COMPLICATIONS OF RADIATION THERAPY FOR CHILDHOOD …videoserver1.iaea.org/media/HHW/Radiotherapy/ICARO...COMPLICATIONS OF RADIATION THERAPY. FOR. CHILDHOOD CANCERS. Siddhartha Laskar.

COMPLICATIONS OF RADIATION THERAPYFOR

CHILDHOOD CANCERS

Siddhartha LaskarAssociate Professor

Department of Radiation OncologyTata Memorial Hospital, Mumbai

INDIA([email protected], www.tatamemorialcenter.com)

S Laskar ICARO 2009

* WHO Projection - 2005

YEAR GLOBAL DEVELOPING WORLD PERCENT.(Millions) (Millions) OF GLOBAL

1985 7.6 3.9 52%1990 8.1 4.1 51%2000 10.1 5.4 53%

2020* 20.0 14.0 70%

CANCER BURDENCANCER BURDENCANCER BURDEN

NEW CASES OF CANCER

“Paediatric Malignancies account for 3-5% of the burden”

S Laskar ICARO 2009

AVERAGE ANNUAL INCIDENCE OF CHILDHOOD CANCERS

IARC 2005S Laskar ICARO 2009

RELATIVE FREQUENCIES OF MAJOR TUMOUR TYPES

IARC 2005S Laskar ICARO 2009

ROLE OF RADIOTHERAPY IN CHILDHOOD CANCERS

Hodgkin’s LymphomaEarly StageAdvanced Stage

> 90%Poor Prognostic Group

Nasopharyngeal Carcinoma 100%

CNS Tumors > 90%

Ewings Sarcoma/ PNETDefinitivePost Operative

40%30-40%

Rhabdomyosarcoma IRS Gr III, Unfav. Histology

NR- Soft Tissue Sarcoma > 80%

Wilms Tumor Stage III FH, All UH

Retinoblastoma Non Amenable to Focal Th.Vitreous Seeding

Leukemia (CNS Prophylaxis) Depends upon type of CTh

Neuroblastoma Residual, Unfavourable

S Laskar ICARO 2009

5 YEAR SURVIVAL AT St JUDE CHILDRENS HOSPITAL

Courtesy: Dr Raul RiberioS Laskar ICARO 2009

UNITED STATES DATA

1 in 640 persons between the ages of 20 and 39years is a childhood cancer survivor (~300,000)

Courtesy: Dr Raul RiberioS Laskar ICARO 2009

ACUTE TOXICITIES

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Dermatitis

Mucositis

Enteritis

Cystitis

Dysphagia

Xerostomia

Impaired Taste

Hoarseness of Voice

Headache

Nausea & Vomiting

Hematological

Radiation Dose: 50-60Gy @ 1.8-2.0Gy/ fr

Potentiating Factors:Skin Condition/ Connective Tissue DisordersPrior Interventions: Surgery/ ChemotherapyConcurrent ChemotherapyPoor Nutrition & HyegienePoor Orodental HyegienePoor Skin Care

Management:Optimal Sequencing with Chemo Optimal Dose/ Fractionation & RT Volume Optimal Radiotherapy Plan (skin dose)Skin CareMaintain Nutrition & HyegieneMaintain Orodental Hyegiene

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RADIOTHERAPYPrimary: 66 – 70 GyNeck: 50 Gy/ 25 fr

CHEMOTHERAPYNeoadjuvantConcomittant

Adjuvant

CARCINOMA OF NASOPHARYNX

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IMRT CONVENTIONAL RT

DOSIMETRIC COMPARISION OF TREATMENT PLANS

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PTV70 (70.2Gy/ 33# @ 2.12Gy/#)

PTV59.4 (59.4Gy/ 33# 1.8Gy/#)

PTV52.8 (52.8Gy/ 33# 1.6Gy/#)

PTV70

PTV59.4

PTV52.8

IMRT FOR CA NASOPHARYNX

S Laskar NPX IMRT 03

IJROBP DEC 2008S Laskar ICARO 2009

42.8

53.447.2

52

32.1

55.4

41.9

57.4

0

10

20

30

40

50

60

Dos

e in

Gy

Spinal Cord Brain stem ContralateralParotid

IpsilateralParotid

IMRTConventional RT

COMPARATIVE DVH FOR CRITICAL ORGANS

Laskar, IJROBP Dec 2008S Laskar ICARO 2009

Laskar, IJROBP Sept 2008S Laskar ICARO 2009

TIME TO DEVELOPMENT OF GRADE II TOXICITY

Laskar, IJROBP Dec 2008S Laskar ICARO 2009

HELICAL TOMOTHERAPY

Significant Improvement in Normal Tissue SparingS Laskar ICARO 2009

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PHOTON IMRT PROTON IMRT

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LATE TOXICITIES

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Cardiovascular

Visual

Psychosocial

Dental

Musculoskeletal Pulmo

nary

Gastrointestinal

Genitourinary

SecondTumor

Endocrine

Auditory

Neurocognitive

LateEffects

S Laskar ICARO 2009

CHRONIC CONDITIONS IN ADULT SURVIVORS OF CHILDHOOD CANCER

Condition Relative Risk of Grade 3 or 4 Complication as Compared to 

Siblings

Major Joint Replacement 54. 0

Congestive Heart Failure 15.1

Second malignant neoplasm 14.8

Cognitive dysfunction, severe 10.5

Coronary artery disease 10.4

Cerebrovascular Accident 9.3

Renal failure or dialysis 8.9

Hearing loss not corrected by aid 6.3

Legally blind or loss of eye 5.8

Ovarian failure 3.5

Oeffinger et al, NEJM 2006S Laskar ICARO 2009

CAUSE OF MORTALITY IN SURVIVORS CANCER

Recurrent 

Cancer

Second

Malignancy/ 

Neoplasm

Cardiac 

Toxicity

Pulmonary 

Disease

Other

Sequelae

Non‐

Treatment

Related

Childhood 

Cancer 

Survivor Study

N = 2823

57% 15% 7% 2% 4% 15%

Piedmont 

Region, Italy

N = 143

62.2% 12.6% 1.4% NA 8.4% 15.4%

British 

Columbia, 

Canada

N = 181

69.1% 7.7% 4.4% 2.2% 5.5% 11.1%

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TIMELINE OF LATE EFFECTS

Paulino AC, IJROBP 2004S Laskar ICARO 2009

EFFECT OF RT ON MUSCULOSKELETAL DEVELOPMENT

Factors Influencing Growth

• Chronological age at treatment• RT volume• Total RT dose• RT dose per fraction• Site of treatment• Homogeneity of growth plate irradiated• Surgery• Chemotherapy

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RELATIVE LOSS OF ADULT HEIGHT

• 7.7% (13cm) with RT dose > 33Gy, Entire spine (pre-pubertal age)• No clinically significant loss of height with low dose RT • IFRT associated with clinically insignificant height loss• No disproportion between sitting & standing height

William KY, IJROBP 1993;28:85StanfordS Laskar ICARO 2009

HEIGHT DEFICIT FROM RADIOTHERAPY

Age at treatment (yrs)

Height deficit (cm) after 10Gy

Height deficit (cm) after 20Gy

Height deficit (cm) after 30Gy

2 2.4 4.8 7.2

4 1.8 3.5 5.3

6 1.2 2.4 3.6

8 0.8 1.5 2.3

Hogeboom et al, Med Pediar Oncol 2001S Laskar ICARO 2009

• Hypoplasia of right flank secondary to hemiabdomen RT at age 3 years for FH Wilms’ tumor

• Dose: 36Gy in 20 fractions

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BOWEL OBSTRUCTION

• 131 of 1,910 children (6.9%) enrolled in NWTS-3 at median follow-up of 5.1 years

• Etiology was bowel adhesions in 104, intussusception in 17, internal hernia in 2

• Risk factors: higher local tumor stage, extrarenal intravascular involvement, en bloc resection of other organs

• Postoperative RT not a risk factor

Ritchey ML et al, Ann Surg 1993S Laskar ICARO 2009

BOWEL OBSTRUCTION

• At University of Iowa, SBO was seen in 6 of 42 children who received RT with median follow-up of 15.1 years for Wilms’ tumor

• 5 yrs:9.5%

• 10 yrs:13%

• 15 yrs:17%

• Time from surgery to RT borderline significant (< 10 days vs. > 10 days)

Paulino et al, IJROBP 2000S Laskar ICARO 2009

PNEUMONITIS: NWTS-3 EXPERIENCE

• 153 pts with Stage IV, FH received whole lung RT

• 19 (13%) developed diffuse interstitial pneumonitis

• 15 unknown etiology, 3 pneumocystis, 1 varicella

• Only 4 of 15 (27%) with pneumonia of unknown etiology survived

Green DM et al, Cancer 1989

CARDIOVASCULAR LATE EFFECTS

STANFORD(1960-1995)

2498 Pts. 754 Deaths 16% CV disease

JCRT(1969-1996)

794 Pts. 124 Deaths 14%CV disease

EORTC(1963-1986)

1449 Pts. 240 Deaths 7%CV disease

BNLI 1043 Pts. 43 Deaths 14%CV disease

Decreasing CV deaths with improving therapy (CT & RT)

Stage I & II at Stanford (CV deaths after 15yrs of treatment)1962 - 1980: 812 pts. ------ 5.4%1980 – 1996: 628 pts. ------ 0.8%

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No of pts No of pts with renal failure

Incidence of Renal Failure (%)

2 years 4 years 16 years

Unilateral 5312 15 0.1 0.2 0.6

Bilateral - - - - -

NWTS-1 41 7 9.8 9.8 16.6

NWTS-2 43 7 14.6 14.6 22.3

NWTS-3 181 18 6.6 8.3 12.7

NWTS-4 177 7 2.6 5.8 _

RENAL FAILURE

Ritchey ML et al, Med Pediatr Oncol, 1996S Laskar ICARO 2009

PREGNANCY OUTCOME

• Increased frequency of following were seen in female patients who have received prior flank or tumor bed RT on NWTS 1-4

Fetal malpositionPremature laborOffspring with low birthweight, premature birth (< 36 weeks of gestation) and congenital anomalies

Green DM et al, JCO 2002S Laskar ICARO 2009

Hong et al., IJROBP 2004

3D-CRT vs. IMRT FOR EXTREMITY SARCOMAS

S Laskar ICARO 2009

CAX

10cm SUP

3D-CRT IMRT

Hong et al., IJROBP 2004S Laskar ICARO 2009

Reduction of Volumes receiving 100% dose using IMRTFemur: 57%Normal Soft Tissue: 78%Normal Skin: 45%Mean Skin Dose: Decreased by 14%

Hong et al., IJROBP 2004S Laskar ICARO 2009

a) 3D CRT b) IMRT c) PROTONS

3D CRT vs. IMRT vs. PROTONS FOR PELVIC SARCOMA

Lee et al, IJROBP 2005S Laskar ICARO 2009

IJROBP 2002S Laskar ICARO 2009

Significant Reduction in Volume of Bony Wall of Orbit inHigh Dose Region

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2002 2008

S Laskar STS CRT S Laskar ICARO 2009

2004

2008

S Laskar STS Brachy 04S Laskar ICARO 2009

TYPE/ SITE RELATIVE RISK ABSOLUTE RISK /10,000 pts,Per Yr.

RELATIVE RISKIn 10yr survivor

ABSOLUTE RISK In 10yr survivor Per 10,000 pts,Per Yr.

All cancers 3.5 (3.1 – 3.8) 56.2 4.7 (3.8 – 5.7) 111.7

Leukemia 32.4 (25.5 – 40.6) 16.8 16.2 (6.5 – 33.3) 9.9

NHL 18.6 (13.8 – 24.6) 10.7 32.7 (19.7 – 51.1) 27.8

Solid tumorsFemale breastLung

2.4 (2.1 – 2.7)2.5 (1.8 – 3.4)4.2 (3.3 – 5.2)

29.3 11.3 13.5

3.6 (2.8 – 4.6)4.6 (3.0 – 6.6)7.3 (4.7 – 10.6)

74.439.533.8

RISK OF SECOND CANCERS

Van Leeuwen FE, J Clin Oncol 1994;12:312Swerdlow AJ, Br Med J 1992;304:1137Tucker MA, NEJM 1988;318:76

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SECOND CANCERS ??????????????????

IJROBP 2003S Laskar ICARO 2009

Its 15 Years after the first clinical use of IMRT“NO REPORT OF 2ND MALIGNANCIES TILL DATE”

S Laskar ICARO 2009

Lancet Oncology 2006S Laskar ICARO 2009

Lancet Oncology 2005S Laskar ICARO 2009

ISSUES……………..

Exact mechanism of radiation induced second cancers

Which is more harmful ??Low Dose RadiationHigh Dose Radiation

Who is the culprit ??RadiationChemotherapy

S Laskar ICARO 2009

IMRT!!

S Laskar ICARO 2009

SUMMARY

Radiation therapy associated with both acute & late sequlae

Severity influenced by:Patient Related/ Tumor Related/ Treatment Related Factors

RT Related Acute Sequelae: Self Limiting

RT Related Late Sequelae: Site Irradiated, Volume, Dose, FractionationConcurrent Therapies

Optimal Sequencing Essential for Favorable Outcome

S Laskar ICARO 2009

Thank YouS Laskar ICARO 2009