chest wall toxicity in sabr : predictors and contouring of chest wall
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Dr Vimoj J. Nair, SABR Fellow, Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Chest Wall Toxicity In Stereotactic Ablative Body
Radiotherapy (SABR): Current Evidence
Dr Vimoj J NairSABR Fellow
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Introduction
• Despite the increasing popularity of SBRT, concern persists regarding late normal tissue toxicity.
• Reports of increased frequency of rib fracture and chest wall pain after SABR treatment of peripherally located lesions compared to conventionally fractionated therapy
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
MAJOR CLINICAL TRIALS NO RIB CONSTRAINTS
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Incidence of Chest wall Syndrome/Toxicity
Modality Incidence
Conventional radiotherapy 1-6%
Hypofractionated RT [Overgaard et al]
19%
SABRSevere chest wall pain 5-33%
rib fractures – 2-21%
Thoracotomy ~30-50%,
VATS None / mild 63%
Severe 6%
McKenna RJ, Houck W, Beeman Fuller C. Video-assisted thoracic surgery lobectomy: experience with 1,100 cases. The Annals of Thoracic Surgery, February 2006. 81(2):421-426.
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Chest wall toxicity
• Dermatologic (erythema, ulceration and fibrosis)
• Chest wall pain – focal or neuropathic
• Rib fracture– symptomatic and
asymptomatic
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Spectrum of CW toxicity
CTCAE v 3.0
Grade
Short name
1 2 3 4 5
Pain Mild pain not interfering with function
Moderate pain, pain or
analgesics interfering with
function, but not with ADL
Severe pain, pain or
analgesics severely
interfering with ADL
Disabling -
Fracture Asymptomatic, radiographic findings
only (e.g. Asymptomatic rib
fracture on plain x-ray, pelvic insufficinecy, fracture on MRI, etc)
Symptomatic, but not
displaced; immobilization
indicated
Symptomatic and displaced or open wound with bone exposure;
operative intervention
indicated
Disabling, amputation indicated
Death
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
• 61% Rib # asymptomatic, revealed ONLY through imaging• 19% of all episodes of CW pain coincided with a documented
rib fracture.
Andolino et al, IJROBP 2011
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
CHEST WALL CONTOURING
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Studies Pros/Retr
o
N chest wall
{CW} lesion
definition
Chest wall Contouring
criteria
Dose fractionati
on
Median f/u
{mths}
Chest wall [Toxicity Pain and Fracture]
rates
Median Time of toxicity {mths}
1 Dunlap et al, Virginia/Colorado,
ASTRO 2008, IJROBP 2010
Retro
60 < 2.5 cm from CW OR Dmax >20 Gy
CW 3cm 60 Gy/30Fr
11 21% pain and 8% fractures
7.1
2 Voroney et al, Alberta,/PMH J
Thor Oncol 2009
Retro
42 NA NA 54-60 Gy /3 Fr
NA 21% rib #, 26% CW pain 1.5 to
5% rib .
17
3 Petterssen et al, Sweden,
Radiother Oncol, 2009
Retro
33 NA Individual Ribs
45Gy/3Fr 29 13 rib fractures 8.8
4 Welsh et al , MDACC, Astro 2009,
IJROBP 2010
Retro
265 (268 TX)
NA All soft tissue minus lungs
50Gy/4Fr 10.3 22% pain, 3% fractures
6
5 Stephans et al , Cleveland, IJROBP
2011
Retro
134 NA Unspecified arc of tissues
60Gy/3 18.8 7% chest wall toxicity ; # not
reported
8.8
6 Andolino et al, Indiana, IJROBP
2011
Retro
347 [203 CW]
CW within ≥
50% isodose
CW3cm + ribs
separately
54-60 Gy/ 2-5 Fr
19 CW 21%, NCW 3.5%
10% CW required
Prescription
8
7 Mutter et al, MSKCC, NY, 2011
Pros 126 NA CW2cm, CW 3cm
compared; 1.2 cm sup/inf
40-60Gy/3-5Fr
16 4% rib #, 51% grade 2 pain
9
Studies on chest wall toxicity in SABR
CW2cm correlated with toxicity
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
CHEST WALL CONTOURING
• 2-cm expansion in the LAT/ANT & POST from the lung edges
• Exclude lung volume, mediastinal soft tissue, and anterior vertebral body
• Include intercostal muscles and exclude other muscles and skin.
• To avoid cumbersome contouring of the entire rib/chest wall, one can define the rib contours arbitrarily within a 3-cm limit from the PTV.
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
CHEST WALL CONTOURING
2cm
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
CHEST WALL TOXICITY PREDICTORS AND PARAMETERS: CURRENT EVIDENCE
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Studies Pros/Retro
N chest wall {CW} vs NCW
lesion definition
Dose fraction
ation
1 Dunlap et al, Virginia/Colorado,
ASTRO 2008, IJROBP 2010
Retro 60 < 2.5 cm from CW OR Dmax
>20 Gy
60 Gy/30Fr
•Volume threshold of 30 cm3 •Recommended V30Gy < 30cc
2 Voroney et al, Alberta,/PMH J
Thor Oncol 2009
Retro 42 NA 54-60 Gy /3 Fr
•Median dose to # site 46-50 Gy
3 Petterssen et al, Sweden, Radiother Oncol,
2009
Retro 33 NA 45Gy/3Fr •Risk of # : 5% if D2CC =27Gy ; 50% if D2CC = 50Gy • 37 % if V40 Gy >2cc
4 Welsh et al , MDACC, Astro 2009,
IJROBP 2010
Retro 265 (268
TX)
NA 50Gy/4Fr •V30 Gy relevant •BMI >29 Doubles risk of c/c pain
5 Stephans et al , Cleveland,
IJROBP 2011
Retro 134 NA 60Gy/3 •V30 ≤ 30cc & V60 ≤ 3cc ~ ≤10-15% risk of late chest wall toxicity
6 Andolino et al, Indiana, IJROBP
2011
Retro 347 [203
CW]
CW within ≥ 50% isodose
54-60 Gy/ 2-5
Fr
•10% if V30 Gy ≥ 15 cc and V40 Gy ≥ 5cc•30% risk of toxicity when V30 ≥ 40cc & V40 ≥ 15 cc. •Dmax >50Gy significant increase in pain and fracture.
7 Mutter et al, MSKCC, NY, 2011
Pros 126 < 2.5 cm from CW
40-60Gy/3-
5Fr
•CW2 V30 ≥ 70cc, significant correlation with Grade 2 CW pain
Studies on chest wall toxicity in SBRT
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
• Prospective . 126 pts with primary, clinically node-negative NSCLC received 40–60 Gy / 3-5 # of SBRT
• DVH dosimetry of CW3cm vs CW2cm.
• Results: Median f/u 16 months, the 2-year estimated actuarial incidence of Grade 2 CW pain : 39%.
• Median time to onset of Grade 2 CWpain was 9 months.
• CW2cm consistently enabled better prediction of CW toxicity.
• CW volume receiving 30 Gy (V30) as one of the strongest predictors (p < 0.001).
• Physical dose of 30 Gy was received by >70cc -significant correlation with Grade 2 CW pain (p =
0.004) so keep V30<70cc
• Only 19/126 pts met previous cutoff V30<30Gy
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
VUmc DATA
• Prospective • 500 pts with T1-2N0 (2003-2009)• Median f/u 33 Months
Chest wall toxicity following risk-adapted stereotactic radiotherapy for early stage lung cancer E. M. Bongers, C. J. Haasbeek, F. J. Lagerwaard, B. Slotman, S. Senan
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
• Results will be presented in ASTRO 2011/IJROBP (in press)
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
Conclusion
• Tumor size and distance from chest wall is correlated to risk of chest wall toxicity.
• Contour 2cm expansion upto 3 cm cranio-caudally.
• V30Gy : useful as a guideline for estimating the likelihood of chest wall toxicity– <70cc optimum– <30 cc ??? feasible
• Dmax 50Gy ~ above which pain and fracture increase.
• Longer f/u needed – Late toxicity
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
CONCLUSION: STRATEGIES FOR CHEST WALL TOXICITY MANAGEMENT
• Reducing the total tumor dose
• ? Risk adapted fractionation/ increase no of Fr
• Increasing the number of noncoplanar beams• Patient selection is vital• Tumor coverage and other normal tissue
constraints should NOT be compromised.
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
HOWEVER THERE ARE SOME TOXICITIES THAT WE CAN’T AVOID
Dr Vimoj J. Nair MBBS MD Department of Radiation Oncology, The Ottawa Hospital Cancer Centre, ON, Canada
THANK YOU
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