Upfront Oxaliplatin-Fluoropyrimidine Chemotherapy and Somatostatin Analogues in Advanced Well-Differentiated Gastro-Entero-Pancreatic Neuroendocrine Tumors

被引:0
作者
Maratta, Maria Grazia [1 ,2 ]
Sparagna, Ileana [1 ,2 ,5 ]
Occhipinti, Denis [1 ,2 ]
Roca, Luigi [1 ,2 ]
Sgambato, Margherita [1 ,2 ]
Raia, Salvatore [3 ]
Bianchi, Antonio [2 ,3 ]
Chiloiro, Sabrina [2 ,3 ]
Rossi, Ernesto [1 ]
Rindi, Guido [2 ,4 ]
Tortora, Giampaolo [1 ,2 ]
Schinzari, Giovanni [1 ,2 ]
机构
[1] Fdn Policlin Univ Agostino Gemelli IRCCS, Comprehens Canc Ctr, Med Oncol Unit, I-00168 Rome, Italy
[2] Univ Cattolica Sacro Cuore, Fac Med & Surg, I-00168 Rome, Italy
[3] Fdn Policlin Univ Agostino Gemelli IRCCS, Div Endocrinol & Metab, I-00168 Rome, Italy
[4] Fdn Policlin Univ A Gemelli IRCCS, Anat Ophthalmol Unit, I-00168 Rome, Italy
[5] Osped SS Annunziata AUSL Ferrara, Med Oncol Dept, Via Giovanni Vicini,2 Ctr, I-44042 Ferrara, Italy
关键词
neuroendocrine tumor; gastroenteropancreatic NET; chemotherapy; LIVER METASTASES; FLUOROURACIL; STREPTOZOCIN; DOXORUBICIN; CAPECITABINE; TEMOZOLOMIDE; DACARBAZINE; RESECTION; SURVIVAL;
D O I
10.3390/cancers17091561
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
(1) Background: GEP-NETs are frequently diagnosed at advanced stage. For well-differentiated somatostatin receptor-positive (SSTR+) NETs, SSA are the preferred first-line therapy. However, in newly diagnosed patients with G2/G3 and a high tumor burden, SSA alone might not be enough; (2) Methods: We conducted a retrospective analysis to assess the effectiveness of combining oxaliplatin-fluoropyrimidine chemotherapy with SSA as an upfront strategy in newly diagnosed metastatic G2/G3 GEP-NET patients treated with oxaliplatin-fluoropyrimidine-based chemotherapy; (3) Results: Between March 2017 and October 2023, 32 pts (19 males, 13 females; M:F = 1.5:1; median age 54 years, range 31-82) were deemed eligible to receive oxaliplatin-fluoropyrimidine chemotherapy in addition to SSA; 14 received XELOX and 18 FOLFOX. After a median follow-up of 26 mo., each patient had completed at least two cycles of chemotherapy. The ORR was 25%, with a median DoR of 21.3 mo. The DCR was 87.5%. Notably, 28.1% of patients experienced tumor shrinkage sufficient for radical surgery on residual tumor lesions, encompassing both primary tumors and metastases; (4) Conclusions: Upfront treatment with the combination of oxaliplatin-fluoropyrimidine and SSA demonstrated effectiveness and safety. This approach may be considered to facilitate conversion surgery in eligible patients.
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