Basal cell carcinoma medical therapy: Difference between revisions

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**The complete [[cure]] rate was around 80%.
**The complete [[cure]] rate was around 80%.
*[[Photodynamic therapy]]
*[[Photodynamic therapy]]
**The other available option for BCC is [[photodynamic therapy]] (PDT) with [[Levulinic acid|5-amino levulinic acid]] or with its methyl [[Esters|ester]] plus red light.  
**The other available option for BCC is [[photodynamic therapy]] (PDT) with [[Levulinic acid|5-amino levulinic acid]](MAL) or with its methyl [[Esters|ester]] plus red light.  
**The MAL cream is applied to the [[tumor]] and covered with an [[Occlusive dressing|occlusive]] [[Dressing (medical)|dressing]] for three hours.  
**The MAL [[Cream (pharmaceutical)|cream]] is applied to the [[tumor]] and covered with an [[Occlusive dressing|occlusive]] [[Dressing (medical)|dressing]] for three hours.  
**The [[Tumor cell|tumor cells]] then form increasing amounts of [[protoporphyrin IX]], which is stimulated by [[irradiation]] with red [[light]] to form [[reactive oxygen species]] which are in turn [[cytotoxic.]]  
**The [[Tumor cell|tumor cells]] then form increasing amounts of [[protoporphyrin IX]], which is stimulated by [[irradiation]] with red [[light]] to form [[reactive oxygen species]] which are in turn [[cytotoxic.]]  
**It should be repeated after 1–4 weeks.
**It should be repeated after 1–4 weeks.
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**The main disadvantages of [[photodynamic therapy]] are the [[pain]] during the [[irradiation]] and the local [[inflammatory]] [[reaction]] ([[erythema]], erosions, [[pustules]], and crusts).
**The main disadvantages of [[photodynamic therapy]] are the [[pain]] during the [[irradiation]] and the local [[inflammatory]] [[reaction]] ([[erythema]], erosions, [[pustules]], and crusts).
*5-flurouracil
*5-flurouracil
**It is a cytostatic agent which is available as a 5% prescription cream that is designed to be applied twice daily for 3–12 weeks until erosions develop.
**It is a [[cytostatic]] agent which is available as a 5% [[prescription]] [[Cream (pharmaceutical)|cream]] that is designed to be applied twice daily for 3–12 weeks until erosions develop.
'''Systemic therapy'''
'''Systemic therapy'''
*Hedgehog pathway inhibitors(vismodegib,sonidegib)  
*[[Sonic hedgehog|Sonic hedgehog pathway]] inhibitors([[vismodegib]], [[sonidegib]])  
**They are markedly teratogenic and embryotoxic.
**They are markedly [[teratogenic]] and embryotoxic.
**The commonest adverse effects of vismodegib include muscle cramps, hair loss, taste disturbances and weight loss.
**The commonest [[adverse effects]] of [[vismodegib]] include [[muscle cramps]], [[hair loss]], [[Taste alteration|taste disturbances]] and [[weight loss]].
'''Cryotherapy'''
'''Cryotherapy'''
*Small and superficial BCC are occasionally still treated with liquid nitrogen (–196°C) either with direct contact or using a spray.
*Small and [[superficial]] basal cell carcinoma is occasionally still treated with [[liquid nitrogen]] (–196°C) either with direct contact or using a [[Spray-on skin|spray]].
*The wounds may heal with either hypopigmentation or scarring so making it a major disadvantage.
*The [[wounds]] may [[Healing|heal]] with either [[hypopigmentation]] or [[scarring]] so making it a major disadvantage.


==References==
==References==

Revision as of 16:28, 1 March 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Saarah T. Alkhairy, M.D.

Overview

After the suspicious lesion is evaluated, the medical therapy is divided into low-risk and high-risk basal cell carcinoma patients. Medical therapy consists of surgery, radiation therapy, and follow-up for recurrence.

Basal Cell Carcinoma Medical Therapy

Once the suspicious lesion is evaluated, the medical therapy is based upon the low-risk and high-risk basal cell carcinoma patients.

The table below summarizes the characteristics in low-risk and high-risk lesions[1].

H&P Low Risk High Risk
Location/size Area L < 20 mm; Area M < 10 mm; Area H < 6 mm Area L ≥ 20 mm; Area M ≥ 10 mm; Area H ≥ 6 mm
Borders Well defined Poorly defined
Primary vs. recurrent Primary Recurrent
Immunosuppression (-) (+)
Site of prior radiation therapy (-) (+)
Subtype Nodular, superficial Aggressive growth pattern
Perineural involvement (-) (+)

Area H = “mask areas” of face (central face, eyelids, eyebrows, periorbital, nose, lips [cutaneous and vermilion], chin, mandible, preauricular and postauricular skin/sulci, temple, ear), genitalia, hands, and feet

Area M = cheeks, forehead, scalp, neck, and pre-tibial area

Area L = trunk and extremities (excluding pre-tibial area, hands, feet, nail units, and ankles)


The algorithm below demonstrates a treatment protocol for low-risk lesions[2].

The algorithm below demonstrates a treatment protocol for high-risk lesions[3].

After the primary treatment, a follow-up is performed to evaluate for recurrence of the tumor.

The algorithm below demonstrates a follow-up protocol[4].

The medical therapy for basal cell carcinoma is divided into[5][6]:

  • Toipcal
  • Systemic

Topical therapy

Systemic therapy

Cryotherapy

References

  1. http://www.nccn.org/professionals/physician_gls/PDF/nmsc.pdf
  2. http://www.nccn.org/professionals/physician_gls/PDF/nmsc.pdf
  3. http://www.nccn.org/professionals/physician_gls/PDF/nmsc.pdf
  4. http://www.nccn.org/professionals/physician_gls/PDF/nmsc.pdf
  5. Berking C, Hauschild A, Kölbl O, Mast G, Gutzmer R (May 2014). "Basal cell carcinoma-treatments for the commonest skin cancer". Dtsch Arztebl Int. 111 (22): 389–95. doi:10.3238/arztebl.2014.0389. PMID 24980564.
  6. Wong CS, Strange RC, Lear JT (October 2003). "Basal cell carcinoma". BMJ. 327 (7418): 794–8. doi:10.1136/bmj.327.7418.794. PMC 214105. PMID 14525881.