RAS突变横结肠癌伴多发肝转移,术后使用aflibercept + FOLFIRI维持治疗并重复进行四次根治性切除术,实现长期无病生存:病例报告。

IF 0.7 Q4 SURGERY
Yasushi Tanaka, Ryota Nakanishi, Shota Sato, Akihiko Otake, Keiichiro Ryujin, Shinichiro Ikeda, Yuho Ebata, Tomoya Harima, Keita Natsugoe, Takayuki Yoshiyama, Yuki Shin, Tetsuro Kawazoe, Kensuke Kudo, Yoko Zaitsu, Yuichi Hisamatsu, Koji Ando, Yuichiro Nakashima, Shinji Itoh, Eiji Oki, Yoshinao Oda, Tomoharu Yoshizumi
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引用次数: 0

摘要

背景:结直肠肝转移(CRLM)患者的治疗需要采用多学科方法。对于 RAS 突变肿瘤进展期患者,血管生成抑制剂的选择可能存在争议。在此,我们报告了一名RAS突变型肝转移瘤患者,通过反复R0切除和围手术期治疗,特别是aflibercept + FOLFIRI(5-氟尿嘧啶、左亚叶酸、伊立替康),患者获得了长期无病生存,这可能避免了长期复发:患者是一名37岁的女性,被诊断为RAS突变横结肠癌,伴有19个LM。由于转移灶局限于肝脏,我们采用了全身化疗,旨在转换手术。在接受了六个周期的贝伐单抗+FOLFOXIRI(5-氟尿嘧啶、左氧氟沙星、奥沙利铂、伊立替康)治疗后,我们对所有肝转移灶进行了肝部分切除术,并在又接受了四个周期的贝伐单抗+FOLFIRI治疗后对原发肿瘤进行了左半结肠切除术。术后三个月,患者出现大量卵巢转移并伴有癌性腹水。我们进行了双侧卵巢切除术,并考虑到贝伐珠单抗耐药的可能性,启动了aflibercept + FOLFIRI疗法。在阿弗利百普+FOLFIRI治疗期间,患者2年无复发。停药后,出现了两个远处转移灶。这两个转移灶均可切除,患者在最后一次手术后获得了2年零3个月的无复发生存期(自开始治疗至今已有6年),且未进行额外化疗:我们认为,以完全切除为目标的多学科治疗即使在 CRLM 反复复发的患者中也能获得长期生存。即使在贝伐单抗治疗后,Aflibercept + FOLFIRI 仍能有效控制 RAS 突变结肠癌的转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RAS mutant transverse colon cancer with multiple liver metastases achieving long-term disease-free survival with postoperative maintenance therapy with aflibercept + FOLFIRI and four repeated radical resections: a case report.

Background: Management of patients with colorectal liver metastases (CRLMs) requires a multidisciplinary approach. For patients with progression of RAS mutant tumors, the choice of angiogenesis inhibitors can be controversial. Here, we report a patient with RAS mutant CRLMs achieving long-term disease-free survival with repeated R0 resections and perioperative treatment, especially aflibercept + FOLFIRI (5-fluorouracil, levofolinate, irinotecan), which may have prevented long-term recurrence.

Case presentation: The patient was a 37 year-old woman diagnosed with RAS mutant transverse colon cancer with 19 LMs. As the metastases were limited to the liver, we introduced systemic chemotherapy aiming at conversion surgery. After six cycles of bevacizumab + FOLFOXIRI (5-fluorouracil, levofolinate, oxaliplatin, irinotecan), we performed partial hepatectomy for all LMs, and left hemicolectomy for the primary tumor after another four cycles of bevacizumab + FOLFIRI. Three months after surgery, the patient presented with massive ovarian metastases with carcinomatous ascites. We conducted bilateral oophorectomy, and initiated aflibercept + FOLFIRI therapy considering the possibility of resistance to bevacizumab. The patient was recurrence-free for 2 years during aflibercept + FOLFIRI treatment. After its discontinuation, two distant metastases developed. Both were resectable and the patient achieved recurrence-free survival of 2 years and 3 months after the last operation (6 years since initiation of treatment), without additional chemotherapy.

Conclusions: We believe that multidisciplinary treatment aimed at complete resection could lead to long-term survival even in patients with repeated recurrence of CRLMs. Aflibercept + FOLFIRI could be effective in controlling metastasis of RAS mutant colon cancer even after treatment with bevacizumab.

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