Simultaneous Gemcitabine/Cisplatin and Radiotherapy for Patients with Locally Advanced Pancreatic Adenocarcinoma using a Strict GEM/RT Time Schedule. A Phase I/II Study

Diana Stripp, MD
University of Pennsylvania Cancer Center
Ultima Vez Modificado: 5 de noviembre del 2001

Share article


English

Presenter: T. Brunner
Presenter's Affiliation: University Hospitals Erlangen, Erlangen, Germany
Type of Session: Scientific

Background

  • Patients with locally advanced pancreatic cancer treated with induction chemoradiation (CRT) prior to surgery have a survival advantage as compared to patients treated with resection at diagnosis. Snady et al. (Cancer 2000)
  • Gemcitabine (GEM) and cisplatin (cDDP) individually are radiosensitizers and have activity in pancreatic cancer.
  • Experimental studies and clinical data suggest that (1) response of pancreatic cancer to GEM/cDDP is better than GEM alone, (2) normal tissues recover more quickly than tumor tissues from GEM&RT and (3) enhancement of tumor radioresponsivness lasts at least 72 h after GEM.
  • This study aimed to evaluate the feasibility and the efficacy at the recommended dose level of gemcitabine (GEM)/ cisplatin (cDDP) with RT

    Materials and Methods

  • 33 patients with locally advanced pancreatic cancer and peripancreatic vessel involvement (VI), periampullary carcinoma (1 pt), and cancer of the biliary system (2 pts) have been enrolled.
  • 3D-conformal RT was prescribed to the involved field and lymphatics concomitantly with cDDP at 20 mg/m2/d (I.V. bolus 20') on days 1-5, 29-33 and GEM (I.V. bolus 30') was administered at 5 dose levels (DL).
  • Patients received radiation to a dose of 50.4 Gy plus a 5.4 Gy boost
  • To avoid sensitization of normal tissue, GEM was administered consistently on Fridays 6 h after RT.
  • Dose limiting toxicity (DLT) was defined as grade 4 toxicity.

    Results

  • Non-hematologic toxicity was relatively mild with 5 pts developing grade 3 nausea/vomiting and 1 patient developing grade 3 diarrhea
  • 1 patient at dose level 1 who died 4.5 months after completion of therapy from duodenal ulcer bleeding regarded as DLT.
  • 9 of 20 (45 %) initially unresectable patients with pancreatic cancer but vessel involvement were resectable 6 weeks after chemoradiation.
  • Reasons against resection were: continued vessel involvement (8 pts), liver metastasis (3 pts), peritoneal seeding (1 pt), refusal of resection (1 pt).

    Author's Conclusions

  • Toxicity is pronounced at higher dose levels with one lethal late GI bleeding and non-lethal grade 4 hematotoxicity.
  • The maximal tolerated dose in this combined modality schedule was 400 mg/m2 and the dose level of 300 mg/m2 was deemed to be safe and used for the ongoing phase II study.
  • Response was good with a significant downstaging in 9/20 pts (45 %) entering the neoadjuvant treatment group.

    Clinical/Scientific Implications

  • Increased toxicity of chemoradiation with gemcitabine is dose related.
  • Use of gemcitabine as a XRT sensitizer should be only consider under investigational settings until further data is available with the use of this potent XRT sensitizer

    Oncolink's ASTRO Coverage made possible by an unrestricted Educational Grant from Bristol-Myers Squibb Oncology and Pharmacia Oncology.

    English
    News
    Induction Chemo Beneficial in Locally Advanced Pancreatic CA

    Jul 18, 2012 - For most patients with locally advanced pancreatic carcinoma (LAPC), induction with a combination of gemcitabine and oxaliplatin (GEMOX) followed by chemoradiotherapy (CRT) is feasible, resulting in clinical benefit, a chance of resectability, and improved survival, according to a study published online July 6 in Cancer.



  • I Wish You Knew

    How cancer patients have changed my life

    View More



    Blogs and Web Chats

    OncoLink Blogs give our readers a chance to react to and comment on key cancer news topics and provides a forum for OncoLink Experts and readers to share opinions and learn from each other.




    OncoLink OncoPilot

    Frente a un nuevo diagnóstico de cáncer o de cambiar el curso de su tratamiento actual? Deje que nuestro personal de enfermería cáncer que ayudan a pasar!

    Más información