Примери за използване на Cuscc на Английски и техните преводи на Български
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Common cuSCC a New Primary Melanoma*.
Cutaneous squamous cell carcinoma(cuSCC).
CuSCC was most commonly treated by local excision.
It has not been determined whether cuSCC is related to Odomzo treatment.
Patients with advanced BCC have an increased risk of developing cuSCC.
Cases of cuSCC have been reported in patients treated with vemurafenib.
Monitoring for skin lesions should occur as described for cuSCC.
Cases of cuSCC have been reported in advanced BCC patients treated with Odomzo.
Patients with advanced BCC have an increased risk of developing cuSCC.
Cases of cuSCC can be managed with excision and do not require treatment modification.
In the pooled encorafenib 300 population, cuSCC was reported in 7.4%(16/217) patients.
The incidence of cuSCC in vemurafenib-treated patients across studies was approximately 20%.
The prescriber should examine the patient monthly during andup to six months after treatment for cuSCC.
In patients who develop cuSCC, it is recommended to continue the treatment without dose adjustment.
Up to 1 in 10 people taking Tafinlar may develop a different type of skin cancer called cutaneous squamous cell carcinoma(cuSCC).
CuSCC usually occurred early in the course of treatment with a median time to the first appearance of 7 to 8 weeks.
The median time to onset of the first event of cuSCC(all grades) was 6.5 months(range 1.0 to 22.8 months).
Cases of cuSCC(including keratoacanthoma) have been reported in patients treated with trametinib in combination with dabrafenib.
Older patients(≥ 65 years) may be more likelyto experience adverse reactions, including cuSCC, decreased appetite, and cardiac disorders.
Up to 3 in 100 people taking Mekinist in combination with dabrafenib may develop a different type of skin cancer called cutaneous squamous cell carcinoma(cuSCC).
Therefore, all patients should be monitored routinely while taking Erivedge, and cuSCC should be treated according to the standard of care.
Cases of cuSCC(including keratoacanthoma) have been reported in patients treated with dabrafenib alone and in combination with trametinib(see section 4.8).
Therefore, all patients should be monitored routinely while taking Odomzo, and cuSCC should be treated according to the standard of care.
Patients taking Tafinlar may commonly(may affect up to 1 in 10 people)develop a different type of skin cancer called cutaneous squamous cell carcinoma(cuSCC).
All patients receiving dabrafenib as monotherapy orin combination with trametinib who developed cuSCC continued on treatment without dose modification.
Cases of cuSCC(which include those classified as keratoacanthoma or mixed keratoacanthoma subtype) have been reported in patients treated with vemurafenib(see section 4.8).
It is recommended that skin examination be performed prior to initiation of therapy with dabrafenib and monthly throughout treatment andfor up to six months after treatment for cuSCC.
Cutaneous malignancies such as cutaneous squamous cell carcinoma(cuSCC) including kerathoacanthoma has been observed in patients treated with BRAF-inhibitors including encorafenib.
Dose modifications or interruptions are not recommended for adverse reactions of cutaneous squamous cell carcinoma(cuSCC) or new primary melanoma(see section 4.4).
In the event the patient develops Cutaneous Squamous Cell Carcinoma(cuSCC), it is recommended to continue the treatment without modifying the dose of vemurafenib(see sections 4.4 and 4.8).