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18.05.2024 | Case Report

Pathological complete response with FOLFIRINOX therapy for recurrence of pancreatic acinar cell carcinoma

verfasst von: Katsuhito Teramatsu, Nao Fujimori, Masatoshi Murakami, Sho Yasumori, Kazuhide Matsumoto, Kohei Nakata, Masafumi Nakamura, Yutaka Koga, Yoshinao Oda, Yoshihiro Ogawa

Erschienen in: Clinical Journal of Gastroenterology

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Abstract

Pancreatic acinar cell carcinoma (PACC) is a very rare subtype of pancreatic cancer. Due to small number of patients, no standard chemotherapy protocol has been established. We experienced an extremely rare case of PACC with liver metastasis that showed a pathological complete response after modified FOLFIRINOX (mFFX) therapy. A 42-year-old man who underwent distal pancreatectomy for an 80 mm tumor at the pancreatic tail 3 years ago was referred to our hospital in September 2017 for the treatment of a recurrent liver tumor. Percutaneous biopsy revealed an acinar-neuroendocrine carcinoma, similar to the surgical specimen. He received eight cycles of irinotecan plus cisplatin chemotherapy. However, the tumor increased in size, and treatment was switched to mFFX therapy. The tumor in the liver shrank remarkably after nine cycles of mFFX therapy. Conversion surgery was selected, and the patient underwent hepatic left and caudate lobectomy 8 months after administration of mFFX. The resected specimen showed no viable tumor cells, indicating a pathological complete response. The histological diagnosis was reconsidered, and PACC was finally diagnosed via an additional immunohistological review. The patient has remained well with no recurrence for 6 years after surgery. This study is the first to report a case of pathological complete response with mFFX therapy for the recurrence of PACC.
Literatur
3.
Zurück zum Zitat Glazer ES, Neill KG, Frakes JM, et al. Systematic review and case series report of acinar cell carcinoma of the pancreas. Cancer Control. 2016;23:446–54.CrossRefPubMed Glazer ES, Neill KG, Frakes JM, et al. Systematic review and case series report of acinar cell carcinoma of the pancreas. Cancer Control. 2016;23:446–54.CrossRefPubMed
4.
Zurück zum Zitat Sridharan V, Mino-Kenudson M, Cleary JM, et al. Pancreatic acinar cell carcinoma: a multi-center series on clinical characteristics and treatment outcomes. Pancreatology. 2021;21:1119–26.CrossRef Sridharan V, Mino-Kenudson M, Cleary JM, et al. Pancreatic acinar cell carcinoma: a multi-center series on clinical characteristics and treatment outcomes. Pancreatology. 2021;21:1119–26.CrossRef
5.
Zurück zum Zitat Siegel RL, Miller KD, Fuchs HE, et al. Cancer statistics, 2021. CA Cancer J Clin. 2021;71:7–33.CrossRefPubMed Siegel RL, Miller KD, Fuchs HE, et al. Cancer statistics, 2021. CA Cancer J Clin. 2021;71:7–33.CrossRefPubMed
6.
Zurück zum Zitat Zhou W, Han X, Fang Y, et al. Clinical analysis of acinar cell carcinoma of the pancreas: a single-center experience of 45 consecutive cases. Cancer Control. 2020;27:1073274820969447.CrossRefPubMedPubMedCentral Zhou W, Han X, Fang Y, et al. Clinical analysis of acinar cell carcinoma of the pancreas: a single-center experience of 45 consecutive cases. Cancer Control. 2020;27:1073274820969447.CrossRefPubMedPubMedCentral
7.
Zurück zum Zitat Takahashi H, Ikeda M, Shiba S, et al. Multicenter retrospective analysis of chemotherapy for advanced pancreatic acinar cell carcinoma: potential efficacy of platinum- and irinotecan-containing regimens. Pancreas. 2021;50:77–82.CrossRefPubMed Takahashi H, Ikeda M, Shiba S, et al. Multicenter retrospective analysis of chemotherapy for advanced pancreatic acinar cell carcinoma: potential efficacy of platinum- and irinotecan-containing regimens. Pancreas. 2021;50:77–82.CrossRefPubMed
8.
Zurück zum Zitat Wang Y, Wang S, Zhou X, et al. Acinar cell carcinoma: a report of 19 cases with a brief review of the literature. World J Surg Oncol. 2016;14:172.CrossRefPubMedPubMedCentral Wang Y, Wang S, Zhou X, et al. Acinar cell carcinoma: a report of 19 cases with a brief review of the literature. World J Surg Oncol. 2016;14:172.CrossRefPubMedPubMedCentral
9.
Zurück zum Zitat Hartwig W, Denneberg M, Bergmann F, et al. Acinar cell carcinoma of the pancreas: is resection justified even in limited metastatic disease? Am J Surg. 2011;202:23–7.CrossRefPubMed Hartwig W, Denneberg M, Bergmann F, et al. Acinar cell carcinoma of the pancreas: is resection justified even in limited metastatic disease? Am J Surg. 2011;202:23–7.CrossRefPubMed
10.
Zurück zum Zitat Yoshida N, Kanno A, Masamune A, et al. Pancreatic acinar cell carcinoma with multiple liver metastases effectively treated by S-1 chemotherapy. Intern Med. 2018;57:3529–35.CrossRefPubMedPubMedCentral Yoshida N, Kanno A, Masamune A, et al. Pancreatic acinar cell carcinoma with multiple liver metastases effectively treated by S-1 chemotherapy. Intern Med. 2018;57:3529–35.CrossRefPubMedPubMedCentral
11.
Zurück zum Zitat Yoo C, Kim BJ, Kim KP, et al. Efficacy of chemotherapy in patients with unresectable or metastatic pancreatic acinar cell carcinoma: potentially improved efficacy with oxaliplatin-containing regimen. Cancer Res Treat. 2017;49:759–65.CrossRefPubMed Yoo C, Kim BJ, Kim KP, et al. Efficacy of chemotherapy in patients with unresectable or metastatic pancreatic acinar cell carcinoma: potentially improved efficacy with oxaliplatin-containing regimen. Cancer Res Treat. 2017;49:759–65.CrossRefPubMed
12.
Zurück zum Zitat Sugimoto M, Hines OJ, Dawson DW, et al. Preoperative treatment with FOLFIRINOX and successful resection for a patient with mixed acinar-endocrine carcinoma of the pancreas. Pancreas. 2017;46:e32–4.CrossRefPubMedPubMedCentral Sugimoto M, Hines OJ, Dawson DW, et al. Preoperative treatment with FOLFIRINOX and successful resection for a patient with mixed acinar-endocrine carcinoma of the pancreas. Pancreas. 2017;46:e32–4.CrossRefPubMedPubMedCentral
13.
Zurück zum Zitat Yoshihiro T, Nio K, Tsuchihashi K, et al. Pancreatic acinar cell carcinoma presenting with panniculitis, successfully treated with FOLFIRINOX: a case report. Mol Clin Oncol. 2017;6:866–70.CrossRefPubMedPubMedCentral Yoshihiro T, Nio K, Tsuchihashi K, et al. Pancreatic acinar cell carcinoma presenting with panniculitis, successfully treated with FOLFIRINOX: a case report. Mol Clin Oncol. 2017;6:866–70.CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Hashimoto M, Hikichi T, Suzuki T, et al. Successful chemotherapy with modified FOLFIRINOX for pancreatic acinar cell carcinoma. Clin J Gastroenterol. 2017;10:564–9.CrossRefPubMed Hashimoto M, Hikichi T, Suzuki T, et al. Successful chemotherapy with modified FOLFIRINOX for pancreatic acinar cell carcinoma. Clin J Gastroenterol. 2017;10:564–9.CrossRefPubMed
15.
Zurück zum Zitat Callata-Carhuapoma HR, Pato Cour E, Garcia-Paredes B, et al. Pancreatic acinar cell carcinoma with bilateral ovarian metastases, panniculitis and polyarthritis treated with FOLFIRINOX chemotherapy regimen. A case report and review of the literature. Pancreatology. 2015;15:440–4.CrossRefPubMed Callata-Carhuapoma HR, Pato Cour E, Garcia-Paredes B, et al. Pancreatic acinar cell carcinoma with bilateral ovarian metastases, panniculitis and polyarthritis treated with FOLFIRINOX chemotherapy regimen. A case report and review of the literature. Pancreatology. 2015;15:440–4.CrossRefPubMed
16.
Zurück zum Zitat Schempf U, Sipos B, König C, et al. FOLFIRINOX as first-line treatment for unresectable acinar cell carcinoma of the pancreas: a case report. Z Gastroenterol. 2014;52:200–3.CrossRefPubMed Schempf U, Sipos B, König C, et al. FOLFIRINOX as first-line treatment for unresectable acinar cell carcinoma of the pancreas: a case report. Z Gastroenterol. 2014;52:200–3.CrossRefPubMed
17.
Zurück zum Zitat Di Marco M, Carloni R, De Lorenzo S, et al. Long-term survival of two patients with recurrent pancreatic acinar cell carcinoma treated with radiofrequency ablation: a case report. World J Clin Cases. 2020;8:1241–50.CrossRefPubMedPubMedCentral Di Marco M, Carloni R, De Lorenzo S, et al. Long-term survival of two patients with recurrent pancreatic acinar cell carcinoma treated with radiofrequency ablation: a case report. World J Clin Cases. 2020;8:1241–50.CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Sumiyoshi T, Shima Y, Okabayashi T, et al. Long-term survival following pancreatectomy and S-1 chemotherapy for pancreatic acinar cell carcinoma with peritoneal dissemination: a case report and literature review. Medicine (Baltimore). 2015;94: e378.CrossRefPubMed Sumiyoshi T, Shima Y, Okabayashi T, et al. Long-term survival following pancreatectomy and S-1 chemotherapy for pancreatic acinar cell carcinoma with peritoneal dissemination: a case report and literature review. Medicine (Baltimore). 2015;94: e378.CrossRefPubMed
19.
Zurück zum Zitat Minakawa K, Oka K, Nihei T, et al. Pancreatic endocrine tumor with partial acinar cell differentiation. APMIS. 2006;114:720–5.CrossRefPubMed Minakawa K, Oka K, Nihei T, et al. Pancreatic endocrine tumor with partial acinar cell differentiation. APMIS. 2006;114:720–5.CrossRefPubMed
20.
Zurück zum Zitat Martin SK, Agarwal G, Lynch GR. Subcutaneous fat necrosis as the presenting feature of a pancreatic carcinoma: the challenge of differentiating endocrine and acinar pancreatic neoplasms. Pancreas. 2009;38:219–22.CrossRefPubMed Martin SK, Agarwal G, Lynch GR. Subcutaneous fat necrosis as the presenting feature of a pancreatic carcinoma: the challenge of differentiating endocrine and acinar pancreatic neoplasms. Pancreas. 2009;38:219–22.CrossRefPubMed
21.
Zurück zum Zitat Ohike N, Kosmahl M, Kloppel G. Mixed acinar-endocrine carcinoma of the pancreas. a clinicopathological study and comparison with acinar-cell carcinoma. Virchows Arch. 2004;445:231–5.CrossRefPubMed Ohike N, Kosmahl M, Kloppel G. Mixed acinar-endocrine carcinoma of the pancreas. a clinicopathological study and comparison with acinar-cell carcinoma. Virchows Arch. 2004;445:231–5.CrossRefPubMed
22.
Zurück zum Zitat La Rosa S, Adsay V, Albarello L, et al. Clinicopathologic study of 62 acinar cell carcinomas of the pancreas: insights into the morphology and immunophenotype and search for prognostic markers. Am J Surg Pathol. 2012;36:1782–95.CrossRefPubMed La Rosa S, Adsay V, Albarello L, et al. Clinicopathologic study of 62 acinar cell carcinomas of the pancreas: insights into the morphology and immunophenotype and search for prognostic markers. Am J Surg Pathol. 2012;36:1782–95.CrossRefPubMed
23.
Zurück zum Zitat La Rosa S, Franzi F, Marchet S, et al. The monoclonal anti-BCL10 antibody (clone 331.1) is a sensitive and specific marker of pancreatic acinar cell carcinoma and pancreatic metaplasia. Virchows Arch. 2009;454:133–42.CrossRefPubMed La Rosa S, Franzi F, Marchet S, et al. The monoclonal anti-BCL10 antibody (clone 331.1) is a sensitive and specific marker of pancreatic acinar cell carcinoma and pancreatic metaplasia. Virchows Arch. 2009;454:133–42.CrossRefPubMed
24.
Zurück zum Zitat Hosoda W, Sasaki E, Murakami Y, et al. BCL10 as a useful marker for pancreatic acinar cell carcinoma, especially using endoscopic ultrasound cytology specimens. Pathol Int. 2013;63:176–82.CrossRefPubMed Hosoda W, Sasaki E, Murakami Y, et al. BCL10 as a useful marker for pancreatic acinar cell carcinoma, especially using endoscopic ultrasound cytology specimens. Pathol Int. 2013;63:176–82.CrossRefPubMed
25.
Zurück zum Zitat Ide Y, Otsuka T, Shimokawa M, et al. Conversion surgery for unresectable pancreatic cancer treated with FOLFIRINOX or gemcitabine plus nab-paclitaxel. Anticancer Res. 2023;43:1817–26.CrossRefPubMed Ide Y, Otsuka T, Shimokawa M, et al. Conversion surgery for unresectable pancreatic cancer treated with FOLFIRINOX or gemcitabine plus nab-paclitaxel. Anticancer Res. 2023;43:1817–26.CrossRefPubMed
26.
Zurück zum Zitat Furuse J, Shibahara J, Sugiyama M. Development of chemotherapy and significance of conversion surgery after chemotherapy in unresectable pancreatic cancer. J Hepatobiliary Pancreat Sci. 2018;25:261–8.CrossRefPubMed Furuse J, Shibahara J, Sugiyama M. Development of chemotherapy and significance of conversion surgery after chemotherapy in unresectable pancreatic cancer. J Hepatobiliary Pancreat Sci. 2018;25:261–8.CrossRefPubMed
27.
Zurück zum Zitat Schneitler S, Kropil P, Riemer J, et al. Metastasized pancreatic carcinoma with neoadjuvant FOLFIRINOX therapy and R0 resection. World J Gastroenterol. 2015;21:6384–90.CrossRefPubMedPubMedCentral Schneitler S, Kropil P, Riemer J, et al. Metastasized pancreatic carcinoma with neoadjuvant FOLFIRINOX therapy and R0 resection. World J Gastroenterol. 2015;21:6384–90.CrossRefPubMedPubMedCentral
Metadaten
Titel
Pathological complete response with FOLFIRINOX therapy for recurrence of pancreatic acinar cell carcinoma
verfasst von
Katsuhito Teramatsu
Nao Fujimori
Masatoshi Murakami
Sho Yasumori
Kazuhide Matsumoto
Kohei Nakata
Masafumi Nakamura
Yutaka Koga
Yoshinao Oda
Yoshihiro Ogawa
Publikationsdatum
18.05.2024
Verlag
Springer Nature Singapore
Erschienen in
Clinical Journal of Gastroenterology
Print ISSN: 1865-7257
Elektronische ISSN: 1865-7265
DOI
https://doi.org/10.1007/s12328-024-01983-2

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