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E-Poster Display

1535P - Paclitaxel based intraperitoneal chemotherapy for gastric and pancreatic cancer with peritoneal metastases achieves higher conversion surgery rate and longer survival

Date

17 Sep 2020

Session

E-Poster Display

Topics

Cytotoxic Therapy

Tumour Site

Pancreatic Adenocarcinoma

Presenters

Koya Sawai

Citation

Annals of Oncology (2020) 31 (suppl_4): S881-S897. 10.1016/annonc/annonc285

Authors

K. Sawai, S. Shindo, T. Takayama, R. honma, Y. Tsuji

Author affiliations

  • Medical Oncology, KKR Tonan Hospital, 060-0004 - Sapporo/JP

Resources

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Abstract 1535P

Background

Peritoneal metastases (PM) represent one of the most refractory disease states. It frequently develops in patients (pts) with gastric (GC) or pancreatic (PC) cancer, significantly impacting their prognosis. Many types of systematic chemotherapies have been evaluated for PC but the results were not satisfactory. Recently, the use of intraperitoneal paclitaxel (ipPTX) plus systemic chemotherapy for GC with PM has shown promising clinical results, especially in pts who underwent conversion surgery after disappearance of PM due to ipPTX (Ishigami H, et al. J. Clin Oncol. 2018). We have studied ipPTX for GC and PC with PM since 2012. In this analysis, we focus on cases resulting in successful conversion surgery.

Methods

142 pts with GC and 34 pts with PC with PM have been treated with ipPTX since February 2012 to December 2019. Systemic chemotherapies were selected from standard regimens for GC or PC, such as DCS (docetaxel/CDDP/S-1), SP (S-1/CDDP), or FOLFORINOX, gemcitabine/nab-paclitaxel, depending on the patient’s condition. IpPTX was administered at 20mg/m2 weekly, 2-weeks or 3-weeks in a row with 1-week rest, according to the schedule of systemic regimens. Patients whose metastases were limited to peritoneum became candidates for conversion surgery.

Results

Of the 46 candidates in GC and 15 in PC, 25 and 6 cases, respectively, achieved conversion surgery after confirmed complete disappearance of PM. Progression free survival and overall survival were 20.9 months and 47.4 months in GC, and 21.8 months and not reached in PC.

Conclusions

Our retrospective analysis showed that the combination of ipPTX with systemic chemotherapy for both GC and PC with PM increases the probability of achieving conversion surgery, which in turn provides significantly better survival benefits than conventional chemotherapy.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

Yasushi Tsuji.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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