Record in Scopus | Cited By in Scopus (16)

3 S.S. Hwang, V.T. Chang and B. Kasimis, Cancer breakthrough pain characteristics and responses to treatment at a VA medical center, Pain 101 (2003), pp. 55–64. Article |

PDF (98 K)
| View Record in Scopus | Cited By in Scopus (71)

4 American Pain Foundation, Breakthrough Cancer Pain Survey Fact Sheet http://www.painfoundation.org/learn/programs/spotlight-on-cancer-pain/breakthrough-pain/btcp-fact-sheet.pdf (2009).

5 Actiq (oral transmucosal fentanyl citrate lozenge) prescribing information. Cephalon, Inc. Revised 2007.

6 Fentora (fentanyl buccal tablet) prescribing information. Cephalon, Inc. Revised 2007.

7 , Onsolis (fentanyl buccal soluble film) prescribing information, Meda Pharmaceuticals, Inc (2009).

8 K. Forbes, Opioids: beliefs and myths, J Pain Palliat Care Pharmacother 20 (2006), pp. 33–35. Full Text via CrossRef | View Record in Scopus | Cited By in Scopus (8)

Commentary on “Cancer Breakthrough Pain in the Presence of Cancer-Related Chronic Pain: Fact versus Perceptions of Health-Care Providers and Patients” by Michelle I. Rhiner, RN, MSN, ACHPN, and Charles F. von Gunten, MD, PhD (page 232)

Conflicts of interest: Dr. Karver serves on Speaker's Bureaus for Meda Pharmaceutical and Pfizer Pharmaceutical.

Correspondence to: Sloan Karver, MD, 12902 Magnolia Drive, Tampa, FL 33612; telephone: (813) 745-8483


1 PubMed ID in brackets

Vitae

Dr. Karver is an assistant professor of oncologic sciences, University of South Florida, Tampa, Florida.

Ms Berger is a masters candidate in health education and behavior, University of Florida, Gainesville, Florida.


The Journal of Supportive Oncology
Volume 8, Issue 6, November-December 2010, Pages 239-240
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The Challenges of Treating Patients with Cancer Pain
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