Corrigendum to “Necitumumab plus gemcitabine and cisplatin versus gemcitabine and cisplatin alone as first-line treatment for stage IV squamous non-small cell lung cancer: A phase 1b and randomized, open-label, multicenter, phase 2 trial in Japan” [Lung Cancer, 129 (March) (2019) 55–62](S0169500219300212)(10.1016/j.lungcan.2019.01.005)

Satoshi Watanabe, Hiroshige Yoshioka, Hiroshi Sakai, Katsuyuki Hotta, Mitsuhiro Takenoyama, Kazuhiko Yamada, Shunichi Sugawara, Yuichi Takiguchi, Yukio Hosomi, Keisuke Tomii, Seiji Niho, Nobuyuki Yamamoto, Makoto Nishio, Yuichiro Ohe, Terufumi Kato, Toshiaki Takahashi, Ami Kamada, Kazumi Suzukawa, Yukie Omori, Sotaro EnatsuKazuhiko Nakagawa, Tomohide Tamura

Research output: Contribution to journalComment/debate

Abstract

The authors regret that despite our best care and attention, we have discovered three errors in Table 3, as well as two corresponding errors in the text. In Table 3, Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events, one error on the AESI row for Skin reactions and two errors on the AESI row for Conjunctivitis have been corrected in Table 3 below. The corresponding text in the second sentence of the third paragraph in section 3.3. Safety should therefore read: Any-grade skin reactions (98% overall vs 44%), hypomagnesemia (39% overall vs 9%), conjunctivitis (11% overall vs 2%), arterial thromboembolic events (7% overall vs 2%), and venous thromboembolic events (6% overall vs 2%) were the most common AESIs observed more often in patients with GC + N than with GC. We have also noticed that the MedDRA preferred terms are not indented in Table 3 in the published version of the manuscript, and therefore cannot be differentiated from the AESI terms. The MedDRA preferred terms should be indented as shown in Table 3 below. The authors would like to apologise for any inconvenience caused. Table 3 Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events.[Table presented] AESIs of any grade in at least two patients in the overall phase are presented in order of any grade incidence in the GC + N group. There were no grade 5 adverse events in either treatment group. Adverse events were graded according to National Cancer Institute-Common Terminology Criteria for Adverse Events version 4.0. The chemotherapy phase was defined as the period of time during which patients received chemotherapy in the GC + N group. AESI, adverse event of special interest; GC, gemcitabine and cisplatin; GC + N, gemcitabine and cisplatin plus necitumumab; IRR, infusion-related reaction; MedDRA, Medical Dictionary for Regulatory Activities; PPES, palmar-plantar erythrodysesthesia syndrome; TEAEs, treatment-emergent adverse events.

Original languageEnglish
JournalLung Cancer
DOIs
Publication statusPublished - Jan 1 2019

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gemcitabine
Non-Small Cell Lung Carcinoma
Cisplatin
Lung Neoplasms
Japan
Anniversaries and Special Events
Conjunctivitis
Medical Dictionaries
Therapeutics
Drug Therapy
Skin
National Cancer Institute (U.S.)
Manuscripts
Terminology
necitumumab
corrigendum
Emotions
Safety

ASJC Scopus subject areas

  • Oncology
  • Pulmonary and Respiratory Medicine
  • Cancer Research

Cite this

Corrigendum to “Necitumumab plus gemcitabine and cisplatin versus gemcitabine and cisplatin alone as first-line treatment for stage IV squamous non-small cell lung cancer : A phase 1b and randomized, open-label, multicenter, phase 2 trial in Japan” [Lung Cancer, 129 (March) (2019) 55–62](S0169500219300212)(10.1016/j.lungcan.2019.01.005). / Watanabe, Satoshi; Yoshioka, Hiroshige; Sakai, Hiroshi; Hotta, Katsuyuki; Takenoyama, Mitsuhiro; Yamada, Kazuhiko; Sugawara, Shunichi; Takiguchi, Yuichi; Hosomi, Yukio; Tomii, Keisuke; Niho, Seiji; Yamamoto, Nobuyuki; Nishio, Makoto; Ohe, Yuichiro; Kato, Terufumi; Takahashi, Toshiaki; Kamada, Ami; Suzukawa, Kazumi; Omori, Yukie; Enatsu, Sotaro; Nakagawa, Kazuhiko; Tamura, Tomohide.

In: Lung Cancer, 01.01.2019.

Research output: Contribution to journalComment/debate

Watanabe, Satoshi ; Yoshioka, Hiroshige ; Sakai, Hiroshi ; Hotta, Katsuyuki ; Takenoyama, Mitsuhiro ; Yamada, Kazuhiko ; Sugawara, Shunichi ; Takiguchi, Yuichi ; Hosomi, Yukio ; Tomii, Keisuke ; Niho, Seiji ; Yamamoto, Nobuyuki ; Nishio, Makoto ; Ohe, Yuichiro ; Kato, Terufumi ; Takahashi, Toshiaki ; Kamada, Ami ; Suzukawa, Kazumi ; Omori, Yukie ; Enatsu, Sotaro ; Nakagawa, Kazuhiko ; Tamura, Tomohide. / Corrigendum to “Necitumumab plus gemcitabine and cisplatin versus gemcitabine and cisplatin alone as first-line treatment for stage IV squamous non-small cell lung cancer : A phase 1b and randomized, open-label, multicenter, phase 2 trial in Japan” [Lung Cancer, 129 (March) (2019) 55–62](S0169500219300212)(10.1016/j.lungcan.2019.01.005). In: Lung Cancer. 2019.
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title = "Corrigendum to “Necitumumab plus gemcitabine and cisplatin versus gemcitabine and cisplatin alone as first-line treatment for stage IV squamous non-small cell lung cancer: A phase 1b and randomized, open-label, multicenter, phase 2 trial in Japan” [Lung Cancer, 129 (March) (2019) 55–62](S0169500219300212)(10.1016/j.lungcan.2019.01.005)",
abstract = "The authors regret that despite our best care and attention, we have discovered three errors in Table 3, as well as two corresponding errors in the text. In Table 3, Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events, one error on the AESI row for Skin reactions and two errors on the AESI row for Conjunctivitis have been corrected in Table 3 below. The corresponding text in the second sentence of the third paragraph in section 3.3. Safety should therefore read: Any-grade skin reactions (98{\%} overall vs 44{\%}), hypomagnesemia (39{\%} overall vs 9{\%}), conjunctivitis (11{\%} overall vs 2{\%}), arterial thromboembolic events (7{\%} overall vs 2{\%}), and venous thromboembolic events (6{\%} overall vs 2{\%}) were the most common AESIs observed more often in patients with GC + N than with GC. We have also noticed that the MedDRA preferred terms are not indented in Table 3 in the published version of the manuscript, and therefore cannot be differentiated from the AESI terms. The MedDRA preferred terms should be indented as shown in Table 3 below. The authors would like to apologise for any inconvenience caused. Table 3 Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events.[Table presented] AESIs of any grade in at least two patients in the overall phase are presented in order of any grade incidence in the GC + N group. There were no grade 5 adverse events in either treatment group. Adverse events were graded according to National Cancer Institute-Common Terminology Criteria for Adverse Events version 4.0. The chemotherapy phase was defined as the period of time during which patients received chemotherapy in the GC + N group. AESI, adverse event of special interest; GC, gemcitabine and cisplatin; GC + N, gemcitabine and cisplatin plus necitumumab; IRR, infusion-related reaction; MedDRA, Medical Dictionary for Regulatory Activities; PPES, palmar-plantar erythrodysesthesia syndrome; TEAEs, treatment-emergent adverse events.",
author = "Satoshi Watanabe and Hiroshige Yoshioka and Hiroshi Sakai and Katsuyuki Hotta and Mitsuhiro Takenoyama and Kazuhiko Yamada and Shunichi Sugawara and Yuichi Takiguchi and Yukio Hosomi and Keisuke Tomii and Seiji Niho and Nobuyuki Yamamoto and Makoto Nishio and Yuichiro Ohe and Terufumi Kato and Toshiaki Takahashi and Ami Kamada and Kazumi Suzukawa and Yukie Omori and Sotaro Enatsu and Kazuhiko Nakagawa and Tomohide Tamura",
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T1 - Corrigendum to “Necitumumab plus gemcitabine and cisplatin versus gemcitabine and cisplatin alone as first-line treatment for stage IV squamous non-small cell lung cancer

T2 - A phase 1b and randomized, open-label, multicenter, phase 2 trial in Japan” [Lung Cancer, 129 (March) (2019) 55–62](S0169500219300212)(10.1016/j.lungcan.2019.01.005)

AU - Watanabe, Satoshi

AU - Yoshioka, Hiroshige

AU - Sakai, Hiroshi

AU - Hotta, Katsuyuki

AU - Takenoyama, Mitsuhiro

AU - Yamada, Kazuhiko

AU - Sugawara, Shunichi

AU - Takiguchi, Yuichi

AU - Hosomi, Yukio

AU - Tomii, Keisuke

AU - Niho, Seiji

AU - Yamamoto, Nobuyuki

AU - Nishio, Makoto

AU - Ohe, Yuichiro

AU - Kato, Terufumi

AU - Takahashi, Toshiaki

AU - Kamada, Ami

AU - Suzukawa, Kazumi

AU - Omori, Yukie

AU - Enatsu, Sotaro

AU - Nakagawa, Kazuhiko

AU - Tamura, Tomohide

PY - 2019/1/1

Y1 - 2019/1/1

N2 - The authors regret that despite our best care and attention, we have discovered three errors in Table 3, as well as two corresponding errors in the text. In Table 3, Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events, one error on the AESI row for Skin reactions and two errors on the AESI row for Conjunctivitis have been corrected in Table 3 below. The corresponding text in the second sentence of the third paragraph in section 3.3. Safety should therefore read: Any-grade skin reactions (98% overall vs 44%), hypomagnesemia (39% overall vs 9%), conjunctivitis (11% overall vs 2%), arterial thromboembolic events (7% overall vs 2%), and venous thromboembolic events (6% overall vs 2%) were the most common AESIs observed more often in patients with GC + N than with GC. We have also noticed that the MedDRA preferred terms are not indented in Table 3 in the published version of the manuscript, and therefore cannot be differentiated from the AESI terms. The MedDRA preferred terms should be indented as shown in Table 3 below. The authors would like to apologise for any inconvenience caused. Table 3 Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events.[Table presented] AESIs of any grade in at least two patients in the overall phase are presented in order of any grade incidence in the GC + N group. There were no grade 5 adverse events in either treatment group. Adverse events were graded according to National Cancer Institute-Common Terminology Criteria for Adverse Events version 4.0. The chemotherapy phase was defined as the period of time during which patients received chemotherapy in the GC + N group. AESI, adverse event of special interest; GC, gemcitabine and cisplatin; GC + N, gemcitabine and cisplatin plus necitumumab; IRR, infusion-related reaction; MedDRA, Medical Dictionary for Regulatory Activities; PPES, palmar-plantar erythrodysesthesia syndrome; TEAEs, treatment-emergent adverse events.

AB - The authors regret that despite our best care and attention, we have discovered three errors in Table 3, as well as two corresponding errors in the text. In Table 3, Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events, one error on the AESI row for Skin reactions and two errors on the AESI row for Conjunctivitis have been corrected in Table 3 below. The corresponding text in the second sentence of the third paragraph in section 3.3. Safety should therefore read: Any-grade skin reactions (98% overall vs 44%), hypomagnesemia (39% overall vs 9%), conjunctivitis (11% overall vs 2%), arterial thromboembolic events (7% overall vs 2%), and venous thromboembolic events (6% overall vs 2%) were the most common AESIs observed more often in patients with GC + N than with GC. We have also noticed that the MedDRA preferred terms are not indented in Table 3 in the published version of the manuscript, and therefore cannot be differentiated from the AESI terms. The MedDRA preferred terms should be indented as shown in Table 3 below. The authors would like to apologise for any inconvenience caused. Table 3 Treatment-emergent adverse events of special interest and hematologic treatment-emergent adverse events.[Table presented] AESIs of any grade in at least two patients in the overall phase are presented in order of any grade incidence in the GC + N group. There were no grade 5 adverse events in either treatment group. Adverse events were graded according to National Cancer Institute-Common Terminology Criteria for Adverse Events version 4.0. The chemotherapy phase was defined as the period of time during which patients received chemotherapy in the GC + N group. AESI, adverse event of special interest; GC, gemcitabine and cisplatin; GC + N, gemcitabine and cisplatin plus necitumumab; IRR, infusion-related reaction; MedDRA, Medical Dictionary for Regulatory Activities; PPES, palmar-plantar erythrodysesthesia syndrome; TEAEs, treatment-emergent adverse events.

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