TY - JOUR
T1 - Severity and Persistency of Late Gastrointestinal Morbidity in Locally Advanced Cervical Cancer: Lessons Learned From EMBRACE-I and Implications for the Future
AU - Spampinato, S.
AU - Jensen, N.B.K.
AU - Potter, R.
AU - Fokdal, L.U.
AU - Chargari, C.
AU - Lindegaard, J.C.
AU - Schmid, M.P.
AU - Sturdza, A.
AU - Jurgenliemk-Schulz, I.M.
AU - Mahantshetty, U.
AU - Hoskin, P.
AU - Segedin, B.
AU - Rai, B.
AU - Bruheim, K.
AU - Wiebe, E.
AU - Van der Steen-Banasik, E.
AU - Cooper, R.
AU - Van Limbergen, E.
AU - Sundset, M.
AU - Pieters, B.R.
AU - Lutgens, L.C.H.W.
AU - Tan, L.T.
AU - Villafranca, E.
AU - Smet, S.
AU - Jastaniyah, N.
AU - Nout, R.A.
AU - Kirisits, C.
AU - Chopra, S.
AU - Kirchheiner, K.
AU - Tanderup, K.
AU - EMBRACE Collaborative Grp
N1 - Funding Information:
The EMBRACE study was supported by Elekta AB and Varian Medical Systems through unrestricted research grants and study sponsoring through the Medical University of Vienna. The work was also supported by the Danish Cancer Society.
Funding Information:
The EMBRACE study was supported by Elekta AB and Varian Medical Systems through unrestricted research grants and study sponsoring through the Medical University of Vienna. The work was also supported by the Danish Cancer Society. Disclosures: S.S. and N.B.K.J. report grants from Danish Cancer Society. C.C. reports grants from Roche and TrerAguix. R.P., C.K., A.S., and K.K. report grants and sponsoring from Elekta AB and Varian Medial Systems. K.T. reports grants from Varian, Elekta, and Danish Cancer Society. R.N. reports grants from the Dutch Cancer Society, Dutch Research Council, Elekta, Varian Medical Systems, and Accuray. C.C. reports payment or honoraria from MSD. S.C. reports payment or honoraria from Varian. C.K. reports payment or honoraria from Elekta. M.S. reports payment or honoraria from Elekta AB. A.S. reports payment or honoraria from Elekta Brachytherapy. C.C. reports support for attending meetings/travel from GSK. C.K. is a GEC-ESTRO committee past chairman. K.T. is a member of the ESTRO board. The EMBRACE study was supported by Elekta AB and Varian Medical System through unrestricted research grants and study sponsoring through the Medical University of Vienna. The work of this manuscript was supported via grants from the Danish Cancer Society (R101-A685414-S31, R150-A10177-001, R146-A9459-16-S2 and R269-A15548).
Funding Information:
S.S. and N.B.K.J. report grants from Danish Cancer Society. C.C. reports grants from Roche and TrerAguix. R.P., C.K., A.S., and K.K. report grants and sponsoring from Elekta AB and Varian Medial Systems. K.T. reports grants from Varian, Elekta, and Danish Cancer Society. R.N. reports grants from the Dutch Cancer Society, Dutch Research Council, Elekta, Varian Medical Systems, and Accuray. C.C. reports payment or honoraria from MSD. S.C. reports payment or honoraria from Varian. C.K. reports payment or honoraria from Elekta. M.S. reports payment or honoraria from Elekta AB. A.S. reports payment or honoraria from Elekta Brachytherapy. C.C. reports support for attending meetings/travel from GSK. C.K. is a GEC-ESTRO committee past chairman. K.T. is a member of the ESTRO board.
Funding Information:
The EMBRACE study was supported by Elekta AB and Varian Medical System through unrestricted research grants and study sponsoring through the Medical University of Vienna. The work of this manuscript was supported via grants from the Danish Cancer Society (R101-A685414-S31, R150-A10177-001, R146-A9459-16-S2 and R269-A15548).
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2022/3/1
Y1 - 2022/3/1
N2 - Purpose: The purpose was to evaluate patient-and treatment-related risk factors for physician-assessed and patient-reported gastrointestinal (GI) symptoms after radio(chemo)therapy and image guided adaptive brachytherapy in locally advanced cervical cancer.Methods and Materials: Of 1416 patients from the EMBRACE-I study, 1199 and 1002 were prospectively evaluated using physician-assessed (Common Terminology Criteria for Adverse Events [CTCAE]) and patient-reported (European Organization for Research and Treatment of Cancer [EORTC]) GI symptoms, respectively. CTCAE severe grade (grade [G] >3) events were pooled according to the location in the GI tract (anus/rectum, sigmoid, and colon/small bowel). CTCAE G >2 and EORTC "very much" and "quite a bit" plus "very much" scores (> "quite a bit") were analyzed for individual symptoms with Cox regression. Logistic regression was used for persistent G >1 and EORTC > "quite a bit" symptoms, defined if present in at least half of follow-ups.Results: The incidence of G >3 events was 2.8%, 1.8%, and 2.3% for G >3 anus/rectum, sigmoid, and colon/small bowel events, respectively. Among G >2 symptoms, diarrhea and flatulence were the most prevalent (8.5% and 9.9%, respectively). Among patient-related factors, baseline morbidity, increasing age, smoking status, and low body mass index were associated with GI symptoms to varying degrees. Among treatment-related factors, rectum D-2cm3 and the International Commission on Radiation Units and Measurements recto-vaginal reference point (ICRU RV-RP) correlated with G >3 anus/rectum events and moderate/persistent diarrhea, proctitis, bleeding, abdominal cramps, and difficulty in bowel control. Bowel D-2cm3 correlated with G >3 sigmoid and colon/small bowel events and moderate/persistent diarrhea and flatulence. For external beam radiation therapy (EBRT), prescription dose correlated with G >3 anus/rectum, diarrhea, and difficulty in bowel control. Patients with large lymph-node boost (V57Gy) were at higher risk for G >3 sigmoid events, moderate/persistent diarrhea, proctitis, and cramps.Conclusions: The analysis showed that both EBRT and image guided adaptive brachytherapy contribute to GI symptoms after locally advanced cervical cancer treatment. Rectum D-2cm3, ICRU RV-RP , and bowel D2cm3 are risk factors for GI morbidity. The risk for various symptoms was lower with an EBRT prescription of 45 Gy than 50 Gy and increased with larger V57Gy. (C) 2021 Elsevier Inc. All rights reserved.
AB - Purpose: The purpose was to evaluate patient-and treatment-related risk factors for physician-assessed and patient-reported gastrointestinal (GI) symptoms after radio(chemo)therapy and image guided adaptive brachytherapy in locally advanced cervical cancer.Methods and Materials: Of 1416 patients from the EMBRACE-I study, 1199 and 1002 were prospectively evaluated using physician-assessed (Common Terminology Criteria for Adverse Events [CTCAE]) and patient-reported (European Organization for Research and Treatment of Cancer [EORTC]) GI symptoms, respectively. CTCAE severe grade (grade [G] >3) events were pooled according to the location in the GI tract (anus/rectum, sigmoid, and colon/small bowel). CTCAE G >2 and EORTC "very much" and "quite a bit" plus "very much" scores (> "quite a bit") were analyzed for individual symptoms with Cox regression. Logistic regression was used for persistent G >1 and EORTC > "quite a bit" symptoms, defined if present in at least half of follow-ups.Results: The incidence of G >3 events was 2.8%, 1.8%, and 2.3% for G >3 anus/rectum, sigmoid, and colon/small bowel events, respectively. Among G >2 symptoms, diarrhea and flatulence were the most prevalent (8.5% and 9.9%, respectively). Among patient-related factors, baseline morbidity, increasing age, smoking status, and low body mass index were associated with GI symptoms to varying degrees. Among treatment-related factors, rectum D-2cm3 and the International Commission on Radiation Units and Measurements recto-vaginal reference point (ICRU RV-RP) correlated with G >3 anus/rectum events and moderate/persistent diarrhea, proctitis, bleeding, abdominal cramps, and difficulty in bowel control. Bowel D-2cm3 correlated with G >3 sigmoid and colon/small bowel events and moderate/persistent diarrhea and flatulence. For external beam radiation therapy (EBRT), prescription dose correlated with G >3 anus/rectum, diarrhea, and difficulty in bowel control. Patients with large lymph-node boost (V57Gy) were at higher risk for G >3 sigmoid events, moderate/persistent diarrhea, proctitis, and cramps.Conclusions: The analysis showed that both EBRT and image guided adaptive brachytherapy contribute to GI symptoms after locally advanced cervical cancer treatment. Rectum D-2cm3, ICRU RV-RP , and bowel D2cm3 are risk factors for GI morbidity. The risk for various symptoms was lower with an EBRT prescription of 45 Gy than 50 Gy and increased with larger V57Gy. (C) 2021 Elsevier Inc. All rights reserved.
KW - GUIDED ADAPTIVE BRACHYTHERAPY
KW - RISK-FACTORS
KW - PELVIC RADIOTHERAPY
KW - FECAL INCONTINENCE
KW - RADIATION
KW - VOLUME
KW - SYMPTOMS
KW - IMPACT
KW - BOWEL
KW - RADIOCHEMOTHERAPY
U2 - 10.1016/j.ijrobp.2021.09.055
DO - 10.1016/j.ijrobp.2021.09.055
M3 - Article
C2 - 34678431
SN - 0360-3016
VL - 112
SP - 681
EP - 693
JO - International Journal of Radiation Oncology Biology Physics
JF - International Journal of Radiation Oncology Biology Physics
IS - 3
ER -