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Poster Display session

375P - Landscape of pancreatic squamous cell carcinoma: A Polish multicenter study

Date

27 Jun 2024

Session

Poster Display session

Presenters

Malgorzata Osmola

Citation

Annals of Oncology (2024) 35 (suppl_1): S119-S161. 10.1016/annonc/annonc1481

Authors

M.N. Osmola1, J. Kiszka2, P.T. Wysocki3, M. Gajda4, J. Mitus5, K. Pawlewicz6, T. Matysiak Budnik7

Author affiliations

  • 1 Medical University of Warsaw, Warsaw/PL
  • 2 Subcarpatian Cancer Center, Brzozow/PL
  • 3 Medical University of Gdansk, Gdansk/PL
  • 4 National Oncology Institute Maria Sklodowskiej-Curie National Research Institute, Gliwice Branch, Gliwice/PL
  • 5 Maria Sklodowska - Curie National Research Institute of Oncology, Cracow Branch, Cracow/PL
  • 6 Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw/PL
  • 7 CHU du Nantes - Hôtel-Dieu, Nantes/FR

Resources

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Abstract 375P

Background

With the increasing global prevalence of pancreatic cancer, rare subtypes like squamous cell pancreatic carcinoma (SCPC) are also on the rise. SCPC is known for its aggressiveness and poor prognosis, even surpassing that of adenocarcinoma. Given no established treatment guidelines for SCPC, we aimed to retrospectively analyze the clinical presentation of SCPC, prevailing treatment modalities, and patients’ survival.

Methods

Retrospective analysis of SCPC patients treated in 5 oncological centers in Poland between 2004 and 2021. Inclusion criteria: at least one type of oncological treatment: chemotherapy or surgery. Exclusion criteria: diagnoses based on fine needle aspiration.

Results

24 patients with SPPC were identified, and 19 met the inclusion criteria. The mean age of the patients was 61.22 ± 7.93 y (range 44 -71), and a slight male predominance (57.9%). Most SCPC were diagnosed at stage III (n=7, 36.8%), followed by stage IV (n=5, 26.3%), II (n=5, 26.3%), and I (n=2, 10.5%). Mixed histology was common, with a median percentage of squamous differentiation of 70% (range 5-100). Pure squamous histology was noted in 21% of patients (n=4). Most tumors were of grade 3 (n=11, 57.9%). The most frequent location of the primary tumor was the pancreatic tail (n=9, 47.4%), followed by the pancreatic body and head (n=5, 26.3%, for each location). 84.2% (n=16) of patients underwent surgical resection. Of them, 9 (57.8%) received adjuvant chemotherapy (FOLFIRINOX n=1; gemcitabine n=3; and chemoradiotherapy with 5-FU n=5). 81.2% (n=13) of patients who underwent surgery relapsed. 9 patients were referred to palliative chemotherapy: FOLFIRINOX n=1, gemcitabine-based regimens (monotherapy n=2; + nab-paclitaxel n=2; + cisplatin n=2) or FOLFOX n=2. The median number of chemotherapy lines was 1 (one patient received 3 lines). Median progression-free survival on the palliative treatment was 5.7 mo (range 0.4-12.7), while the median overall survival was 10.91 mo (range 1.2-21.4).

Conclusions

Our study provides insights into the clinical presentation, treatment patterns, and survival of SCPC patients, highlighting the need for further research and a standardized therapeutic approach in SCPC.

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

M.N. Osmola: Financial Interests, Personal, Funding: Angelini Pharma, Amgen; Financial Interests, Personal, Writing Engagements: Sandoz. J. Kiszka: Financial Interests, Personal, Funding: AstraZeneca, Roche, Pfizer, Merck, BMS, Amgen, Bayer, Novartis; Financial Interests, Personal, Writing Engagements: Sandoz, Gilead. All other authors have declared no conflicts of interest.

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