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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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1463087 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" W* i! H" E1 R! N1 i) Y6 _
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 5 `  u& h: Y6 c
+ Author Affiliations+ q" a' C) [+ {  ~8 y  v
4 Q- K/ P3 X% Z# {5 T, y
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 1 s7 H6 r$ q- ]$ T
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
$ [) k  e  B' \1 |0 F3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
0 K  q' \' V/ n4 N/ K4 M0 i4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 0 v% f1 w3 ?. F& z7 C1 q
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
$ Z# S2 Y1 e0 X6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
! c! Z. @' p/ c# M" {5 f$ ~7Kinki University School of Medicine, Osaka 589-8511, Japan
) G- p: i/ A/ I" q$ u. _8Izumi Municipal Hospital, Osaka 594-0071, Japan 4 W4 b5 m4 g+ U3 V9 l
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan + C$ E+ F6 Q8 w& b) u4 w/ u; W$ Z
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 5 J. e& j$ r, Y1 v
AbstractBackground: 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
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7 n0 k: W& F# k: M( A) DAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 2 b0 w+ M9 a1 d, b
7 N8 N4 y/ S- [6 Z
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
2 g: l& ?0 ~& M8 C# x
0 C, `/ `  |$ E' IPublished online on: Thursday, December 1, 2011 " n& F9 y3 A& n$ M2 E
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Doi: 10.3892/ol.2011.507 4 Y  l6 O7 b0 O1 b0 i$ _

4 c  L9 Y1 d0 u$ CPages: 405-410
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( T6 R1 o: \. G9 v  J9 i8 ~0 LAbstract:
. n& S) n9 i+ R3 \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.9 t# p) N+ v4 P9 G
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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
' `3 v, l* R1 C7 yF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 / A7 k8 o' b# l* U
+ Author Affiliations9 g# }- ^5 `- g, h0 ]" Y9 M
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
2 w2 e- E* ]8 U2Department of Thoracic Surgery, Kyoto University, Kyoto % i4 g* Q: R( _0 [
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
( n3 X0 `  ]/ M&#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
/ \6 a5 x6 B! H* Z+ h7 d7 AReceived September 3, 2010.
& W$ V4 u) z; @0 a- nRevision received November 11, 2010.
& l/ U2 f& A/ }2 E% ~Accepted November 17, 2010. 3 s: D% p2 a: n7 H2 a
Abstract
) M& w% e: p. ~) _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. 6 h! t4 N! Q. d! f5 t
Patients 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. # d& c( R; P. n% t* C
Results: 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. + H0 d4 @$ d, I9 V& I! X* S0 b
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. % ]9 R7 \! ^; w8 y8 P) S
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。
) X3 j# O# O1 }' _. {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?( B8 d  G& |3 m1 _3 b
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* A; ]; U7 X. Z! X9 t
http://clinicaltrials.gov/ct2/show/NCT01523587
4 y$ `6 Q5 x4 ]" ?' c  x
$ J* u( [% C+ g, cBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ ]1 U' v1 r! {" Thttp://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 " `7 v5 X1 K- |9 `. C' O

  C& {6 b+ D: D0 p- [. e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。8 A4 m9 R( v( ^' h. R1 o4 H6 O
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
! L  u* k  e  m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。
: R% k5 F# s9 o% ^1 `; r$ ]5 Q2 @! t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。
" \/ z* n4 \' M4 i% I5 g不错。

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