Session Item

Monday
May 24
08:00 - 18:00
Mining the radiotherapy dose: exploring dose-response patterns in radiation therapy (no online session)
Choice of workshop
Ultra-hypofractionated whole breast radiotherapy with integrated boost for early breast cancer
Angel Montero, Spain
PO-1135

Abstract

Ultra-hypofractionated whole breast radiotherapy with integrated boost for early breast cancer
Authors:

Angel Montero1, Raquel Ciervide1, Mariola Garcia-Aranda1, Beatriz Alvarez1, Alejandro Prado2, Xin Chen-Zhao1, Rosa Alonso1, Mercedes Lopez1, Emilio Sanchez1, Ovidio Hernando1, Jeannette Valero1, Monica Nuñez1, Marta Izquierdo1, Karla Rossi1, Carmen Cañadillas1, Pedro Fernandez-Leton2, Carmen Rubio1

1HM Hospitales, Radiation Oncology, Madrid, Spain; 2HM Hospitales, Medical Physics, Madrid, Spain

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Purpose or Objective

Whole breast irradiation (WBI) after breast conserving surgery (BCS) is indicated to improve loco-regional control and survival. Former studies showed that addition of tumor bed boost in all age groups significantly improved local control although no apparent impact on overall survival but with an increased risk of worse cosmetic outcome.

Although hypofractioned regimens in 3 weeks are considered the standard, recent studies have shown the non-inferiority of a treatment regimen of 5 fractions in one-week in both locoregional control and toxicity profile. We present our preliminary results of acute toxicity of a ultra-hypofractionated 5 fractions in one-week WBI schedule with simultaneous integrated boost (SIB) in early breast cancer.

Material and Methods

FromMarch-2020 to January-2021, 138 patients with a median age of 58.5years (range 31-87) were treated according to our institution ultra-hypofractionated radiotherapy schedule after breast conserving surgery (BCS).Clinical staging (AJCC): Tis 29p (21%) , T1a 10p (7.5%), T1b% 36p (26%), T1c 54p (39%), T2 9p (6.5%). All patients were pN0

Radiotherapy comprises whole breast receiving 26Gy@5.2Gy/day with a simultaneous integrated boost (SIB) to all patients up to a total dose of 29Gy@5.8Gy/day in 111p (80%) and 30Gy@6Gy/day in 27p (20%) with close/focally affected margins. WBI+SIB was delivered by conformal 3-D technique in 130p (94%), VMAT in 6p (4%) and 3-D with deep inspiration breath hold (DIBH) in 2p (1.5%).Treatment beam arrangement for SIB comprised of coplanar 2 beams in 1p (1%), 3 beams in 43p (31%), 4 beams in 77p (56%), 5 beams in 11p (8%) and 2 arcs in 6p (4%). Dose constraints are detailed in table 1

Systemic therapy: 136p (98.5%) received hormone therapy and 12p (9%) systemic or targeted chemotherapy.

OAR

Ipsilateral lung

V12<20%

Contralateral lung

Dmean<5.6 Gy

V3.6 <10%

Heart

V12 <5%

V7<5%

V1.5 < 30%

Contralateral Breast

V3.6 < 30 %

Spinal Canal

Dmax< 27 Gy       

D0.01 cc< 22.5 Gy

OAR: organs at risk;, Dmean: mean dose; Dmax: maximal dose

Results

With a median follow-up of 3.5months (range1-11), acute tolerance was acceptable with null o mild toxicity: 69p (50%) developed skin toxicity grade 1 and 3p (2%) grade 2. No other acute toxicities were observed

A comparative analysis was performed with the Chi-Square test. We found a weak but significant relation between age (< 56 years-old) and dermitis G1-2 (p = 0,048), however w3e could not demonstrate any relation with use  of chemotherapy (p = 0.33), homonotherapy (p = 0.06), breast PTV ( p = 0.12), boost PTV (p = 0.47) or ratio boost PTV/breast PTV (p = 0.27) and tolerance. 

Conclusion

Ultra-hypofractionated WBI with SIB in 5 fractions along one-week is feasible and well tolerated although longer follow-up is necessary to confirm these results.