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Outcomes After Secondary Cytoreductive Surgery With or Without Carboplatin Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Followed by Systemic Combination Chemotherapy for Recurrent Platinum-Sensitive Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

NCT01767675 on ClinicalTrials.gov Phase 2 Memorial Sloan Kettering Cancer Center (academic or other) Started 2013-01-08 Completed
Riskier than 33% of active trials
this trial: 14% 0% 36%

Model scores of the 29,894 trials active now.

Model score 14% for any early termination, 6% for termination due to slow enrollment. Past trials like this one (phase, sponsor type and disease area, started 2008–2016) ended terminated 26% of the time (3,728 trials).

Finished trial that started 2008–2014: scored by a model trained without any trial from its start year, so its own outcome was never used.

How it ended

Completed on 2025-08-26, after 2013-01-08 start.

The score above never used this outcome: finished trial that started 2008–2014: scored by a model trained without any trial from its start year, so its own outcome was never used.

Termination over time, as the model saw it at the start

0% 6% 13% 19% 26% 0123456 yr completed 22% terminated 16%

Cumulative chance of ending terminated (red) or completed (green) by each year from its start; it actually ended on 2025-08-26. The rest of the way to 100% is still running.

From the competing-risks survival model (termination vs completion, still-running trials censored), fit to trials that started 2008–2014 and recalibrated to termination rates over 2022–2024, since termination has become more common. Checked on past years, it still ran a little low when the rise continued.

What moved the score

Every input that moved this score, largest first: SHAP contributions in log-odds, red raising risk and green lowering it. They describe the model, not causes of termination. Phrases are traced from the text features back to this registration's words, approximately.

The trial

Design

Phase
2
Number of arms
2
Allocation
randomized
Design
parallel
Primary purpose
treatment
Blinding
none
Has a data monitoring committee
not given (typical: 56% yes)
Responsible party
sponsor
Collaborators
5 (typical: 0)
Keywords listed
4 (typical: 1)

Who can join

Minimum age
21 (typical: 18)
Maximum age
not given (typical: 71)
Sex
female (typical: all)
Accepts healthy volunteers
No (typical: 9% yes)

Sponsor's track record

Sponsor type
academic or other
Sponsor's past trials
342 (typical: 32)
Sponsor's past termination rate
3.8% (typical: 9.9%)
Trials the sponsor started in the prior 2 years
81 (typical: 19)

Drug's FDA history

Drugs with FDA adverse-event history
2 (typical: 1)
Drug has FAERS history
Yes (typical: 64% yes)
Drug's FAERS reports before start
16462 (typical: 2148)
Drug's FAERS reports in the prior 12 months
3443 (typical: 412.5)
Drug's FAERS reports marked serious
93.4% (typical: 85.6%)
Drug's FAERS reports with a death
22.1% (typical: 15.9%)

Disease area and drugs

Disease areas
cancer, urogenital, endocrine
Drugs matched to FDA substances
carboplatin, platinum

Typical values are among the trials active now. Sponsor and drug history are counted only up to this trial's start date.

Similar finished trials

Closest by meaning of the registration text (PubMedBERT embeddings), among finished trials. How they ended is context, not an input to this trial's score.