Bevacizumab for non‐small‐cell lung cancer: A nested case control study of risk factors for hemoptysis
Potentially life‐threatening, serious hemoptysis is an adverse event associated with bevacizumab in non‐squamous non‐small‐cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is stil...
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Published in | Cancer science Vol. 107; no. 12; pp. 1837 - 1842 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
John Wiley & Sons, Inc
01.12.2016
John Wiley and Sons Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1347-9032 1349-7006 1349-7006 |
DOI | 10.1111/cas.13096 |
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Abstract | Potentially life‐threatening, serious hemoptysis is an adverse event associated with bevacizumab in non‐squamous non‐small‐cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case‐control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab‐treated patients in a real‐world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade ≥3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade ≥2 drug‐related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step‐wise multivariate analysis, prior thoracic radiotherapy (P = 0.1844), presence of tumor exposure in the central airway (P = 0.0256) and concomitant radiotherapy (P = 0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real‐world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case‐control study was a non‐interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be.
This manuscript reports the incidence of hemoptysis in 6774 Japanese patients, which was low in this real‐world setting, and the resulting uni‐ and multivariate analysis to identify associated risk factors. Prior thoracic radiotherapy, presence of a tumor mass in the central airway and concomitant radiotherapy, were identified as risk factors for hemoptysis and should be considered before starting bevacizumab treatment, in order to ensure patients are receiving the most appropriate therapy. |
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AbstractList | Potentially life‐threatening, serious hemoptysis is an adverse event associated with bevacizumab in non‐squamous non‐small‐cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case‐control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab‐treated patients in a real‐world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade ≥3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade ≥2 drug‐related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step‐wise multivariate analysis, prior thoracic radiotherapy (
P =
0.1844), presence of tumor exposure in the central airway (
P =
0.0256) and concomitant radiotherapy (
P =
0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real‐world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case‐control study was a non‐interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be. Potentially life‐threatening, serious hemoptysis is an adverse event associated with bevacizumab in non‐squamous non‐small‐cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case‐control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab‐treated patients in a real‐world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade ≥3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade ≥2 drug‐related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step‐wise multivariate analysis, prior thoracic radiotherapy (P = 0.1844), presence of tumor exposure in the central airway (P = 0.0256) and concomitant radiotherapy (P = 0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real‐world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case‐control study was a non‐interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be. Potentially life‐threatening, serious hemoptysis is an adverse event associated with bevacizumab in non‐squamous non‐small‐cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case‐control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab‐treated patients in a real‐world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade ≥3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade ≥2 drug‐related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step‐wise multivariate analysis, prior thoracic radiotherapy (P = 0.1844), presence of tumor exposure in the central airway (P = 0.0256) and concomitant radiotherapy (P = 0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real‐world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case‐control study was a non‐interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be. This manuscript reports the incidence of hemoptysis in 6774 Japanese patients, which was low in this real‐world setting, and the resulting uni‐ and multivariate analysis to identify associated risk factors. Prior thoracic radiotherapy, presence of a tumor mass in the central airway and concomitant radiotherapy, were identified as risk factors for hemoptysis and should be considered before starting bevacizumab treatment, in order to ensure patients are receiving the most appropriate therapy. Potentially life-threatening, serious hemoptysis is an adverse event associated with bevacizumab in non-squamous non-small-cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case-control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab-treated patients in a real-world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade ≥3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade ≥2 drug-related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step-wise multivariate analysis, prior thoracic radiotherapy (P = 0.1844), presence of tumor exposure in the central airway (P = 0.0256) and concomitant radiotherapy (P = 0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real-world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case-control study was a non-interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be.Potentially life-threatening, serious hemoptysis is an adverse event associated with bevacizumab in non-squamous non-small-cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case-control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab-treated patients in a real-world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade ≥3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade ≥2 drug-related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step-wise multivariate analysis, prior thoracic radiotherapy (P = 0.1844), presence of tumor exposure in the central airway (P = 0.0256) and concomitant radiotherapy (P = 0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real-world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case-control study was a non-interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be. Potentially life-threatening, serious hemoptysis is an adverse event associated with bevacizumab in non-squamous non-small-cell lung cancer (NSCLC) trials. Suggested risk factors include central tumor location and cavitation; however, the profile of hemoptysis occurrence in clinical practice is still unclear. A nested case-control study was conducted to assess the onset profile and risk factors for hemoptysis in bevacizumab-treated patients in a real-world setting in Japan. After bevacizumab was approved for NSCLC, physicians registered all NSCLC patients scheduled for bevacizumab therapy, from November 2009 to August 2011. Patients developing grade 2 hemoptysis requiring an injectable hemostatic agent or grade greater than or equal to 3 hemoptysis were selected as case subjects, matched with four control subjects each. Case report forms were collected after an observation period of 24 weeks. Radiologists assessed blinded thoracic images. Risk factors for hemoptysis were assessed by univariate and stepwise multivariate analysis. Of 6774 patients registered, 23 (0.3%) experienced grade greater than or equal to 2 drug-related hemoptysis. A total of 104 patients (21 cases, 83 controls) were analyzed by central reviewers for risk factors of hemoptysis occurrence. In the univariate analysis seven factors were associated with hemoptysis. In the step-wise multivariate analysis, prior thoracic radiotherapy (P = 0.1844), presence of tumor exposure in the central airway (P = 0.0256) and concomitant radiotherapy (P = 0.1169) were identified as risk factors for hemoptysis. While the incidence of hemoptysis was low in the real-world setting in Japan, the three risk factors identified, prior thoracic radiotherapy, presence of tumor exposure in the central airway and concomitant radiotherapy, should be considered when selecting patients for bevacizumab treatment. Although technically classed as a clinical trial, a nested case-control study was a non-interventional surveillance study analyzing all NSCLC patients receiving bevacizumab in Japan, therefore it was not registered as a phase II/III clinical trial would be. This manuscript reports the incidence of hemoptysis in 6774 Japanese patients, which was low in this real-world setting, and the resulting uni- and multivariate analysis to identify associated risk factors. Prior thoracic radiotherapy, presence of a tumor mass in the central airway and concomitant radiotherapy, were identified as risk factors for hemoptysis and should be considered before starting bevacizumab treatment, in order to ensure patients are receiving the most appropriate therapy. |
Author | Yamamoto, Nobuyuki Ohe, Yuichiro Fukuoka, Masahiro Goto, Koichi Endo, Masahiro Kusumoto, Masahiko Shimizu, Ayaka |
AuthorAffiliation | 2 Department of Diagnostic Radiology Shizuoka Cancer Center Shizuoka Japan 6 Chugai Pharmaceutical Co., Ltd Tokyo Japan 1 Department of Thoracic Oncology National Cancer Center Hospital East Chiba Japan 3 Department of Diagnostic Radiology National Cancer Center Hospital East Chiba Japan 4 3 rd Department of Internal Medicine Wakayama Medical University Wakayama Japan 5 Division of Thoracic Oncology National Cancer Center Hospital Tokyo Japan 7 Cancer Center Izumi Municipal Hospital Osaka Japan |
AuthorAffiliation_xml | – name: 1 Department of Thoracic Oncology National Cancer Center Hospital East Chiba Japan – name: 3 Department of Diagnostic Radiology National Cancer Center Hospital East Chiba Japan – name: 4 3 rd Department of Internal Medicine Wakayama Medical University Wakayama Japan – name: 2 Department of Diagnostic Radiology Shizuoka Cancer Center Shizuoka Japan – name: 6 Chugai Pharmaceutical Co., Ltd Tokyo Japan – name: 7 Cancer Center Izumi Municipal Hospital Osaka Japan – name: 5 Division of Thoracic Oncology National Cancer Center Hospital Tokyo Japan |
Author_xml | – sequence: 1 givenname: Koichi surname: Goto fullname: Goto, Koichi email: kgoto@east.ncc.go.jp organization: National Cancer Center Hospital East – sequence: 2 givenname: Masahiro surname: Endo fullname: Endo, Masahiro organization: Shizuoka Cancer Center – sequence: 3 givenname: Masahiko surname: Kusumoto fullname: Kusumoto, Masahiko organization: National Cancer Center Hospital East – sequence: 4 givenname: Nobuyuki surname: Yamamoto fullname: Yamamoto, Nobuyuki organization: Wakayama Medical University – sequence: 5 givenname: Yuichiro surname: Ohe fullname: Ohe, Yuichiro organization: National Cancer Center Hospital – sequence: 6 givenname: Ayaka surname: Shimizu fullname: Shimizu, Ayaka organization: Chugai Pharmaceutical Co., Ltd – sequence: 7 givenname: Masahiro surname: Fukuoka fullname: Fukuoka, Masahiro organization: Izumi Municipal Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27714941$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1080_0284186X_2021_1942545 crossref_primary_10_1080_09553002_2019_1552375 crossref_primary_10_1016_j_ajem_2024_09_013 crossref_primary_10_3389_fphar_2024_1339505 crossref_primary_10_1016_j_asjsur_2020_05_013 crossref_primary_10_1186_s12967_023_04212_5 crossref_primary_10_1159_000487477 crossref_primary_10_1186_s13014_024_02458_x crossref_primary_10_1016_j_esmoop_2023_101156 crossref_primary_10_1007_s11604_018_0776_6 crossref_primary_10_1007_s40278_017_26964_0 crossref_primary_10_3389_fonc_2024_1434326 crossref_primary_10_1007_s10147_019_01552_5 crossref_primary_10_1159_000502156 |
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Copyright | 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. Copyright John Wiley & Sons, Inc. 2016 |
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Keywords | real-world hemoptysis Japanese Bevacizumab non-small-cell lung cancer |
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License | Attribution-NonCommercial-NoDerivs http://creativecommons.org/licenses/by-nc-nd/4.0 2016 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
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Notes | This study was funded by Chugai Pharmaceutical Co. Ltd. Funding Information ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Koichi Goto, Nobuyuki Yamamoto, Yuichiro Ohe and Masahiro Fukuoka are members in Independent Appropriate use Advisory Board for Bevacizumab. Koichi Goto, Masahiro Endo and Masahiko Kusumoto are members in Computed Tomography Imaging Review Committtee for Bevacizumab. |
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SubjectTerms | Aged Aged, 80 and over Angiogenesis Angiogenesis Inhibitors - administration & dosage Angiogenesis Inhibitors - adverse effects Angiogenesis Inhibitors - therapeutic use Antineoplastic Agents - administration & dosage Antineoplastic Agents - adverse effects Antineoplastic Agents - therapeutic use Bevacizumab Bevacizumab - administration & dosage Bevacizumab - adverse effects Bevacizumab - therapeutic use Carcinoma, Non-Small-Cell Lung - complications Carcinoma, Non-Small-Cell Lung - diagnosis Carcinoma, Non-Small-Cell Lung - drug therapy Case-Control Studies Cavitation Chemotherapy Clinical trials Combined Modality Therapy Drug dosages Female Hemoptysis Hemoptysis - diagnosis Hemoptysis - epidemiology Hemoptysis - etiology Hemorrhage Humans Immunotherapy Incidence Japanese Lung cancer Lung Neoplasms - complications Lung Neoplasms - diagnosis Lung Neoplasms - drug therapy Male Middle Aged Monoclonal antibodies Multivariate analysis Neoplasm Staging Non-small cell lung carcinoma non‐small‐cell lung cancer Original Patients Pharmaceuticals Population Surveillance Pulmonary arteries Radiation therapy real‐world Respiratory tract Risk Factors Targeted cancer therapy Thorax Tomography Tumors Vascular endothelial growth factor Veins & arteries |
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Title | Bevacizumab for non‐small‐cell lung cancer: A nested case control study of risk factors for hemoptysis |
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