TY - JOUR
T1 - Integrative medicine during the intensive phase of chemotherapy in pediatric oncology in Germany
T2 - a randomized controlled trial with 5-year follow up
AU - Seifert, Georg
AU - Blakeslee, Sarah B.
AU - Calaminus, Gabriele
AU - Kandil, Farid I.
AU - Barth, Andrea
AU - Bernig, Toralf
AU - Classen, Carl Friedrich
AU - Corbacioglu, Selim
AU - Föll, Jürgen
AU - Gottschling, Sven
AU - Gruhn, Bernd
AU - vom Hoff-Heise, Claudia
AU - Lode, Holger N.
AU - Martin, David
AU - Nathrath, Michaela
AU - Neunhoeffer, Felix
AU - Pekrun, Arnulf
AU - Wulff, Beate
AU - Zuzak, Tycho
AU - Henze, Günter
AU - Längler, Alfred
N1 - Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: Integrative medicine is used frequently alongside chemotherapy treatment in pediatric oncology, but little is known about the influence on toxicity. This German, multi-center, open-label, randomized controlled trial assessed the effects of complementary treatments on toxicity related to intensive-phase chemotherapy treatment in children aged 1–18 with the primary outcome of the toxicity sum score. Secondary outcomes were chemotherapy-related toxicity, overall and event-free survival after 5 years in study patients. Methods: Intervention and control were given standard chemotherapy according to malignancy & tumor type. The intervention arm was provided with anthroposophic supportive treatment (AST); given as anthroposophic base medication (AMP), as a base medication for all patients and additional on-demand treatment tailored to the intervention malignancy groups. The control was given no AMP. The toxicity sum score (TSS) was assessed using NCI-CTC scales. Results: Data of 288 patients could be analyzed. Analysis did not reveal any statistically significant differences between the AST and the control group for the primary endpoint or the toxicity measures (secondary endpoints). Furthermore, groups did not differ significantly in the five-year overall and event-free survival follow up. Discussion: In this trial findings showed that AST was able to be safely administered in a clinical setting, although no beneficial effects of AST between group toxicity scores, overall or event-free survival were shown.
AB - Background: Integrative medicine is used frequently alongside chemotherapy treatment in pediatric oncology, but little is known about the influence on toxicity. This German, multi-center, open-label, randomized controlled trial assessed the effects of complementary treatments on toxicity related to intensive-phase chemotherapy treatment in children aged 1–18 with the primary outcome of the toxicity sum score. Secondary outcomes were chemotherapy-related toxicity, overall and event-free survival after 5 years in study patients. Methods: Intervention and control were given standard chemotherapy according to malignancy & tumor type. The intervention arm was provided with anthroposophic supportive treatment (AST); given as anthroposophic base medication (AMP), as a base medication for all patients and additional on-demand treatment tailored to the intervention malignancy groups. The control was given no AMP. The toxicity sum score (TSS) was assessed using NCI-CTC scales. Results: Data of 288 patients could be analyzed. Analysis did not reveal any statistically significant differences between the AST and the control group for the primary endpoint or the toxicity measures (secondary endpoints). Furthermore, groups did not differ significantly in the five-year overall and event-free survival follow up. Discussion: In this trial findings showed that AST was able to be safely administered in a clinical setting, although no beneficial effects of AST between group toxicity scores, overall or event-free survival were shown.
KW - Anthroposophic medicine
KW - Complementary cancer treatment
KW - Mistletoe
KW - Pediatric oncology trial
KW - RCT
KW - Randomized controlled trial
UR - http://www.scopus.com/inward/record.url?scp=85131805739&partnerID=8YFLogxK
U2 - 10.1186/s12885-022-09703-0
DO - 10.1186/s12885-022-09703-0
M3 - Article
C2 - 35698215
AN - SCOPUS:85131805739
SN - 1471-2407
VL - 22
JO - BMC Cancer
JF - BMC Cancer
IS - 1
M1 - 652
ER -