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Definitive and Postoperative Radiation Therapy for Basal and Squamous Cell Cancers of - PPT Presentation

Developed in Collaboration with the American Society of Clinical Oncology and Society of Surgical Oncology Endorsed by the American Association of Physicists in Medicine American Brachytherapy Society American College of Radiology American Head and Neck Society and the Society of Surgical Onco ID: 774820

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Slide1

Definitive and Postoperative Radiation Therapy for Basal and Squamous Cell Cancers of the Skin: An ASTRO Clinical Practice Guideline

Developed in Collaboration with the American Society of Clinical Oncology and Society of Surgical Oncology

Endorsed by the American Association of Physicists in Medicine, American Brachytherapy Society, American College of Radiology, American Head and Neck Society, and the Society of Surgical Oncology

Slide2

Citation

This slide set is adapted from the

Definitive and Postoperative Radiation Therapy for Basal and Squamous Cell Cancers of the Skin Guideline

,

published in the January/February

2020 issue of Practical Radiation Oncology (PRO).

The guideline was e-published (

https://doi.org/10.1016/j.prro.2019.10.014

) on

December 9, 2019, and is also available on the

ASTRO website:

www.astro.org

Slide3

Guideline Task Force

Chairs:Phillip M. Devlin, MDAnna Likhacheva, MD, MPH

Members:

Musaddiq Awan, MD

Christopher A. Barker, MD

Ajay Bhatnagar, MD

Lisa Bradfield

Mary Sue Brady, MD

Ivan Buzurovic, PhD

Jessica L. Geiger, MD

Upendra Parvathaneni, MBBS

Sandra Zaky, MD

Slide4

Task Force Composition

Radiation oncology

Drawn from academic practice, private or community practice, and the Veterans Health Administration system

Include a RO resident and a member of the Guidelines Subcommittee

Related specialties/disciplines*

radiation, medical, and surgical oncologists

Medical physicist

*Non-RO physicians are nominated by their respective societies

Patient representative

Slide5

Guideline Scope

To review the evidence and provide recommendations for the use of definitive and postoperative radiation therapy (RT) in patients with basal cell carcinoma (BCC) and cutaneous squamous cell carcinoma (

cSCC

) as well as dose-fractionation schemes, target volumes, basic aspects of treatment planning, choice of radiation modality and the role of systemic therapy in combination with radiation.

Slide6

Systematic Review

MEDLINE® PubMed - 5/01/1988 – 6/31/2018

Both

MeSH

terms and text words used and then supplemented with hand searches

Outcomes

:

local and regional recurrence risk,

d

isease-free survival, overall survival,

toxicity, quality of life (QoL)

Inclusion

: Age ≥18 years, diagnosis of nonmetastatic invasive BCC and

cSCC

, RT delivered with curative intent.

KQ1 included studies with ≥100 patients, KQs 2-4 used ≥50 patients and KQ5 reduced the patient number to ≥15 since minimal evidence exists on chemotherapy, biologic, and immunotherapy agents

Exclusion

:

metastatic BCC and

cSCC

;

dermatopathologic

aspects of diagnosis, surgical nuances, technical details of RT,

mucosal head and neck SCC, vulvar, penile, and perianal skin carcinoma;

preclinical and

dosimetric

studies, publications addressing re-irradiation or palliation, non-English, case reports, not relevant to KQs

1515 citations identified

193 articles assessed

 143 articles included and abstracted into evidence tables

Slide7

Rating Strength of Recommendation

Strength of Recommendation

Definition

Overall QoE

Grade

Recommendation Wording

Strong

Benefits clearly outweigh risks and burden, or risks and burden clearly outweigh benefits.

All or almost all informed people would make the recommended choice.

Any

(usually high, moderate, or expert opinion)

“Recommend/ Should”

Conditional

Benefits are finely balanced with risks and burden or appreciable uncertainty exists about the magnitude of benefits and risks.

Most informed people would choose the recommended course of action, but a substantial number would not.

A shared decision-making approach regarding patient values and preferences is particularly important.

Any

(usually moderate, low, or expert opinion)

“Conditionally Recommend”

Slide8

Rating Quality of Evidence

Overall QoE Grade

Type/Quality of Study

Evidence Interpretation

High

2 or more

well-conducted and highly-generalizable RCTs or meta-analyses of such trials.

The true effect is very likely to lie close to the estimate of the effect based on the body of evidence.

Moderate

1

well-conducted and highly-generalizable RCT or a meta-analysis of such trials

OR

2 or more

RCTs with some weaknesses of procedure or generalizability

OR

2 or more

strong observational studies with consistent findings

.

The true effect is likely to be close to the estimate of the effect based on the body of evidence, but it is possible that it is substantially different.

Low

1 RCT with some weaknesses of procedure or generalizability

OR

1 or more RCTs with serious deficiencies of procedure or generalizability or extremely small sample sizes

OR

2 or more observational studies with inconsistent findings, small sample sizes, or other problems that potentially confound interpretation of data.

The true effect may be substantially different from the estimate of the effect. There is a risk that future research may significantly alter the estimate of the effect size or the interpretation of the results.

Expert Opinion

*

Consensus of the panel based on clinical judgement and experience, due to absence of evidence or limitations in evidence.

Strong consensus (≥90%) of the panel guides the recommendation despite insufficient evidence to discern the true magnitude and direction of the net effect. Further research may better inform the topic.

Slide9

Consensus Methodology

Modified Delphi approach

Task force members rated their agreement with each recommendation using an online consensus survey

5-point Likert scale from “strongly disagree” to “strongly agree”

Consensus defined using pre-specified threshold of ≥75% (≥90% for expert opinion recommendations) agreement

Recommendations for which consensus is not achieved are removed or are revised and re-surveyed.

Recommendations achieving consensus edited with substantive changes after the first round are also re-surveyed.

Slide10

KQ 1: What are the appropriate indications for definitive RT for BCC and cSCC?

KQ1 Recommendations

Strength of Recommendation

Quality of Evidence

In patients with BCC and cSCC who cannot undergo or decline surgical resection, definitive RT is recommended as a curative treatment modality.

Strong

Moderate

Slide11

Randomized evidence to support the use of definitive RT

A randomized study comparing surgery and RT for treatment of early stage BCC of the face.347 patients (174 patients in the surgery group and 173 patients in the RT group) started in 1982.The 4-year actuarial failure rate was 0.7% in the surgery group compared with 7.5% in the RT group (p=0.003).87% of the surgery-treated patients and 69% of the radiation-treated patients considered the cosmetic result as good (p<0.01).

Avril MF, Auperin A, Margulis A, et al. Basal cell carcinoma of the face: surgery or radiotherapy? Results of a randomized study.

British journal of cancer.

1997;76(1):100-106.

Slide12

Evidence to support the use of definitive RT for cSCC and BCC

Retrospective and single-arm prospective evidence characterizing outcomes for skin carcinomas after treatment with modern RT:A meta-analysis of 9729 patients (21 studies) with BCC and cSCC confirmed excellent control with RT.1 Median 1-year LR rate was 2% and the 5-year LR rate was 14% when combining all fractionation regimens. A meta-analysis of 40 randomized and 5 nonrandomized studies of various available interventions for primary cutaneous BCC.2 LR rates were similar for excision (3.8%), Mohs surgery (3.8%), and EBRT(3.5%).LR rates for cryotherapy (22.3%) curettage and cryotherapy (19.9%), 5-fluorouracil (18.8%), imiquimod (14.1%), and photodynamic therapy using methyl-aminolevulinic acid (18.8) or aminolevulinic acid (16.6).

1. Zaorsky NG, Lee CT, Zhang E, Keith SW, Galloway TJ. Hypofractionated radiation therapy for basal and squamous cell skin cancer: A meta-analysis. Radiotherapy & Oncology. 2017;125:13-20.

2. Drucker AM, Adam GP, Rofeberg V, et al. Treatments of Primary Basal Cell Carcinoma of the Skin: A Systematic Review and Network Meta-analysis.

Ann Intern Med.

2018;169(7):456-466.

Slide13

KQ 1: What are the appropriate indications for definitive RT for BCC and cSCC?

KQ1 Recommendations

Strength of Recommendation

Quality of Evidence

2. In patients with BCC and cSCC in anatomical locations where surgery can compromise function or cosmesis, definitive RT is conditionally recommended as a curative treatment modality.

Conditional

Moderate

Slide14

Cosmetic and functional aspect of definitive RT for BCC and cSCC

Good functional outcomes are especially relevant for commonly sun exposed area of the face where surgical deformity can cause decreased QoL.

Nose

Lips

Eyelids

Ears

Slide15

Cosmetic and functional aspect of definitive RT for BCC and cSCC

Zaorsky meta-analysis found “good” or “better” cosmesis in the 21 studies to be 80% at 5 years.Single arm studies reporting excellent functional preservation inPeri-orbital targetsLipNose

Zaorsky NG, Lee CT, Zhang E, Keith SW, Galloway TJ. Hypofractionated radiation therapy for basal and squamous cell skin cancer: A meta-analysis. Radiotherapy & Oncology. 2017;125:13-20.

de Visscher JG, Botke G, Schakenraad JA, van der Waal I. A comparison of results after radiotherapy and surgery for stage I squamous cell carcinoma of the lower lip.

Head & neck.

1999;21(6):526-530.

Mazeron JJ, Chassagne D, Crook J, et al. Radiation therapy of carcinomas of the skin of nose and nasal vestibule: a report of 1676 cases by the Groupe Europeen de Curietherapie.

Radiotherapy & Oncology.

1988;13(3):165-173.

Krengli M, Masini L, Comoli AM, et al. Interstitial brachytherapy for eyelid carcinoma. Outcome analysis in 60 patients.

Strahlentherapie und Onkologie.

2014;190:245-249.

Slide16

KQ 1: What are the appropriate indications for definitive RT for BCC and cSCC?

KQ1 Recommendations

Strength of Recommendation

Quality of Evidence

3. Definitive RT for BCC and cSCC is conditionally

not

recommended in patients with genetic diseases predisposing to heightened radiosensitivity.

Conditional

Expert Opinion

Slide17

Contraindications to definitive RT

The use of definitive RT is discouraged for the treatment of cSCC or BCC in patients with genetic conditions predisposing to heightened radiosensitivity, such as ataxia telangiectasia, nevoid basal cell carcinoma syndrome (Gorlin Syndrome) and Li Fraumeni syndrome.Poorly controlled connective tissue disorders are a relative contraindication to treatment.Overall life expectancy should be considered and discussed with younger patients, for whom a larger lifetime risk of developing secondary malignancy in the treatment field is expected.

Baker S, Joseph K, Tai P. Radiotherapy in Gorlin Syndrome: Can It Be Safe and Effective in Adult Patients?

Journal of cutaneous medicine and surgery.

2016;20(2):159-162.

Martin F. Lavin. Ataxia-telangiectasia: from a rare disorder to a paradigm for cell signalling and cancer. Nature Reviews Molecular Cell Biology volume 9, pages 759–769 (2008)

Heymann, et al. Radio-induced malignancies after breast cancer postoperative radiotherapy in patients with Li-Fraumeni syndrome. Radiat Oncol. 2010 Nov 8;5:104. doi: 10.1186/1748-717X-5-104.

Slide18

KQ 2: Indications for postoperative radiation therapy (PORT)

KQ2 Recommendations

Strength of Recommendation

Strength of Recommendation

Quality of Evidence

Both BCC and cSCC

PORT is recommended for gross perineural spread that is clinically or radiologically apparent.

Strong

Moderate

Slide19

Indications for PORT in cSCC

Cutaneous SCC is a much more aggressive entity than BCC with a far greater risk for regional and nodal spread. Thus, the task force recommends more wide-ranging utilization of PORT in the SCC population.

Lin C, Tripcony L, Keller J, Poulsen M, Dickie G. Cutaneous carcinoma of the head and neck with clinical features of perineural infiltration treated with radiotherapy.

Clinical oncology (Royal College of Radiologists (Great Britain)).

2013;25(6):362-367.

Jackson JE, Dickie GJ, Wiltshire KL, et al. Radiotherapy for perineural invasion in cutaneous head and neck carcinomas: toward a risk-adapted treatment approach.

Head & neck.

2009;31(5):604-610.

Slide20

KQ 2: Indications for PORT (Con’t)

KQ2 Recommendations

Strength of Recommendation

Quality of Evidence

cSCC

1. PORT is recommended for patients with cSCC having close/positive margins that cannot be corrected with further surgery (secondary to morbidity and/or adverse cosmetic outcome).

Strong

Low

2. PORT is recommended for patients with cSCC in the setting of recurrence following a prior margin negative resection.

Strong

Moderate

3. In patients with cSCC, PORT is recommended for T3 and T4 tumors.

*

Strong

Moderate

4. In patients with cSCC, PORT is recommended for desmoplastic

/infiltrative tumors in the setting of chronic immunosuppression.

Strong

Moderate

Slide21

Perineural invasion

Retrospective review of patients with HN cSCC with perineural involvement: gross cranial nerve involvement (GCNI), microscopic focal perineural invasion (MFPNI), and microscopic extensive perineural invasion (MEPNI), managed with or without RT.102 patients were observed or treated with RT from 2000 through 2013. The pattern of relapse was predominantly local, with a low rate of successful salvage.

Sapir E, Tolpadi A, McHugh J, et al. Skin cancer of the head and neck with gross or microscopic perineural involvement: Patterns of failure. Radiotherapy and oncology. 2016;120(1):81-86.

Type of PNI

Definition

2 year RFS

2 year DFS

Gross cranial nerve involvement, 100% definitive RT

64%

56%

Microscopic

extensive

perineural invasion, 63% adjuvant RT

Involvement of >2 nerves with diameter >0.1 mm

94% (RT) vs 25% (no RT)

73% (RT) vs 40% (no RT)

Microscopic

focal

PNI, 27% adjuvant RT

Involvement of 1–2 nerves with diameter >0.1 mm

86% (RT) vs 83% (no RT)

61% (RT) vs 74% (no RT)

Slide22

Other high-risk features for recurrence

Retrospective analysis of stage I through IV head and neck cSCC who underwent surgery and also received PORT for primary or recurrent disease. 205 patients treated between 1995 and 2015On MVA, immunosuppressed status (hazard ratio [HR]: 3.79), recurrent disease (HR: 2.67), poor differentiation (HR: 2.08), and PNI (HR: 2.05) were significantly associated with locoregional recurrence

Manyam BV, Garsa AA, Chin RI, et al. A multi-institutional comparison of outcomes of immunosuppressed and immunocompetent patients treated with surgery and radiation therapy for cutaneous squamous cell carcinoma of the head and neck.

Cancer.

2017;123(11):2054-2060.

Slide23

KQ 2: Indications for PORT (Con’t)

KQ2 Recommendations

Strength of Recommendation

Quality of Evidence

BCC

6. PORT is conditionally recommended in patients with BCC with close/positive margins that cannot be corrected with further surgery (secondary to morbidity and/or adverse cosmetic outcome).

Conditional

Low

7. PORT is conditionally recommended in patients with BCC in the setting of recurrence following a prior margin negative resection.

Conditional

Low

8. PORT is conditionally recommended in patients with BCC with locally advanced or neglected tumors involving bone or infiltrating into muscle.

Conditional

Low

Slide24

KQ 3: What are the appropriate indications for RT for treating regional nodes? What dose and fractionation should be used for management of regional disease?

KQ3 Recommendations

Strength of Recommendation

Quality of Evidence

1. For patients with cSCC or BCC that metastasized to clinically apparent regional lymph nodes, therapeutic lymphadenectomy followed by adjuvant RT is recommended, with the exception of patients that have a single, small (<3 cm) cervical lymph node harboring carcinoma, without extracapsular extension.

Strong

Moderate

2. For patients with cSCC or BCC that metastasized to clinically apparent regional lymph nodes, definitive RT is only recommended for patients who are medically inoperable or surgically unresectable.

Strong

Moderate

Slide25

Best outcomes associated with therapeutic lymphadenectomy and adjuvant radiation

Median 2-year regional relapse free survival rates from literature review:

RT alone: 63%

Therapeutic lymphadenectomy alone: 72%

Therapeutic lymphadenectomy and adjuvant RT: 87%

Median 2-year overall survival rates from literature review:

RT alone: 50%

Therapeutic lymphadenectomy alone: 62%

Therapeutic lymphadenectomy and adjuvant RT: 77%

Slide26

Best outcomes associated with therapeutic lymphadenectomy and adjuvant radiation

However, in medically inoperable or surgically unresectable nodal metastases, radiation therapy is recommended

In addition, patients with a single, small (<3 cm) cervical lymph node were found to be at low risk for regional recurrence after therapeutic lymphadenectomy alone, and may not need RT

Slide27

KQ 3: What are the appropriate indications for RT for treating regional nodes? What dose and fractionation should be used for management of regional disease?

KQ3 Recommendations

Strength of Recommendation

Quality of Evidence

3. For patients with cSCC at high risk of regional nodal metastasis, imaging and sentinel lymph node biopsy are conditionally recommended to guide the need for and target of lymph node basin RT.

Implementation Remark

:

Close clinical follow-up of the lymph node basin is important for patients in whom sentinel lymph node biopsy is unlikely to be accurate due to: 1) an extensive initial primary resection and/or reconstruction or 2) tumor location in the head and neck area.

Conditional

Expert Opinion

4. For patients with cSCC at high risk of regional nodal metastasis (thickness >6 mm), elective lymph node basin RT is conditionally recommended only for those undergoing RT to the primary site with overlap of the adjacent nodal basin.

Conditional

Low

Slide28

Regional recurrence most strongly associated with tumor thickness (>6 mm)

VariableCrude risk of recurrenceMultivariable model HR (p=)Tumor thickness≤2 mm: 0%2.1-6.0 mm: 4%>6.0 mm: 16%4.92 (<0.001)Tumor siteEar: 10%Lip: 5%Non-ear: 3%Non-lip: 4%3.37 (<0.01)Immune statusImmunocompetent: 4%Immunosuppressed: 16%3.36 (<0.05)Tumor horizontal size≤20 mm: 2%21-50 mm: 8%>50 mm: 20%2.10 (<0.05)Desmoplastic Not desmoplastic: 4%Desmoplastic: 12%1.80 (0.26)Number of tumors1: 3%>1: 8%1.21 (0.66)DifferentiationGood/moderate: 3%Poor: 7%1.06 (0.88)

Prospective, multivariable analysis of risk factors for regional recurrence after margin-negative excision of cSCC in 615 patients

Brantsch KD et al, Lancet Oncology 2008

Slide29

KQ 3: What are the appropriate indications for RT for treating regional nodes? What dose and fractionation should be used for management of regional disease?

KQ3 Recommendations

Strength of Recommendation

Quality of Evidence

5. For patients with BCC or cSCC undergoing

adjuvant

RT after therapeutic lymphadenectomy, a dose of 6000–6600 cGy (conventional fractionation [180–200 cGy/fx]) is recommended.

Strong

Moderate

6. For patients with cSCC undergoing

elective

RT in the absence of a lymphadenectomy, a dose of 5000–5400 cGy (conventional fractionation [180–200 cGy/fx]) is recommended.

Strong

Moderate

Slide30

KQ 4: What is the preferred dose-fractionation schedules & radiation techniques for management of the primary site in BCC and cSCC?

KQ4 Recommendations

Strength of Recommendation

Quality of Evidence

1. In patients with BCC and

cSCC

receiving RT in the definitive setting, the following dose-fractionation schemes* are recommended:

Conventional (180–200 cGy/fx): BED

10

70–93.5

Hypofractionation (210–500 cGy/fx): BED

10

56–88

 Implementation Remark

: Conventional fractionation is delivered 5 days per week; hypofractionation is delivered daily or 2

–4

times/wk.

Strong

Low

2. In patients with BCC and

cSCC

receiving RT in the postoperative setting, the following dose-fractionation schemes* are recommended:

Conventional (180–200 cGy/fx): BED

10

59.5–79.2

Hypofractionation (210-500 cGy/fx): BED

10

56–70.2

 Implementation Remark:

Conventional fractionation is delivered 5 days per week; hypofractionation is delivered daily or 2

–4

times/wk.

Strong

Low

Slide31

Why Biological Effective Dose (BED10) instead of Total Dose?

To address the wide variation in dosing schemes within the literature. BED calculations involve the use of an established radiobiological equation to compare different fractionation regimens by converting them to comparable values for a given tissue of interest.

Slide32

Radiation modalities

ELS (electronically generated low-energy source) utilize x-ray sources with peak voltage up to 120 kVp:OrthovoltageContact x-raysSoft x-raysIntermediate x-raysElectronic brachytherapySuperficial x-rays

HDR and LDR brachytherapy

Megavoltage Electrons

Megavoltage Photons

Slide33

Local control with varying radiation modalities

5-year local control for ELS, brachytherapy and electrons: 75%-100%

5-year local control for photon therapy: 54%-80%

No long-term studies (>10 years) for electronic brachytherapy in regards to local control and toxicity

Slide34

Tumor characteristics with varying radiation modalities

Stage

Depth

Bolus

Margin

Treatment Planning

ELS

T1/T2

0.5 cm

Yes/No

1 cm

Mostly 2-D; 3-D may be needed to evaluate critical structures

HDR/LDR brachytherapy

T1/T2

0.3-0.5 cm

No

0.5 cm

Nomograms or 3-D planning

Electrons

T1-T3

N/A

Yes

1-2 cm

Clinical set-up with MU calculations or

3-D planning

Photons

T3-T4

N/A

Yes

2 cm

3-D planning

Slide35

Conventional fractionation dose schemes

Total dose (cGy)

# fx

Fx size (cGy)

Weekly

fx

BED

10

Definitive

Postop

ELS

5040

28

180

5

59.5

---

X

6000

30

200

5

72

---

X

6600

33

200

5

79.2

X

X

7000

35

200

5

84

X

---

7400

37

200

5

88.8

X

---

Slide36

Conventional fractionation dose schemes

Total dose (cGy)

# fx

Fx size (cGy)

Weekly fx

BED

10

Definitive

Postop

HDR Brachytherapy

5940

33

180

5

70.1

X

---

6480

36

180

5

76.5

X

---

7920

44

180

5

93.5

X

---

Electrons

6000

30

200

5

72

---

X

Photons

6000

30

200

5

72

---

X

6600

33

200

5

79.2

X

X

7000

35

200

5

84

X

---

Slide37

Hypofractionation dose schemes - ELS

Total dose (cGy)

# fx

Fx size (cGy)

Weekly fx

BED

10

Definitive

Postop

ELS

4500

15

300

5

58.5

X

X

4500

10

450

4

65.3

X

X

5000

20

250

5

62.5

X

X

5100

17

300

5

66.3

X

---

5400

18

300

4–5

70.2

X

X

5500

20

275

5

70.1

X

X

6120

18

340

5

82

X

X

Slide38

Hypofractionation dose schemes - HDR

Total dose (cGy)

# fx

Fx size (cGy)

Weekly fx

BED

10

Definitive

Postop

HDR Brachytherapy

4000

8

500

2

60

X

---

4050

9

450

BID for 9 fx/wk

58.7

X

X

4400

14

300 (1

st

dose); 400 (last dose)

BID for 10 fx/wk

58.0

X

---

4500

9

500

BID for 9 fx/wk

67.5

X

X

4800

16

300

5

62.4

X

---

6120

18

340

5

82

X

X

Slide39

Hypofractionation dose schemes - electrons and photons

Total dose (cGy)

# fx

Fx size (cGy)

Weekly fx

BED

10

Definitive

Postop

Electrons

4400

10

440

4

63.4

X

X

4500

15

300

5

58.5

X

X

5000

20

250

5

62.5

X

X

5400

18

300

4–5

70.2

X

X

Photons

4500

15

300

5

58.5

X

X

5000

20

250

5

62.5

X

X

5500

20

275

5

70.1

X

X

6120

18

340

5

82

X

X

Slide40

KQ 5: When is it appropriate to use chemotherapy, biologic, and immunotherapy agents before, during or after RT in the treatment of BCC or cSCC?

KQ5 Recommendations

Strength of Recommendation

Quality of Evidence

1. In patients with resected locally advanced cSCC, the addition of concurrent carboplatin to adjuvant RT is

not

recommended.

Strong

Moderate

2. In patients with unresected locally advanced cSCC, the addition of concurrent drug therapies to definitive RT is conditionally recommended.

Conditional

Low

Slide41

Postoperative concurrent chemoradiation with carboplatin in cSCC

Phase III randomized study comparing PORT alone versus chemoradiation with weekly carboplatin in patients with high-risk cSCC of the head and neck310 patientsMedian RT dose 60 GyCarboplatin AUC 2

Porceddu et al.

J Clin Oncol

36:1275-1283

Slide42

Postoperative concurrent chemoradiation with carboplatin in cSCC

FFLRR

DFS

OS

Porceddu et al.

J Clin Oncol

36:1275-1283

Slide43

Postoperative concurrent chemoradiation with carboplatin in cSCC

No significant differences in DFS or OS with the addition of carboplatin to PORT compared with PORT alone2- and 5-year freedom from locoregional relapse rates were 88% and 83% for RT vs 89% and 87% for chemoradiationNo observed enhancement of RT toxicity with carboplatin

Porceddu et al.

J Clin Oncol

36:1275-1283

Slide44

Key take away messages

Definitive RT for BCC and cSCC is associated with high rates of disease control

High-risk features for recurrence after surgery may warrant PORT to the primary bed or regional nodal basins

Several dose and fractionation schemes for treatment of BCC and cSCC are preferred

Concurrent carboplatin with adjuvant RT is not recommended