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Re-challenge with catumaxomab in patients with malignant ascites: results from the SECIMAS study

Pietzner, Klaus (author)
Charite, Germany
Vergote, Ignace (author)
University Hospital Leuven, Belgium; Leuven Cancer Institute, Belgium
Santoro, Armando (author)
Ist Clin Humanitas, Italy
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Chekerov, Radoslav (author)
Charite, Germany
Marme, Frederik (author)
University of Frauenklin Heidelberg, Germany
Rosenberg, Per (author)
Östergötlands Läns Landsting,Linköpings universitet,Avdelningen för kliniska vetenskaper,Hälsouniversitetet,Onkologiska kliniken US
Martinius, Holger (author)
Neovu Biotech GmbH, Germany
Friccius-Quecke, Hilke (author)
Neovu Biotech GmbH, Germany
Sehouli, Jalid (author)
Charite, Germany; North Eastern German Soc Gynecol NOGGO, Germany
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 (creator_code:org_t)
2014-11-04
2014
English.
In: Medical Oncology. - : Humana Press. - 1357-0560 .- 1559-131X. ; 31:12, s. 308-
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Malignant ascites is a common phenomenon in cancer patients. It poses a great challenge to the clinician, because of limited treatment options and strong impairment of the quality of life of the often palliative patients. The SECIMAS study investigated the feasibility of a re-challenge with four catumaxomab intraperitoneal infusions in patients who had already received a first cycle of four infusions in the phase III CASIMAS study, which compared catumaxomab with and without prednisolone premedication. The primary endpoint was the proportion of patients who received at least three catumaxomab infusions. Secondary endpoints included a composite safety score (CSS) summarising the worst grades for the main catumaxomab-related adverse events (pyrexia, nausea, vomiting and abdominal pain), safety, efficacy and the occurrence of anti-drug antibodies (ADAs). Eight of nine screened patients received a second catumaxomab cycle. Compliance with a catumaxomab re-challenge was high: all eight patients (100 %) received all four infusions. The median CSS was 3.0 versus 3.4 in CASIMAS. The tolerability profile of the second catumaxomab cycle was comparable to that of the first cycle. Median puncture-free survival (48 days) and overall survival (407 days) were longer than in CASIMAS (35 and 103 days, respectively), although median time to next puncture was shorter (60 vs. 97 days). Of six patients sampled, all were ADA positive at screening and remained ADA positive until the end of the study. The presence of ADAs did not affect catumaxomabs safety or efficacy. The CSS and tolerability profile for catumaxomab in SECIMAS were comparable to those in CASIMAS. The majority of patients benefitted from a second cycle of catumaxomab. A re-challenge seems to be feasible and safe for selected patients with recurrent malignant ascites due to carcinoma after a first cycle of catumaxomab.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Catumaxomab; Second cycle; Malignant ascites; Anti-drug antibodies; Re-challenge

Publication and Content Type

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