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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1391835 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
& q; L' ]. [+ o) a9 Y5 ~NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ) \7 {. u9 _# f9 i) a+ ]
+ Author Affiliations3 Z0 Z1 a2 m8 j

" y1 N- \6 x( o) E1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan . k, b6 {; _2 I6 Y" _1 |0 C7 u
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan " N) {: \4 }) }
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" m7 @1 {& O8 T! D9 b2 G* w2 y4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 8 a; V0 i, k4 d+ F% Z
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
8 f" u3 A1 o+ w* r6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan ' j7 G! {/ h$ q' _& g/ p  B
7Kinki University School of Medicine, Osaka 589-8511, Japan
6 R5 ]! B% Q, Z  m3 ^; b0 ?8Izumi Municipal Hospital, Osaka 594-0071, Japan
. q. ]4 `; n9 |: K/ W! Q+ c+ a9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ) d+ o/ `" Y  x$ k$ c
Correspondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp
+ ?4 o8 P" Q0 F/ k& c2 oAbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type 5 Y" r. j- k4 S- f# v, P  P  O
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato - |- l" _$ A9 v5 k1 V

3 n/ u9 O1 d# ?+ UAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  3 |% ~' @$ S9 @# K7 D/ v
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Published online on: Thursday, December 1, 2011 " d9 L3 `2 G3 p& |* S8 X0 y2 }

4 n  O8 g9 |: ~6 z$ X+ x. _; W* QDoi: 10.3892/ol.2011.507
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Pages: 405-410
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: ~. Q: X+ q% K9 K/ ]8 rAbstract:; |9 d) ^. V1 U# d
S-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population, i. I5 i' ?6 f4 M$ k% w' R" E1 m# A* T- e
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
6 m+ m# s, l( O9 _' g5 l2 P; ^+ n+ Author Affiliations* N5 d# V) I. l7 \+ l* D' q
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
" X, j4 H" C) K: V( h& n) ]2Department of Thoracic Surgery, Kyoto University, Kyoto 0 A: |0 B, j# g* }
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
8 H  ?  Q/ V& ?7 Y# C8 p$ o&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp
' K& ^- e7 v* Q4 l: j! v. m. }Received September 3, 2010.
' I7 i3 y; W9 jRevision received November 11, 2010.
$ A- y$ K7 p6 Q) _: o5 J2 {Accepted November 17, 2010. . O; c" m9 @  M; F1 S
Abstract/ E. i% a0 C. V" T$ L2 _1 r
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
& \# m& W8 l# kPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
# \1 g) A. W: KResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression.
9 t. G. I  b3 w3 C- K6 Z+ N- HConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. + ?: h# {/ X+ ~( s! ^4 x: B
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。
2 v; \2 n+ n/ y+ C9 }/ |今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?; Y$ b- {! ?9 O; x
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy. F- ^5 b+ \. i, E0 Q
http://clinicaltrials.gov/ct2/show/NCT01523587
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4 }: ~3 v9 ^* R; kBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC$ ~3 `) e- Z  W! {) Z
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑 4 L3 q3 {2 T% _  e7 v" `. m
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从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。% c. r$ H' V" d9 K# k
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 ) g* l8 X, ~- Y9 d( B/ c  g% o
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
) F: M! |- h! }- g( c# n3 v至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。: Q  {, \. w; r# s% {  ]5 g4 y
不错。

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