eISSN: 1897-4309
ISSN: 1428-2526
Contemporary Oncology/Współczesna Onkologia
Current issue Archive Manuscripts accepted About the journal Supplements Addendum Special Issues Editorial board Reviewers Abstracting and indexing Subscription Contact Instructions for authors Ethical standards and procedures
Editorial System
Submit your Manuscript
SCImago Journal & Country Rank
3/2011
vol. 15
 
Share:
Share:
Review paper

Palmar-plantar erythrodysaesthesia during pegylated liposomal doxorubicin treatment – case report

Bożena Cybulska-Stopa
,
Marek Ziobro
,
Marta Skoczek
,
Ida Cedrych

Współcz Onkol 2011; 15 (3): 164–167
Online publish date: 2011/07/04
Article file
- Palmar.pdf  [1.02 MB]
Get citation
 
PlumX metrics:
 

Introduction

Palmar-plantar erythrodysaesthesia (PPE), otherwise known as the hand-foot syndrome, is a characteristic dermatological complication which may occur after administration of certain cytotoxic drugs. It was observed and described for the first time in 1974 after administration of mitotane [1]. Later there was an increase in reports concerning the development of PPE after prolonged infusions of 5-fluorouracil [2]. At the moment it is known that palmar-plantar erythrodysaesthesia can be caused by a number of other anticancer drugs. It is most frequently observed after administration of capecitabine [3], pegylated liposomal doxorubicin (PLD) [4], sorafenib [5], sunitinib [5], 5-fluorouracil [8], vinorelbine [8], tegafur [6], emitefur [7] and after prolonged exposure to irinotecan [8], doxorubicin [8], cytarabine [8], floxuridine [8], and high doses of interleukin [4], or gemcitabine [4].

The precise mechanism which leads to the onset of the PPE associated with the administration of certain drugs is not yet known. It was observed that pegylated liposomal form of doxorubicin (PLD) accumulates in greater amounts in the eccrine sweat glands, located mainly on the palms and soles of the feet, which may explain the frequent location of the skin changes in this area [4, 9]. An individual tendency to excessive sweating of hands and feet can also contribute to the occurrence of PPE [10]. It is hypothesized that PLD emerges from the capillaries in the deeper layers of the skin due to the local trauma associated with daily activities, which may explain the occurrence of PPE in other areas of the body such as the axillary, inguinal, and sacral region [11].

Clinical signs of PPE are: dysaesthesia defined as unpleasant sensory sensations, tingling, itching, connected with swelling and redness (erythema) of the palms of the hands and soles of the feet, appearing about 2-12 days after initiation of chemotherapy. These symptoms may worsen within 3-4 days after onset, leading to blistering, painful skin cracking and deep ulcerations. Dysaesthesia and erythema may also occur in other areas of the body, particularly those exposed to pressure or higher temperature, but it is much less frequent.

Histological examination of the affected foot skin reveals hyperkeratosis and parakeratosis in the cornified layer (stratum corneum) of the epidermis and intercellular oedema (spongiosis) with numerous pyknotic cells without associated lymphocytes in the Malpighian layer. A focal vacuolization in the basal layer, perivascular lymphocytic infiltration and deposits of melanin in the dermis are also observed [12].

Description

We report a case of palmar-plantar erythrodysaesthesia in a 56-year-old breast cancer patient with metastatic lesions located in the liver and lungs, treated with pegylated liposomal doxorubicin. During the second cycle of the cytotoxic therapy the patient developed a classic form of hand-foot skin lesions with the clinical features of erythrodysaesthesia located on the skin of the armpit, groin, back and the abdomen.

The patient started treatment with pegylated liposomal doxorubicin and docetaxel at doses of 30 mg/m2 and 75 mg/m2 respectively, administered in 3-week intervals. Since the initiation of the chemotherapy, vitamin B6 (pyridoxine) in a dose of 100 mg twice daily as a hand-foot syndrome prevention, and dexamethasone in doses of 2 × 8 mg on three consecutive days, as a premedication for dace taxel were administered. After three series of the chemotherapy the patient developed grade 1 hand-foot syndrome (according to the NCI CTCAE v3 scale) [17]. Initially the changes were limited to the hands and feet and were described as dysaesthesia (unpleasant sensory experiences) and tingling, with redness and swollen, cyanosed areas on the hands and feet (Fig. 1). The application of a skin barrier cream and cooling of the changed areas was recommended, which gave relief to the patient. The chemotherapy was continued in full doses, until the worsening of the skin lesions. Redness and desquamation of the skin on the palm appeared (Fig. 2), followed by changes around the armpits, groin, and on the skin of the back and abdomen (Fig. 3, 4). The described symptoms were connected with severe pain. Due to the severity of the changes – grade 3 (according to the NCI CTCv3 scale) [17], after the fourth cycle the chemotherapy was stopped and symptomatic treatment to relieve the pain was implemented. The topical application of the grease cream a few times a day and ice-cooling of the hands and feet was continued. To relieve the pain we used non-steroidal anti-inflammatory drugs, as well as oral formulations of morphine. The skin changes of such severity lasted for about four weeks. After this time, a decrease in symptoms to grade 1 was observed (only local erythema and paraesthesia) (Fig. 5). Chemotherapy was resumed with doses reduced by 25% in accordance with the recommendations for dose modification (Table 1). The chemotherapy was continued for a further four courses, after which, due to worsening of skin symptoms on the hands, armpits and abdomen, the therapy was completed. We administered the symptomatic treatment as mentioned above. The symptoms resolved in about three weeks after the end of treatment, leaving a brown discoloration that remained for a period of several months (Fig. 6, 7).

Summary

Palmar-plantar erythrodysaesthesia in most cases is confined to the hands and feet, but dysaesthesia, erythema, skin desquamation and sores may appear in other areas of the body, especially those exposed to pressure or increased temperature [11]. In the presented case the PPE affected the axillary and inguinal region, the skin of the back and abdomen. These changes, however, may also appear on the buttocks, inframammary region, vulva or scrotum [13], deteriorating the quality of life of the patient, and impairing normal activities of daily living. Prevention strategies of palmar-plantar erythrodysaesthesia onset include the patient’s education on the care of the body areas most exposed to the hand-foot changes, which includes: to avoid pressure, skin abrasions and circumstances leading to vasodilatation such as hot baths and solar radiation [9]. The use of moisturizing creams, cool baths and wearing loose clothing and footwear are also recommended [9, 15]. The list of pharmacological agents includes vitamin B6 (pyridoxine) and oral corticosteroids; however, the efficacy of these drugs in the prevention of PPE has not been confirmed by randomized clinical trials [9].

Treatment delay or chemotherapy dose reductions in accordance with the recommendations for dose modification remain the most important action in PPE treatment. Adequate hygiene of the affected skin areas, the use of moisturizing creams (containing petrolatum and lanolin), the application of antibiotic ointment in case of infection and analgesic drugs is also crucial [9]. Palmar-plantar erythrodysaesthesia is a common and very inconvenient complication of chemotherapy, which significantly impairs the patient’s quality of life. Unfortunately there are no effective methods of prevention and treatment of this complication, so we are forced to lengthen the time interval between courses and reduce drug doses, which often limits the possibility of effective treatment of oncological patients.

References

 1. Zuehlke RL. Erythematous eruption of the palms and soles associated with mitotane therapy. Dermatologica 1974; 148: 90-2.  

2. Lokich JJ, Moore C. Chemotherapy associated palmar-plantar erythrodysesthesia syndrome. Ann Intern Med 1984; 101: 798-9.  

3. Van Cutsem E, Hoff PM, Harper P, Bukowski RM, et al. Oral capecitabine vs intravenosus 5-fluorouracil and leucovorin: integrated efficacy data and novel analyses from two, randomized, phase II trials. Br J Cancer 2004; 90: 1190-7.  

4. Lorusso D, Stefano Di, Carone V, et al. Pegylated liposomal doxorubici-related palmar-plantar erythrodysestesia (“hand-foot” syndrome). Ann Oncol 2007; 18: 1159-64.  

5. Lipworth AD, Robert C, Zhu AX. Hand-foot syndrome (hand-foot skin reaction, palmar-plantar erythrodysesthesia): focus on sorafenib and sunitinib. Oncology 2009; 77: 257-71.  

6. Jucgla A, Sais G, Navarro M. Palmoplantar keratoderma secondary to chronic acral erythema due to tegafur. Arch Dermatol 1995; 131: 364-5.  

7. Nemunaitis J, Eager R, Twadell T. Phase I assessment of the pharmacokinetics, metabolism, and safety of emitur in patients with refractory tumors. J Clin Oncol 2000; 18: 3423-34.  

8. Janusch M, Fischer M, et al. The hand-hood syndrome – a frequent secondary manifestation in antineoplastic chemotherapy. Eur J Dermatol 2006; 16: 494-9.  

9. Moos R, Thuerlimann BJ, Aapro M, et al. Pegylated liposomal doxorubicin-associated hand-foot syndrome: recommendations of an international panel of experts. Eur J Cancer 2008; 44: 781-90.

10. Jacobi U, Waibler E, Schulze P, et al. Release of doxorubicin in sweat: first step to induce the palmar-plantar erythrodysesthesia syndrome? Ann Oncol 2005; 16: 1210-1.

11. Lyass O, Uziely B, Ben-Yosef R, et al. Correlation of toxity with pharmacokinetics of pegylated liposomal doxorybicin (Doxil) in metastatic breast carcinoma. Cancer 2000; 89: 1037-47.

12. Nagore E, Insa A, Sanmartin O. Antineoplastic therapy-induced palmar plantar erythrodysestesia (“hand-foot”) syndrome: incidence, recognition and management. Am J Clin Dermatol 2000; 1: 225-34.

13. Marini A, Hengge UR. Hand-foot syndrome with capecytabine therapy. Hautzartz 2007; 58: 532-6.

14. Edwards SJ. Prevention and treatment of adverse effects related to chemotherapy for recurrent ovarian cancer. Semin Oncol Nurs 2003; 19: 19-39.

15. Wilkes GM, Doyle D. Palmar-plantar erythrodysesthesia. Clin J Oncol Nurs 2005; 9: 103-6.

16. Doxil (doxorubicin HCI liposome injection) prescribing information. Brigewater NJ. Tibotec Therapeutics/Division of Ortho Biotech Products 2005.

17. NCI CTC v3, COMMON TOXICITY CRITERIA (NCI CTC-3).

Address for correspondence



Bożena Cybulska-Stopa

Department of Systemic and Generalized Malignancies

Department of Centre of Oncology

Maria Sklodowska-Curie Memorial Centre

Garncarska 11

31-115 Kraków, Poland

e-mail: bcybulskastopa@vp.pl
Copyright: © 2011 Termedia Sp. z o. o. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.