TY - JOUR
T1 - Preoperative bevacizumab and volumetric recovery after resection of colorectal liver metastases
AU - Margonis, Georgios Antonios
AU - Buettner, Stefan
AU - Andreatos, Nikolaos
AU - Sasaki, Kazunari
AU - Pour, Manijeh Zargham
AU - Deshwar, Ammar
AU - Wang, Jane
AU - Ghasebeh, Mounes Aliyari
AU - Damaskos, Christos
AU - Rezaee, Neda
AU - Pawlik, Timothy M.
AU - Wolfgang, Christopher L.
AU - Kamel, Ihab R.
AU - Weiss, Matthew J.
PY - 2017
Y1 - 2017
N2 - Background and Objectives: While preoperative treatment is frequently administered to CRLM patients, the impact of chemotherapy, with or without bevacizumab, on liver regeneration remains controversial. Methods: The early and late regeneration indexes were defined as the relative increase in liver volume (RLV) within 2 and 9 months from surgery. Regeneration rates of the preoperative treatment groups were compared. Results: Preoperative chemotherapy details and volumetric data were available for 185 patients; 78 (42.2%) received preoperative chemotherapy with bevacizumab (Bev+), 46 (24.8%) received chemotherapy only (Bev-), and 61 (33%) received no chemotherapy. Patients in the Bev+ and Bev- groups received similar chemotherapy cycles (4 [3-6] vs 4 [4-6]; P=0.499). Despite the comparable clinicopathological characteristics and Resected Volume/Total Liver Volume (TLV) at surgery (P=0.944) of both groups, Bev+ group had higher early and late regeneration (17.2% vs 4.3%; P=0.035 and 14.0% vs 9.4%; P=0.091, respectively). Of note, early and late regeneration rates (3.7% and 10.9% vs 6.6% and 5.5%, respectively) were comparable between the no chemotherapy and Bev- groups (all P>0.05). In multivariable analysis -adjusted for gender, age, portal vein embolization, preoperative chemotherapy, resected liver volume, tumor number, postoperative chemotherapy, fibrosis, steatosis- bevacizumab independently predicted early liver regeneration (P=0.019). Conclusion: Our findings suggest that preoperative bevacizumab administered along with chemotherapy was associated with enhanced volumetric restoration. Interestingly, this effect was more pronounced among patients who received oxaliplatin-based regimens and bevacizumab compared to those treated with irinotecan-based regimens and bevacizumab.
AB - Background and Objectives: While preoperative treatment is frequently administered to CRLM patients, the impact of chemotherapy, with or without bevacizumab, on liver regeneration remains controversial. Methods: The early and late regeneration indexes were defined as the relative increase in liver volume (RLV) within 2 and 9 months from surgery. Regeneration rates of the preoperative treatment groups were compared. Results: Preoperative chemotherapy details and volumetric data were available for 185 patients; 78 (42.2%) received preoperative chemotherapy with bevacizumab (Bev+), 46 (24.8%) received chemotherapy only (Bev-), and 61 (33%) received no chemotherapy. Patients in the Bev+ and Bev- groups received similar chemotherapy cycles (4 [3-6] vs 4 [4-6]; P=0.499). Despite the comparable clinicopathological characteristics and Resected Volume/Total Liver Volume (TLV) at surgery (P=0.944) of both groups, Bev+ group had higher early and late regeneration (17.2% vs 4.3%; P=0.035 and 14.0% vs 9.4%; P=0.091, respectively). Of note, early and late regeneration rates (3.7% and 10.9% vs 6.6% and 5.5%, respectively) were comparable between the no chemotherapy and Bev- groups (all P>0.05). In multivariable analysis -adjusted for gender, age, portal vein embolization, preoperative chemotherapy, resected liver volume, tumor number, postoperative chemotherapy, fibrosis, steatosis- bevacizumab independently predicted early liver regeneration (P=0.019). Conclusion: Our findings suggest that preoperative bevacizumab administered along with chemotherapy was associated with enhanced volumetric restoration. Interestingly, this effect was more pronounced among patients who received oxaliplatin-based regimens and bevacizumab compared to those treated with irinotecan-based regimens and bevacizumab.
KW - Bevacizumab
KW - Liver resection
KW - Regeneration
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U2 - 10.1002/jso.24769
DO - 10.1002/jso.24769
M3 - Article
C2 - 28743167
AN - SCOPUS:85026311631
SN - 0022-4790
JO - Journal of Surgical Oncology
JF - Journal of Surgical Oncology
ER -