TY - JOUR
T1 - Enhancement of intratumoral chemotherapy with cisplatin with or without microwave ablation and lipiodol. future concept for local treatment in lung cancer
AU - Hohenforst-Schmidt, Wolfgang
AU - Zarogoulidis, Paul
AU - Stopek, Joshua
AU - Kosmidis, Efstratios
AU - Vogl, Thomas
AU - Linsmeier, Bernd
AU - Tsakiridis, Kosmas
AU - Lampaki, Sofia
AU - Lazaridis, George
AU - Mpakas, Andreas
AU - Browning, Robert
AU - Papaiwannou, Antonis
AU - Drevelegas, Antonis
AU - Baka, Sofia
AU - Karavasilis, Vasilis
AU - Mpoukovinas, Ioannis
AU - Turner, J. Francis
AU - Zarogoulidis, Konstantinos
AU - Brachmann, Johannes
N1 - Publisher Copyright:
© 2015 Ivyspring International Publisher.
PY - 2015
Y1 - 2015
N2 - Novel therapies for lung cancer are being explored nowadays with local therapies being the tip of the arrow. Intratumoral chemotherapy administration and local microwave ablation have been investigated in several studies. It has been previously proposed that lipiodol has the ability to modify the microenvironment matrix. In our current study we investigated this theory in BALBC mice. In total 160 BALBC mice were divided in eight groups: a) control, b) cisplatin, c) microwave, d) microwave and lipiodol, e) cisplatin and lipiodol, f) microwave and cisplatin, g) lipiodol and h) lipiodol, cisplatin and microwave. Lewis lung carcinoma cell lines (106) were injected into the right back leg of each mouse. After the 8th day, when the tumor volume was about 100mm3 the therapy application was initiated, once per week for four weeks. Magnetic resonance imaging was performed for each tumor when a mouse died or when sacrificed if they were still alive by the end of the experiment (8-Canal multifunctional spool; NORAS MRI products, Gmbh, Germany). Imaging and survival revealed efficient tumor apoptosis for the groups b,c,d,e and f. However; severe toxicity was observed in group h and no follow up was available for this group after the second week of therapy administration. Lipiodol in its current form does assist in a more efficient way the distribution of cisplatin, as the microwave apoptotic effect. Future modification of lipiodol might provide a more efficient method of therapy enhancement. Combination of drug and microwave ablation is possible and has an efficient apoptotic effect.
AB - Novel therapies for lung cancer are being explored nowadays with local therapies being the tip of the arrow. Intratumoral chemotherapy administration and local microwave ablation have been investigated in several studies. It has been previously proposed that lipiodol has the ability to modify the microenvironment matrix. In our current study we investigated this theory in BALBC mice. In total 160 BALBC mice were divided in eight groups: a) control, b) cisplatin, c) microwave, d) microwave and lipiodol, e) cisplatin and lipiodol, f) microwave and cisplatin, g) lipiodol and h) lipiodol, cisplatin and microwave. Lewis lung carcinoma cell lines (106) were injected into the right back leg of each mouse. After the 8th day, when the tumor volume was about 100mm3 the therapy application was initiated, once per week for four weeks. Magnetic resonance imaging was performed for each tumor when a mouse died or when sacrificed if they were still alive by the end of the experiment (8-Canal multifunctional spool; NORAS MRI products, Gmbh, Germany). Imaging and survival revealed efficient tumor apoptosis for the groups b,c,d,e and f. However; severe toxicity was observed in group h and no follow up was available for this group after the second week of therapy administration. Lipiodol in its current form does assist in a more efficient way the distribution of cisplatin, as the microwave apoptotic effect. Future modification of lipiodol might provide a more efficient method of therapy enhancement. Combination of drug and microwave ablation is possible and has an efficient apoptotic effect.
KW - Cisplatin
KW - Intratumoral
KW - Lipiodol
KW - Lung cancer
KW - Microwave ablation
UR - http://www.scopus.com/inward/record.url?scp=84923687137&partnerID=8YFLogxK
U2 - 10.7150/jca.10970
DO - 10.7150/jca.10970
M3 - Article
AN - SCOPUS:84923687137
SN - 1837-9664
VL - 6
SP - 218
EP - 226
JO - Journal of Cancer
JF - Journal of Cancer
IS - 3
ER -