ALK Inhibitors or Chemotherapy for Third Line in ALK-positive NSCLC? Real-world Data

Author:

Moskovitz Mor1,Dudnik Elizabeth2ORCID,Shamai Sivan3,Rotenberg Yakir4,Popovich-Hadari Noa5,Wollner Mira1,Zer Alona2,Gottfried Maya6,Mishaeli Moshe6,Rosenberg Shoshana Keren5,Onn Amir7,Merimsky Ofer3,Urban Damien7,Peled Nir2,Maimon Natalie6,Bar Jair7ORCID

Affiliation:

1. Thoracic Cancer Service, Rambam Health Care Campus, Haifa, Israel

2. Thoracic Cancer Service, Davidoff Cancer Center, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel

3. Oncology Division, Tel Aviv Sourasky Medical Center, Affiliated with Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

4. Sharett Oncology Institute, Hadassah Hebrew University Medical Center, Jerusalem, Israel

5. Department of Oncology, Lin Medical Center, Haifa, Israel

6. Department of Oncology, Meir Medical Center, Kfar-Saba, Israel

7. Thoracic Oncology Service, Institute of Oncology, Sheba Medical Center, Tel HaShomer, Ramat Gan, Israel

Abstract

Abstract Objectives ALK inhibitors (ALKi) are the standard-of-care treatment for metastatic ALK-rearranged non-small cell lung cancer (NSCLC) in the first- and second-line setting. We conducted a real-world multi-institutional analysis, aiming to compare the efficacy of third-line ALKi versus chemotherapy in these patients. Methods Consecutive ALK-positive metastatic NSCLC patients treated with at least one ALKi were identified in the working databases of 7 Israeli oncology centers (the full cohort). Demographic and clinical data were collected. Patients receiving any systemic treatment beyond 2 ALKi comprised the third-line cohort, whether a third ALKi (group A) or chemotherapy (group B). Groups A and B were compared in terms of overall survival (OS) and time-to-next-treatment line (TNT). Results At a median follow-up of 41 months (95% confidence interval [CI]: 32-55), 80 (47.1%) have died. Median OS (mOS) in the full cohort (n = 170) was 52 months (95% CI: 32-65). Number of ALKi (hazard ratio [HR] 0.765; 95% CI: 0.61-0.95; P = .024) and age (HR 1.02, 95% CI: 1.01-1.04, P = .009) significantly associated with OS in the full cohort. The third-line cohort included 40 patients, of which 27 were treated with third ALKi (group A) and 13 treated with chemotherapy (group B). mOS from third-line initiation was 27 months in group A (95% CI: 13-NR) and 13 months for group B (95% CI: 3-NR); the difference was not significant (NS; P = .12). Chemotherapy as first line (HR 0.17, 95% CI: 0.05-0.52, P = .002) and a higher number of ALKi (HR 0.38, 95% CI: 0.20-0.86, P = .011) associated significantly with longer OS of the third-line cohort. TNT was 10 months for group A (95% CI: 5-19) and 3 months for group B (95% CI: 0-NR); the difference was NS (P = .079). Conclusion We report mature real-world data of more than 4-year mOS in ALK-positive patients. The number of ALKi given was associated with a better outcome. OS and TNT demonstrated a statistically nonsignificant trend for a better outcome in patients receiving a third-line ALKi.

Funder

Boehringer Ingelheim

Pfizer

Merck Sharp and Dohme

Abbvie

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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