Phase II clinical trial of nab-paclitaxel plus gemcitabine in elderly patients with previously untreated locally advanced or metastatic pancreatic adenocarcinoma: BIBABRAX study.

Authors

null

Jaime Feliu Batlle

Medical Oncology Department, La Paz University Hospital, Madrid, Spain

Jaime Feliu Batlle , Monica Jorge Fernandez , Teresa Macarulla , Bartomeu Massuti , Ana Albero , Federico Gonzalez , Guillermo Alfonso Quintero Aldana , J. Ignacio Delgado Mingorance , Ana Fernandez Montes , Carmen Garcia Piernavieja , Manuel Valladares-Ayerbes , Carlos García Girón , Rebeca Mondejar , Pilar Vicente , Esther Casado , Irene Gonzalez Cebrian , Guillermo Lopez-Vivanco

Organizations

Medical Oncology Department, La Paz University Hospital, Madrid, Spain, Hospital Xeral Cies de Vigo, Vigo, Spain, Vall d’Hebron University Hospital, Barcelona, Spain, Alicante University Hospital ISABIAL, Alicante, Spain, Hospital Virgen Macarena, Seville, Spain, Hospital Universitario Quirón Madrid, Madrid, Spain, Hospital Universitario Lucus Augusti, Lugo, Spain, Hospital Infanta Cristina, Badajoz, Spain, Medical Oncology Department, Complexo Hospitalario Universitario, Ourense, Spain, Hospital Universitario Insular de Gran Canaria, Las Palmas De Gran Canaria, Spain, Medical Oncology, IMIBIC, Reina Sofía Hospital, CIBERONC, Instituto de Salud Carlos III, Córdoba, Spain, Hospital Universitario de Burgos, Burgos, Spain, Medical Oncology. Hospital Universitario de la Princesa, Instituto de Investigacion Sanitaria La Princesa, Madrid, Spain, Hospital General de Granollers, Granollers, Spain, Hospital Althaia, Manresa, Spain, Hospital Virgen de las Nieves, Granada, Spain, Department of Medical Oncology, Hospital de Cruces, Barakaldo, Spain

Research Funding

Pharmaceutical/Biotech Company
Celgene

Background: FOLFIRINOX and nab-paclitaxel plus gemcitabine (nab-P+G) are the standard of care in the first-line treatment of mPC patients (pt) with good performance status. However, no standards of care exist for elderly ( > 70 years) pt as they are usually excluded in clinical trials. This study aimed to evaluate whether the clinical benefit of nab-P+G could be extended to elderly pt with mPC. Methods: This was an open-label, single-arm, multicenter, phase II trial, to assess the efficacy and safety of Nab-P+G in elderly pt (≥ 70 years) with ECOG PS 0–1 and untreated unresectable locally advanced or metastatic PC. Pt received four-week cycles of intravenous (i.v.) nab-paclitaxel 125 mg/m2, followed by i.v. gemcitabine 1,000 mg/m2, on days 1, 8 and 15, until disease progression. Efficacy was evaluated according RECIST v 1.1 criteria and safety according NCI-CTCAE v 4.0 criteria. Results: Eighty pt were enrolled in the study. Median age was 74.6 years (range 70-87.9), 57.5% were men, 71% had ECOG PS 1 and 86% metastatic disease. 16.3% of patients had a history of prior tumor surgical resection, 12.5% received chemotherapy and 3.8% radiotherapy. Primary tumor was located in head (32.5%), tail (25.0%) and body (22.5%). Nab-P and G was reduced in 49% and 41% of pt respectively. 15 pt definitely interrupt study treatment due to toxicity: neurotoxicity (7), asthenia (5), neutropenia (1), leukocytosis (1) and hepatotoxicity (1). Time until definite deterioration (reduction ≥10 points as compared to baseline in EORTC-QLQ C30) was 1.6 months and deterioration-free rate at 3 months was 54.3%. Overall response rate was 13.8%, clinical benefit rate 67.5%, median PFS 7.2 months and median OS 9.2 months. The most common treatment-related adverse events were asthenia (60.0%), diarrhea (40.0%), neutropenia (33.8%), hair loss (28.8%), thrombocytopenia (26.3%), and nausea (23.8%). Only asthenia and neutropenia presented a relatively high incidence of grade 3 and 4 toxicities (21.3%). At least 1 SAE was reported in 55% of pt. Conclusions: BIBABRAX study confirms the clinical benefit of nab-P+G in an elderly population with mPC, in terms of survival, clinical response and tolerance, therefore it could be considered a treatment option for elderly patients. However, it was unable to demonstrate the preplanned benefit on the quality of life. Further research is needed on treatment strategies that could reduce deterioration of the quality of life in these pt. Clinical trial information: NCT02391662.

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Poster Session

Session Title

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Pancreatic Cancer

Clinical Trial Registration Number

NCT02391662

Citation

J Clin Oncol 38: 2020 (suppl; abstr 4615)

DOI

10.1200/JCO.2020.38.15_suppl.4615

Abstract #

4615

Poster Bd #

223

Abstract Disclosures