Skin Flashcards

1
Q

What are the most important history for skin cancer?

A

Immunosuppression - more aggressive, can influence treatment field
Previous skin cancer history

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2
Q

What are the 5 types of BCC?

A

Superficial
Nodular

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3
Q

Why is Morpheic type BCC more aggressive?

A
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4
Q

What is Gorelin’s syndrome?

A
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5
Q

What are difficult area to treat ?

A

Eye lids
Pre-tibial region of leg
Tendon of hands
Lacriminal gland

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6
Q

What is the C-POST trial evaluating?

A

The adjuvant immunotherapy trial evaluating Siniplimab (anti-PD-1) vs. placebo after surgery and post-operative radiotherapy for high-risk cutaneous squamous cell carcinoma (CSCC)

C-POST stands for TROG 17.11

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7
Q

What was the rationale behind the C-POST trial?

A

No proven systemic therapy had previously shown benefit in this setting, and anti-PD-1 therapies showed strong activity in recurrent/metastatic CSCC

The hypothesis was that adjuvant Siniplimab could improve disease-free survival (DFS)

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8
Q

What was the primary endpoint of the C-POST trial?

A

Disease-Free Survival (DFS)

Secondary endpoints included overall survival, freedom from loco-regional and distant recurrence, second primary tumors, and safety/tolerability

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9
Q

What were the high-risk criteria for patients in the C-POST trial?

A
  • Nodal disease with ≥20mm node & extracapsular extension
  • ≥3 lymph nodes involved
  • In-transit metastases
  • Clinical or radiologic main nerve perineural invasion
  • T4 tumors
  • Recurrent disease with additional risk factors
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10
Q

What was the randomization process in the C-POST trial?

A

Patients were randomized to 1 year of Siniplimab or placebo

Patients who relapsed could receive Siniplimab in Part 2

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11
Q

How many patients were enrolled in the C-POST trial?

A

415 patients

Enrollment was initially planned for 112 patients but was delayed due to COVID-19

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12
Q

What percentage of participants in the C-POST trial were contributed by TROG?

A

43%

This contribution came from 24 TROG sites

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13
Q

What was the significant result regarding recurrence risk from the C-POST trial?

A

68% reduction in recurrence risk (Hazard Ratio: 0.32)

This was based on the primary endpoint being met

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14
Q

What was the median follow-up duration for the C-POST trial?

A

24 months

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15
Q

What was the treatment-related discontinuation rate in the Siniplimab arm?

A

10%

This was compared to 1.5% in the placebo group

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16
Q

What ongoing review is being conducted as part of the C-POST trial?

A

Retrospective review of 20% of radiation plans to analyze patterns of practice and potential correlations with outcomes

This review is led by Sandro Porceddu

17
Q

What are the future plans for the C-POST trial results?

A

Planned mid-year presentation at a major oncology conference with simultaneous high-impact journal publication

18
Q

What conclusion can be drawn from the C-POST trial?

A

The trial demonstrated a significant DFS benefit for adjuvant Siniplimab in high-risk CSCC, supporting its potential role as a new standard of care in this population