Expanded NAPOLI-1 Analysis Further Characterizes MM-398 Benefit in Metastatic Pancreatic Cancer

Sandra Hanner
Published: Saturday, Jan 17, 2015

Dr. Li-Tzong Chen

Li-Tzong Chen, MD, PhD

An analysis of the per-protocol population in the phase III NAPOLI-1 trial supports the benefits of adding MM-398 to 5-fluorouracil plus leucovorin (5-FU/LV) for the treatment of patients with metastatic pancreatic cancer who were previously treated with gemcitabine.

In the per-protocol assessment, treatment with the nanoliposomal encapsulation of irinotecan MM-398 plus 5-FU/LV improved overall survival (OS) by 53% compared with 5-FU/LV alone. In the full intent-to-treat (ITT) population of NAPOLI-1, MM-398 plus 5-FU/LV improved OS by 43% as reported in 2014.

“In the per-protocol population, the MM-398 plus 5-FU/LV combination regimen achieved a median overall survival of 8.9 months,” said Li-Tzong Chen, MD, PhD, of the National Institute of Cancer Research in Tainan City, Taiwan, who reported the expanded pre-specified per-protocol and sensitivity analyses of the NAPOLI-1 data at the 2015 Gastrointestinal Cancers Symposium.

MM-398 contains about 80,000 molecules of irinotecan stably encapsulated in a 100-mm liposome. MM-398 at 120 mg/m2 has extended circulation and achieves 9.6 ng/g of the active metabolite, SN-38, in the tumor, compared with 1.7 ng/mL in blood at 72 hours.

The open-label NAPOLI-1 study randomized 417 patients to receive MM-398 as a single agent, 5-FU/LV (control), or MM-398 prior to 5-FU and racemic LV. The primary endpoint was overall survival.

In the monotherapy arm, MM-398 was administered at 120 mg/m2 every 3 weeks. In the control, 5-FU was administered at 2000 mg/m2 over 24 hours with racemic LV at 200 mg/m2 over 30 minutes for 4 weeks followed by 2 weeks off. In the combination arm, MM-398 was administered at 80 mg/m2 every 3 weeks prior to 5-FU at 2400 mg/m2 over 46 hours and racemic LV at 400 mg/m2 over 30 minutes.

The ITT analysis explored all patients randomized to MM-398 plus 5-FU/LV (n - 117) and those in the control (n = 119). The per-protocol population included patients who received at least 80% of the target dose in the first 6 weeks and did not violate any inclusion or exclusion criteria. There were 66 patients in the per-protocol MM-398 arm and 71 in the control. The non-per-protocol population (n = 99) included those not qualifying for per-protocol analysis.

In the ITT population, the median PFS was 3.1 months for the combination compared with 1.5 months with the control (HR = 0.56; 95% CI, 0.41-0.75; P = .0001). The partial response rate was 16% versus 1% (P <.001). The disease control rate with MM-398 was 57%.

Analysis of the per-protocol population confirmed the favorable OS found with the combination in the ITT analysis. Additionally, the median OS appeared longer in the per-protocol arm than in the ITT population (Table). This was also reflected by the progression-free survival (PFS), objective response rate, and CA19-9 level for the combination over the control arm, Chen reported.

Table. Median OS in Per-Protocol and ITT Populations

  MM-398 + 5-FU/LV 5-FU/LV Stratified HR
Intent-to-Treat 6.1 months 4.2 months 0.57 (95% CI, 0.41-0.80)
P = .0009
Per-Protocol 8.9 months 5.1 months 0.47 (95% CI, 0.29-0.77)
P = .0018
Non-Per-Protocol 4.4 months 2.8 months 0.56 (95% CI, 0.33-0.97)
P = .0365
“Not surprisingly, the combination achieved a highly significant improvement in overall survival in the per-protocol analysis. But more surprisingly, it also significantly improved overall survival in the non-per-protocol population, versus the control arm,” Chen said. “Analysis of the subgroups consistently favored overall survival for the MM-398 plus 5-FU/LV arm over 5-FU/LV alone.”

Analysis by pretreatment characteristics included age at diagnosis, time since initial histological diagnosis, prior lines of therapy, time since last prior therapy, and CA1909 levels. In the ITT arms, CA19-9 levels were decreased by ≥50% in 36% versus 12% of patients in the combination and control arms, respectively.

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TitleExpiration DateCME Credits
Oncology Briefings™: Integrating Novel Targeted Treatment Strategies to Advance Pancreatic Cancer CareNov 30, 20181.0
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